Run ID: SRR1181328
Sample name:
Date: 03-04-2023 04:48:42
Number of reads: 3363989
Percentage reads mapped: 79.09
Strain: lineage2.2.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.99 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.99 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
embB | 4247448 | p.His312Arg | missense_variant | 0.17 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6250 | c.1011A>G | synonymous_variant | 0.15 |
gyrA | 6307 | c.-995T>G | upstream_gene_variant | 0.16 |
gyrA | 6700 | c.-602T>C | upstream_gene_variant | 0.17 |
gyrA | 6703 | c.-599G>C | upstream_gene_variant | 0.17 |
gyrA | 6706 | c.-596G>A | upstream_gene_variant | 0.15 |
gyrA | 6709 | c.-593A>G | upstream_gene_variant | 0.17 |
gyrA | 6721 | c.-581C>T | upstream_gene_variant | 0.14 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7595 | c.294C>G | synonymous_variant | 0.16 |
gyrA | 7601 | c.300C>G | synonymous_variant | 0.17 |
gyrA | 7784 | c.483A>G | synonymous_variant | 0.16 |
gyrA | 7799 | c.498A>G | synonymous_variant | 0.15 |
gyrA | 8121 | c.820T>C | synonymous_variant | 0.2 |
gyrA | 8156 | c.855T>C | synonymous_variant | 0.16 |
gyrA | 8168 | c.867A>G | synonymous_variant | 0.15 |
gyrA | 8177 | c.876A>C | synonymous_variant | 0.14 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 0.17 |
gyrA | 8339 | c.1038A>G | synonymous_variant | 0.16 |
gyrA | 8340 | p.Ala347Ser | missense_variant | 0.15 |
gyrA | 8375 | c.1074G>C | synonymous_variant | 0.14 |
gyrA | 8603 | c.1302A>G | synonymous_variant | 0.17 |
gyrA | 8609 | c.1308G>C | synonymous_variant | 0.17 |
gyrA | 8619 | c.1318T>C | synonymous_variant | 0.16 |
gyrA | 8645 | c.1344C>T | synonymous_variant | 0.17 |
gyrA | 8655 | p.Ile452Val | missense_variant | 0.19 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490863 | c.81C>A | synonymous_variant | 0.13 |
fgd1 | 491542 | c.760T>C | synonymous_variant | 0.14 |
fgd1 | 491547 | c.765A>C | synonymous_variant | 0.16 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.99 |
mshA | 575561 | p.Met72Val | missense_variant | 0.13 |
mshA | 575907 | p.Ala187Val | missense_variant | 0.88 |
mshA | 575916 | p.Asp190Ala | missense_variant | 0.13 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.15 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.14 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.16 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.17 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.18 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.13 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.18 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.19 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.13 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.19 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.13 |
rpoB | 761097 | c.1291_1292delAGinsTC | synonymous_variant | 0.18 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.18 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.14 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.16 |
rpoB | 761492 | c.1686G>C | synonymous_variant | 0.17 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.19 |
rpoB | 761561 | c.1755C>G | synonymous_variant | 0.17 |
rpoB | 761564 | c.1758G>C | synonymous_variant | 0.17 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.16 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.16 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 0.13 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.14 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.14 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.14 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 1.0 |
rpoC | 762410 | c.-960T>C | upstream_gene_variant | 0.15 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.16 |
rpoC | 762470 | c.-900G>C | upstream_gene_variant | 0.16 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.14 |
rpoC | 762983 | c.-387C>A | upstream_gene_variant | 0.14 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.23 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.26 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.27 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.27 |
rpoC | 763076 | c.-294C>T | upstream_gene_variant | 0.14 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.23 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.18 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.18 |
rpoC | 763169 | c.-201A>G | upstream_gene_variant | 0.16 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.16 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.19 |
rpoC | 763636 | c.267T>G | synonymous_variant | 0.19 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.19 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.16 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.14 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.16 |
rpoC | 763771 | c.402C>T | synonymous_variant | 0.13 |
rpoC | 763781 | p.Ser138Ala | missense_variant | 0.18 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.19 |
rpoC | 763836 | p.Ala156Val | missense_variant | 0.15 |
rpoC | 763855 | c.486C>T | synonymous_variant | 0.16 |
rpoC | 763858 | c.489A>G | synonymous_variant | 0.14 |
rpoC | 763888 | c.519G>T | synonymous_variant | 0.14 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.14 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.14 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.19 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.18 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.19 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.19 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.22 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.22 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.2 |
rpoC | 764500 | c.1131C>G | synonymous_variant | 0.18 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.19 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.18 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.24 |
rpoC | 764548 | c.1179G>A | synonymous_variant | 0.16 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.19 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.16 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.19 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.14 |
rpoC | 764833 | c.1464A>G | synonymous_variant | 0.14 |
rpoC | 765547 | c.2178C>A | synonymous_variant | 0.19 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.18 |
rpoC | 765562 | c.2193G>C | synonymous_variant | 0.17 |
rpoC | 765685 | c.2316G>A | synonymous_variant | 0.14 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.23 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 0.14 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.18 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.19 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.19 |
rpoC | 765952 | c.2583G>C | synonymous_variant | 0.14 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.16 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.15 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 0.18 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.19 |
rpoC | 766543 | c.3174C>T | synonymous_variant | 0.2 |
rpoC | 766573 | c.3204T>C | synonymous_variant | 0.18 |
rpoC | 766579 | c.3210C>T | synonymous_variant | 0.16 |
rpoC | 766585 | c.3216T>C | synonymous_variant | 0.21 |
rpoC | 766594 | c.3225G>C | synonymous_variant | 0.21 |
rpoC | 766607 | p.Ile1080Leu | missense_variant | 0.18 |
rpoC | 766672 | c.3303T>C | synonymous_variant | 0.13 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.19 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.19 |
rpoC | 766792 | c.3423C>G | synonymous_variant | 0.15 |
rpoC | 766795 | c.3426C>T | synonymous_variant | 0.15 |
rpoC | 766801 | c.3432C>T | synonymous_variant | 0.16 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.2 |
rpoC | 766843 | c.3474T>G | synonymous_variant | 0.18 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.17 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.15 |
rpoC | 767033 | c.3664_3666delTCGinsAGT | synonymous_variant | 0.19 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.21 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.2 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.21 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.17 |
rpoC | 767200 | c.3831G>A | synonymous_variant | 0.17 |
rpoC | 767209 | c.3840T>C | synonymous_variant | 0.14 |
rpoC | 767221 | c.3852C>G | synonymous_variant | 0.2 |
rpoC | 767230 | c.3861G>C | synonymous_variant | 0.18 |
rpoC | 767233 | c.3864T>C | synonymous_variant | 0.2 |
rpoC | 767264 | p.Ala1299Gln | missense_variant | 0.16 |
rpoC | 767275 | c.3906T>A | synonymous_variant | 0.15 |
rpoC | 767281 | c.3912C>G | synonymous_variant | 0.13 |
rpoC | 767284 | c.3915C>T | synonymous_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.98 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 0.98 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.14 |
rplC | 800648 | c.-161A>C | upstream_gene_variant | 0.15 |
rplC | 800693 | c.-116A>C | upstream_gene_variant | 0.18 |
rplC | 800714 | c.-95C>T | upstream_gene_variant | 0.18 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.18 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.19 |
rplC | 800877 | c.69A>C | synonymous_variant | 0.14 |
fbiC | 1303545 | c.615A>G | synonymous_variant | 0.15 |
fbiC | 1304832 | c.1902C>T | synonymous_variant | 0.14 |
fbiC | 1304856 | c.1926C>G | synonymous_variant | 0.13 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 0.98 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471935 | n.90T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472040 | n.195T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473887 | n.230T>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473924 | n.267_268insT | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474061 | n.404T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474083 | n.426C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474111 | n.454T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474717 | n.1060A>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475266 | n.1609T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475273 | n.1616T>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475289 | n.1632G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475290 | n.1633A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475402 | n.1746T>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475487 | n.1830C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475638 | n.1981C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476580 | n.2923G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.15 |
inhA | 1674015 | c.-187C>A | upstream_gene_variant | 0.17 |
inhA | 1674018 | c.-184G>C | upstream_gene_variant | 0.17 |
inhA | 1674024 | c.-178T>C | upstream_gene_variant | 0.16 |
inhA | 1674870 | c.669T>C | synonymous_variant | 0.14 |
rpsA | 1833589 | c.48A>T | synonymous_variant | 0.18 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.15 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.18 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.15 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.15 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.15 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.15 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.15 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.14 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.14 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.18 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.18 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.19 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.22 |
rpsA | 1834495 | c.954G>A | synonymous_variant | 0.19 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.17 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.15 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.2 |
rpsA | 1834615 | c.1074C>T | synonymous_variant | 0.19 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.17 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.14 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 0.97 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.16 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.14 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.15 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.13 |
rpoA | 3878157 | c.351C>G | synonymous_variant | 0.14 |
rpoA | 3878247 | c.261G>C | synonymous_variant | 0.16 |
rpoA | 3878256 | c.252G>C | synonymous_variant | 0.21 |
rpoA | 3878262 | c.246C>T | synonymous_variant | 0.23 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.21 |
rpoA | 3878283 | p.Glu75Asp | missense_variant | 0.21 |
rpoA | 3878295 | c.213A>G | synonymous_variant | 0.17 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.17 |
rpoA | 3878641 | c.-135delG | upstream_gene_variant | 0.14 |
clpC1 | 4038278 | c.2427T>C | synonymous_variant | 0.16 |
clpC1 | 4038289 | p.Asn806Asp | missense_variant | 0.13 |
clpC1 | 4038314 | c.2391T>C | synonymous_variant | 0.14 |
clpC1 | 4038329 | p.Glu792Asp | missense_variant | 0.14 |
clpC1 | 4038350 | c.2355C>G | synonymous_variant | 0.17 |
clpC1 | 4038356 | c.2349T>C | synonymous_variant | 0.16 |
clpC1 | 4038359 | c.2346A>G | synonymous_variant | 0.16 |
clpC1 | 4038368 | c.2337T>C | synonymous_variant | 0.16 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.16 |
clpC1 | 4038839 | c.1866G>C | synonymous_variant | 0.14 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.23 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.14 |
clpC1 | 4038980 | c.1725C>T | synonymous_variant | 0.15 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.14 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.13 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.16 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.15 |
clpC1 | 4039412 | c.1293T>G | synonymous_variant | 0.15 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.14 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.14 |
clpC1 | 4040551 | c.154T>C | synonymous_variant | 0.14 |
embC | 4240783 | c.921G>C | synonymous_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242838 | c.-395C>G | upstream_gene_variant | 0.16 |
embA | 4242844 | c.-389A>G | upstream_gene_variant | 0.14 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embB | 4245683 | c.-831C>T | upstream_gene_variant | 0.13 |
embB | 4246567 | c.54G>T | synonymous_variant | 1.0 |
embB | 4247470 | c.957T>C | synonymous_variant | 0.14 |
embB | 4247497 | c.984T>C | synonymous_variant | 0.16 |
embB | 4247500 | c.987C>G | synonymous_variant | 0.15 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.15 |
aftB | 4267580 | c.1257G>A | synonymous_variant | 0.14 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 0.9 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.99 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |