Run ID: ERR4815550
Sample name:
Date: 01-04-2023 13:55:37
Number of reads: 259591
Percentage reads mapped: 13.21
Strain: lineage4
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.99 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.05 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 1.0 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5488 | c.249C>A | synonymous_variant | 0.67 |
gyrB | 6274 | c.1035C>G | synonymous_variant | 0.5 |
gyrB | 6286 | c.1047T>C | synonymous_variant | 0.5 |
gyrB | 6292 | c.1053G>C | synonymous_variant | 0.5 |
gyrB | 6295 | c.1056A>G | synonymous_variant | 0.5 |
gyrB | 6298 | c.1059C>T | synonymous_variant | 0.5 |
gyrB | 6299 | c.1060C>T | synonymous_variant | 0.5 |
gyrA | 6307 | c.-995T>G | upstream_gene_variant | 0.5 |
gyrA | 6319 | c.-983G>C | upstream_gene_variant | 0.5 |
gyrA | 6325 | c.-977C>G | upstream_gene_variant | 0.5 |
gyrA | 6361 | c.-941G>A | upstream_gene_variant | 0.67 |
gyrA | 6362 | c.-940T>C | upstream_gene_variant | 0.67 |
gyrA | 6379 | c.-923C>G | upstream_gene_variant | 1.0 |
gyrA | 6382 | c.-920A>G | upstream_gene_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 760189 | p.Phe128Tyr | missense_variant | 0.6 |
rpoB | 760199 | c.393C>G | synonymous_variant | 0.71 |
rpoB | 760207 | p.Ile134Thr | missense_variant | 0.71 |
rpoB | 760213 | p.Asn136Ser | missense_variant | 0.71 |
rpoB | 760216 | p.Asn137Met | missense_variant | 0.71 |
rpoB | 760218 | p.Thr138Ser | missense_variant | 0.71 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.71 |
rpoB | 760235 | c.429T>C | synonymous_variant | 1.0 |
rpoB | 760241 | c.435G>C | synonymous_variant | 1.0 |
rpoB | 760244 | c.438G>C | synonymous_variant | 1.0 |
rpoB | 760250 | p.Met148Ile | missense_variant | 1.0 |
rpoB | 760253 | c.447T>C | synonymous_variant | 1.0 |
rpoB | 760271 | c.465C>G | synonymous_variant | 0.92 |
rpoB | 760274 | p.Glu156Asp | missense_variant | 0.92 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.75 |
rpoB | 760389 | c.583_584delAGinsTC | synonymous_variant | 0.5 |
rpoB | 760400 | c.594G>C | synonymous_variant | 0.71 |
rpoB | 760407 | c.601_602delAGinsTC | synonymous_variant | 0.83 |
rpoB | 760412 | c.606C>T | synonymous_variant | 0.83 |
rpoB | 760415 | c.609C>T | synonymous_variant | 0.91 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.91 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.91 |
rpoB | 760457 | c.651C>T | synonymous_variant | 0.8 |
rpoB | 760460 | c.654G>C | synonymous_variant | 0.8 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.67 |
rpoB | 760478 | c.672C>T | synonymous_variant | 0.67 |
rpoB | 760481 | c.675G>T | synonymous_variant | 0.5 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.5 |
rpoB | 760490 | c.684C>G | synonymous_variant | 0.4 |
rpoB | 760493 | c.687C>G | synonymous_variant | 0.4 |
rpoB | 760496 | c.690G>C | synonymous_variant | 0.4 |
rpoB | 760916 | c.1110C>T | synonymous_variant | 0.67 |
rpoB | 760919 | c.1113C>T | synonymous_variant | 0.67 |
rpoB | 760922 | c.1116G>C | synonymous_variant | 0.67 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.67 |
rpoB | 760940 | c.1134G>C | synonymous_variant | 0.62 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.62 |
rpoB | 760953 | p.Ile383Val | missense_variant | 0.5 |
rpoB | 760958 | c.1152G>C | synonymous_variant | 0.43 |
rpoB | 760961 | c.1155C>G | synonymous_variant | 0.43 |
rpoB | 760965 | p.Met387Leu | missense_variant | 0.43 |
rpoB | 760970 | c.1164G>C | synonymous_variant | 0.43 |
rpoB | 760973 | c.1167G>C | synonymous_variant | 0.43 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.5 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.5 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.5 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 1.0 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 1.0 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 1.0 |
rpoB | 761198 | c.1392G>C | synonymous_variant | 1.0 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 1.0 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 1.0 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 1.0 |
rpoB | 761252 | c.1446C>G | synonymous_variant | 0.98 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.98 |
rpoB | 761264 | c.1458C>G | synonymous_variant | 0.98 |
rpoB | 761273 | c.1467T>C | synonymous_variant | 0.88 |
rpoB | 761276 | c.1470G>C | synonymous_variant | 0.88 |
rpoB | 761292 | p.Val496Ser | missense_variant | 0.87 |
rpoB | 761312 | c.1506G>C | synonymous_variant | 0.86 |
rpoB | 761318 | c.1512G>T | synonymous_variant | 0.86 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.8 |
rpoB | 761511 | p.Glu569Gln | missense_variant | 0.67 |
rpoB | 761534 | c.1728G>C | synonymous_variant | 0.96 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.88 |
rpoB | 761540 | c.1734C>G | synonymous_variant | 0.96 |
rpoB | 761549 | c.1743G>C | synonymous_variant | 0.96 |
rpoB | 761552 | c.1746G>C | synonymous_variant | 0.96 |
rpoB | 761558 | c.1752C>G | synonymous_variant | 0.96 |
rpoB | 761561 | c.1755C>G | synonymous_variant | 0.97 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.97 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.97 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.97 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.95 |
rpoB | 761615 | c.1809A>G | synonymous_variant | 0.95 |
rpoB | 761633 | c.1827G>C | synonymous_variant | 0.97 |
rpoB | 761643 | p.Val613Leu | missense_variant | 0.96 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.96 |
rpoB | 761649 | c.1843_1844delAGinsTC | synonymous_variant | 0.96 |
rpoB | 761661 | p.Leu619Phe | missense_variant | 0.96 |
rpoB | 761675 | c.1869G>C | synonymous_variant | 0.95 |
rpoB | 761690 | c.1884G>C | synonymous_variant | 0.83 |
rpoB | 761693 | c.1887G>C | synonymous_variant | 0.83 |
rpoB | 761694 | p.Ile630Tyr | missense_variant | 0.83 |
rpoB | 761712 | p.Val636Ile | missense_variant | 0.75 |
rpoB | 761858 | c.2052G>C | synonymous_variant | 0.5 |
rpoB | 761863 | p.Ala686Glu | missense_variant | 0.5 |
rpoB | 761867 | c.2061C>T | synonymous_variant | 0.71 |
rpoB | 761873 | c.2067A>C | synonymous_variant | 0.83 |
rpoB | 761885 | c.2079T>C | synonymous_variant | 0.86 |
rpoB | 761890 | p.Val695Ala | missense_variant | 0.86 |
rpoB | 761903 | c.2097T>C | synonymous_variant | 0.9 |
rpoB | 761907 | p.Cys701Gly | missense_variant | 0.9 |
rpoB | 761912 | c.2106T>C | synonymous_variant | 0.9 |
rpoB | 761916 | p.Asp704Asn | missense_variant | 0.93 |
rpoB | 761921 | c.2115C>T | synonymous_variant | 0.94 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.98 |
rpoB | 761951 | c.2145G>C | synonymous_variant | 0.98 |
rpoB | 761955 | p.Ile717Phe | missense_variant | 0.98 |
