Run ID: SRR8692893
Sample name:
Date: 13-08-2023 19:59:47
Number of reads: NA
Percentage reads mapped: NA
Strain: lineage4.9
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.99 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.96 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rplC | 801268 | p.Cys154Arg | missense_variant | 0.71 | linezolid |
pncA | 2289081 | p.Pro54Gln | missense_variant | 0.14 | pyrazinamide |
pncA | 2289105 | p.Ala46Glu | missense_variant | 0.14 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6799 | c.-503C>A | upstream_gene_variant | 0.15 |
gyrA | 6826 | c.-476G>T | upstream_gene_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 0.33 |
gyrA | 7524 | c.223C>A | synonymous_variant | 0.25 |
gyrA | 7541 | c.240C>A | synonymous_variant | 0.29 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 0.29 |
gyrA | 7592 | c.291G>C | synonymous_variant | 0.25 |
gyrA | 7595 | c.294C>G | synonymous_variant | 0.25 |
gyrA | 7607 | c.306C>G | synonymous_variant | 0.25 |
gyrA | 7631 | c.330G>C | synonymous_variant | 0.3 |
gyrA | 7637 | c.336C>T | synonymous_variant | 0.33 |
gyrA | 7658 | c.357A>G | synonymous_variant | 0.33 |
gyrA | 7661 | c.360C>T | synonymous_variant | 0.33 |
gyrA | 7664 | c.363T>C | synonymous_variant | 0.33 |
gyrA | 7670 | c.369A>G | synonymous_variant | 0.33 |
gyrA | 7676 | c.375G>C | synonymous_variant | 0.33 |
gyrA | 7679 | c.378G>C | synonymous_variant | 0.33 |
gyrA | 7683 | c.382_384delAGGinsCGC | synonymous_variant | 0.3 |
gyrA | 7694 | c.393A>G | synonymous_variant | 0.27 |
gyrA | 7700 | c.399G>T | synonymous_variant | 0.25 |
gyrA | 7706 | c.405C>T | synonymous_variant | 0.17 |
gyrA | 7709 | c.408G>A | synonymous_variant | 0.17 |
gyrA | 7710 | c.409T>C | synonymous_variant | 0.17 |
gyrA | 7715 | c.414G>C | synonymous_variant | 0.17 |
gyrA | 7728 | c.427_429delAGGinsCGT | synonymous_variant | 0.15 |
gyrA | 8016 | p.Gly239Cys | missense_variant | 0.15 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 0.18 |
gyrA | 9218 | c.1917C>T | synonymous_variant | 0.29 |
gyrA | 9230 | c.1929T>C | synonymous_variant | 0.29 |
gyrA | 9236 | c.1935G>C | synonymous_variant | 0.29 |
gyrA | 9242 | c.1941A>C | synonymous_variant | 0.25 |
gyrA | 9248 | c.1947G>C | synonymous_variant | 0.22 |
gyrA | 9252 | p.Val651Ile | missense_variant | 0.2 |
gyrA | 9266 | p.Asp655Glu | missense_variant | 0.22 |
gyrA | 9267 | p.Asn656Gly | missense_variant | 0.25 |
gyrA | 9275 | c.1974G>A | synonymous_variant | 0.22 |
gyrA | 9296 | c.1995T>C | synonymous_variant | 0.2 |
gyrA | 9299 | c.1998G>C | synonymous_variant | 0.22 |
gyrA | 9304 | p.Gly668Glu | missense_variant | 0.22 |
gyrA | 9311 | c.2010C>T | synonymous_variant | 0.22 |
gyrA | 9324 | c.2023_2025delTCGinsAGC | synonymous_variant | 0.2 |
gyrA | 9335 | c.2034G>T | synonymous_variant | 0.17 |
gyrA | 9345 | c.2044A>C | synonymous_variant | 0.17 |
gyrA | 9783 | p.Val828Met | missense_variant | 0.22 |
fgd1 | 491019 | p.Phe79Leu | missense_variant | 0.18 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.27 |
mshA | 575166 | c.-182G>T | upstream_gene_variant | 0.2 |
mshA | 575240 | c.-108G>T | upstream_gene_variant | 0.2 |
mshA | 576476 | p.Leu377Met | missense_variant | 0.17 |
mshA | 576508 | c.1161C>A | synonymous_variant | 0.14 |
rpoB | 760172 | c.366G>C | synonymous_variant | 0.14 |
rpoB | 760181 | c.375T>G | synonymous_variant | 0.15 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.15 |
rpoB | 760234 | p.Ser143Ile | missense_variant | 0.14 |
rpoB | 760244 | c.438G>C | synonymous_variant | 0.14 |
rpoB | 760256 | c.450C>T | synonymous_variant | 0.18 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.17 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.17 |
rpoB | 760502 | c.696C>G | synonymous_variant | 0.12 |
rpoB | 760508 | c.702G>C | synonymous_variant | 0.13 |
rpoB | 760511 | c.705G>C | synonymous_variant | 0.19 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.19 |
rpoB | 760532 | c.726T>C | synonymous_variant | 0.27 |
rpoB | 760535 | c.729C>G | synonymous_variant | 0.29 |
rpoB | 760541 | c.735G>C | synonymous_variant | 0.27 |
rpoB | 760547 | c.741G>C | synonymous_variant | 0.25 |
rpoB | 760561 | c.757_758delCG | frameshift_variant | 0.25 |
rpoB | 760567 | p.Ser254Trp | missense_variant | 0.27 |
rpoB | 760568 | c.762_763insGC | frameshift_variant | 0.27 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.33 |
rpoB | 760601 | c.795C>T | synonymous_variant | 0.2 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.22 |
rpoB | 761051 | c.1245G>T | synonymous_variant | 0.15 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.17 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.17 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.17 |
rpoB | 761063 | c.1257C>G | synonymous_variant | 0.17 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.2 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.17 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.22 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.24 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.19 |
rpoB | 761150 | c.1344A>T | synonymous_variant | 0.19 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.2 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.21 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.15 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.15 |
rpoB | 761198 | c.1392G>T | synonymous_variant | 0.2 |
rpoB | 761217 | p.Pro471Ser | missense_variant | 0.19 |
rpoB | 761220 | c.1414_1416delTCGinsAGC | synonymous_variant | 0.17 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.17 |
rpoB | 761261 | c.1455G>C | synonymous_variant | 0.17 |
rpoB | 761264 | c.1458C>G | synonymous_variant | 0.17 |
rpoB | 761655 | p.Ala617Ser | missense_variant | 0.18 |
rpoB | 761990 | c.2184G>C | synonymous_variant | 0.2 |
rpoB | 761999 | c.2193G>C | synonymous_variant | 0.2 |
rpoB | 762002 | c.2196C>G | synonymous_variant | 0.22 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.12 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.12 |
rpoC | 762596 | c.-774G>T | upstream_gene_variant | 0.5 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.15 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.12 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.15 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.17 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.17 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.2 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.18 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.18 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.31 |
rpoC | 762989 | c.-381G>A | upstream_gene_variant | 0.31 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.29 |
rpoC | 763004 | c.-366G>A | upstream_gene_variant | 0.21 |
rpoC | 763007 | c.-363C>T | upstream_gene_variant | 0.21 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.12 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.14 |
rpoC | 763414 | c.45T>G | synonymous_variant | 0.12 |
rpoC | 763423 | p.Glu18Asp | missense_variant | 0.12 |
rpoC | 763430 | c.61_63delAGGinsCGC | synonymous_variant | 0.15 |
rpoC | 763433 | p.Gln22Asn | missense_variant | 0.15 |
rpoC | 763443 | p.Tyr25Phe | missense_variant | 0.14 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.2 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.17 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.17 |
rpoC | 763495 | c.126G>A | synonymous_variant | 0.15 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.13 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.12 |
rpoC | 764071 | c.702G>C | synonymous_variant | 0.12 |
rpoC | 764077 | c.708C>G | synonymous_variant | 0.13 |
rpoC | 764083 | c.714A>G | synonymous_variant | 0.14 |
rpoC | 764084 | p.Asn239Val | missense_variant | 0.15 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.17 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.4 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 0.5 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.2 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.22 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.2 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.18 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.2 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.18 |
