Run ID: SRR16156832
Sample name:
Date: 03-04-2023 16:42:15
Number of reads: 484229
Percentage reads mapped: 12.11
Strain:
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.97 | rifampicin |
rpoB | 761196 | p.Leu464Met | missense_variant | 0.94 | rifampicin |
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.99 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 1.0 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.97 | kanamycin, capreomycin, aminoglycosides, amikacin |
embB | 4247429 | p.Met306Val | missense_variant | 0.29 | ethambutol |
ethA | 4326333 | p.Ala381Pro | missense_variant | 1.0 | ethionamide |
gid | 4407967 | p.Leu79Ser | missense_variant | 1.0 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6659 | p.Met474Leu | missense_variant | 0.4 |
gyrB | 6737 | p.Thr500Ala | missense_variant | 0.5 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8755 | p.Glu485Val | missense_variant | 0.25 |
gyrA | 8787 | p.Thr496Ala | missense_variant | 0.22 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9593 | c.2292G>A | synonymous_variant | 0.67 |
fgd1 | 491139 | p.Glu119Asp | missense_variant | 0.67 |
fgd1 | 491504 | p.Leu241Pro | missense_variant | 0.22 |
fgd1 | 491563 | p.Ser261Gly | missense_variant | 0.18 |
fgd1 | 491581 | p.Glu267* | stop_gained | 0.2 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576304 | c.957G>T | synonymous_variant | 0.2 |
ccsA | 620082 | c.192G>A | synonymous_variant | 0.5 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.17 |
rpoB | 760769 | c.963C>G | synonymous_variant | 0.25 |
rpoB | 760776 | c.970_972delTCGinsAGC | synonymous_variant | 0.2 |
rpoB | 760793 | c.987A>G | synonymous_variant | 0.22 |
rpoB | 760805 | c.999G>C | synonymous_variant | 0.29 |
rpoB | 760916 | c.1110C>T | synonymous_variant | 0.94 |
rpoB | 760920 | p.Leu372Ile | missense_variant | 0.91 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.9 |
rpoB | 760926 | p.Thr374Ala | missense_variant | 0.94 |
rpoB | 760931 | c.1125C>G | synonymous_variant | 0.93 |
rpoB | 760944 | p.Gln380Glu | missense_variant | 0.94 |
rpoB | 760958 | c.1152G>C | synonymous_variant | 0.94 |
rpoB | 760959 | p.Val385Thr | missense_variant | 0.94 |
rpoB | 760965 | p.Met387Leu | missense_variant | 0.94 |
rpoB | 760970 | c.1164G>C | synonymous_variant | 0.94 |
rpoB | 760973 | c.1167G>C | synonymous_variant | 0.92 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.92 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.92 |
rpoB | 760988 | c.1182C>G | synonymous_variant | 0.97 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.97 |
rpoB | 760997 | c.1191G>C | synonymous_variant | 0.97 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.97 |
rpoB | 761027 | c.1221A>C | synonymous_variant | 0.97 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.96 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.96 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.86 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.88 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.88 |
rpoB | 761063 | c.1257C>G | synonymous_variant | 0.88 |
rpoB | 761088 | c.1282_1284delAGCinsTCG | synonymous_variant | 0.94 |
rpoB | 761097 | c.1291_1292delAGinsTC | synonymous_variant | 0.9 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.96 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.97 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.97 |
rpoB | 761138 | c.1332C>G | synonymous_variant | 0.97 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.94 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.94 |
rpoB | 761156 | c.1350G>C | synonymous_variant | 0.94 |
rpoB | 761162 | c.1356G>C | synonymous_variant | 0.94 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.94 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.94 |
rpoB | 761174 | c.1368T>C | synonymous_variant | 0.94 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.94 |
rpoB | 761183 | c.1377T>C | synonymous_variant | 0.94 |
rpoB | 761186 | p.Glu460Asp | missense_variant | 0.94 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.94 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.94 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.94 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.88 |
rpoB | 761243 | c.1437G>C | synonymous_variant | 0.85 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.85 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.4 |
rpoB | 761258 | c.1452G>A | synonymous_variant | 0.4 |
rpoB | 761261 | c.1455G>C | synonymous_variant | 0.5 |
rpoB | 761264 | c.1458C>G | synonymous_variant | 0.5 |
rpoB | 761273 | c.1467T>C | synonymous_variant | 0.5 |
rpoB | 761477 | c.1671C>G | synonymous_variant | 0.33 |