rpoB | 761998 | c.2193_2195delGTC | disruptive_inframe_deletion | 0.97 |
rpoB | 762005 | c.2200_2201insAGC | disruptive_inframe_insertion | 0.97 |
rpoB | 762009 | p.Leu735Met | missense_variant | 0.97 |
rpoB | 762014 | c.2208C>G | synonymous_variant | 0.97 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 0.97 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.98 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 1.0 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 1.0 |
rpoB | 762074 | c.2268C>G | synonymous_variant | 1.0 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 1.0 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 1.0 |
rpoB | 762084 | p.Ala760Pro | missense_variant | 1.0 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 1.0 |
rpoB | 762114 | p.Ile770Val | missense_variant | 1.0 |
rpoB | 762117 | p.Ser771Gly | missense_variant | 1.0 |
rpoB | 762122 | p.Asp772Glu | missense_variant | 1.0 |
rpoB | 762125 | p.Glu773Asp | missense_variant | 1.0 |
rpoB | 762128 | c.2322G>C | synonymous_variant | 1.0 |
rpoB | 762134 | c.2328C>G | synonymous_variant | 1.0 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 1.0 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 1.0 |
rpoB | 762146 | p.Glu780Asp | missense_variant | 1.0 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 1.0 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.93 |
rpoB | 762173 | p.Glu789Asp | missense_variant | 1.0 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 1.0 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 1.0 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 1.0 |
rpoB | 762209 | c.2403C>G | synonymous_variant | 1.0 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.6 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.6 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.6 |
rpoB | 762251 | c.2445G>C | synonymous_variant | 0.6 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.6 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 0.6 |
rpoB | 762278 | c.2472C>T | synonymous_variant | 0.6 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.6 |
rpoB | 762293 | c.2487T>G | synonymous_variant | 0.6 |
rpoB | 762297 | p.Leu831Met | missense_variant | 0.6 |
rpoB | 762305 | c.2499G>C | synonymous_variant | 0.6 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 1.0 |
rpoB | 762799 | p.Ala998Asp | missense_variant | 1.0 |
rpoB | 762801 | p.Asp999Tyr | missense_variant | 1.0 |
rpoB | 762813 | p.Met1003Glu | missense_variant | 1.0 |
rpoB | 762819 | p.Phe1005Ile | missense_variant | 1.0 |
rpoC | 762827 | c.-543G>C | upstream_gene_variant | 1.0 |
rpoC | 762830 | c.-540C>G | upstream_gene_variant | 1.0 |
rpoC | 762831 | c.-539_-538delAGinsTC | upstream_gene_variant | 1.0 |
rpoC | 762842 | c.-528G>C | upstream_gene_variant | 1.0 |
rpoC | 762857 | c.-513C>G | upstream_gene_variant | 1.0 |
rpoB | 762858 | p.Thr1018Ser | missense_variant | 1.0 |
rpoC | 762863 | c.-507T>G | upstream_gene_variant | 1.0 |
rpoB | 762878 | p.Ile1024Met | missense_variant | 1.0 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 1.0 |
rpoC | 762896 | c.-474G>C | upstream_gene_variant | 1.0 |
rpoB | 762905 | p.Asp1033Glu | missense_variant | 1.0 |
rpoC | 762926 | c.-444C>G | upstream_gene_variant | 1.0 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 1.0 |
rpoC | 762938 | c.-432G>C | upstream_gene_variant | 1.0 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 1.0 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 1.0 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 1.0 |
rpoC | 762983 | c.-387C>A | upstream_gene_variant | 1.0 |
rpoC | 762989 | c.-381G>T | upstream_gene_variant | 1.0 |
rpoC | 762995 | c.-375G>C | upstream_gene_variant | 1.0 |
rpoB | 763005 | p.Cys1067Val | missense_variant | 1.0 |
rpoC | 763022 | c.-348C>G | upstream_gene_variant | 1.0 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 1.0 |
rpoC | 763043 | c.-327G>C | upstream_gene_variant | 0.95 |
rpoC | 763049 | c.-321G>A | upstream_gene_variant | 0.95 |
rpoC | 763052 | c.-318G>C | upstream_gene_variant | 0.94 |
rpoC | 763053 | c.-317_-315delTTGinsCTC | upstream_gene_variant | 0.94 |
rpoC | 763058 | c.-312C>G | upstream_gene_variant | 0.94 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.94 |
rpoB | 763074 | p.Thr1090Val | missense_variant | 0.94 |
rpoC | 763085 | c.-285C>T | upstream_gene_variant | 0.94 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 0.94 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.95 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.92 |
rpoB | 763130 | p.Glu1108Asp | missense_variant | 0.97 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.97 |
rpoC | 763157 | c.-213G>C | upstream_gene_variant | 0.95 |
rpoC | 763160 | c.-210G>C | upstream_gene_variant | 0.95 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.91 |
rpoC | 763169 | c.-201A>G | upstream_gene_variant | 0.91 |
rpoC | 763172 | c.-198G>C | upstream_gene_variant | 0.91 |
rpoC | 763367 | c.-3_-2insC | upstream_gene_variant | 0.92 |
rpoC | 763375 | c.6C>G | synonymous_variant | 0.93 |
rpoC | 763393 | c.24T>C | synonymous_variant | 0.81 |
rpoC | 763396 | c.27A>G | synonymous_variant | 0.76 |
rpoC | 763399 | c.30C>T | synonymous_variant | 0.76 |
rpoC | 763411 | c.42T>G | synonymous_variant | 0.76 |
rpoC | 763414 | c.45T>G | synonymous_variant | 0.76 |
rpoC | 763417 | c.48C>G | synonymous_variant | 0.72 |
rpoC | 763420 | c.51G>C | synonymous_variant | 0.68 |
rpoC | 763423 | p.Glu18Asp | missense_variant | 0.68 |
rpoC | 763430 | c.61_63delAGGinsCGC | synonymous_variant | 0.68 |
rpoC | 763434 | p.Gln22Arg | missense_variant | 0.68 |
rpoC | 763442 | p.Tyr25Lys | missense_variant | 0.78 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.87 |
rpoC | 763462 | c.93G>C | synonymous_variant | 0.88 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.88 |
rpoC | 763483 | c.114G>C | synonymous_variant | 0.89 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.89 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.9 |
rpoC | 763517 | p.Lys50Arg | missense_variant | 0.94 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.94 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.94 |
rpoC | 763537 | c.168C>G | synonymous_variant | 0.95 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.95 |
rpoC | 763550 | p.Tyr61Ala | missense_variant | 0.95 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.99 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.99 |
rpoC | 763576 | c.207C>T | synonymous_variant | 0.99 |
rpoC | 763578 | p.Phe70Tyr | missense_variant | 0.99 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.97 |
rpoC | 763630 | c.261G>C | synonymous_variant | 0.97 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.97 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.97 |
