Run ID: ERR4822101
Sample name:
Date: 01-04-2023 17:38:20
Number of reads: 2202581
Percentage reads mapped: 78.9
Strain: lineage4.1.3;lineage1.1.2
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.54 |
lineage1 | Indo-Oceanic | EAI | RD239 | 0.49 |
lineage4.1 | Euro-American | T;X;H | None | 0.5 |
lineage1.1 | Indo-Oceanic | EAI3;EAI4;EAI5;EAI6 | RD239 | 0.47 |
lineage4.1.3 | Euro-American | T;X;H | None | 0.44 |
lineage1.1.2 | Indo-Oceanic | EAI3;EAI5 | RD239 | 0.52 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6112 | p.Met291Ile | missense_variant | 0.25 |
gyrB | 6124 | c.885C>T | synonymous_variant | 0.25 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7391 | c.90C>T | synonymous_variant | 0.17 |
gyrA | 7394 | c.93T>C | synonymous_variant | 0.18 |
gyrA | 7427 | c.126G>C | synonymous_variant | 0.18 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8435 | c.1134C>G | synonymous_variant | 0.54 |
gyrA | 8452 | p.Ala384Val | missense_variant | 0.57 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 0.49 |
gyrA | 9191 | c.1890G>C | synonymous_variant | 0.13 |
gyrA | 9200 | c.1899A>G | synonymous_variant | 0.14 |
gyrA | 9204 | p.Ser635Thr | missense_variant | 0.14 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 490812 | c.30A>G | synonymous_variant | 0.14 |
fgd1 | 490815 | c.33G>C | synonymous_variant | 0.14 |
fgd1 | 490827 | c.45C>T | synonymous_variant | 0.14 |
fgd1 | 490851 | c.69A>T | synonymous_variant | 0.13 |
fgd1 | 490868 | p.Ala29Gly | missense_variant | 0.15 |
fgd1 | 491313 | c.531C>G | synonymous_variant | 0.15 |
fgd1 | 491319 | c.537G>C | synonymous_variant | 0.17 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.47 |
mshA | 575376 | p.Ser10Leu | missense_variant | 0.65 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.16 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.14 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.13 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.14 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.14 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.17 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.18 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.18 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.14 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.14 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.15 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.16 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.2 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.19 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.17 |
rpoB | 761306 | c.1500C>G | synonymous_variant | 0.18 |
rpoB | 761312 | c.1506G>C | synonymous_variant | 0.19 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.17 |
rpoB | 761330 | c.1524G>C | synonymous_variant | 0.17 |
rpoB | 761354 | c.1548C>T | synonymous_variant | 0.13 |
rpoB | 761360 | c.1554T>C | synonymous_variant | 0.13 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.13 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.15 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.15 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.14 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.13 |
rpoB | 762008 | c.2202C>T | synonymous_variant | 0.16 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.16 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.13 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.16 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 0.16 |
rpoB | 762338 | c.2532T>C | synonymous_variant | 0.13 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.46 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.14 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.15 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.17 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.16 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.16 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.15 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.15 |
rpoC | 763884 | p.Ala172Val | missense_variant | 0.57 |
rpoC | 763886 | c.517C>A | synonymous_variant | 0.6 |
rpoC | 764083 | c.714A>G | synonymous_variant | 0.15 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.15 |
rpoC | 764131 | c.762T>C | synonymous_variant | 0.14 |
rpoC | 764140 | c.771C>T | synonymous_variant | 0.14 |
rpoC | 764215 | c.846A>G | synonymous_variant | 0.13 |
rpoC | 764236 | c.867G>A | synonymous_variant | 0.19 |
rpoC | 764248 | c.879C>G | synonymous_variant | 0.17 |
rpoC | 764257 | c.888G>C | synonymous_variant | 0.17 |
rpoC | 764266 | c.897T>C | synonymous_variant | 0.14 |
rpoC | 764269 | c.900G>C | synonymous_variant | 0.14 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.15 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.14 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.14 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.15 |
rpoC | 764510 | c.1141C>T | synonymous_variant | 0.12 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 0.14 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.14 |
rpoC | 764554 | c.1185C>T | synonymous_variant | 0.22 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.19 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.25 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.22 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.17 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.22 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.13 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.21 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.17 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.18 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.13 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.17 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.14 |
rpoC | 764872 | c.1503A>G | synonymous_variant | 0.13 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.16 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 0.18 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 0.13 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.16 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.16 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 0.53 |
rpoC | 765171 | p.Pro601Leu | missense_variant | 0.42 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.16 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.2 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.25 |
rpoC | 765529 | c.2160C>T | synonymous_variant | 0.25 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.28 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.27 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.24 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.25 |
rpoC | 765580 | c.2211G>C | synonymous_variant | 0.23 |
rpoC | 765613 | p.His748Gln | missense_variant | 0.2 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.17 |
rpoC | 765631 | p.Asp754Glu | missense_variant | 0.16 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.16 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.14 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.14 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.16 |
rpoC | 765982 | c.2613C>G | synonymous_variant | 0.17 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.18 |
rpoC | 766021 | c.2652G>C | synonymous_variant | 0.15 |
rpoC | 766027 | c.2658G>C | synonymous_variant | 0.16 |
rpoC | 766030 | c.2661C>G | synonymous_variant | 0.14 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.13 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.36 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781421 | c.-139C>A | upstream_gene_variant | 0.5 |
fbiC | 1303914 | c.984C>G | synonymous_variant | 0.17 |
fbiC | 1303920 | c.990C>T | synonymous_variant | 0.18 |
fbiC | 1304142 | c.1212G>C | synonymous_variant | 0.15 |
fbiC | 1304161 | p.Arg411Ser | missense_variant | 0.15 |
fbiC | 1304169 | c.1239T>C | synonymous_variant | 0.14 |
fbiC | 1304174 | p.Val415Ala | missense_variant | 0.14 |
fbiC | 1304184 | c.1254G>C | synonymous_variant | 0.15 |
fbiC | 1304187 | c.1257T>C | synonymous_variant | 0.15 |
fbiC | 1304208 | c.1278C>T | synonymous_variant | 0.12 |
fbiC | 1304610 | c.1680C>T | synonymous_variant | 0.44 |
fbiC | 1304784 | c.1854T>C | synonymous_variant | 0.15 |
fbiC | 1304808 | c.1878C>G | synonymous_variant | 0.14 |
fbiC | 1304811 | c.1881C>G | synonymous_variant | 0.15 |
fbiC | 1304817 | c.1887T>C | synonymous_variant | 0.18 |
fbiC | 1304829 | c.1899T>C | synonymous_variant | 0.25 |
fbiC | 1304832 | c.1902C>T | synonymous_variant | 0.19 |
fbiC | 1304853 | c.1923C>G | synonymous_variant | 0.12 |
fbiC | 1304856 | c.1926C>G | synonymous_variant | 0.33 |
fbiC | 1304869 | c.1939C>T | synonymous_variant | 0.15 |
fbiC | 1304875 | p.Ile649Val | missense_variant | 0.16 |
fbiC | 1304883 | p.Glu651Asp | missense_variant | 0.15 |
fbiC | 1304891 | p.Ile654Thr | missense_variant | 0.15 |
fbiC | 1304893 | p.Gly655Ser | missense_variant | 0.15 |
fbiC | 1304907 | c.1977C>G | synonymous_variant | 0.15 |
fbiC | 1304910 | c.1980G>C | synonymous_variant | 0.15 |
fbiC | 1304916 | c.1986T>C | synonymous_variant | 0.14 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 0.33 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472242 | n.397C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472251 | n.406G>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472252 | n.407G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472256 | n.411T>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472754 | n.909G>T | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1473660 | n.3G>A | non_coding_transcript_exon_variant | 0.37 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474507 | n.850G>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475170 | n.1513A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.13 |
rpsA | 1833595 | c.54T>C | synonymous_variant | 0.13 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.15 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.16 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.15 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.13 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.15 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.14 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.14 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.13 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.15 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.15 |
rpsA | 1834690 | c.1149T>C | synonymous_variant | 0.15 |
rpsA | 1834732 | c.1191T>C | synonymous_variant | 0.15 |
rpsA | 1834738 | c.1197A>G | synonymous_variant | 0.13 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.15 |
rpsA | 1834765 | p.Glu408Asp | missense_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.29 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 0.41 |
PPE35 | 2167983 | p.Gly877Asp | missense_variant | 0.31 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 0.51 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 0.5 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 0.5 |
Rv2752c | 3064632 | c.1560C>T | synonymous_variant | 0.42 |
thyX | 3067355 | c.591A>C | synonymous_variant | 0.13 |
thyX | 3067367 | c.579G>C | synonymous_variant | 0.15 |
thyX | 3067373 | c.573C>G | synonymous_variant | 0.15 |
thyX | 3067376 | c.570G>A | synonymous_variant | 0.13 |
thyX | 3067391 | c.555G>C | synonymous_variant | 0.14 |
thyX | 3067394 | c.552G>C | synonymous_variant | 0.15 |
thyX | 3067439 | c.507A>G | synonymous_variant | 0.17 |
thyX | 3067445 | c.501C>G | synonymous_variant | 0.16 |
thyX | 3067457 | c.489C>G | synonymous_variant | 0.18 |
thyX | 3067465 | p.Ile161Val | missense_variant | 0.18 |
thyX | 3067475 | c.471A>G | synonymous_variant | 0.19 |
thyX | 3067490 | c.456C>G | synonymous_variant | 0.2 |
thyX | 3067493 | c.453A>G | synonymous_variant | 0.2 |
thyX | 3067515 | p.Ser144Thr | missense_variant | 0.13 |
thyX | 3067685 | c.261A>C | synonymous_variant | 0.14 |
thyA | 3073860 | c.612C>G | synonymous_variant | 0.14 |
thyA | 3073872 | p.Ile200Met | missense_variant | 0.13 |
thyA | 3073920 | c.552C>G | synonymous_variant | 0.15 |
thyA | 3073929 | c.543T>C | synonymous_variant | 0.12 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.12 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.98 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 0.42 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 0.97 |
fprA | 3474597 | c.591C>A | synonymous_variant | 0.56 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 0.49 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.12 |
rpoA | 3877656 | c.852T>G | synonymous_variant | 0.14 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.15 |
rpoA | 3877679 | p.Ala277Ser | missense_variant | 0.17 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.16 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.19 |
rpoA | 3877704 | c.804G>C | synonymous_variant | 0.19 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.2 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.18 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.19 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.15 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.13 |
rpoA | 3877848 | c.660C>T | synonymous_variant | 0.13 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.14 |
rpoA | 3877875 | c.633T>G | synonymous_variant | 0.16 |
rpoA | 3877878 | c.630G>C | synonymous_variant | 0.15 |
rpoA | 3877890 | c.618C>T | synonymous_variant | 0.13 |
rpoA | 3877896 | c.612G>C | synonymous_variant | 0.13 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.18 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.19 |
rpoA | 3877923 | c.585C>T | synonymous_variant | 0.19 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.15 |
clpC1 | 4038770 | c.1935C>T | synonymous_variant | 0.15 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.15 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.16 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.21 |
clpC1 | 4038845 | c.1860G>C | synonymous_variant | 0.18 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.18 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.17 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.15 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.14 |
clpC1 | 4039562 | c.1143C>G | synonymous_variant | 0.13 |
clpC1 | 4039589 | c.1116G>C | synonymous_variant | 0.13 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.14 |
clpC1 | 4039622 | c.1083C>T | synonymous_variant | 0.13 |
clpC1 | 4039661 | c.1044T>G | synonymous_variant | 0.12 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.16 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.15 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.15 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.22 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.13 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 0.43 |
embC | 4240671 | p.Thr270Ile | missense_variant | 0.46 |
embC | 4241042 | p.Asn394Asp | missense_variant | 0.51 |
embC | 4241719 | c.1857G>C | synonymous_variant | 0.12 |
embC | 4241727 | p.Phe622Tyr | missense_variant | 0.12 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 0.5 |
embA | 4243848 | p.Val206Met | missense_variant | 0.68 |
embA | 4245083 | c.1851A>C | synonymous_variant | 0.15 |
embA | 4245089 | c.1857G>C | synonymous_variant | 0.19 |
embA | 4245092 | c.1860C>G | synonymous_variant | 0.18 |
embA | 4245101 | c.1869G>C | synonymous_variant | 0.2 |
embA | 4245137 | c.1905T>C | synonymous_variant | 0.23 |
embA | 4245146 | c.1914G>A | synonymous_variant | 0.23 |
embA | 4245149 | c.1917C>G | synonymous_variant | 0.24 |
embA | 4245153 | p.Ile641Val | missense_variant | 0.21 |
embA | 4245182 | c.1950T>C | synonymous_variant | 0.13 |
embA | 4245969 | p.Pro913Ser | missense_variant | 0.61 |
embB | 4247356 | c.843C>T | synonymous_variant | 0.53 |
embB | 4247646 | p.Glu378Ala | missense_variant | 0.56 |
aftB | 4268602 | p.Leu79Met | missense_variant | 0.12 |
aftB | 4268608 | p.Met77Leu | missense_variant | 0.12 |
aftB | 4268612 | c.225G>C | synonymous_variant | 0.12 |
aftB | 4268618 | c.219G>C | synonymous_variant | 0.13 |
aftB | 4268626 | p.Gly71Ser | missense_variant | 0.13 |
aftB | 4268683 | p.Gly52Ser | missense_variant | 0.33 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 0.48 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 0.51 |
whiB6 | 4338441 | p.Tyr27* | stop_gained | 0.36 |
whiB6 | 4338449 | p.Ala25Pro | missense_variant | 0.39 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 0.33 |
gid | 4407588 | c.615A>G | synonymous_variant | 0.36 |
gid | 4407873 | c.330G>T | synonymous_variant | 0.36 |