rpoB | 761916 | p.Asp704His | missense_variant | 0.43 |
rpoB | 761925 | p.Met707Leu | missense_variant | 0.43 |
rpoB | 761933 | c.2127G>C | synonymous_variant | 0.38 |
rpoB | 761945 | c.2139G>C | synonymous_variant | 0.5 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.5 |
rpoB | 761951 | c.2145G>C | synonymous_variant | 0.5 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 0.5 |
rpoB | 761955 | p.Ile717Phe | missense_variant | 0.69 |
rpoB | 761963 | c.2157G>C | synonymous_variant | 0.8 |
rpoB | 761974 | p.His723Leu | missense_variant | 0.97 |
rpoB | 762003 | p.Asn733Gln | missense_variant | 0.97 |
rpoB | 762009 | p.Leu735Met | missense_variant | 0.97 |
rpoB | 762015 | p.Glu737Ser | missense_variant | 0.97 |
rpoB | 762026 | c.2220G>C | synonymous_variant | 0.97 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.98 |
rpoB | 762057 | p.Ile751Val | missense_variant | 0.98 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.98 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.97 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 1.0 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 1.0 |
rpoB | 762098 | c.2292C>G | synonymous_variant | 1.0 |
rpoB | 762101 | c.2295C>T | synonymous_variant | 1.0 |
rpoB | 762110 | c.2304G>C | synonymous_variant | 1.0 |
rpoB | 762114 | p.Ile770Val | missense_variant | 1.0 |
rpoB | 762122 | p.Asp772Glu | missense_variant | 1.0 |
rpoC | 762383 | c.-987C>G | upstream_gene_variant | 0.75 |
rpoB | 762387 | p.Glu861Gln | missense_variant | 0.85 |
rpoC | 762398 | c.-972T>C | upstream_gene_variant | 0.88 |
rpoC | 762401 | c.-969G>C | upstream_gene_variant | 0.88 |
rpoC | 762404 | c.-966T>C | upstream_gene_variant | 0.89 |
rpoC | 762410 | c.-960T>G | upstream_gene_variant | 0.89 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.89 |
rpoB | 762426 | p.Ser874Thr | missense_variant | 0.89 |
rpoC | 762434 | c.-936T>C | upstream_gene_variant | 0.89 |
rpoB | 762441 | p.Leu879Met | missense_variant | 0.85 |
rpoC | 762452 | c.-918G>C | upstream_gene_variant | 0.85 |
rpoC | 762470 | c.-900G>C | upstream_gene_variant | 0.85 |
rpoB | 762474 | p.Gly890Ser | missense_variant | 0.85 |
rpoB | 762489 | p.Val895Leu | missense_variant | 0.89 |
rpoC | 762509 | c.-861T>G | upstream_gene_variant | 0.89 |
rpoC | 762512 | c.-858C>G | upstream_gene_variant | 0.89 |
rpoC | 762533 | c.-837T>C | upstream_gene_variant | 0.6 |
rpoC | 762818 | c.-552C>G | upstream_gene_variant | 0.67 |
rpoC | 762827 | c.-543G>C | upstream_gene_variant | 0.77 |
rpoB | 762832 | p.Ser1009Thr | missense_variant | 0.86 |
rpoB | 762849 | p.Tyr1015Asp | missense_variant | 0.91 |
rpoC | 762857 | c.-513C>G | upstream_gene_variant | 0.91 |
rpoB | 762858 | p.Thr1018Ser | missense_variant | 0.91 |
rpoC | 762863 | c.-507T>G | upstream_gene_variant | 0.95 |
rpoC | 762866 | c.-504C>T | upstream_gene_variant | 0.95 |
rpoB | 762878 | p.Ile1024Met | missense_variant | 0.91 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.91 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.96 |
rpoC | 762926 | c.-444C>G | upstream_gene_variant | 0.96 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.96 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 0.96 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.94 |
rpoC | 762980 | c.-390T>A | upstream_gene_variant | 0.85 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.8 |
rpoC | 762995 | c.-375G>C | upstream_gene_variant | 0.67 |
rpoC | 763430 | c.61_63delAGGinsCGC | synonymous_variant | 0.73 |
rpoC | 763434 | p.Gln22Arg | missense_variant | 0.73 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.83 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.94 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.96 |
rpoC | 763483 | c.114G>C | synonymous_variant | 0.97 |
rpoC | 763486 | c.117T>G | synonymous_variant | 0.97 |
rpoC | 763504 | c.135C>A | synonymous_variant | 0.99 |
rpoC | 763507 | c.138G>C | synonymous_variant | 0.99 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.99 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.99 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.99 |
rpoC | 763537 | c.168C>T | synonymous_variant | 0.99 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.98 |
rpoC | 763550 | p.Tyr61Ala | missense_variant | 0.98 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.96 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 0.94 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.93 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.93 |
rpoC | 763639 | p.Glu90Asp | missense_variant | 0.93 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.93 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.92 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.92 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.9 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.92 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.92 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.92 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.92 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.93 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.92 |
rpoC | 763765 | c.396T>G | synonymous_variant | 0.88 |
rpoC | 763772 | p.Val135Met | missense_variant | 0.87 |
rpoC | 763786 | c.417C>G | synonymous_variant | 0.89 |
rpoC | 763796 | p.Met143Val | missense_variant | 0.6 |
rpoC | 764140 | c.771C>T | synonymous_variant | 0.4 |
rpoC | 764344 | c.975C>T | synonymous_variant | 0.84 |
rpoC | 764359 | c.990C>G | synonymous_variant | 0.87 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.94 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 0.96 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.96 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.96 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.99 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.97 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.97 |
rpoC | 764435 | c.1066A>C | synonymous_variant | 0.97 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 0.96 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.96 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.96 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.95 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.97 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.97 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.97 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.96 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.96 |
rpoC | 764507 | p.Ala380Ser | missense_variant | 0.97 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.98 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.98 |
rpoC | 764542 | c.1173C>G | synonymous_variant | 0.98 |
rpoC | 764548 | c.1179G>C | synonymous_variant | 0.98 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.99 |
rpoC | 764575 | c.1206T>C | synonymous_variant | 0.99 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.99 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.99 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.97 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.97 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.96 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 0.98 |
rpoC | 764650 | c.1281G>C | synonymous_variant | 0.98 |
rpoC | 764665 | c.1296C>G | synonymous_variant | 0.98 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.96 |
rpoC | 764671 | c.1302G>C | synonymous_variant | 0.96 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.96 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.95 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.97 |
rpoC | 764749 | c.1380G>C | synonymous_variant | 0.97 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.97 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.97 |
rpoC | 764780 | c.1411_1412delAGinsTC | synonymous_variant | 0.97 |
rpoC | 764804 | p.Gln479Phe | missense_variant | 0.94 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.96 |
rpoC | 764812 | c.1443C>G | synonymous_variant | 0.94 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.96 |
rpoC | 764818 | c.1449G>C | synonymous_variant | 0.96 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.98 |
rpoC | 764833 | c.1464A>G | synonymous_variant | 0.98 |
rpoC | 764843 | p.Ala492Thr | missense_variant | 0.97 |
rpoC | 764857 | c.1488G>C | synonymous_variant | 0.95 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.97 |
rpoC | 764872 | c.1503A>C | synonymous_variant | 0.96 |
rpoC | 764887 | c.1518G>T | synonymous_variant | 0.83 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.83 |
rpoC | 764893 | c.1524T>C | synonymous_variant | 0.83 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.67 |
rpoC | 764912 | p.Met515Gln | missense_variant | 0.67 |
rpoC | 764917 | c.1548G>C | synonymous_variant | 0.67 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 0.67 |
rpoC | 764933 | p.Ile522Leu | missense_variant | 0.44 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.5 |
rpoC | 764953 | c.1584G>C | synonymous_variant | 0.44 |
rpoC | 764956 | c.1587T>C | synonymous_variant | 0.5 |
rpoC | 764957 | p.Glu530Ser | missense_variant | 0.44 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.44 |
rpoC | 764971 | c.1602C>G | synonymous_variant | 0.44 |