rpoC | 764500 | c.1131C>G | synonymous_variant | 0.18 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.17 |
rpoC | 764527 | c.1158C>T | synonymous_variant | 0.17 |
rpoC | 764530 | c.1161C>T | synonymous_variant | 0.17 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.18 |
rpoC | 764602 | c.1233C>A | synonymous_variant | 0.17 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.15 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.15 |
rpoC | 764719 | c.1350G>A | synonymous_variant | 0.25 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.3 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.33 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.33 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.33 |
rpoC | 764800 | c.1431G>A | synonymous_variant | 0.6 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.5 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.5 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.4 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.33 |
rpoC | 765808 | p.Gln813His | missense_variant | 0.33 |
rpoC | 766171 | c.2802C>A | synonymous_variant | 0.18 |
rpoC | 766632 | p.Val1088Ala | missense_variant | 0.12 |
rpoC | 767155 | c.3786C>G | synonymous_variant | 0.18 |
rpoC | 767162 | p.Asn1265Ala | missense_variant | 0.17 |
rpoC | 767173 | c.3804C>G | synonymous_variant | 0.17 |
rpoC | 767174 | p.Asn1269Asp | missense_variant | 0.17 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.17 |
rpoC | 767185 | c.3816G>C | synonymous_variant | 0.17 |
rpoC | 767186 | p.Gln1273Asn | missense_variant | 0.17 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.17 |
rpoC | 767197 | c.3828G>A | synonymous_variant | 0.18 |
rpoC | 767221 | c.3852C>G | synonymous_variant | 0.17 |
mmpL5 | 775758 | p.Thr908Asn | missense_variant | 0.22 |
mmpL5 | 775768 | p.Gln905Lys | missense_variant | 0.27 |
mmpL5 | 777121 | p.His454Asn | missense_variant | 0.14 |
mmpL5 | 777232 | p.Asp417Tyr | missense_variant | 0.22 |
mmpL5 | 778227 | p.Gly85Glu | missense_variant | 0.13 |
mmpS5 | 778537 | p.Lys123Asn | missense_variant | 0.14 |
mmpR5 | 779215 | p.Gln76Lys | missense_variant | 0.14 |
mmpR5 | 779359 | p.Ala124Thr | missense_variant | 0.18 |
mmpR5 | 779449 | p.Leu154Met | missense_variant | 0.13 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.17 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.14 |
rplC | 800628 | c.-181G>C | upstream_gene_variant | 0.15 |
rplC | 800633 | c.-176T>C | upstream_gene_variant | 0.17 |
rplC | 800639 | c.-170C>T | upstream_gene_variant | 0.15 |
rplC | 800759 | c.-50C>A | upstream_gene_variant | 0.25 |
fbiC | 1302956 | p.Ser9Tyr | missense_variant | 0.17 |
fbiC | 1303097 | p.Ala56Asp | missense_variant | 0.22 |
fbiC | 1303367 | p.Thr146Asn | missense_variant | 0.18 |
fbiC | 1303503 | c.573G>C | synonymous_variant | 0.17 |
fbiC | 1303509 | c.579G>C | synonymous_variant | 0.17 |
fbiC | 1303512 | c.582T>G | synonymous_variant | 0.17 |
fbiC | 1303525 | p.Ser199Thr | missense_variant | 0.18 |
fbiC | 1303531 | p.Met201Leu | missense_variant | 0.17 |
fbiC | 1303536 | c.606G>C | synonymous_variant | 0.14 |
fbiC | 1303542 | c.612C>G | synonymous_variant | 0.13 |
fbiC | 1303548 | c.618G>C | synonymous_variant | 0.13 |
fbiC | 1303806 | c.876G>T | synonymous_variant | 0.25 |
fbiC | 1303992 | p.Trp354Cys | missense_variant | 0.2 |
fbiC | 1304746 | p.Asp606Tyr | missense_variant | 0.17 |
fbiC | 1305310 | p.Arg794Trp | missense_variant | 0.25 |
Rv1258c | 1406113 | p.Asp410Tyr | missense_variant | 0.22 |
Rv1258c | 1406686 | p.Val219Ile | missense_variant | 1.0 |
embR | 1416382 | p.Ser322Arg | missense_variant | 0.29 |
embR | 1416535 | c.813C>T | synonymous_variant | 0.14 |
