Run ID: ERR4820833
Sample name:
Date: 01-04-2023 16:54:23
Number of reads: 242034
Percentage reads mapped: 33.12
Strain:
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.14 | streptomycin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.67 | streptomycin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.16 | kanamycin, capreomycin, aminoglycosides, amikacin |
katG | 2156007 | c.104delA | frameshift_variant | 0.33 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575280 | c.-67delC | upstream_gene_variant | 0.5 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.4 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.4 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.5 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.5 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.25 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 0.29 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.29 |
rpoB | 762024 | p.Val740Ile | missense_variant | 0.22 |
rpoB | 762029 | c.2223C>G | synonymous_variant | 0.22 |
rpoB | 762051 | p.His749Tyr | missense_variant | 0.38 |
rpoB | 762057 | p.Ile751Val | missense_variant | 0.38 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.5 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.5 |
rpoB | 762071 | p.Asp755Glu | missense_variant | 0.5 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.5 |
rpoB | 762085 | p.Ala760Glu | missense_variant | 0.5 |
rpoB | 762089 | c.2283G>A | synonymous_variant | 0.38 |
rpoB | 762110 | c.2304G>C | synonymous_variant | 0.33 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.33 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.22 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.22 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.2 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.2 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.25 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.55 |
rpoB | 762200 | c.2394C>T | synonymous_variant | 0.55 |
rpoB | 762212 | c.2406G>C | synonymous_variant | 0.4 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.64 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.64 |
rpoB | 762234 | p.Pro810Ser | missense_variant | 0.64 |
rpoB | 762239 | c.2433G>A | synonymous_variant | 0.36 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.58 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.54 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.33 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoB | 762855 | p.Val1017Ile | missense_variant | 0.3 |
rpoB | 762858 | p.Thr1018Ser | missense_variant | 0.3 |
rpoC | 762863 | c.-507T>G | upstream_gene_variant | 0.2 |
rpoB | 762871 | p.Met1022Thr | missense_variant | 0.2 |
rpoB | 762878 | p.Ile1024Met | missense_variant | 0.17 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.42 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.14 |
rpoC | 762902 | c.-468C>T | upstream_gene_variant | 0.33 |
rpoC | 762911 | c.-459C>T | upstream_gene_variant | 0.35 |
rpoC | 762917 | c.-453C>T | upstream_gene_variant | 0.35 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.4 |
rpoC | 762926 | c.-444C>G | upstream_gene_variant | 0.13 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.43 |
rpoC | 762944 | c.-426C>T | upstream_gene_variant | 0.29 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 0.13 |
rpoC | 762956 | c.-414G>C | upstream_gene_variant | 0.31 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.27 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.15 |
rpoC | 762980 | c.-390T>C | upstream_gene_variant | 0.17 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.18 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.33 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.25 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763038 | p.Thr1078Ala | missense_variant | 0.27 |
rpoC | 763043 | c.-327G>C | upstream_gene_variant | 0.33 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.38 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.43 |
rpoB | 763077 | p.Val1091Thr | missense_variant | 0.5 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.47 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.4 |
rpoB | 763119 | p.Asn1105Asp | missense_variant | 0.4 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.38 |
rpoC | 763133 | c.-237G>C | upstream_gene_variant | 0.33 |
rpoC | 763160 | c.-210G>A | upstream_gene_variant | 0.22 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.25 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.25 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.25 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.22 |
rpoC | 763550 | p.Tyr61Ala | missense_variant | 0.2 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.22 |
rpoC | 763578 | p.Phe70Tyr | missense_variant | 0.22 |
rpoC | 763647 | p.Gly93Ala | missense_variant | 0.25 |
rpoC | 763655 | p.Glu96Lys | missense_variant | 0.2 |
rpoC | 763660 | c.291T>C | synonymous_variant | 0.22 |
rpoC | 763666 | c.297G>C | synonymous_variant | 0.2 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.17 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.23 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.16 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.44 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.53 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.44 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.44 |
rpoC | 763718 | p.Leu117Val | missense_variant | 0.33 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.44 |
rpoC | 763724 | p.Asp119Asn | missense_variant | 0.44 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.5 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.5 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.5 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.43 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.54 |
rpoC | 763772 | p.Val135Met | missense_variant | 0.29 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 0.5 |
rpoC | 764446 | p.Asp359Glu | missense_variant | 0.5 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.6 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.6 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.73 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.73 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.45 |
rpoC | 764503 | c.1134G>T | synonymous_variant | 0.91 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.18 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.93 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.94 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 0.69 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.93 |
rpoC | 764543 | p.Thr392Ala | missense_variant | 0.93 |
rpoC | 764548 | c.1179G>T | synonymous_variant | 0.79 |
rpoC | 764551 | c.1182G>C | synonymous_variant | 0.26 |
rpoC | 764573 | p.Leu402Ile | missense_variant | 0.59 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.59 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.56 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.56 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.25 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.74 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.74 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.71 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.32 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.5 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.69 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.65 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.52 |
rpoC | 764656 | c.1287C>T | synonymous_variant | 0.64 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.68 |
rpoC | 764665 | c.1296C>T | synonymous_variant | 0.14 |
rpoC | 764677 | c.1308C>A | synonymous_variant | 0.59 |
rpoC | 764678 | p.Lys437Gln | missense_variant | 0.7 |
rpoC | 764683 | c.1314G>C | synonymous_variant | 0.39 |
rpoC | 764692 | c.1323C>T | synonymous_variant | 0.56 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.62 |
rpoC | 764713 | c.1344G>C | synonymous_variant | 0.38 |
rpoC | 764731 | c.1362G>C | synonymous_variant | 0.36 |
rpoC | 764737 | c.1368G>C | synonymous_variant | 0.36 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.4 |
rpoC | 764755 | p.Asp462Glu | missense_variant | 0.4 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.4 |
rpoC | 764760 | p.Asn464Ser | missense_variant | 0.33 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.33 |
rpoC | 764767 | c.1398G>T | synonymous_variant | 0.31 |
rpoC | 764776 | c.1407C>T | synonymous_variant | 0.36 |
rpoC | 764785 | c.1416C>T | synonymous_variant | 0.33 |
rpoC | 764791 | c.1422C>T | synonymous_variant | 0.31 |
rpoC | 764797 | c.1428G>T | synonymous_variant | 0.2 |
rpoC | 765923 | p.Asn852Ala | missense_variant | 0.17 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.23 |
rpoC | 765940 | c.2571A>T | synonymous_variant | 0.25 |
rpoC | 765947 | c.2578T>C | synonymous_variant | 0.23 |
rpoC | 765952 | c.2583G>C | synonymous_variant | 0.23 |
rpoC | 765958 | c.2589C>G | synonymous_variant | 0.23 |
rpoC | 765962 | c.2593T>C | synonymous_variant | 0.23 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.21 |
rpoC | 765988 | c.2619G>C | synonymous_variant | 0.21 |
rpoC | 765991 | c.2622C>G | synonymous_variant | 0.21 |
rpoC | 765994 | c.2625A>C | synonymous_variant | 0.21 |
rpoC | 766003 | c.2634G>C | synonymous_variant | 0.23 |
rpoC | 766009 | c.2640G>C | synonymous_variant | 0.2 |
rpoC | 766354 | c.2985C>G | synonymous_variant | 0.25 |
rpoC | 766366 | c.2997C>T | synonymous_variant | 0.22 |
rpoC | 766369 | c.3000C>G | synonymous_variant | 0.22 |
rpoC | 766378 | c.3009C>T | synonymous_variant | 0.25 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.29 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.29 |
rpoC | 766390 | c.3021C>T | synonymous_variant | 0.29 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.29 |
rpoC | 766429 | c.3060C>T | synonymous_variant | 0.29 |
rpoC | 766432 | c.3063T>C | synonymous_variant | 0.29 |
rpoC | 766434 | p.Glu1022Gly | missense_variant | 0.29 |
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 | 781616 | c.57C>G | synonymous_variant | 0.29 |
rpsL | 781623 | p.Ala22Pro | missense_variant | 0.29 |
rpsL | 781628 | c.69T>G | synonymous_variant | 0.25 |
rpsL | 781638 | c.79_80delAGinsTC | synonymous_variant | 0.22 |
rpsL | 781643 | c.84G>C | synonymous_variant | 0.22 |
rpsL | 781652 | c.93T>C | synonymous_variant | 0.25 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.29 |
rpsL | 781658 | c.99A>G | synonymous_variant | 0.25 |
rpsL | 781667 | c.108C>T | synonymous_variant | 0.25 |
rpsL | 781682 | c.123T>G | synonymous_variant | 0.25 |
rpsL | 781703 | c.144G>T | synonymous_variant | 0.22 |
rpsL | 781706 | c.147T>G | synonymous_variant | 0.22 |
rpsL | 781709 | c.150G>A | synonymous_variant | 0.25 |
rpsL | 781751 | c.192G>C | synonymous_variant | 0.38 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.46 |
rpsL | 781766 | c.207C>T | synonymous_variant | 0.5 |
rpsL | 781768 | p.Glu70Val | missense_variant | 0.21 |
rpsL | 781772 | c.213C>T | synonymous_variant | 0.18 |
rpsL | 781793 | c.234G>C | synonymous_variant | 0.14 |
rpsL | 781796 | p.Met79Ile | missense_variant | 0.53 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.53 |
rpsL | 781805 | c.246G>T | synonymous_variant | 0.32 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.57 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.52 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.52 |
rpsL | 781829 | c.270G>C | synonymous_variant | 0.2 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.47 |
rpsL | 781835 | c.276T>C | synonymous_variant | 0.26 |
rpsL | 781838 | c.279G>T | synonymous_variant | 0.17 |
rpsL | 781841 | c.282C>T | synonymous_variant | 0.29 |
rpsL | 781845 | p.Lys96Arg | missense_variant | 0.29 |
rpsL | 781851 | p.Ile98Val | missense_variant | 0.36 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.36 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.36 |
fbiC | 1305492 | c.2562T>C | synonymous_variant | 0.2 |
rrs | 1472068 | n.223T>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472285 | n.440A>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472396 | n.551A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472426 | n.581T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472427 | n.582T>G | non_coding_transcript_exon_variant | 0.4 |
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 | 1472447 | n.602C>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 | 1.0 |
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 | 1472484 | n.639_640insC | non_coding_transcript_exon_variant | 0.67 |
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 | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.16 |
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 | 0.61 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472687 | n.842_843insC | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472840 | n.995A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472875 | n.1030T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.23 |
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 | 0.98 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.98 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.98 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473101 | n.1256C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.41 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473163 | n.1318C>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473270 | n.1425G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473294 | n.1449A>G | non_coding_transcript_exon_variant | 0.59 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473305 | n.1460G>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474163 | n.506C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474183 | n.526T>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.91 |
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 | 1474363 | n.706A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474365 | n.708G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474383 | n.726G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474384 | n.727C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474487 | n.830G>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474497 | n.840G>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474503 | n.846G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474506 | n.849C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474517 | n.860C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474634 | n.977T>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474637 | n.980C>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474643 | n.986A>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474658 | n.1001A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474692 | n.1035G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474706 | n.1049G>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474717 | n.1060A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474734 | n.1077G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474806 | n.1149A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474819 | n.1162T>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474823 | n.1166C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474825 | n.1168G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474837 | n.1180A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475059 | n.1403_1404insTA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475062 | n.1405A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475065 | n.1409_1411delCAA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475079 | n.1422T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475080 | n.1425_1426delCC | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475104 | n.1447T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475124 | n.1467A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475171 | n.1514C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475703 | n.2046A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475715 | n.2058G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475756 | n.2099T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475767 | n.2110_2111insT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476130 | n.2473G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476164 | n.2507A>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476179 | n.2522C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476194 | n.2537A>T | 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 | 0.41 |
rrl | 1476204 | n.2547C>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476207 | n.2550T>C | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476267 | n.2610G>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.15 |
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 | 0.89 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476535 | n.2878G>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476536 | n.2879G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476594 | n.2937C>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476600 | n.2943A>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476603 | n.2946G>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476628 | n.2971T>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476633 | n.2976A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476664 | n.3007T>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476665 | n.3008T>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476668 | n.3011C>T | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.57 |
rpsA | 1833667 | c.126C>T | synonymous_variant | 0.57 |
rpsA | 1833668 | p.Ile43Val | missense_variant | 0.57 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.71 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.6 |
rpsA | 1833684 | p.Arg48His | missense_variant | 0.57 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 0.71 |
rpsA | 1833700 | c.159C>T | synonymous_variant | 0.67 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.83 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.83 |
rpsA | 1833732 | p.Pro64Leu | missense_variant | 0.8 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.6 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.8 |
rpsA | 1834189 | c.648G>T | synonymous_variant | 0.29 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.5 |
rpsA | 1834216 | c.675C>T | synonymous_variant | 0.25 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.75 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.7 |
rpsA | 1834246 | c.705G>T | synonymous_variant | 0.4 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.8 |
rpsA | 1834258 | c.717G>A | synonymous_variant | 0.25 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.91 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.83 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.55 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.55 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.55 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.55 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.55 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.5 |
rpsA | 1834345 | c.804C>T | synonymous_variant | 0.33 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.33 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.18 |
rpsA | 1834459 | c.918G>C | synonymous_variant | 0.2 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103227 | c.-185T>A | upstream_gene_variant | 0.2 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223053 | p.Glu38Lys | 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 |
pncA | 2289572 | c.-331C>A | upstream_gene_variant | 0.5 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449966 | p.Ala488Val | missense_variant | 0.25 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612674 | c.442delA | frameshift_variant | 0.15 |
fbiA | 3640522 | c.-20delG | upstream_gene_variant | 0.5 |
alr | 3841262 | c.159T>C | synonymous_variant | 0.4 |
alr | 3841473 | c.-53G>A | upstream_gene_variant | 1.0 |
clpC1 | 4038859 | p.Arg616Ser | missense_variant | 0.4 |
clpC1 | 4040010 | p.Ala232Arg | missense_variant | 0.29 |
clpC1 | 4040015 | c.690G>C | synonymous_variant | 0.29 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.33 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.33 |
clpC1 | 4040036 | c.669C>T | synonymous_variant | 0.33 |
clpC1 | 4040063 | c.642G>C | synonymous_variant | 0.29 |
clpC1 | 4040066 | c.639G>C | synonymous_variant | 0.33 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embB | 4247507 | p.Trp332Arg | missense_variant | 0.29 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |