Run ID: ERR9285979
Sample name:
Date: 02-04-2023 11:48:21
Number of reads: 2979905
Percentage reads mapped: 81.33
Strain: lineage3.1.1
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
lineage3.1 | East-African-Indian | Non-CAS1-Delhi | RD750 | 1.0 |
lineage3.1.1 | East-African-Indian | CAS1-Kili | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761099 | p.Ser431Arg | missense_variant | 0.11 | rifampicin |
rpoB | 761196 | p.Leu464Met | missense_variant | 0.13 | rifampicin |
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.24 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.21 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.17 | 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 | 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 | 761123 | c.1317G>C | synonymous_variant | 0.16 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.16 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.16 |
rpoB | 761138 | c.1332C>G | synonymous_variant | 0.17 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.15 |
rpoB | 761150 | c.1344A>T | synonymous_variant | 0.16 |
rpoB | 761156 | c.1350G>C | synonymous_variant | 0.16 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.16 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.16 |
rpoB | 761171 | c.1365C>T | synonymous_variant | 0.16 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.16 |
rpoB | 761186 | p.Glu460Asp | missense_variant | 0.15 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.12 |
rpoB | 761204 | c.1398C>T | synonymous_variant | 0.12 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.12 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.12 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.11 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.11 |
rpoB | 762209 | c.2403C>G | synonymous_variant | 0.12 |
rpoB | 762212 | c.2406G>C | synonymous_variant | 0.12 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.12 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.1 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.11 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.11 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.16 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.16 |
rpoC | 762995 | c.-375G>C | upstream_gene_variant | 0.17 |
rpoB | 763005 | p.Cys1067Val | missense_variant | 0.17 |
rpoB | 763014 | p.Met1070Leu | missense_variant | 0.19 |
rpoB | 763017 | p.Gln1071Glu | missense_variant | 0.19 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.19 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.24 |
rpoC | 763053 | c.-317_-315delTTGinsCTC | upstream_gene_variant | 0.22 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.19 |
rpoB | 763074 | p.Thr1090Val | missense_variant | 0.19 |
rpoB | 763077 | p.Val1091Pro | missense_variant | 0.15 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.16 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.13 |
rpoC | 764491 | c.1122G>C | synonymous_variant | 0.13 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.12 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.12 |
rpoC | 764551 | c.1182G>T | synonymous_variant | 0.12 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.15 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.14 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.14 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.14 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.13 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.14 |
rpoC | 764620 | c.1251G>C | synonymous_variant | 0.13 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.15 |
rpoC | 764644 | c.1275G>C | synonymous_variant | 0.19 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.18 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.18 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.15 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.18 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.15 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.12 |
rpoC | 764759 | p.Asn464Asp | missense_variant | 0.12 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.12 |
rpoC | 764780 | p.Ser471Cys | missense_variant | 0.11 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpR5 | 778451 | c.-539C>T | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472288 | n.443A>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472289 | n.444T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472290 | n.445C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472293 | n.448C>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472326 | n.481T>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472582 | n.737G>A | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472591 | n.746G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472597 | n.752G>A | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472674 | n.829T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472685 | n.840G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473122 | n.1277T>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473127 | n.1282G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474253 | n.596A>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474583 | n.926C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474664 | n.1007G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474676 | n.1019T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474823 | n.1166C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474830 | n.1173A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474869 | n.1212G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474904 | n.1247G>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475696 | n.2039T>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475697 | n.2040C>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475702 | n.2045G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475703 | n.2046A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475740 | n.2083G>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475747 | n.2090A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475758 | n.2101A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475764 | n.2107A>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475766 | n.2109G>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475781 | n.2124T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475788 | n.2131C>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476213 | n.2556G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476251 | n.2594T>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476288 | n.2631T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.1 |
rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.13 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.13 |
rpsA | 1833994 | c.453G>C | synonymous_variant | 0.12 |
rpsA | 1833997 | c.456G>C | synonymous_variant | 0.12 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.12 |
rpsA | 1834009 | c.468C>T | synonymous_variant | 0.12 |
rpsA | 1834012 | c.471G>T | synonymous_variant | 0.12 |
rpsA | 1834024 | c.483G>C | synonymous_variant | 0.12 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.13 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 0.12 |
rpsA | 1834039 | c.498C>A | synonymous_variant | 0.12 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.12 |
rpsA | 1834336 | c.795C>G | synonymous_variant | 0.12 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.12 |
rpsA | 1834395 | p.Arg285Gln | missense_variant | 0.12 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.1 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.11 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.11 |
rpsA | 1834427 | p.Ile296Val | 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 | 2170461 | p.Gly51Glu | 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 | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
clpC1 | 4039586 | c.1119G>C | synonymous_variant | 0.11 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.13 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.13 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.11 |
clpC1 | 4040063 | c.642G>C | synonymous_variant | 0.11 |
clpC1 | 4040069 | c.636G>C | synonymous_variant | 0.11 |
clpC1 | 4040087 | c.618G>C | synonymous_variant | 0.11 |
clpC1 | 4040090 | c.615T>C | synonymous_variant | 0.12 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.11 |
embC | 4240172 | p.Val104Met | missense_variant | 1.0 |
embC | 4241562 | p.Arg567His | missense_variant | 1.0 |
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 | 1.0 |