embR | 1416668 | p.Ala227Val | missense_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471931 | n.87delA | non_coding_transcript_exon_variant | 0.17 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1471979 | n.134T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472019 | n.174G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472023 | n.178G>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472029 | n.184C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472030 | n.185G>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472033 | n.188A>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472035 | n.190G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472040 | n.195T>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472043 | n.198T>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472102 | n.257G>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472204 | n.359G>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472206 | n.361G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472289 | n.444T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472290 | n.445C>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472324 | n.479G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472337 | n.492C>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472380 | n.535G>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472502 | n.657G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472847 | n.1002G>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472848 | n.1003T>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472849 | n.1004C>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472850 | n.1005T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472857 | n.1012A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472858 | n.1013G>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472859 | n.1014G>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472860 | n.1015C>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.45 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473515 | n.-143G>T | upstream_gene_variant | 0.25 |
rrl | 1473554 | n.-104G>T | upstream_gene_variant | 0.2 |
rrl | 1473633 | n.-25C>A | upstream_gene_variant | 0.22 |
rrl | 1473668 | n.11C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473697 | n.40C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473717 | n.60G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473746 | n.89T>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1473757 | n.100T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1473814 | n.157A>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473815 | n.158T>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473816 | n.159C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473828 | n.171G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473829 | n.172G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473830 | n.173T>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473831 | n.174G>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474011 | n.354G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474135 | n.478G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474185 | n.528G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474232 | n.575C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474473 | n.816C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474552 | n.895C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474672 | n.1015C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474753 | n.1096A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474810 | n.1153G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474888 | n.1231C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474946 | n.1289C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475108 | n.1451C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475358 | n.1701T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475363 | n.1706C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475380 | n.1723C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475381 | n.1724G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475382 | n.1725A>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475395 | n.1738T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475396 | n.1739C>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475397 | n.1740G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475402 | n.1745C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475544 | n.1887A>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1475759 | n.2102C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475764 | n.2107A>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475775 | n.2118G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1475991 | n.2334T>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475995 | n.2338G>A | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476018 | n.2361G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476088 | n.2431A>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476095 | n.2438C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476105 | n.2448G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476106 | n.2449A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476259 | n.2602C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476583 | n.2926G>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476674 | n.3017T>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476679 | n.3022T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476689 | n.3032A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476690 | n.3033C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476693 | n.3036G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476695 | n.3038T>A | non_coding_transcript_exon_variant | 0.2 |
fabG1 | 1673324 | c.-116G>T | upstream_gene_variant | 0.21 |
inhA | 1674228 | c.27G>T | synonymous_variant | 0.2 |
inhA | 1674376 | p.Pro59Thr | missense_variant | 0.17 |
inhA | 1674659 | p.Arg153Leu | missense_variant | 0.13 |
inhA | 1674835 | p.Gly212Arg | missense_variant | 0.18 |
rpsA | 1833595 | c.54T>G | synonymous_variant | 0.14 |
rpsA | 1833596 | p.Ser19Ala | missense_variant | 0.14 |
rpsA | 1833616 | c.75A>G | synonymous_variant | 0.14 |
rpsA | 1833619 | c.78A>C | synonymous_variant | 0.14 |
rpsA | 1833625 | c.84A>G | synonymous_variant | 0.13 |
rpsA | 1833628 | c.87G>C | synonymous_variant | 0.13 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.19 |
rpsA | 1833679 | c.138G>C | synonymous_variant | 0.19 |
rpsA | 1833685 | c.144G>T | synonymous_variant | 0.19 |
rpsA | 1833694 | c.153G>T | synonymous_variant | 0.19 |
rpsA | 1833697 | c.156C>G | synonymous_variant | 0.18 |
rpsA | 1833703 | c.162C>T | synonymous_variant | 0.19 |
rpsA | 1833709 | c.168C>T | synonymous_variant | 0.17 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.14 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.17 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.17 |
rpsA | 1833793 | c.252C>T | synonymous_variant | 0.17 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.19 |
rpsA | 1833808 | c.267G>C | synonymous_variant | 0.19 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.17 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 0.2 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 0.2 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.19 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.19 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.18 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.18 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.17 |
rpsA | 1833892 | c.351G>A | synonymous_variant | 0.17 |
rpsA | 1833894 | p.Ala118Glu | missense_variant | 0.17 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.2 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.18 |
rpsA | 1833976 | c.435C>T | synonymous_variant | 0.18 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.18 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.2 |
rpsA | 1834213 | c.672G>C | synonymous_variant | 0.15 |
rpsA | 1834216 | p.Phe225Leu | missense_variant | 0.15 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.14 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.14 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.23 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.23 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.25 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.25 |
rpsA | 1834279 | c.738C>T | synonymous_variant | 0.22 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.21 |
rpsA | 1834298 | p.Gln253Thr | missense_variant | 0.21 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.22 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.22 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.2 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.19 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.19 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.26 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.22 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.19 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.2 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.22 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.19 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.19 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.19 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.17 |
rpsA | 1834513 | c.972C>G | synonymous_variant | 0.26 |
rpsA | 1834520 | p.Ala327Ser | missense_variant | 0.23 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.21 |
rpsA | 1834540 | c.999G>C | synonymous_variant | 0.21 |
rpsA | 1834543 | c.1002C>G | synonymous_variant | 0.21 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.21 |
rpsA | 1834554 | c.1014_1015delTG | frameshift_variant | 0.21 |
rpsA | 1834558 | c.1017_1018insAG | frameshift_variant | 0.22 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 0.26 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.26 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 0.25 |
rpsA | 1834622 | c.1081_1083delTCGinsAGC | synonymous_variant | 0.25 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.28 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.28 |
rpsA | 1834666 | c.1125G>C | synonymous_variant | 0.18 |
rpsA | 1834667 | p.Ala376Ser | missense_variant | 0.18 |
rpsA | 1834690 | c.1149T>C | synonymous_variant | 0.2 |
rpsA | 1834700 | p.Gln387Ala | missense_variant | 0.22 |
rpsA | 1834705 | c.1164C>G | synonymous_variant | 0.22 |
rpsA | 1834732 | c.1191T>C | synonymous_variant | 0.2 |
tlyA | 1918247 | p.Arg103His | missense_variant | 0.18 |
ndh | 2102575 | p.Glu156Asp | missense_variant | 0.2 |
katG | 2153975 | p.Ala713Ser | missense_variant | 0.2 |
katG | 2154439 | p.Ala558Glu | missense_variant | 0.29 |
katG | 2155452 | c.660G>T | synonymous_variant | 0.22 |
katG | 2155471 | p.Arg214Leu | missense_variant | 0.2 |
katG | 2155626 | c.486G>A | synonymous_variant | 0.33 |
katG | 2155800 | c.312G>A | synonymous_variant | 0.14 |
katG | 2156334 | c.-223G>T | upstream_gene_variant | 0.38 |
katG | 2156560 | c.-449C>A | upstream_gene_variant | 0.19 |
PPE35 | 2168178 | p.Pro812Leu | missense_variant | 0.29 |
PPE35 | 2170046 | c.567C>A | synonymous_variant | 0.5 |
PPE35 | 2170568 | p.Ile15Met | missense_variant | 0.33 |
Rv1979c | 2222560 | p.Ala202Glu | missense_variant | 0.22 |
Rv1979c | 2223022 | p.Pro48Gln | missense_variant | 0.22 |
Rv1979c | 2223031 | p.Pro45His | missense_variant | 0.25 |
Rv1979c | 2223059 | p.Pro36Thr | missense_variant | 0.25 |
Rv1979c | 2223250 | c.-86C>A | upstream_gene_variant | 0.14 |
Rv1979c | 2223262 | c.-98C>A | upstream_gene_variant | 0.14 |
Rv1979c | 2223275 | c.-111C>A | upstream_gene_variant | 0.13 |
kasA | 2517941 | c.-174C>G | upstream_gene_variant | 0.16 |
kasA | 2518315 | c.201G>T | synonymous_variant | 0.17 |
kasA | 2518527 | p.Ser138Tyr | missense_variant | 0.14 |
kasA | 2518946 | p.Val278Leu | missense_variant | 0.29 |
eis | 2714337 | p.Lys332Asn | missense_variant | 0.14 |
eis | 2714871 | c.462G>T | synonymous_variant | 0.2 |
ahpC | 2726323 | p.Pro44Gln | missense_variant | 0.13 |
folC | 2746692 | p.Val303Leu | missense_variant | 0.18 |
folC | 2746794 | p.Gln269Lys | missense_variant | 0.5 |
folC | 2746918 | c.681G>T | synonymous_variant | 0.2 |
pepQ | 2859548 | p.Gly291Cys | missense_variant | 0.2 |
pepQ | 2859557 | p.Glu288* | stop_gained | 0.2 |
pepQ | 2859940 | p.Arg160Leu | missense_variant | 0.14 |
pepQ | 2860422 | c.-4G>T | upstream_gene_variant | 0.17 |
ribD | 2987533 | p.Gly232Val | missense_variant | 0.25 |
Rv2752c | 3064895 | p.Ala433Thr | missense_variant | 0.18 |
Rv2752c | 3065931 | c.261C>T | synonymous_variant | 0.29 |
thyA | 3074037 | c.435C>A | synonymous_variant | 0.18 |
ald | 3087767 | c.948G>T | synonymous_variant | 0.2 |
fbiD | 3339332 | p.Ala72Glu | missense_variant | 0.13 |
Rv3083 | 3448358 | c.-146G>T | upstream_gene_variant | 0.15 |
Rv3083 | 3449030 | p.Ser176Tyr | missense_variant | 0.4 |
Rv3083 | 3449063 | p.Ala187Glu | missense_variant | 0.18 |
Rv3083 | 3449507 | p.Arg335Leu | missense_variant | 0.14 |
Rv3083 | 3449682 | c.1179G>A | synonymous_variant | 0.2 |
fprA | 3475046 | p.Arg347Leu | missense_variant | 0.15 |
Rv3236c | 3611991 | p.Gly376Trp | missense_variant | 0.14 |
Rv3236c | 3612577 | p.Glu180Asp | missense_variant | 0.17 |
Rv3236c | 3612871 | p.Phe82Leu | missense_variant | 0.18 |
fbiB | 3641939 | c.405G>T | synonymous_variant | 0.4 |
fbiB | 3642030 | p.Gly166Cys | missense_variant | 0.25 |
fbiB | 3642164 | c.630C>A | synonymous_variant | 0.33 |
fbiB | 3642627 | p.Arg365Ser | missense_variant | 0.17 |
alr | 3840333 | p.Ala363Glu | missense_variant | 0.15 |
alr | 3841180 | p.Ala81Thr | missense_variant | 0.22 |
alr | 3841458 | c.-38G>T | upstream_gene_variant | 0.14 |
ddn | 3986794 | c.-50G>T | upstream_gene_variant | 0.33 |
ddn | 3987192 | p.Glu117* | stop_gained | 0.25 |
clpC1 | 4038318 | p.Pro796Gln | missense_variant | 0.15 |
clpC1 | 4038647 | c.2058T>C | synonymous_variant | 0.15 |
clpC1 | 4038650 | c.2055C>T | synonymous_variant | 0.15 |
clpC1 | 4039064 | c.1641C>T | synonymous_variant | 0.18 |
clpC1 | 4039067 | c.1638G>C | synonymous_variant | 0.18 |
clpC1 | 4039079 | c.1626C>G | synonymous_variant | 0.18 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.2 |
clpC1 | 4039091 | c.1614G>C | synonymous_variant | 0.2 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.2 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.3 |
clpC1 | 4039118 | c.1587C>G | synonymous_variant | 0.3 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.3 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.27 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.27 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.15 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.17 |
clpC1 | 4039187 | c.1518G>C | synonymous_variant | 0.17 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.33 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.22 |
clpC1 | 4039448 | c.1257A>G | synonymous_variant | 0.22 |
clpC1 | 4039454 | c.1251A>T | synonymous_variant | 0.22 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.15 |
clpC1 | 4039622 | c.1083C>T | synonymous_variant | 0.15 |
clpC1 | 4039640 | c.1065C>G | synonymous_variant | 0.14 |
clpC1 | 4039649 | c.1056G>C | synonymous_variant | 0.15 |
clpC1 | 4039652 | c.1053G>C | synonymous_variant | 0.15 |
clpC1 | 4039661 | c.1044T>C | synonymous_variant | 0.19 |
clpC1 | 4039664 | c.1041G>C | synonymous_variant | 0.19 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.16 |
clpC1 | 4039718 | c.987C>G | synonymous_variant | 0.17 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.16 |
clpC1 | 4039733 | c.972G>C | synonymous_variant | 0.15 |
clpC1 | 4040232 | p.Arg158His | missense_variant | 0.2 |
clpC1 | 4040540 | c.165G>C | synonymous_variant | 0.12 |
panD | 4044037 | p.Gly82Val | missense_variant | 0.22 |
panD | 4044039 | c.243G>T | synonymous_variant | 0.22 |
embC | 4239978 | p.Leu39Pro | missense_variant | 0.17 |
embC | 4240324 | c.462G>T | synonymous_variant | 0.14 |
embC | 4240425 | p.Arg188Pro | missense_variant | 0.2 |
embC | 4240819 | c.957A>C | synonymous_variant | 0.33 |
embC | 4240822 | c.960C>G | synonymous_variant | 0.33 |
embC | 4240831 | c.969T>G | synonymous_variant | 0.33 |
embC | 4240934 | p.Val358Ile | missense_variant | 0.2 |
embC | 4240945 | c.1083T>C | synonymous_variant | 0.2 |
embC | 4240954 | c.1092T>C | synonymous_variant | 0.2 |
embC | 4241434 | p.Met524Ile | missense_variant | 0.2 |
embC | 4242545 | p.Glu895* | stop_gained | 0.25 |
embC | 4242794 | p.Ala978Ser | missense_variant | 0.13 |
embC | 4243065 | p.Pro1068His | missense_variant | 0.18 |
embC | 4243073 | p.Gln1071Lys | missense_variant | 0.17 |
embA | 4243078 | c.-155C>A | upstream_gene_variant | 0.17 |
embA | 4244272 | p.Leu347Pro | missense_variant | 0.17 |
embA | 4244486 | c.1254C>A | synonymous_variant | 0.18 |
embA | 4245009 | p.Ala593Ser | missense_variant | 0.17 |
embA | 4245230 | p.Phe666Leu | missense_variant | 0.29 |
embA | 4246180 | p.Thr983Ile | missense_variant | 0.12 |
embB | 4247176 | c.663G>T | synonymous_variant | 0.14 |
embB | 4247964 | p.Ala484Val | missense_variant | 0.2 |
embB | 4248705 | p.Pro731Gln | missense_variant | 0.14 |
embB | 4248957 | p.Trp815Leu | missense_variant | 0.29 |
embB | 4248986 | p.Gly825Cys | missense_variant | 0.22 |
embB | 4249167 | p.Gly885Asp | missense_variant | 0.18 |
embB | 4249299 | p.Trp929Leu | missense_variant | 0.15 |
embB | 4249596 | p.Trp1028Leu | missense_variant | 0.2 |
embB | 4249666 | c.3153C>A | synonymous_variant | 0.2 |
aftB | 4267181 | c.1656C>A | synonymous_variant | 0.13 |
aftB | 4267222 | p.Ala539Ser | missense_variant | 0.15 |
aftB | 4267263 | p.Arg525Leu | missense_variant | 0.2 |
aftB | 4267329 | p.Arg503Leu | missense_variant | 0.15 |
aftB | 4267641 | p.Ala399Asp | missense_variant | 0.15 |
aftB | 4267969 | p.Leu290Met | missense_variant | 0.14 |
aftB | 4268258 | c.579C>A | synonymous_variant | 0.17 |
aftB | 4268614 | p.Gly75Trp | missense_variant | 0.25 |
ubiA | 4269069 | p.Phe255Leu | missense_variant | 0.14 |
aftB | 4269117 | c.-281G>A | upstream_gene_variant | 0.15 |
ubiA | 4269120 | p.Phe238Leu | missense_variant | 0.17 |
aftB | 4269123 | c.-287T>G | upstream_gene_variant | 0.17 |
aftB | 4269129 | c.-293G>C | upstream_gene_variant | 0.17 |
aftB | 4269141 | c.-307_-305delTTGinsCTC | upstream_gene_variant | 0.25 |
aftB | 4269144 | c.-308C>G | upstream_gene_variant | 0.22 |
ubiA | 4269149 | p.Val229Leu | missense_variant | 0.22 |
aftB | 4269156 | c.-320C>A | upstream_gene_variant | 0.22 |
aftB | 4269171 | c.-335C>G | upstream_gene_variant | 0.25 |
aftB | 4269177 | c.-341G>C | upstream_gene_variant | 0.25 |
ubiA | 4269186 | p.Thr216Ser | missense_variant | 0.29 |
ubiA | 4269199 | p.Ser212Asn | missense_variant | 0.29 |
aftB | 4269201 | c.-365A>G | upstream_gene_variant | 0.29 |
aftB | 4269210 | c.-374G>A | upstream_gene_variant | 0.33 |
ubiA | 4269220 | p.Ala205Lys | missense_variant | 0.29 |
aftB | 4269222 | c.-386T>C | upstream_gene_variant | 0.29 |
aftB | 4269234 | c.-398A>G | upstream_gene_variant | 0.29 |
ubiA | 4269238 | p.Ala199Val | missense_variant | 0.29 |
aftB | 4269240 | c.-404G>C | upstream_gene_variant | 0.29 |
ubiA | 4269243 | p.His197Gln | missense_variant | 0.29 |
aftB | 4269249 | c.-413G>A | upstream_gene_variant | 0.29 |
aftB | 4269258 | c.-422C>T | upstream_gene_variant | 0.29 |
aftB | 4269264 | c.-428C>T | upstream_gene_variant | 0.25 |
aftB | 4269375 | c.-539G>A | upstream_gene_variant | 0.2 |
ubiA | 4269695 | p.Asp47Tyr | missense_variant | 0.22 |
ubiA | 4269756 | p.Trp26Cys | missense_variant | 0.2 |
ubiA | 4269924 | c.-91G>A | upstream_gene_variant | 0.14 |
ethA | 4326570 | p.Phe302Leu | missense_variant | 0.33 |
ethR | 4326907 | c.-642C>G | upstream_gene_variant | 0.2 |
ethA | 4327428 | p.Gly16Cys | missense_variant | 0.22 |
ethA | 4327436 | p.Gly13Val | missense_variant | 0.33 |
whiB6 | 4338193 | p.Arg110Leu | missense_variant | 0.22 |
whiB6 | 4338215 | p.Gly103Cys | missense_variant | 0.22 |
whiB6 | 4338319 | p.Glu68Gly | missense_variant | 0.2 |
whiB6 | 4338324 | c.198C>A | synonymous_variant | 0.2 |
whiB6 | 4338347 | c.175C>A | synonymous_variant | 0.2 |
whiB6 | 4338692 | c.-171G>T | upstream_gene_variant | 0.2 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.19 |
gid | 4407942 | p.Gln87His | missense_variant | 0.22 |