rpoC | 764983 | c.1614T>C | synonymous_variant | 0.36 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.33 |
rpoC | 764998 | c.1629G>C | synonymous_variant | 0.33 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.4 |
rpoC | 765488 | p.Ile707Val | missense_variant | 0.4 |
rpoC | 765493 | c.2124G>C | synonymous_variant | 0.4 |
rpoC | 765494 | p.Val709Thr | missense_variant | 0.4 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.4 |
rpoC | 765505 | c.2136C>G | synonymous_variant | 0.4 |
rpoC | 765506 | p.Val713Leu | missense_variant | 0.4 |
rpoC | 765514 | p.Lys715Asn | missense_variant | 0.4 |
rpoC | 765533 | p.Tyr722His | missense_variant | 0.67 |
rpoC | 765875 | p.Val836Ile | missense_variant | 0.73 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.82 |
rpoC | 765888 | p.Phe840Tyr | missense_variant | 0.83 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.86 |
rpoC | 765902 | p.Thr845Ser | missense_variant | 0.9 |
rpoC | 765910 | c.2541G>C | synonymous_variant | 0.88 |
rpoC | 765920 | p.Ile851Ser | missense_variant | 0.84 |
rpoC | 765923 | p.Asn852Ala | missense_variant | 0.86 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.82 |
rpoC | 765940 | c.2571A>C | synonymous_variant | 0.84 |
rpoC | 765947 | c.2578_2580delTTGinsCTC | synonymous_variant | 0.83 |
rpoC | 765962 | c.2593T>C | synonymous_variant | 0.82 |
rpoC | 765965 | p.Arg866Lys | missense_variant | 0.84 |
rpoC | 765973 | c.2604C>G | synonymous_variant | 0.82 |
rpoC | 765974 | p.Asp869Asn | missense_variant | 0.83 |
rpoC | 765979 | c.2610C>G | synonymous_variant | 0.83 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.83 |
rpoC | 766000 | c.2631G>C | synonymous_variant | 0.81 |
rpoC | 766021 | c.2652G>C | synonymous_variant | 0.8 |
rpoC | 766027 | c.2658G>C | synonymous_variant | 0.76 |
rpoC | 766034 | p.His889Asp | missense_variant | 0.72 |
mmpL5 | 775617 | p.Pro955Leu | missense_variant | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777157 | c.1324C>A | synonymous_variant | 0.29 |
mmpS5 | 778748 | p.Pro53His | missense_variant | 0.22 |
mmpS5 | 778755 | p.Phe51Leu | missense_variant | 0.22 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781796 | p.Met79Ile | missense_variant | 0.75 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.5 |
fbiC | 1303667 | p.Thr246Ser | missense_variant | 0.5 |
Rv1258c | 1407219 | p.Ala41Asp | missense_variant | 0.67 |
embR | 1416662 | p.Arg229Leu | missense_variant | 0.67 |
embR | 1417090 | c.258C>G | synonymous_variant | 0.33 |
embR | 1417457 | c.-110C>A | upstream_gene_variant | 1.0 |
atpE | 1461151 | p.Ile36Asn | missense_variant | 0.4 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472287 | n.442C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472293 | n.448C>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472496 | n.651T>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.99 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472674 | n.829T>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472686 | n.841G>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473022 | n.1177G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.98 |
rrs | 1473089 | n.1244A>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473122 | n.1277T>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473252 | n.1407T>C | 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 | 0.98 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473317 | n.1472G>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1473845 | n.188G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474112 | n.455T>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474124 | n.467G>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474125 | n.468C>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474133 | n.476T>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474141 | n.484G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474142 | n.485C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474155 | n.498G>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474186 | n.529A>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474202 | n.545T>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474263 | n.606G>A | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474275 | n.618T>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474280 | n.623C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474281 | n.624A>G | non_coding_transcript_exon_variant | 0.95 |
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 | 1474316 | n.659T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474317 | n.660G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474359 | n.702C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474381 | n.724T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474444 | n.787G>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474451 | n.794T>C | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474662 | n.1005C>A | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474688 | n.1031G>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474710 | n.1053T>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474711 | n.1054_1055insAA | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474714 | n.1058delT | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474717 | n.1060A>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474784 | n.1127C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474830 | n.1173A>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474944 | n.1287G>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474948 | n.1291C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475060 | n.1404delC | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475065 | n.1408G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475067 | n.1410A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475068 | n.1411A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475076 | n.1419C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475078 | n.1421T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475079 | n.1422T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475081 | n.1424C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475088 | n.1431A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475094 | n.1437C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475104 | n.1447T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475108 | n.1451C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475111 | n.1454G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475116 | n.1459G>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475119 | n.1462C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475124 | n.1467A>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475129 | n.1472G>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475285 | n.1628G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475499 | n.1842C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475538 | n.1881T>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1475548 | n.1891C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1475549 | n.1892T>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475655 | n.1998T>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.69 |
rrl | 1475672 | n.2015C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475673 | n.2016T>C | non_coding_transcript_exon_variant | 0.87 |
rrl | 1475688 | n.2031G>A | non_coding_transcript_exon_variant | 0.92 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475713 | n.2056C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475747 | n.2090A>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475757 | n.2101_2104delACCC | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475764 | n.2107A>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475765 | n.2108A>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475766 | n.2109G>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475781 | n.2124T>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.96 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1475963 | n.2306G>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475997 | n.2340A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475998 | n.2341C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476130 | n.2473G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.98 |
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 | 1.0 |
rrl | 1476221 | n.2564T>C | 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 | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476253 | n.2596A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476257 | n.2600G>C | 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 | 0.98 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476299 | n.2642C>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476308 | n.2651G>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476540 | n.2883C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.71 |
fabG1 | 1673608 | p.Gly57Ser | missense_variant | 0.67 |
rpsA | 1833628 | c.87G>C | synonymous_variant | 0.71 |
rpsA | 1833653 | p.Ile38Leu | missense_variant | 0.9 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.9 |
rpsA | 1833668 | p.Ile43Val | missense_variant | 0.9 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.92 |
rpsA | 1833685 | c.144G>C | synonymous_variant | 0.95 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 1.0 |
rpsA | 1833697 | c.156C>G | synonymous_variant | 1.0 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 1.0 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 1.0 |
rpsA | 1833733 | c.192C>G | synonymous_variant | 1.0 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 1.0 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 1.0 |
rpsA | 1833763 | c.222C>G | synonymous_variant | 1.0 |
rpsA | 1833769 | c.228C>G | synonymous_variant | 1.0 |
rpsA | 1833770 | p.Asn77Asp | missense_variant | 1.0 |
rpsA | 1833781 | c.240T>G | synonymous_variant | 1.0 |
rpsA | 1833782 | p.Ser81Ala | missense_variant | 1.0 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 1.0 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 1.0 |
rpsA | 1833794 | p.Glu85Thr | missense_variant | 1.0 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 1.0 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 1.0 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 1.0 |
rpsA | 1833835 | c.294C>T | synonymous_variant | 1.0 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 1.0 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 1.0 |
rpsA | 1833850 | c.309C>G | synonymous_variant | 1.0 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 1.0 |
rpsA | 1833862 | c.321G>C | synonymous_variant | 1.0 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.89 |
rpsA | 1833877 | c.336C>G | synonymous_variant | 0.83 |
rpsA | 1833884 | p.Thr115Asp | missense_variant | 0.84 |
rpsA | 1833893 | p.Ala118Lys | missense_variant | 0.83 |
rpsA | 1833896 | p.Leu119Ile | missense_variant | 0.83 |
rpsA | 1833905 | p.Lys122Glu | missense_variant | 0.83 |
rpsA | 1833912 | p.Glu124Gly | missense_variant | 0.83 |
rpsA | 1833915 | p.Ala125Val | missense_variant | 0.79 |
rpsA | 1833920 | p.Lys127Glu | missense_variant | 0.84 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.91 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.92 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.94 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 0.94 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.93 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.94 |
rpsA | 1833985 | c.444G>C | synonymous_variant | 0.94 |
rpsA | 1833988 | c.447C>G | synonymous_variant | 0.94 |
rpsA | 1833994 | c.453G>C | synonymous_variant | 0.94 |
rpsA | 1833997 | c.456G>C | synonymous_variant | 0.94 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.94 |
rpsA | 1834025 | p.Gln162Ala | missense_variant | 0.96 |
rpsA | 1834040 | p.Lys167Gln | missense_variant | 0.97 |
rpsA | 1834043 | p.Glu168Lys | missense_variant | 0.97 |
rpsA | 1834046 | p.Ile169Leu | missense_variant | 0.97 |
rpsA | 1834054 | c.513C>G | synonymous_variant | 0.96 |
rpsA | 1834093 | c.552G>C | synonymous_variant | 0.93 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.9 |
rpsA | 1834114 | c.573G>C | synonymous_variant | 0.89 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.9 |
rpsA | 1834213 | c.672G>C | synonymous_variant | 1.0 |
rpsA | 1834219 | c.678C>G | synonymous_variant | 1.0 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 1.0 |
rpsA | 1834225 | c.684C>G | synonymous_variant | 1.0 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.96 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.96 |
rpsA | 1834243 | c.702G>C | synonymous_variant | 0.97 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.98 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.98 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.98 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.97 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.97 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.97 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.97 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.97 |
rpsA | 1834327 | c.786G>C | synonymous_variant | 0.98 |
rpsA | 1834333 | p.Asp264Glu | missense_variant | 0.98 |
rpsA | 1834336 | c.795C>G | synonymous_variant | 0.97 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.97 |
rpsA | 1834354 | c.813G>T | synonymous_variant | 0.97 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.97 |
rpsA | 1834360 | c.819G>C | synonymous_variant | 0.97 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.97 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.97 |
rpsA | 1834369 | c.828C>G | synonymous_variant | 0.98 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.98 |
rpsA | 1834384 | c.843A>G | synonymous_variant | 0.99 |
rpsA | 1834395 | p.Arg285Gln | missense_variant | 0.99 |
rpsA | 1834398 | p.His286Leu | missense_variant | 0.98 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.99 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.98 |
rpsA | 1834418 | p.Ile293Leu | missense_variant | 0.96 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.98 |
rpsA | 1834427 | p.Ile296Val | missense_variant | 0.98 |
rpsA | 1834451 | c.910_912delTTGinsCTC | synonymous_variant | 1.0 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.98 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.98 |
rpsA | 1834480 | c.939C>G | synonymous_variant | 0.96 |
rpsA | 1834486 | p.Glu315Asp | missense_variant | 0.98 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.97 |
rpsA | 1834501 | c.960G>C | synonymous_variant | 0.97 |
rpsA | 1834513 | c.972C>G | synonymous_variant | 0.96 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101697 | p.Ala449Gly | missense_variant | 0.22 |
katG | 2153966 | p.Ala716Thr | missense_variant | 0.25 |
katG | 2154410 | p.Thr568Ala | missense_variant | 0.67 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155794 | c.318G>A | synonymous_variant | 0.5 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169100 | p.Gly505Trp | missense_variant | 0.5 |
PPE35 | 2170761 | c.-149G>T | upstream_gene_variant | 0.25 |
Rv1979c | 2222232 | c.933G>T | synonymous_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289059 | c.183A>T | synonymous_variant | 0.5 |
kasA | 2518702 | c.588C>T | synonymous_variant | 0.4 |
pepQ | 2859596 | p.Ala275Thr | missense_variant | 0.67 |
ribD | 2987548 | p.Arg237Leu | missense_variant | 0.33 |
Rv2752c | 3064735 | p.Pro486Leu | missense_variant | 0.2 |
thyX | 3067726 | p.Glu74* | stop_gained | 0.5 |
thyA | 3073693 | p.Pro260Leu | missense_variant | 0.22 |
thyA | 3074276 | p.Asp66Tyr | missense_variant | 0.17 |
ald | 3086729 | c.-91A>G | upstream_gene_variant | 0.5 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086935 | p.Ala39Val | missense_variant | 0.29 |
ald | 3087697 | p.Thr293Met | missense_variant | 0.18 |
fbiD | 3339565 | p.Val150Leu | missense_variant | 0.25 |
Rv3083 | 3448743 | c.240G>A | synonymous_variant | 0.4 |
Rv3083 | 3448763 | p.Asp87Val | missense_variant | 0.4 |
Rv3083 | 3449815 | p.Gln438Lys | missense_variant | 0.67 |
fprA | 3473877 | c.-130G>A | upstream_gene_variant | 0.29 |
fprA | 3473984 | c.-23G>T | upstream_gene_variant | 0.29 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568643 | p.Gln13* | stop_gained | 0.33 |
Rv3236c | 3612150 | c.966delG | frameshift_variant | 0.29 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
Rv3236c | 3612866 | p.Ser84Thr | missense_variant | 0.4 |
fbiA | 3640658 | p.His39Arg | missense_variant | 1.0 |
fbiB | 3640962 | c.-573C>A | upstream_gene_variant | 1.0 |
fbiB | 3641124 | c.-411C>T | upstream_gene_variant | 0.33 |
alr | 3840822 | p.Ala200Val | missense_variant | 0.25 |
rpoA | 3877587 | c.921A>C | synonymous_variant | 0.75 |
rpoA | 3877601 | p.Gln303Glu | missense_variant | 0.75 |
rpoA | 3877602 | p.His302Gln | missense_variant | 0.75 |
rpoA | 3877605 | c.903G>C | synonymous_variant | 0.75 |
rpoA | 3877611 | p.Ile299Glu | missense_variant | 0.75 |
rpoA | 3877617 | c.891G>C | synonymous_variant | 0.75 |
rpoA | 3877636 | p.Gln291Ala | missense_variant | 0.9 |
rpoA | 3877638 | c.870T>C | synonymous_variant | 0.9 |
rpoA | 3877656 | p.Leu284Met | missense_variant | 0.9 |
rpoA | 3877667 | p.Ser281Ala | missense_variant | 0.9 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.9 |
rpoA | 3877671 | p.Thr279Ser | missense_variant | 0.9 |
rpoA | 3877674 | c.834C>G | synonymous_variant | 0.9 |
rpoA | 3877677 | p.Ala277Gly | missense_variant | 0.9 |
rpoA | 3877683 | c.825G>C | synonymous_variant | 0.9 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.9 |
rpoA | 3877701 | p.Val269Ile | missense_variant | 0.75 |
rpoA | 3877704 | c.804G>C | synonymous_variant | 0.75 |
rpoA | 3877728 | c.780C>G | synonymous_variant | 0.67 |
ddn | 3987003 | p.Arg54Ser | missense_variant | 0.25 |
ddn | 3987017 | c.174G>A | synonymous_variant | 0.25 |
clpC1 | 4038744 | p.Thr654Val | missense_variant | 0.5 |
clpC1 | 4038746 | c.1959C>T | synonymous_variant | 0.5 |
clpC1 | 4038756 | p.Gly650Ser | missense_variant | 0.89 |
clpC1 | 4038764 | c.1941C>G | synonymous_variant | 0.86 |
clpC1 | 4038767 | c.1938G>A | synonymous_variant | 0.86 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.86 |
clpC1 | 4038782 | p.Val641Ile | missense_variant | 0.86 |
clpC1 | 4038795 | c.1909_1910delAGinsTC | synonymous_variant | 0.9 |
clpC1 | 4038801 | p.Tyr635Phe | missense_variant | 0.86 |
clpC1 | 4038805 | p.Ile634Leu | missense_variant | 0.86 |
clpC1 | 4038806 | p.Glu633Asp | missense_variant | 0.86 |
clpC1 | 4038815 | c.1890G>C | synonymous_variant | 0.87 |
clpC1 | 4038824 | p.Ile627Val | missense_variant | 0.87 |
clpC1 | 4038845 | c.1860G>C | synonymous_variant | 0.9 |
clpC1 | 4038854 | p.Lys617Arg | missense_variant | 0.9 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.86 |
clpC1 | 4038863 | c.1842G>C | synonymous_variant | 0.86 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.85 |
clpC1 | 4038899 | c.1806C>G | synonymous_variant | 0.62 |
clpC1 | 4038905 | c.1800A>C | synonymous_variant | 0.4 |
clpC1 | 4039125 | p.Ala527Asp | missense_variant | 0.18 |
clpC1 | 4039513 | p.Lys398Glu | missense_variant | 0.4 |
clpC1 | 4039691 | c.1014G>C | synonymous_variant | 0.67 |
clpC1 | 4039714 | p.Tyr331His | missense_variant | 0.88 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.91 |
clpC1 | 4039730 | c.975C>G | synonymous_variant | 0.91 |
clpC1 | 4039748 | c.957G>C | synonymous_variant | 0.93 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.93 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.95 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.95 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.95 |
clpC1 | 4039773 | p.Lys311Met | missense_variant | 0.95 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.95 |
clpC1 | 4039781 | c.924G>C | synonymous_variant | 0.95 |
clpC1 | 4039787 | c.916_918delTCGinsAGC | synonymous_variant | 0.95 |
clpC1 | 4039814 | c.891C>G | synonymous_variant | 0.97 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 0.97 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.92 |
clpC1 | 4039823 | c.882T>G | synonymous_variant | 0.94 |
clpC1 | 4039829 | c.874_876delTTGinsCTC | synonymous_variant | 0.89 |
clpC1 | 4039838 | p.Leu289Ile | missense_variant | 0.93 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.95 |
clpC1 | 4039865 | c.840T>G | synonymous_variant | 0.94 |
clpC1 | 4039871 | c.834C>G | synonymous_variant | 0.94 |
clpC1 | 4039875 | p.Asn277Arg | missense_variant | 0.93 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.87 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.87 |
clpC1 | 4039916 | c.789T>C | synonymous_variant | 0.89 |
clpC1 | 4039929 | c.775_776delAGinsTC | synonymous_variant | 0.88 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.88 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.88 |
clpC1 | 4039940 | c.765G>C | synonymous_variant | 0.88 |
clpC1 | 4039943 | c.762G>C | synonymous_variant | 0.88 |
clpC1 | 4039946 | c.759A>C | synonymous_variant | 0.88 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.88 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.91 |
clpC1 | 4039960 | p.Thr249Ser | missense_variant | 0.94 |
clpC1 | 4039977 | p.Lys243Arg | missense_variant | 0.97 |
clpC1 | 4039988 | c.717C>G | synonymous_variant | 0.98 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.98 |
clpC1 | 4039994 | p.Glu237Asp | missense_variant | 0.98 |
clpC1 | 4040001 | p.His235Arg | missense_variant | 0.98 |
clpC1 | 4040003 | p.Val234Asp | missense_variant | 0.98 |
clpC1 | 4040009 | c.696C>G | synonymous_variant | 0.96 |
clpC1 | 4040015 | c.690G>C | synonymous_variant | 0.96 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.96 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.96 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.98 |
clpC1 | 4040063 | c.642G>C | synonymous_variant | 0.95 |
clpC1 | 4040069 | c.636G>C | synonymous_variant | 0.93 |
clpC1 | 4040087 | c.618G>C | synonymous_variant | 0.9 |
clpC1 | 4040090 | c.615T>C | synonymous_variant | 0.9 |
clpC1 | 4040108 | c.597G>C | synonymous_variant | 0.83 |
clpC1 | 4040114 | p.Ile197Met | missense_variant | 0.56 |
clpC1 | 4040117 | c.588A>G | synonymous_variant | 0.33 |
clpC1 | 4040724 | c.-20G>T | upstream_gene_variant | 0.4 |
embC | 4240055 | p.Gly65Cys | missense_variant | 0.4 |
embC | 4240117 | c.255C>T | synonymous_variant | 0.22 |
embC | 4241998 | c.2136G>A | synonymous_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4243644 | p.Ala138Ser | missense_variant | 0.5 |
embA | 4245107 | p.Phe625Leu | missense_variant | 0.5 |
embA | 4245462 | p.Asp744Asn | missense_variant | 0.4 |
embB | 4247985 | p.Thr491Asn | missense_variant | 0.5 |
embB | 4248121 | c.1608G>A | synonymous_variant | 0.29 |
embB | 4249264 | c.2751G>A | synonymous_variant | 0.67 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4267652 | p.Met395Ile | missense_variant | 0.29 |
aftB | 4268872 | c.-36G>T | upstream_gene_variant | 0.25 |
ethA | 4326184 | c.1290C>A | synonymous_variant | 0.2 |
ethA | 4326205 | c.1269C>T | synonymous_variant | 0.22 |
ethR | 4327285 | c.-264A>T | upstream_gene_variant | 0.29 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |
gid | 4408378 | c.-176G>A | upstream_gene_variant | 0.18 |