Run ID: SRR6981961
Sample name:
Date: 04-04-2023 18:23:12
Number of reads: 435058
Percentage reads mapped: 91.07
Strain: lineage2.2.1
Drug-resistance: Sensitive
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 | 0.98 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7499 | c.198G>A | synonymous_variant | 0.13 |
gyrA | 7523 | c.222C>A | synonymous_variant | 0.13 |
gyrA | 7526 | c.225G>T | synonymous_variant | 0.14 |
gyrA | 7532 | c.231T>C | synonymous_variant | 0.14 |
gyrA | 7541 | c.240C>G | synonymous_variant | 0.14 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7595 | c.294C>G | synonymous_variant | 0.12 |
gyrA | 7614 | c.313C>T | synonymous_variant | 0.17 |
gyrA | 7865 | c.564T>C | synonymous_variant | 0.13 |
gyrA | 7886 | c.585T>C | synonymous_variant | 0.11 |
gyrA | 7889 | c.588G>A | synonymous_variant | 0.12 |
gyrA | 7890 | c.589C>T | synonymous_variant | 0.12 |
gyrA | 7898 | p.Asp199Glu | missense_variant | 0.12 |
gyrA | 8339 | c.1038A>G | synonymous_variant | 0.12 |
gyrA | 8340 | p.Ala347Ser | missense_variant | 0.12 |
gyrA | 8375 | c.1074G>C | synonymous_variant | 0.14 |
gyrA | 8382 | p.Leu361Met | missense_variant | 0.12 |
gyrA | 8391 | p.Tyr364His | missense_variant | 0.12 |
gyrA | 8399 | c.1098T>C | synonymous_variant | 0.13 |
gyrA | 8401 | p.Asp367Ala | missense_variant | 0.12 |
gyrA | 8414 | c.1113C>T | synonymous_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575728 | c.381C>A | synonymous_variant | 0.12 |
mshA | 575734 | c.387T>G | synonymous_variant | 0.12 |
mshA | 575737 | c.390T>C | synonymous_variant | 0.12 |
mshA | 575744 | p.Ala133Thr | missense_variant | 0.12 |
mshA | 575749 | c.402C>G | synonymous_variant | 0.12 |
mshA | 575756 | c.409C>T | synonymous_variant | 0.12 |
mshA | 575764 | c.417C>A | synonymous_variant | 0.12 |
mshA | 575771 | p.Val142Thr | missense_variant | 0.12 |
mshA | 575779 | c.432A>G | synonymous_variant | 0.13 |
mshA | 575782 | c.435G>C | synonymous_variant | 0.13 |
mshA | 575785 | c.438T>C | synonymous_variant | 0.12 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 576450 | p.Pro368Gln | missense_variant | 0.11 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.15 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.17 |
rpoB | 760310 | c.504G>C | synonymous_variant | 0.18 |
rpoB | 760316 | c.510C>G | synonymous_variant | 0.19 |
rpoB | 760325 | c.519G>C | synonymous_variant | 0.2 |
rpoB | 760331 | c.525G>C | synonymous_variant | 0.17 |
rpoB | 760334 | c.528G>T | synonymous_variant | 0.15 |
rpoB | 760340 | c.534G>T | synonymous_variant | 0.21 |
rpoB | 760357 | p.Thr184Ser | missense_variant | 0.19 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.2 |
rpoB | 760370 | c.564C>G | synonymous_variant | 0.19 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.19 |
rpoB | 760407 | p.Ser201Gly | missense_variant | 0.2 |
rpoB | 760415 | c.609C>T | synonymous_variant | 0.2 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.2 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.22 |
rpoB | 760457 | c.651C>T | synonymous_variant | 0.17 |
rpoB | 760460 | c.654G>C | synonymous_variant | 0.19 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.18 |
rpoB | 760478 | c.672C>T | synonymous_variant | 0.18 |
rpoB | 760481 | c.675G>T | synonymous_variant | 0.17 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.17 |
rpoB | 760502 | c.696C>G | synonymous_variant | 0.18 |
rpoB | 760561 | c.757_758delCG | frameshift_variant | 0.12 |
rpoB | 760567 | p.Ser254Trp | missense_variant | 0.12 |
rpoB | 760568 | c.762_763insGC | frameshift_variant | 0.12 |
rpoB | 760571 | c.765G>C | synonymous_variant | 0.12 |
rpoB | 760574 | c.768G>C | synonymous_variant | 0.12 |
rpoB | 760585 | p.Asn260Ser | missense_variant | 0.13 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.15 |
rpoB | 760596 | p.Thr264Pro | missense_variant | 0.21 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.18 |
rpoB | 760625 | c.819C>G | synonymous_variant | 0.18 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.16 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.16 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.16 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.16 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.11 |
rpoB | 761345 | c.1539G>T | synonymous_variant | 0.11 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.14 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.14 |
rpoB | 762122 | c.2316C>T | synonymous_variant | 0.14 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.12 |
rpoB | 762137 | c.2331C>T | synonymous_variant | 0.12 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.12 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.12 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.15 |
rpoB | 762158 | c.2352G>C | synonymous_variant | 0.15 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.15 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.15 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.15 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.23 |
rpoB | 762239 | c.2433G>A | synonymous_variant | 0.23 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.24 |
rpoB | 762284 | c.2478G>T | synonymous_variant | 0.25 |
rpoB | 762293 | c.2487T>G | synonymous_variant | 0.27 |
rpoB | 762308 | c.2502G>C | synonymous_variant | 0.2 |
rpoB | 762314 | c.2508C>T | synonymous_variant | 0.2 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.2 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.19 |
rpoB | 762338 | c.2532T>C | synonymous_variant | 0.12 |
rpoB | 762341 | c.2535G>C | synonymous_variant | 0.12 |
rpoB | 762347 | c.2541T>C | synonymous_variant | 0.13 |
rpoB | 762353 | c.2547C>T | synonymous_variant | 0.13 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 0.13 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 0.15 |
rpoC | 762374 | c.-996G>C | upstream_gene_variant | 0.15 |
rpoB | 762444 | p.Ala880Ser | missense_variant | 0.17 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.93 |
rpoC | 763621 | c.252C>G | synonymous_variant | 0.11 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.13 |
rpoC | 763666 | c.297G>A | synonymous_variant | 0.13 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.13 |
rpoC | 764344 | c.975C>T | synonymous_variant | 0.15 |
rpoC | 764353 | c.984G>T | synonymous_variant | 0.17 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.16 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.16 |
rpoC | 764374 | c.1005C>T | synonymous_variant | 0.16 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.16 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.17 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.15 |
rpoC | 764692 | c.1323C>T | synonymous_variant | 0.24 |
rpoC | 764701 | c.1332C>G | synonymous_variant | 0.26 |
rpoC | 764713 | c.1344G>T | synonymous_variant | 0.26 |
rpoC | 764719 | c.1350G>A | synonymous_variant | 0.27 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.19 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.18 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.21 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.2 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.24 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.24 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.23 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.18 |
rpoC | 764851 | c.1482C>T | synonymous_variant | 0.17 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.17 |
rpoC | 764869 | c.1500C>T | synonymous_variant | 0.17 |
rpoC | 764875 | c.1506C>T | synonymous_variant | 0.17 |
rpoC | 764878 | c.1509C>G | synonymous_variant | 0.14 |
rpoC | 764887 | c.1518G>C | synonymous_variant | 0.12 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.12 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.12 |
rpoC | 765868 | c.2499G>T | synonymous_variant | 0.12 |
rpoC | 765871 | c.2502T>C | synonymous_variant | 0.12 |
rpoC | 765875 | p.Val836Ile | missense_variant | 0.12 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.12 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.12 |
rpoC | 765899 | c.2530C>T | synonymous_variant | 0.13 |
rpoC | 765904 | c.2535C>G | synonymous_variant | 0.12 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.13 |
rpoC | 766390 | c.3021C>T | synonymous_variant | 0.13 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 0.11 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.12 |
rpoC | 766428 | c.3059_3060insTAC | disruptive_inframe_insertion | 0.12 |
rpoC | 766433 | c.3065delA | frameshift_variant | 0.12 |
rpoC | 766442 | p.Thr1025Val | missense_variant | 0.12 |
rpoC | 766456 | c.3087C>T | synonymous_variant | 0.11 |
rpoC | 766539 | c.3171_3174delCGGC | frameshift_variant | 0.12 |
rpoC | 766548 | c.3179_3180insACAA | frameshift_variant | 0.12 |
rpoC | 766573 | c.3204T>C | synonymous_variant | 0.11 |
rpoC | 766579 | c.3210C>T | synonymous_variant | 0.11 |
rpoC | 766582 | c.3213C>T | synonymous_variant | 0.12 |
rpoC | 766585 | c.3216T>C | synonymous_variant | 0.12 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.9 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 0.96 |
mmpL5 | 779067 | c.-587A>G | upstream_gene_variant | 0.18 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781898 | c.339A>C | synonymous_variant | 0.12 |
rpsL | 781907 | c.348T>C | synonymous_variant | 0.12 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.14 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1407535 | c.-195G>T | upstream_gene_variant | 0.11 |
embR | 1417116 | c.231delT | frameshift_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475602 | n.1945G>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475603 | n.1946G>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475604 | n.1947A>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475612 | n.1955G>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475615 | n.1958C>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475616 | n.1959A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475637 | n.1980T>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475638 | n.1981C>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475639 | n.1982C>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475643 | n.1986C>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475647 | n.1990G>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475764 | n.2107A>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475775 | n.2118G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475991 | n.2334T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475995 | n.2338G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476033 | n.2376T>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476046 | n.2389G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476088 | n.2431A>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476105 | n.2448G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476106 | n.2449A>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.19 |
fabG1 | 1673597 | p.Lys53Thr | missense_variant | 0.17 |
fabG1 | 1673710 | p.Leu91Ile | missense_variant | 0.12 |
fabG1 | 1673716 | p.Ala93Gln | missense_variant | 0.12 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.96 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.12 |
rpsA | 1834423 | c.882G>T | synonymous_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918408 | p.Phe157Leu | missense_variant | 0.12 |
ndh | 2102733 | p.Leu104Ile | missense_variant | 0.14 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223167 | c.-3G>T | upstream_gene_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518365 | p.Gln84Arg | missense_variant | 0.11 |
folC | 2746697 | p.Asn301Ser | missense_variant | 0.12 |
ribD | 2986673 | c.-166C>T | upstream_gene_variant | 0.18 |
ribD | 2987487 | p.Pro217Thr | missense_variant | 0.12 |
Rv2752c | 3065876 | p.Lys106Glu | missense_variant | 0.15 |
thyA | 3073970 | p.Ala168Pro | missense_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339583 | p.Thr156Ala | missense_variant | 0.17 |
Rv3083 | 3449168 | p.Ala222Glu | missense_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiA | 3640766 | p.Pro75His | missense_variant | 0.15 |
rpoA | 3878028 | c.480G>C | synonymous_variant | 0.12 |
ddn | 3986987 | c.144G>A | synonymous_variant | 0.12 |
clpC1 | 4038721 | c.1984C>T | synonymous_variant | 0.14 |
clpC1 | 4038725 | c.1980C>G | synonymous_variant | 0.14 |
clpC1 | 4038740 | c.1965G>C | synonymous_variant | 0.12 |
clpC1 | 4038755 | c.1950G>C | synonymous_variant | 0.12 |
clpC1 | 4038767 | c.1938G>C | synonymous_variant | 0.12 |
clpC1 | 4038770 | c.1935C>T | synonymous_variant | 0.13 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.13 |
clpC1 | 4038779 | c.1926C>G | synonymous_variant | 0.13 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.13 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.13 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.16 |
clpC1 | 4038815 | c.1890G>C | synonymous_variant | 0.17 |
clpC1 | 4038842 | c.1863G>C | synonymous_variant | 0.14 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.17 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.2 |
clpC1 | 4038890 | c.1815G>A | synonymous_variant | 0.2 |
clpC1 | 4038905 | c.1800A>G | synonymous_variant | 0.24 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.24 |
clpC1 | 4038911 | c.1794G>T | synonymous_variant | 0.24 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.24 |
clpC1 | 4038917 | c.1788C>T | synonymous_variant | 0.24 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.25 |
clpC1 | 4038941 | c.1764G>C | synonymous_variant | 0.22 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.15 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.14 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.14 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.12 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.11 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.11 |
panD | 4044146 | p.Ile46Val | missense_variant | 0.17 |
embC | 4239733 | c.-130_-129insC | upstream_gene_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4245026 | p.His598Gln | missense_variant | 0.14 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338710 | c.-189A>G | upstream_gene_variant | 0.12 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407620 | p.Tyr195His | missense_variant | 1.0 |
gid | 4407783 | c.420C>T | synonymous_variant | 0.15 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |
gid | 4408430 | c.-228G>T | upstream_gene_variant | 0.17 |