rpoC | 763660 | c.291T>C | synonymous_variant | 0.98 |
rpoC | 763666 | c.297G>C | synonymous_variant | 0.98 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.97 |
rpoC | 763672 | c.303C>G | synonymous_variant | 0.98 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.97 |
rpoC | 763711 | c.342G>C | synonymous_variant | 0.96 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.96 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.96 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.96 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.92 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.88 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.85 |
rpoC | 763765 | c.396T>G | synonymous_variant | 0.57 |
rpoC | 763768 | c.399C>G | synonymous_variant | 0.57 |
rpoC | 763769 | p.Tyr134Asn | missense_variant | 0.57 |
rpoC | 763772 | p.Val135Ile | missense_variant | 0.57 |
rpoC | 763780 | c.411C>G | synonymous_variant | 0.57 |
rpoC | 763783 | c.414G>C | synonymous_variant | 0.57 |
rpoC | 764239 | c.870T>C | synonymous_variant | 1.0 |
rpoC | 764257 | c.888G>C | synonymous_variant | 1.0 |
rpoC | 764263 | c.894G>C | synonymous_variant | 1.0 |
rpoC | 764266 | c.897T>C | synonymous_variant | 1.0 |
rpoC | 764277 | p.Gln303Leu | missense_variant | 1.0 |
rpoC | 764280 | p.Gln304Arg | missense_variant | 1.0 |
rpoC | 764291 | p.Ser308Asp | missense_variant | 1.0 |
rpoC | 764297 | p.Met310Ala | missense_variant | 1.0 |
rpoC | 764308 | c.939G>C | synonymous_variant | 1.0 |
rpoC | 764315 | p.Ala316Cys | missense_variant | 1.0 |
rpoC | 764318 | p.Val317Ile | missense_variant | 1.0 |
rpoC | 764326 | c.957G>C | synonymous_variant | 1.0 |
rpoC | 764344 | c.975C>G | synonymous_variant | 1.0 |
rpoC | 764353 | c.984G>C | synonymous_variant | 1.0 |
rpoC | 764371 | c.1002G>T | synonymous_variant | 0.86 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 0.9 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.91 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.92 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 0.92 |
rpoC | 764419 | c.1050C>G | synonymous_variant | 0.92 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.92 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.92 |
rpoC | 764435 | c.1066_1068delAGGinsCGC | synonymous_variant | 0.92 |
rpoC | 764438 | p.Leu357Met | missense_variant | 0.92 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 0.92 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.92 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.92 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.92 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 1.0 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 1.0 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.98 |
rpoC | 764491 | c.1122G>C | synonymous_variant | 0.99 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.99 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.98 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.95 |
rpoC | 764527 | c.1158C>G | synonymous_variant | 0.95 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 0.96 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.96 |
rpoC | 764545 | c.1176C>G | synonymous_variant | 0.96 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.96 |
rpoC | 764572 | c.1203G>C | synonymous_variant | 0.96 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.97 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.97 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.96 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.96 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.97 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.97 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 0.96 |
rpoC | 764644 | c.1275G>C | synonymous_variant | 0.92 |
rpoC | 764647 | c.1278C>G | synonymous_variant | 0.92 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.95 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.96 |
rpoC | 764660 | p.Val431Ile | missense_variant | 0.96 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.95 |
rpoC | 764701 | c.1332C>G | synonymous_variant | 0.88 |
rpoC | 764707 | c.1338G>C | synonymous_variant | 0.87 |
rpoC | 764713 | c.1344G>C | synonymous_variant | 0.85 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.84 |
rpoC | 764737 | c.1368G>C | synonymous_variant | 0.71 |
rpoC | 764749 | c.1380G>C | synonymous_variant | 0.37 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.57 |
rpoC | 764833 | c.1464A>G | synonymous_variant | 0.75 |
rpoC | 764838 | p.Val490Ala | missense_variant | 0.77 |
rpoC | 764843 | p.Ala492Ser | missense_variant | 0.83 |
rpoC | 764857 | c.1488G>C | synonymous_variant | 0.91 |
rpoC | 764858 | p.Leu497Met | missense_variant | 0.91 |
rpoC | 764863 | c.1494G>C | synonymous_variant | 0.92 |
rpoC | 764869 | c.1500C>T | synonymous_variant | 0.93 |
rpoC | 764872 | c.1503A>G | synonymous_variant | 0.93 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.95 |
rpoC | 764893 | c.1524T>C | synonymous_variant | 0.95 |
rpoC | 764902 | c.1533C>G | synonymous_variant | 1.0 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 1.0 |
rpoC | 764914 | p.Met515Ile | missense_variant | 1.0 |
rpoC | 764917 | c.1548G>C | synonymous_variant | 1.0 |
rpoC | 764920 | c.1551G>C | synonymous_variant | 1.0 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 1.0 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 1.0 |
rpoC | 764941 | c.1572G>C | synonymous_variant | 1.0 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 1.0 |
rpoC | 764952 | p.Val528Ala | missense_variant | 1.0 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 1.0 |
rpoC | 764998 | c.1629G>C | synonymous_variant | 1.0 |
rpoC | 765491 | p.Val708Thr | missense_variant | 1.0 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 1.0 |
rpoC | 765508 | c.2139C>G | synonymous_variant | 1.0 |
rpoC | 766309 | c.2940G>C | synonymous_variant | 1.0 |
rpoC | 766312 | c.2943T>C | synonymous_variant | 1.0 |
rpoC | 766321 | c.2952C>G | synonymous_variant | 1.0 |
rpoC | 766331 | p.Leu988Lys | missense_variant | 1.0 |
rpoC | 766348 | c.2979A>G | synonymous_variant | 1.0 |
rpoC | 766354 | c.2985C>G | synonymous_variant | 1.0 |
rpoC | 766363 | c.2994G>C | synonymous_variant | 1.0 |
rpoC | 766369 | c.3000C>G | synonymous_variant | 1.0 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 1.0 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 1.0 |
rpoC | 766390 | c.3021C>T | synonymous_variant | 1.0 |
rpoC | 766393 | c.3024C>G | synonymous_variant | 1.0 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 1.0 |
rpoC | 766411 | c.3042C>G | synonymous_variant | 1.0 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 1.0 |
