Run ID: ERR2509886
Sample name:
Date: 31-03-2023 18:32:56
Number of reads: 408496
Percentage reads mapped: 61.54
Strain: lineage3
Drug-resistance: RR-TB
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 |
---|---|---|---|---|---|
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.25 | rifampicin |
rpoB | 761196 | p.Leu464Met | missense_variant | 0.12 | rifampicin |
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.13 | streptomycin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.33 | streptomycin |
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 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.12 |
rpoB | 761030 | c.1224G>C | synonymous_variant | 0.16 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.24 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.19 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.18 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.18 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.18 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.15 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.19 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 0.19 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.2 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.25 |
rpoB | 761123 | c.1317G>C | synonymous_variant | 0.12 |
rpoB | 761126 | c.1320G>C | synonymous_variant | 0.17 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.22 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.25 |
rpoB | 761150 | c.1344A>T | synonymous_variant | 0.17 |
rpoB | 761159 | c.1353G>C | synonymous_variant | 0.22 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.22 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.13 |
rpoB | 761186 | p.Glu460Asp | missense_variant | 0.13 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.12 |
rpoB | 761954 | c.2148C>T | synonymous_variant | 1.0 |
rpoB | 762134 | c.2328C>T | synonymous_variant | 0.14 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.25 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.25 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.21 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.15 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.22 |
rpoB | 762177 | p.Arg791Thr | missense_variant | 0.22 |
rpoB | 762181 | p.Asp792Ala | missense_variant | 0.22 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.22 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.24 |
rpoB | 762200 | c.2394C>T | synonymous_variant | 0.19 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.19 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.25 |
rpoB | 762234 | p.Pro810Ser | missense_variant | 0.25 |
rpoB | 762239 | c.2433G>A | synonymous_variant | 0.25 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.36 |
rpoB | 762248 | c.2442G>C | synonymous_variant | 0.18 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.4 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763043 | c.-327G>C | upstream_gene_variant | 0.17 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.14 |
rpoC | 763067 | c.-303C>G | upstream_gene_variant | 0.13 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.13 |
rpoB | 763077 | p.Val1091Thr | missense_variant | 0.14 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.14 |
rpoC | 763109 | c.-261C>T | upstream_gene_variant | 0.13 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.14 |
rpoB | 763119 | p.Asn1105Asp | missense_variant | 0.15 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.13 |
rpoC | 763133 | c.-237G>C | upstream_gene_variant | 0.14 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.12 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.18 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.2 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.27 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.18 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.23 |
rpoC | 763550 | p.Tyr61Ala | missense_variant | 0.23 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.31 |
rpoC | 763578 | p.Phe70Tyr | missense_variant | 0.36 |
rpoC | 763606 | c.237C>A | synonymous_variant | 0.18 |
rpoC | 763615 | c.246G>C | synonymous_variant | 0.23 |
rpoC | 763618 | c.249C>T | synonymous_variant | 0.14 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 0.27 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.2 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.14 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.38 |
rpoC | 763647 | p.Gly93Ala | missense_variant | 0.12 |
rpoC | 763655 | p.Glu96Asn | missense_variant | 0.11 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.33 |
rpoC | 763666 | c.297G>C | synonymous_variant | 0.35 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.32 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.4 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.44 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.38 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.38 |
rpoC | 763718 | p.Leu117Val | missense_variant | 0.31 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.38 |
rpoC | 763724 | p.Asp119Asn | missense_variant | 0.38 |
rpoC | 763729 | c.360G>C | synonymous_variant | 0.38 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.38 |
rpoC | 763735 | c.366G>C | synonymous_variant | 0.38 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.36 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.46 |
rpoC | 763772 | p.Val135Met | missense_variant | 0.4 |
rpoC | 763781 | p.Ser138Glu | missense_variant | 0.36 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.38 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.36 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.42 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.15 |
rpoC | 764503 | c.1134G>T | synonymous_variant | 0.27 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.42 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.29 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.29 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 0.24 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.32 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.14 |
rpoC | 764543 | p.Thr392Ala | missense_variant | 0.27 |
rpoC | 764548 | c.1179G>C | synonymous_variant | 0.35 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.29 |
rpoC | 764572 | c.1203G>C | synonymous_variant | 0.13 |
rpoC | 764573 | p.Leu402Ile | missense_variant | 0.35 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.35 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.43 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.43 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.35 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.24 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.46 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.44 |
rpoC | 764620 | c.1251G>C | synonymous_variant | 0.2 |
rpoC | 764623 | c.1254C>G | synonymous_variant | 0.12 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.25 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.33 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.27 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.33 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.36 |
rpoC | 764656 | c.1287C>T | synonymous_variant | 0.25 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.38 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.26 |
rpoC | 764678 | p.Lys437Gln | missense_variant | 0.26 |
rpoC | 764683 | c.1314G>C | synonymous_variant | 0.2 |
rpoC | 764692 | c.1323C>T | synonymous_variant | 0.28 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.27 |
rpoC | 764731 | c.1362G>C | synonymous_variant | 0.14 |
rpoC | 764737 | c.1368G>C | synonymous_variant | 0.14 |
rpoC | 764746 | c.1377G>C | synonymous_variant | 0.16 |
rpoC | 764749 | c.1380G>C | synonymous_variant | 0.11 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.11 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.12 |
rpoC | 765988 | c.2619G>C | synonymous_variant | 0.14 |
rpoC | 765991 | c.2622C>G | synonymous_variant | 0.14 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.14 |
rpoC | 766003 | c.2634G>C | synonymous_variant | 0.11 |
rpoC | 766009 | c.2640G>C | synonymous_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpS5 | 778970 | c.-65A>G | upstream_gene_variant | 0.17 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.11 |
rpsL | 781835 | c.276T>C | synonymous_variant | 0.11 |
fbiC | 1305067 | p.Val713Met | missense_variant | 0.12 |
atpE | 1461086 | c.42A>G | synonymous_variant | 0.33 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472686 | n.841G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472707 | n.862A>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.34 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472954 | n.1109T>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472973 | n.1128A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472974 | n.1129A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472992 | n.1147A>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473101 | n.1256C>T | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.66 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.66 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.54 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.66 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 0.63 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.51 |
rrs | 1473294 | n.1449A>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1473384 | n.-274A>G | upstream_gene_variant | 0.26 |
rrl | 1473534 | n.-124T>A | upstream_gene_variant | 0.12 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474901 | n.1244A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474921 | n.1264C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475713 | n.2056C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475751 | n.2094C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475757 | n.2101_2104delACCC | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476429 | n.2772A>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476542 | n.2885T>C | non_coding_transcript_exon_variant | 0.12 |
fabG1 | 1673800 | p.Gln121Lys | missense_variant | 0.14 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.17 |
rpsA | 1833884 | p.Thr115Asp | missense_variant | 0.16 |
rpsA | 1833893 | p.Ala118Lys | missense_variant | 0.16 |
rpsA | 1833896 | p.Leu119Ile | missense_variant | 0.17 |
rpsA | 1833905 | p.Lys122Glu | missense_variant | 0.22 |
rpsA | 1833912 | p.Glu124Gly | missense_variant | 0.21 |
rpsA | 1833915 | p.Ala125Val | missense_variant | 0.21 |
rpsA | 1833920 | p.Lys127Glu | missense_variant | 0.17 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.21 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.19 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 0.24 |
rpsA | 1833961 | c.420C>G | synonymous_variant | 0.17 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.22 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.23 |
rpsA | 1833985 | c.444G>C | synonymous_variant | 0.11 |
rpsA | 1833988 | c.447C>G | synonymous_variant | 0.11 |
rpsA | 1833994 | c.453G>C | synonymous_variant | 0.12 |
rpsA | 1833997 | c.456G>C | synonymous_variant | 0.12 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.24 |
rpsA | 1834024 | c.483G>C | synonymous_variant | 0.14 |
rpsA | 1834040 | p.Lys167Gln | missense_variant | 0.14 |
rpsA | 1834046 | p.Ile169Leu | missense_variant | 0.13 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.13 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.11 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.11 |
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 |
PPE35 | 2170082 | c.531T>G | synonymous_variant | 0.4 |
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 |
eis | 2715193 | p.Val47Glu | missense_variant | 0.15 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
pepQ | 2859578 | p.Ile281Leu | missense_variant | 0.15 |
Rv2752c | 3065602 | p.Asp197Gly | missense_variant | 0.18 |
thyA | 3073756 | p.Phe239Ser | missense_variant | 0.17 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
Rv3083 | 3449883 | p.Trp460* | stop_gained | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474809 | p.Val268Ala | missense_variant | 0.15 |
Rv3236c | 3612835 | c.282T>G | synonymous_variant | 0.29 |
alr | 3841473 | c.-53G>A | upstream_gene_variant | 1.0 |
ddn | 3986878 | c.36delG | frameshift_variant | 1.0 |
embC | 4240648 | c.786C>T | synonymous_variant | 0.25 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245927 | p.Thr899Ala | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407775 | p.Asp143Gly | missense_variant | 1.0 |