Run ID: SRR6046376
Sample name:
Date: 04-04-2023 12:15:47
Number of reads: 2619519
Percentage reads mapped: 61.25
Strain: lineage3
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.73 | streptomycin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.23 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.75 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.7 | kanamycin, capreomycin, aminoglycosides, amikacin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 0.99 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 761973 | p.His723Tyr | missense_variant | 0.15 |
rpoB | 762002 | c.2196C>G | synonymous_variant | 0.13 |
rpoB | 762003 | p.Asn733Gln | missense_variant | 0.13 |
rpoB | 762011 | c.2205G>C | synonymous_variant | 0.13 |
rpoB | 762014 | c.2208C>G | synonymous_variant | 0.13 |
rpoB | 762015 | p.Glu737Gln | missense_variant | 0.13 |
rpoB | 762020 | p.Glu738Asp | missense_variant | 0.13 |
rpoB | 762024 | p.Val740Thr | missense_variant | 0.13 |
rpoB | 762030 | p.Thr742Ser | missense_variant | 0.14 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.23 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.22 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.23 |
rpoB | 762074 | c.2268C>G | synonymous_variant | 0.21 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.19 |
rpoB | 762084 | p.Ala760Pro | missense_variant | 0.19 |
rpoB | 762098 | c.2292C>G | synonymous_variant | 0.21 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.21 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.2 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.2 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.21 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.2 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.2 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.26 |
rpoB | 762162 | p.Ile786Val | missense_variant | 0.27 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.33 |
rpoB | 762179 | c.2373C>T | synonymous_variant | 0.33 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.27 |
rpoB | 762189 | p.Ile795Leu | missense_variant | 0.27 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.27 |
rpoB | 762209 | c.2403C>G | synonymous_variant | 0.28 |
rpoB | 762212 | c.2406G>C | synonymous_variant | 0.28 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.27 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.25 |
rpoB | 762278 | c.2472C>T | synonymous_variant | 0.18 |
rpoB | 762284 | c.2478G>T | synonymous_variant | 0.15 |
rpoB | 762287 | c.2481C>A | synonymous_variant | 0.16 |
rpoB | 762293 | c.2487T>G | synonymous_variant | 0.16 |
rpoB | 762297 | p.Leu831Met | missense_variant | 0.16 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 0.98 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.11 |
rpoC | 762896 | c.-474G>C | upstream_gene_variant | 0.13 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.14 |
rpoB | 762905 | p.Asp1033Glu | missense_variant | 0.13 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.12 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.12 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.12 |
rpoC | 762926 | c.-444C>G | upstream_gene_variant | 0.12 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.12 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 0.12 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.14 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.16 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.18 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.16 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.16 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763504 | c.135C>A | synonymous_variant | 0.12 |
rpoC | 763507 | c.138G>C | synonymous_variant | 0.11 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.13 |
rpoC | 763534 | c.165T>G | synonymous_variant | 0.13 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.15 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.19 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.2 |
rpoC | 763576 | c.207C>T | synonymous_variant | 0.19 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.22 |
rpoC | 763615 | c.246G>C | synonymous_variant | 0.14 |
rpoC | 763618 | c.249C>G | synonymous_variant | 0.14 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 0.13 |
rpoC | 763625 | p.Lys86Ala | missense_variant | 0.13 |
rpoC | 763630 | c.261G>T | synonymous_variant | 0.15 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.19 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.19 |
rpoC | 763660 | c.291T>C | synonymous_variant | 0.23 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.21 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.19 |
rpoC | 763699 | c.330G>C | synonymous_variant | 0.13 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.12 |
rpoC | 763703 | c.334_336delTCGinsAGC | synonymous_variant | 0.12 |
rpoC | 763708 | c.339G>T | synonymous_variant | 0.12 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.14 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.14 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.14 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.14 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.13 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.13 |
rpoC | 763772 | p.Val135Met | missense_variant | 0.11 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.16 |
rpoC | 764371 | c.1002G>T | synonymous_variant | 0.16 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 0.16 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.18 |
rpoC | 764405 | c.1036_1038delAGGinsCGT | synonymous_variant | 0.31 |
rpoC | 764428 | c.1059G>A | synonymous_variant | 0.29 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.29 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.29 |
rpoC | 764435 | c.1066_1068delAGGinsCGT | synonymous_variant | 0.3 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 0.3 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.29 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.3 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.34 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.36 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.35 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.27 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.25 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.28 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.25 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.26 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 0.24 |
rpoC | 764533 | c.1164C>T | synonymous_variant | 0.23 |
rpoC | 764536 | c.1167G>A | synonymous_variant | 0.23 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.23 |
rpoC | 764542 | c.1173C>G | synonymous_variant | 0.25 |
rpoC | 764548 | c.1179G>T | synonymous_variant | 0.26 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.28 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.31 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.32 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.32 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.35 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.34 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.36 |
rpoC | 764632 | c.1263T>A | synonymous_variant | 0.33 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.28 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.28 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.27 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.27 |
rpoC | 764672 | p.Gln435Thr | missense_variant | 0.27 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.25 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.19 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.11 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.11 |
rpsL | 781860 | p.Ser101Ala | missense_variant | 0.11 |
embR | 1416974 | c.371_373delACG | disruptive_inframe_deletion | 0.98 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472148 | n.303T>C | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472297 | n.453_461delGTCCGGGTT | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472309 | n.464C>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472310 | n.465T>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472312 | n.468_470delGAT | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472412 | n.567A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472416 | n.571C>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472418 | n.573T>C | non_coding_transcript_exon_variant | 0.1 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472426 | n.581T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472427 | n.582T>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472476 | n.631A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472495 | n.650C>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472496 | n.651T>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472496 | n.651T>G | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472582 | n.737G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472584 | n.739A>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472597 | n.752G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472673 | n.828T>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472674 | n.829T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472836 | n.991G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472875 | n.1030T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472970 | n.1126delG | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472974 | n.1129A>C | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472975 | n.1130T>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.77 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473099 | n.1254T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473122 | n.1277T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473127 | n.1282G>A | non_coding_transcript_exon_variant | 0.66 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1473844 | n.187C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473870 | n.213G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473871 | n.214T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473887 | n.230T>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473922 | n.265A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474155 | n.498G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474163 | n.506C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474166 | n.509G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474171 | n.514C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474179 | n.522C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.65 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474185 | n.528G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474186 | n.529A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.74 |
rrl | 1474228 | n.571T>A | non_coding_transcript_exon_variant | 0.74 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474253 | n.596A>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1474281 | n.624A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474289 | n.633_647delTTTTCCTCTCCGGAG | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474306 | n.649A>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.59 |
rrl | 1474316 | n.659T>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474353 | n.696A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474355 | n.698A>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474356 | n.699T>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474359 | n.702C>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474383 | n.726G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474450 | n.793T>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474676 | n.1019T>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474692 | n.1035G>A | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474790 | n.1133C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474830 | n.1173A>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474869 | n.1212G>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474936 | n.1279C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474938 | n.1281G>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474946 | n.1289C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474948 | n.1291C>T | 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 | 1475068 | n.1411A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475076 | n.1419C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475078 | n.1421T>C | 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 | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475091 | n.1434G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475104 | n.1447T>A | 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 | 1475124 | n.1467A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475129 | n.1472G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475173 | n.1516A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475175 | n.1518G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475573 | n.1916G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475655 | n.1998T>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475672 | n.2015C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475673 | n.2016T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475686 | n.2029C>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1475696 | n.2039T>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475697 | n.2040C>A | non_coding_transcript_exon_variant | 0.74 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475702 | n.2045G>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1475703 | n.2046A>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475751 | n.2094C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475752 | n.2095C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475758 | n.2101A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.99 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476076 | n.2419A>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476088 | n.2431A>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476095 | n.2438C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476100 | n.2443A>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476113 | n.2456T>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476130 | n.2473G>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476213 | n.2556G>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476251 | n.2594T>A | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476267 | n.2610G>C | non_coding_transcript_exon_variant | 0.49 |
rrl | 1476276 | n.2619C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476368 | n.2711T>C | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476586 | n.2929C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476613 | n.2956G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476631 | n.2974G>T | non_coding_transcript_exon_variant | 0.24 |
rpsA | 1833952 | c.411C>T | synonymous_variant | 0.15 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 0.18 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.2 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.19 |
rpsA | 1833985 | c.444G>C | synonymous_variant | 0.2 |
rpsA | 1833988 | c.447C>T | synonymous_variant | 0.2 |
rpsA | 1833991 | c.450C>G | synonymous_variant | 0.21 |
rpsA | 1834009 | c.468C>T | synonymous_variant | 0.21 |
rpsA | 1834012 | c.471G>T | synonymous_variant | 0.2 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.22 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.25 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 0.25 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.24 |
rpsA | 1834093 | c.552G>C | synonymous_variant | 0.15 |
rpsA | 1834099 | c.558C>G | synonymous_variant | 0.12 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.16 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.16 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.26 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.25 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.25 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.26 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.26 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.24 |
rpsA | 1834354 | c.813G>C | synonymous_variant | 0.23 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.23 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.23 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.24 |
rpsA | 1834378 | c.837T>G | synonymous_variant | 0.26 |
rpsA | 1834395 | p.Arg285Gln | missense_variant | 0.27 |
rpsA | 1834405 | c.864C>T | synonymous_variant | 0.27 |
rpsA | 1834411 | c.870T>G | synonymous_variant | 0.22 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.21 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.2 |
rpsA | 1834427 | p.Ile296Val | missense_variant | 0.21 |
rpsA | 1834447 | c.906C>G | synonymous_variant | 0.19 |
rpsA | 1834451 | c.910_912delTTGinsCTC | synonymous_variant | 0.18 |
rpsA | 1834456 | c.915T>C | synonymous_variant | 0.19 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.17 |
rpsA | 1834474 | c.933C>G | synonymous_variant | 0.18 |
rpsA | 1834486 | p.Glu315Asp | missense_variant | 0.15 |
rpsA | 1834498 | c.957C>T | synonymous_variant | 0.12 |
rpsA | 1834501 | c.960G>C | synonymous_variant | 0.12 |
rpsA | 1834504 | c.963G>C | synonymous_variant | 0.12 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2222754 | p.Lys137Asn | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 0.98 |
pepQ | 2860448 | c.-30C>A | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.11 |
clpC1 | 4039481 | c.1224T>G | synonymous_variant | 0.12 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.19 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.18 |
clpC1 | 4039871 | c.834C>G | synonymous_variant | 0.18 |
clpC1 | 4039874 | p.Asn277Arg | missense_variant | 0.17 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.21 |
clpC1 | 4039928 | p.Ser259Thr | missense_variant | 0.12 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.98 |