rpoC | 766434 | p.Glu1022Gly | missense_variant | 1.0 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 1.0 |
rpoC | 766453 | c.3084G>C | synonymous_variant | 1.0 |
rpoC | 766456 | c.3087C>G | synonymous_variant | 1.0 |
rpoC | 766459 | c.3090G>T | synonymous_variant | 1.0 |
rpoC | 766462 | c.3093G>C | synonymous_variant | 1.0 |
rpoC | 766483 | c.3114G>C | synonymous_variant | 1.0 |
rpoC | 766486 | c.3117A>G | synonymous_variant | 1.0 |
rpoC | 766783 | c.3414C>G | synonymous_variant | 0.4 |
rpoC | 766787 | p.Glu1140Lys | missense_variant | 0.4 |
rpoC | 766800 | p.Ala1144Asp | missense_variant | 0.57 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.57 |
rpoC | 766811 | p.Ser1148Ala | missense_variant | 0.57 |
rpoC | 766835 | p.Val1156Ile | missense_variant | 0.73 |
rpoC | 766843 | c.3474T>C | synonymous_variant | 0.73 |
rpoC | 766846 | c.3477C>G | synonymous_variant | 0.73 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.7 |
rpoC | 766867 | c.3498C>G | synonymous_variant | 0.7 |
rpoC | 766868 | p.Ile1167Val | missense_variant | 0.7 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781658 | c.99A>C | synonymous_variant | 1.0 |
rpsL | 781664 | c.105C>G | synonymous_variant | 1.0 |
rpsL | 781670 | c.111G>C | synonymous_variant | 1.0 |
rpsL | 781676 | c.117C>G | synonymous_variant | 1.0 |
rpsL | 781682 | c.123T>G | synonymous_variant | 1.0 |
rpsL | 781703 | c.144G>T | synonymous_variant | 1.0 |
rpsL | 781706 | c.147T>C | synonymous_variant | 1.0 |
rpsL | 781793 | c.234G>C | synonymous_variant | 1.0 |
rpsL | 781802 | c.243G>C | synonymous_variant | 1.0 |
rpsL | 781811 | c.252C>T | synonymous_variant | 1.0 |
rpsL | 781814 | c.255C>T | synonymous_variant | 1.0 |
rpsL | 781817 | c.258G>T | synonymous_variant | 1.0 |
rpsL | 781829 | c.270G>C | synonymous_variant | 0.6 |
rpsL | 781832 | c.273T>G | synonymous_variant | 0.6 |
rpsL | 781838 | c.279G>C | synonymous_variant | 0.6 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.6 |
rpsL | 781856 | c.297C>T | synonymous_variant | 0.6 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.6 |
rpsL | 781862 | c.303G>C | synonymous_variant | 0.6 |
rpsL | 781865 | c.306G>C | synonymous_variant | 0.6 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.6 |
rpsL | 781877 | c.318T>C | synonymous_variant | 0.6 |
rpsL | 781884 | p.Asn109Asp | missense_variant | 0.6 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.6 |
rpsL | 781901 | c.342C>T | synonymous_variant | 0.6 |
rpsL | 781902 | c.343_344delAGinsTC | synonymous_variant | 0.6 |
rpsL | 781907 | c.348T>C | synonymous_variant | 0.6 |
rpsL | 781916 | c.357T>G | synonymous_variant | 1.0 |
rplC | 800633 | c.-176T>C | upstream_gene_variant | 1.0 |
rplC | 800648 | c.-161A>G | upstream_gene_variant | 1.0 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 1.0 |
rplC | 800672 | c.-137G>C | upstream_gene_variant | 1.0 |
rplC | 800690 | c.-119C>T | upstream_gene_variant | 0.92 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.92 |
rplC | 800702 | c.-107G>A | upstream_gene_variant | 0.92 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.92 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.92 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.92 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.92 |
rplC | 800726 | c.-83G>C | upstream_gene_variant | 0.92 |
rplC | 800744 | c.-65G>C | upstream_gene_variant | 0.92 |
rplC | 800759 | c.-50C>T | upstream_gene_variant | 0.92 |
rplC | 800780 | c.-29C>G | upstream_gene_variant | 0.8 |
rplC | 800786 | c.-23C>T | upstream_gene_variant | 0.57 |
fbiC | 1304244 | c.1314C>T | synonymous_variant | 0.67 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471852 | n.7T>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471932 | n.87A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471985 | n.140T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472037 | n.192A>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472038 | n.193_194insTA | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472041 | n.196C>G | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472042 | n.197_198insG | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472045 | n.200T>C | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472054 | n.210_212delCGC | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472062 | n.217G>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472068 | n.223T>C | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472069 | n.224G>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472123 | n.278A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472279 | n.434T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472330 | n.485G>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472450 | n.605A>G | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472451 | n.606C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472461 | n.616G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472462 | n.617T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472674 | n.829T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472675 | n.832delC | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472837 | n.992C>G | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472838 | n.993A>G | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472844 | n.999_1000insCG | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472847 | n.1004_1005delCT | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472851 | n.1006A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472856 | n.1011T>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472858 | n.1013G>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472860 | n.1015C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472861 | n.1016G>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472869 | n.1024G>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472873 | n.1028C>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472875 | n.1031delG | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473089 | n.1244A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473109 | n.1264T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473111 | n.1266A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473283 | n.1438T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473292 | n.1447G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473293 | n.1448G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473574 | n.-84G>C | upstream_gene_variant | 0.5 |
rrl | 1473667 | n.11delC | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473679 | n.22T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473696 | n.39T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473697 | n.40C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473698 | n.42dupA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473728 | n.71A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473743 | n.86C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473746 | n.89T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 0.9 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1473899 | n.242A>C | non_coding_transcript_exon_variant | 0.87 |
rrl | 1473905 | n.248T>C | non_coding_transcript_exon_variant | 0.87 |
rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1473922 | n.265A>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474044 | n.387C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474054 | n.397T>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474056 | n.399T>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474074 | n.417C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474083 | n.426C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474110 | n.453A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474130 | n.473C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474182 | n.525C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474185 | n.529delA | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474266 | n.609T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474289 | n.632C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474291 | n.635_649delTTCCTCTCCGGAGGA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474351 | n.694G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474451 | n.794T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474487 | n.830G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474496 | n.839C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474497 | n.840G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474517 | n.860C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474658 | n.1001A>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474688 | n.1031G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474695 | n.1038A>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474709 | n.1053_1056delTGGT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474717 | n.1060_1061insGTGAG | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474774 | n.1117A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474798 | n.1141C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474803 | n.1146G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474825 | n.1168G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474837 | n.1180A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474901 | n.1244A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474921 | n.1264C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474951 | n.1294C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474954 | n.1297A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474959 | n.1302C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474963 | n.1306G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474971 | n.1314T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474974 | n.1317G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474989 | n.1332C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475033 | n.1376G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475060 | n.1404delC | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475063 | n.1406A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475065 | n.1408G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475067 | n.1410A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475076 | n.1419C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475079 | n.1422T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475081 | n.1424C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475088 | n.1431A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475094 | n.1437C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475108 | n.1451C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475111 | n.1454G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475116 | n.1459G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475119 | n.1462C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475120 | n.1463G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475137 | n.1480A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475171 | n.1514C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475202 | n.1545G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475206 | n.1549C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475440 | n.1783T>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 0.99 |
rrl | 1475458 | n.1801C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1475480 | n.1823A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475485 | n.1828C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475486 | n.1829A>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475499 | n.1842C>A | non_coding_transcript_exon_variant | 0.96 |
rrl | 1475500 | n.1843A>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1475538 | n.1881T>A | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475542 | n.1885A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1475550 | n.1893A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1475659 | n.2002_2003insGA | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475696 | n.2039T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475703 | n.2046A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475757 | n.2100_2101insG | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475764 | n.2107A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475765 | n.2108A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475768 | n.2111G>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475900 | n.2243A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476032 | n.2375C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476033 | n.2376T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476046 | n.2389G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476087 | n.2430C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476091 | n.2434_2435insG | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476100 | n.2443A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476113 | n.2456T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476584 | n.2927C>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476595 | n.2938C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476600 | n.2943A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476602 | n.2945G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476624 | n.2967T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476625 | n.2968C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476628 | n.2971T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1833628 | c.87G>C | synonymous_variant | 0.67 |
rpsA | 1833643 | c.102C>T | synonymous_variant | 0.96 |
rpsA | 1833646 | c.105T>C | synonymous_variant | 0.96 |
rpsA | 1833649 | c.108C>T | synonymous_variant | 0.96 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.96 |
rpsA | 1833668 | p.Ile43Val | missense_variant | 0.96 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.96 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.96 |
rpsA | 1833684 | p.Arg48His | missense_variant | 0.89 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.9 |
rpsA | 1833697 | c.156C>G | synonymous_variant | 0.91 |
rpsA | 1833700 | c.159C>G | synonymous_variant | 0.91 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.85 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.89 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.92 |
rpsA | 1833739 | c.198C>T | synonymous_variant | 0.94 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.94 |
rpsA | 1833769 | c.228C>T | synonymous_variant | 0.93 |
rpsA | 1833770 | p.Asn77Asp | missense_variant | 0.93 |
rpsA | 1833778 | c.237C>T | synonymous_variant | 0.92 |
rpsA | 1833781 | c.240T>C | synonymous_variant | 0.91 |
rpsA | 1833782 | p.Ser81Glu | missense_variant | 0.91 |
rpsA | 1833787 | c.246C>T | synonymous_variant | 0.91 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.91 |
rpsA | 1833797 | p.Val86Ile | missense_variant | 0.91 |
rpsA | 1833802 | p.Glu87Asp | missense_variant | 0.92 |
rpsA | 1833805 | c.264C>G | synonymous_variant | 0.93 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 0.93 |
rpsA | 1833817 | c.276C>G | synonymous_variant | 0.94 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 0.95 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 0.97 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.98 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.98 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.99 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.99 |
rpsA | 1833862 | c.321G>C | synonymous_variant | 0.99 |
rpsA | 1833877 | c.336C>G | synonymous_variant | 1.0 |
rpsA | 1833883 | c.342C>T | synonymous_variant | 1.0 |
rpsA | 1833884 | p.Thr115Ala | missense_variant | 1.0 |
rpsA | 1833894 | p.Ala118Glu | missense_variant | 1.0 |
rpsA | 1833914 | p.Ala125Pro | missense_variant | 0.99 |
rpsA | 1833921 | p.Lys127Thr | missense_variant | 0.98 |
rpsA | 1833925 | c.384C>T | synonymous_variant | 0.98 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.98 |
rpsA | 1833952 | c.411C>T | synonymous_variant | 0.98 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 0.97 |
rpsA | 1833970 | c.429G>T | synonymous_variant | 0.97 |
rpsA | 1833973 | c.432G>C | synonymous_variant | 0.96 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.96 |
rpsA | 1833985 | c.444G>C | synonymous_variant | 0.97 |
rpsA | 1833997 | c.456G>C | synonymous_variant | 0.97 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.97 |
rpsA | 1834009 | c.468C>T | synonymous_variant | 0.97 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.97 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.97 |
rpsA | 1834024 | c.483G>C | synonymous_variant | 0.97 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.97 |
rpsA | 1834040 | p.Lys167Gln | missense_variant | 0.97 |
rpsA | 1834076 | p.Asn179His | missense_variant | 0.98 |
rpsA | 1834093 | c.552G>C | synonymous_variant | 0.98 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.97 |
rpsA | 1834105 | c.564C>T | synonymous_variant | 0.97 |
rpsA | 1834108 | c.567C>G | synonymous_variant | 0.97 |
rpsA | 1834114 | c.573G>C | synonymous_variant | 0.96 |
rpsA | 1834135 | c.594G>C | synonymous_variant | 0.95 |
rpsA | 1834139 | c.598_599delAGinsTC | synonymous_variant | 1.0 |
rpsA | 1834151 | p.Asn204His | missense_variant | 1.0 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834183 | c.642T>C | synonymous_variant | 1.0 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 1.0 |
rpsA | 1834213 | c.672G>C | synonymous_variant | 1.0 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 1.0 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 1.0 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 1.0 |
rpsA | 1834243 | c.702G>C | synonymous_variant | 1.0 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 1.0 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 1.0 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 1.0 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.98 |
rpsA | 1834298 | p.Gln253Thr | missense_variant | 0.98 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.98 |
rpsA | 1834318 | c.777C>G | synonymous_variant | 0.98 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.98 |
rpsA | 1834340 | p.Met267Leu | missense_variant | 0.98 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.96 |
rpsA | 1834354 | c.813G>C | synonymous_variant | 0.87 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.87 |
rpsA | 1834360 | c.819G>C | synonymous_variant | 0.87 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.87 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.87 |
rpsA | 1834369 | c.828C>G | synonymous_variant | 0.89 |
rpsA | 1834378 | c.837T>G | synonymous_variant | 0.91 |
rpsA | 1834384 | c.843A>G | synonymous_variant | 0.92 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.91 |
rpsA | 1834397 | p.His286Val | missense_variant | 0.91 |
rpsA | 1834408 | c.867C>G | synonymous_variant | 0.91 |
rpsA | 1834411 | c.870T>G | synonymous_variant | 0.91 |
rpsA | 1834423 | c.882G>T | synonymous_variant | 0.97 |
rpsA | 1834432 | c.891G>C | synonymous_variant | 0.97 |
rpsA | 1834447 | c.906C>G | synonymous_variant | 1.0 |
rpsA | 1834451 | c.910_912delTTGinsCTC | synonymous_variant | 1.0 |
rpsA | 1834456 | c.915T>C | synonymous_variant | 1.0 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 1.0 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 1.0 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.97 |
rpsA | 1834501 | c.960G>C | synonymous_variant | 0.96 |
rpsA | 1834519 | c.978G>C | synonymous_variant | 0.98 |
rpsA | 1834528 | c.987T>G | synonymous_variant | 0.98 |
rpsA | 1834534 | c.993C>G | synonymous_variant | 0.97 |
rpsA | 1834537 | p.Glu332Asp | missense_variant | 0.97 |
rpsA | 1834540 | c.999G>C | synonymous_variant | 0.97 |
rpsA | 1834543 | c.1002C>G | synonymous_variant | 0.96 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.97 |
rpsA | 1834552 | c.1011G>C | synonymous_variant | 0.97 |
rpsA | 1834555 | c.1014T>C | synonymous_variant | 1.0 |
rpsA | 1834556 | p.Ala339Thr | missense_variant | 1.0 |
rpsA | 1834565 | p.Asp342Gln | missense_variant | 1.0 |
rpsA | 1834600 | c.1059G>C | synonymous_variant | 1.0 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 1.0 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 1.0 |
rpsA | 1834618 | c.1077G>C | synonymous_variant | 1.0 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 1.0 |
rpsA | 1834624 | c.1083G>C | synonymous_variant | 1.0 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 1.0 |
rpsA | 1834636 | c.1095C>G | synonymous_variant | 1.0 |
rpsA | 1834637 | p.Asn366Asp | missense_variant | 1.0 |
rpsA | 1834666 | c.1125G>C | synonymous_variant | 1.0 |
rpsA | 1834667 | p.Ala376Ser | missense_variant | 1.0 |
rpsA | 1834688 | c.1147_1149delAGTinsTCC | synonymous_variant | 1.0 |
rpsA | 1834720 | c.1179C>G | synonymous_variant | 0.9 |
rpsA | 1834732 | c.1191T>C | synonymous_variant | 0.75 |
rpsA | 1834733 | p.Ala398Pro | missense_variant | 0.71 |
rpsA | 1834738 | c.1197A>G | synonymous_variant | 0.71 |
rpsA | 1834741 | c.1200C>G | synonymous_variant | 0.71 |
rpsA | 1834747 | c.1206A>G | synonymous_variant | 0.71 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.71 |
pncA | 2289801 | c.-560C>A | upstream_gene_variant | 0.33 |
Rv2752c | 3064998 | c.1194A>C | synonymous_variant | 0.5 |
Rv2752c | 3065004 | c.1188G>C | synonymous_variant | 0.5 |
Rv2752c | 3065014 | p.Val393Ala | missense_variant | 0.5 |
Rv2752c | 3065028 | p.Val388Ala | missense_variant | 0.5 |
Rv2752c | 3065031 | p.Gly387Ala | missense_variant | 0.5 |
Rv2752c | 3065055 | c.1137T>G | synonymous_variant | 0.5 |
Rv2752c | 3065060 | p.Ala378Ser | missense_variant | 0.5 |
thyX | 3067654 | p.His98Asp | missense_variant | 1.0 |
thyA | 3073822 | p.Arg217Lys | missense_variant | 1.0 |
thyA | 3073824 | c.648A>G | synonymous_variant | 1.0 |
thyA | 3073827 | c.645A>G | synonymous_variant | 1.0 |
thyA | 3073839 | c.633T>C | synonymous_variant | 1.0 |
thyA | 3073860 | c.612C>G | synonymous_variant | 0.87 |
thyA | 3073863 | c.609T>C | synonymous_variant | 0.87 |
thyA | 3073872 | p.Ile200Val | missense_variant | 0.76 |
thyA | 3073888 | p.Ser195Glu | missense_variant | 0.76 |
thyA | 3073892 | c.580T>C | synonymous_variant | 0.76 |
thyA | 3073896 | c.576C>G | synonymous_variant | 0.76 |
thyA | 3073902 | p.Ala190Gln | missense_variant | 0.76 |
thyA | 3073908 | p.Met188Phe | missense_variant | 0.76 |
thyA | 3073925 | c.547T>C | synonymous_variant | 0.81 |
thyA | 3073929 | c.543T>C | synonymous_variant | 0.81 |
thyA | 3073932 | c.540C>T | synonymous_variant | 0.81 |
thyA | 3073956 | c.516G>C | synonymous_variant | 0.88 |
thyA | 3073959 | c.513T>C | synonymous_variant | 0.87 |
thyA | 3073964 | p.Leu170Met | missense_variant | 1.0 |
thyA | 3073968 | c.504C>G | synonymous_variant | 1.0 |
thyA | 3073977 | c.495A>G | synonymous_variant | 1.0 |
thyA | 3073989 | c.483T>C | synonymous_variant | 1.0 |
fprA | 3473979 | c.-28C>A | upstream_gene_variant | 1.0 |
fprA | 3474654 | c.648C>T | synonymous_variant | 0.5 |
clpC1 | 4038356 | c.2349T>C | synonymous_variant | 1.0 |
clpC1 | 4038359 | c.2346A>G | synonymous_variant | 1.0 |
clpC1 | 4038368 | c.2337T>G | synonymous_variant | 1.0 |
clpC1 | 4038377 | c.2328C>G | synonymous_variant | 1.0 |
clpC1 | 4038388 | c.2317T>C | synonymous_variant | 1.0 |
clpC1 | 4038398 | c.2307G>T | synonymous_variant | 1.0 |
clpC1 | 4038401 | c.2302_2304delTTGinsCTC | synonymous_variant | 1.0 |
clpC1 | 4038505 | p.Met734Leu | missense_variant | 1.0 |
clpC1 | 4038519 | p.Arg729Gln | missense_variant | 1.0 |
clpC1 | 4038523 | p.Ile728Val | missense_variant | 1.0 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 1.0 |
clpC1 | 4038533 | p.Arg724Gln | missense_variant | 1.0 |
clpC1 | 4038536 | c.2169C>G | synonymous_variant | 1.0 |
clpC1 | 4038539 | c.2166G>C | synonymous_variant | 1.0 |
clpC1 | 4038554 | p.Ile717Val | missense_variant | 1.0 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 1.0 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.8 |
clpC1 | 4038692 | p.Ser671Gln | missense_variant | 0.67 |
clpC1 | 4038704 | c.2001T>C | synonymous_variant | 0.81 |
clpC1 | 4038707 | c.1998C>G | synonymous_variant | 0.81 |
clpC1 | 4038713 | c.1992T>C | synonymous_variant | 0.87 |
clpC1 | 4038719 | c.1986G>C | synonymous_variant | 0.89 |
clpC1 | 4038740 | c.1965G>C | synonymous_variant | 0.92 |
clpC1 | 4038743 | p.Thr654Val | missense_variant | 0.92 |
clpC1 | 4038749 | c.1956C>G | synonymous_variant | 0.93 |
clpC1 | 4038755 | c.1950G>C | synonymous_variant | 0.93 |
clpC1 | 4038767 | c.1938G>T | synonymous_variant | 0.96 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.96 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.96 |
clpC1 | 4038788 | c.1917G>C | synonymous_variant | 0.95 |
clpC1 | 4038791 | c.1914G>C | synonymous_variant | 0.95 |
clpC1 | 4038794 | p.Ser637Thr | missense_variant | 0.95 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.96 |
clpC1 | 4038815 | c.1890G>C | synonymous_variant | 0.96 |
clpC1 | 4038836 | c.1869G>C | synonymous_variant | 0.97 |
clpC1 | 4038842 | c.1863G>C | synonymous_variant | 0.96 |
clpC1 | 4038845 | c.1858_1860delTCGinsAGC | synonymous_variant | 0.96 |
clpC1 | 4038860 | c.1845G>T | synonymous_variant | 0.95 |
clpC1 | 4038863 | c.1842G>C | synonymous_variant | 0.95 |
clpC1 | 4038872 | c.1833C>G | synonymous_variant | 0.94 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.94 |
clpC1 | 4038890 | p.Glu605Asp | missense_variant | 0.93 |
clpC1 | 4038905 | c.1800A>G | synonymous_variant | 0.91 |
clpC1 | 4038911 | c.1794G>C | synonymous_variant | 0.9 |
clpC1 | 4038923 | c.1782A>C | synonymous_variant | 0.88 |
clpC1 | 4038926 | c.1779G>T | synonymous_variant | 0.87 |
clpC1 | 4038929 | c.1776G>C | synonymous_variant | 0.87 |
clpC1 | 4038932 | c.1773G>C | synonymous_variant | 0.87 |
clpC1 | 4038935 | c.1770C>G | synonymous_variant | 0.87 |
clpC1 | 4038941 | c.1764G>C | synonymous_variant | 0.89 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.88 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.69 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.75 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.75 |
clpC1 | 4038989 | c.1716T>G | synonymous_variant | 0.71 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.56 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.56 |
clpC1 | 4039154 | c.1551G>C | synonymous_variant | 0.56 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.56 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.56 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.56 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.56 |
clpC1 | 4039184 | c.1521G>C | synonymous_variant | 0.56 |
clpC1 | 4039187 | c.1518G>T | synonymous_variant | 0.56 |
clpC1 | 4039192 | p.Thr505Ser | missense_variant | 0.56 |
clpC1 | 4039195 | p.Thr504Ser | missense_variant | 0.56 |
clpC1 | 4039199 | p.Ala502Glu | missense_variant | 0.56 |
clpC1 | 4039205 | c.1500C>G | synonymous_variant | 0.64 |
clpC1 | 4039216 | p.Phe497Val | missense_variant | 0.64 |
clpC1 | 4039217 | c.1488G>C | synonymous_variant | 0.64 |
clpC1 | 4039220 | c.1485G>C | synonymous_variant | 0.64 |
clpC1 | 4039226 | c.1479T>C | synonymous_variant | 0.64 |
clpC1 | 4039241 | c.1464G>C | synonymous_variant | 0.7 |
clpC1 | 4039262 | p.Asp481Glu | missense_variant | 0.83 |
clpC1 | 4039265 | p.Asp480Gly | missense_variant | 0.83 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 1.0 |
clpC1 | 4039586 | c.1119G>C | synonymous_variant | 1.0 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.95 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.95 |
clpC1 | 4039639 | p.Ile356Val | missense_variant | 0.91 |
clpC1 | 4039645 | p.His354Asp | missense_variant | 0.91 |
clpC1 | 4039654 | p.Thr351Ser | missense_variant | 0.9 |
clpC1 | 4039661 | p.Gly348Pro | missense_variant | 0.79 |
clpC1 | 4039670 | c.1035G>C | synonymous_variant | 0.79 |
clpC1 | 4039673 | c.1032G>C | synonymous_variant | 0.79 |
clpC1 | 4039682 | c.1023C>G | synonymous_variant | 0.79 |
clpC1 | 4039691 | c.1014G>C | synonymous_variant | 0.75 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.75 |
clpC1 | 4039714 | p.Tyr331His | missense_variant | 0.69 |
clpC1 | 4039718 | c.987C>G | synonymous_variant | 0.62 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.6 |
clpC1 | 4039727 | p.Asp326Glu | missense_variant | 0.5 |
clpC1 | 4039730 | c.975C>G | synonymous_variant | 0.5 |
clpC1 | 4039736 | c.969C>G | synonymous_variant | 0.33 |
clpC1 | 4039739 | c.966C>G | synonymous_variant | 0.33 |
clpC1 | 4039742 | c.963C>T | synonymous_variant | 0.33 |
clpC1 | 4039748 | c.957G>C | synonymous_variant | 0.5 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.5 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.62 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.62 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.5 |
clpC1 | 4039781 | c.924G>C | synonymous_variant | 0.5 |
clpC1 | 4039787 | c.916_918delTCGinsAGC | synonymous_variant | 0.56 |
clpC1 | 4039790 | c.915C>G | synonymous_variant | 0.56 |
clpC1 | 4039805 | c.900C>T | synonymous_variant | 0.73 |
clpC1 | 4039811 | c.894C>G | synonymous_variant | 0.85 |
clpC1 | 4039817 | c.888A>C | synonymous_variant | 0.85 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.85 |
clpC1 | 4039823 | c.882T>C | synonymous_variant | 0.85 |
clpC1 | 4039829 | c.874_876delTTGinsCTC | synonymous_variant | 0.88 |
clpC1 | 4039838 | p.Leu289Ile | missense_variant | 0.89 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.96 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 1.0 |
clpC1 | 4039871 | p.Thr278Gln | missense_variant | 1.0 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.94 |
clpC1 | 4039901 | c.804C>G | synonymous_variant | 0.94 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.92 |
clpC1 | 4039919 | c.786C>G | synonymous_variant | 0.91 |
clpC1 | 4039925 | c.780C>T | synonymous_variant | 0.89 |
clpC1 | 4039929 | c.775_776delAGinsTC | synonymous_variant | 0.83 |
clpC1 | 4039931 | c.774T>G | synonymous_variant | 0.83 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.83 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 0.83 |
clpC1 | 4039940 | c.765G>C | synonymous_variant | 0.83 |
clpC1 | 4039946 | c.759A>C | synonymous_variant | 0.83 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.83 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.83 |
clpC1 | 4039955 | c.750G>C | synonymous_variant | 0.83 |
clpC1 | 4039960 | p.Thr249Ser | missense_variant | 0.83 |
clpC1 | 4039964 | c.741C>G | synonymous_variant | 0.83 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.89 |
clpC1 | 4039988 | c.717C>G | synonymous_variant | 0.89 |
clpC1 | 4039996 | p.Glu237Lys | missense_variant | 0.83 |
clpC1 | 4040002 | p.His235Asn | missense_variant | 0.75 |
clpC1 | 4040003 | c.702G>C | synonymous_variant | 0.75 |
clpC1 | 4040012 | p.Gln231Leu | missense_variant | 0.75 |
clpC1 | 4040015 | c.690G>C | synonymous_variant | 0.75 |
clpC1 | 4040018 | c.687G>C | synonymous_variant | 0.75 |
clpC1 | 4040021 | c.684A>T | synonymous_variant | 0.75 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.75 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.67 |
clpC1 | 4040051 | c.654C>G | synonymous_variant | 0.8 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.8 |
clpC1 | 4040063 | c.642G>C | synonymous_variant | 0.57 |
clpC1 | 4040066 | c.639G>C | synonymous_variant | 0.57 |
clpC1 | 4040081 | c.624C>G | synonymous_variant | 0.57 |
clpC1 | 4040087 | c.618G>C | synonymous_variant | 0.57 |
clpC1 | 4040090 | c.615T>G | synonymous_variant | 0.57 |
clpC1 | 4040096 | c.609G>C | synonymous_variant | 0.57 |
clpC1 | 4040279 | c.426C>G | synonymous_variant | 0.71 |
clpC1 | 4040291 | c.414G>C | synonymous_variant | 0.85 |
clpC1 | 4040300 | c.405C>G | synonymous_variant | 0.85 |
clpC1 | 4040311 | p.Thr132Ser | missense_variant | 0.85 |
clpC1 | 4040312 | c.393G>C | synonymous_variant | 0.85 |
clpC1 | 4040315 | p.Glu130Asp | missense_variant | 0.85 |
clpC1 | 4040318 | c.387C>G | synonymous_variant | 1.0 |
clpC1 | 4040321 | c.384C>G | synonymous_variant | 1.0 |
clpC1 | 4040324 | c.381G>C | synonymous_variant | 1.0 |
clpC1 | 4040333 | c.372G>C | synonymous_variant | 0.93 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 0.88 |
clpC1 | 4040357 | c.348T>C | synonymous_variant | 0.88 |
clpC1 | 4040363 | c.342A>C | synonymous_variant | 0.88 |
clpC1 | 4040375 | c.330G>C | synonymous_variant | 0.88 |
clpC1 | 4040378 | c.325_327delTTGinsCTC | synonymous_variant | 0.76 |
clpC1 | 4040381 | c.324T>C | synonymous_variant | 0.88 |
clpC1 | 4040387 | c.318A>G | synonymous_variant | 0.88 |
clpC1 | 4040393 | c.312G>C | synonymous_variant | 0.72 |
clpC1 | 4040402 | p.Asn101Lys | missense_variant | 0.71 |
clpC1 | 4040411 | c.294T>C | synonymous_variant | 0.8 |
clpC1 | 4040417 | c.288G>C | synonymous_variant | 0.8 |
clpC1 | 4040423 | c.282A>G | synonymous_variant | 0.8 |
clpC1 | 4040431 | c.274T>C | synonymous_variant | 0.5 |
clpC1 | 4040433 | p.Ser91Ala | missense_variant | 0.4 |
clpC1 | 4040435 | c.270G>C | synonymous_variant | 0.4 |
clpC1 | 4040618 | c.87C>G | synonymous_variant | 1.0 |
clpC1 | 4040640 | p.Met22Ala | missense_variant | 1.0 |
clpC1 | 4040642 | c.61_63delAGGinsCGC | synonymous_variant | 1.0 |
clpC1 | 4040651 | c.54A>G | synonymous_variant | 1.0 |
clpC1 | 4040657 | c.48T>G | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4246778 | p.Arg89Cys | missense_variant | 0.67 |
embB | 4247869 | c.1356G>T | synonymous_variant | 0.67 |
embB | 4248006 | p.Thr498Asn | missense_variant | 1.0 |
aftB | 4267342 | p.Gly499Arg | missense_variant | 0.5 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |