Run ID: SRR13861322
Sample name:
Date: 03-04-2023 09:29:03
Number of reads: 864612
Percentage reads mapped: 21.64
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 | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.8 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6856 | c.-446T>C | upstream_gene_variant | 0.14 |
gyrA | 6862 | c.-440C>G | upstream_gene_variant | 0.14 |
gyrA | 6881 | c.-421T>C | upstream_gene_variant | 0.14 |
gyrA | 7626 | c.325C>T | synonymous_variant | 0.16 |
gyrA | 7631 | c.330G>C | synonymous_variant | 0.15 |
gyrA | 7637 | c.336C>G | synonymous_variant | 0.17 |
gyrA | 7649 | c.348C>T | synonymous_variant | 0.2 |
gyrA | 7652 | c.351C>T | synonymous_variant | 0.21 |
gyrA | 7658 | c.357A>G | synonymous_variant | 0.18 |
gyrA | 7664 | c.363T>C | synonymous_variant | 0.18 |
gyrA | 7670 | c.369A>G | synonymous_variant | 0.18 |
gyrA | 7676 | c.375G>C | synonymous_variant | 0.21 |
gyrA | 7683 | c.382A>C | synonymous_variant | 0.21 |
gyrA | 7694 | c.393A>G | synonymous_variant | 0.2 |
gyrA | 7697 | c.396C>G | synonymous_variant | 0.2 |
gyrA | 7710 | c.409T>C | synonymous_variant | 0.17 |
gyrA | 7715 | c.414G>C | synonymous_variant | 0.19 |
gyrA | 7728 | c.427_429delAGGinsCGC | synonymous_variant | 0.15 |
gyrA | 7760 | c.459C>T | synonymous_variant | 0.17 |
gyrA | 7763 | c.462T>C | synonymous_variant | 0.17 |
gyrA | 8111 | c.810G>C | synonymous_variant | 0.21 |
gyrA | 8204 | c.903C>T | synonymous_variant | 0.14 |
gyrA | 8219 | c.918T>C | synonymous_variant | 0.16 |
gyrA | 8225 | c.924T>C | synonymous_variant | 0.16 |
gyrA | 8234 | c.933T>G | synonymous_variant | 0.17 |
gyrA | 8235 | c.934_936delTTAinsCTG | synonymous_variant | 0.17 |
gyrA | 8253 | p.Ile318Leu | missense_variant | 0.17 |
gyrA | 8339 | c.1038A>G | synonymous_variant | 0.17 |
gyrA | 8342 | c.1041G>C | synonymous_variant | 0.17 |
gyrA | 8366 | c.1065G>C | synonymous_variant | 0.15 |
gyrA | 8375 | c.1074G>C | synonymous_variant | 0.15 |
gyrA | 8391 | p.Tyr364His | missense_variant | 0.19 |
gyrA | 8399 | c.1098T>C | synonymous_variant | 0.19 |
gyrA | 8420 | c.1119T>C | synonymous_variant | 0.21 |
gyrA | 8423 | c.1122G>C | synonymous_variant | 0.22 |
gyrA | 8442 | c.1141C>T | synonymous_variant | 0.2 |
gyrA | 8453 | c.1152A>C | synonymous_variant | 0.24 |
gyrA | 8462 | c.1161A>G | synonymous_variant | 0.26 |
gyrA | 8471 | c.1170T>C | synonymous_variant | 0.26 |
gyrA | 8480 | c.1179C>T | synonymous_variant | 0.26 |
gyrA | 8486 | c.1185T>C | synonymous_variant | 0.24 |
gyrA | 8489 | c.1188A>G | synonymous_variant | 0.25 |
gyrA | 8498 | c.1197C>T | synonymous_variant | 0.2 |
gyrA | 8504 | c.1203G>C | synonymous_variant | 0.21 |
gyrA | 8516 | c.1215T>C | synonymous_variant | 0.24 |
gyrA | 8519 | c.1218A>C | synonymous_variant | 0.24 |
gyrA | 8537 | c.1236G>A | synonymous_variant | 0.17 |
gyrA | 8546 | c.1245T>C | synonymous_variant | 0.17 |
gyrA | 8597 | c.1296C>G | synonymous_variant | 0.18 |
gyrA | 8603 | c.1302A>G | synonymous_variant | 0.17 |
gyrA | 8619 | c.1318T>C | synonymous_variant | 0.17 |
gyrA | 8624 | c.1323G>C | synonymous_variant | 0.16 |
gyrA | 8627 | c.1326C>G | synonymous_variant | 0.16 |
gyrA | 8636 | c.1335A>G | synonymous_variant | 0.17 |
gyrA | 8642 | c.1341A>G | synonymous_variant | 0.17 |
gyrA | 8645 | c.1344C>G | synonymous_variant | 0.17 |
gyrA | 8693 | c.1392T>C | synonymous_variant | 0.15 |
gyrA | 8699 | c.1398A>G | synonymous_variant | 0.16 |
fgd1 | 490804 | p.Tyr8Asn | missense_variant | 1.0 |
fgd1 | 490893 | c.111C>T | synonymous_variant | 1.0 |
fgd1 | 491121 | c.339A>G | synonymous_variant | 0.15 |
fgd1 | 491137 | p.Glu119Gln | missense_variant | 0.15 |
fgd1 | 491145 | c.363C>G | synonymous_variant | 0.15 |
fgd1 | 491181 | c.399T>C | synonymous_variant | 0.15 |
mshA | 575498 | p.Ala51Pro | missense_variant | 1.0 |
rpoB | 760730 | c.924T>C | synonymous_variant | 0.16 |
rpoB | 760751 | c.945G>C | synonymous_variant | 0.17 |
rpoB | 760757 | c.951T>C | synonymous_variant | 0.16 |
rpoB | 760759 | p.Val318Ala | missense_variant | 0.16 |
rpoB | 760763 | c.957C>T | synonymous_variant | 0.15 |
rpoB | 760769 | c.963C>G | synonymous_variant | 0.14 |
rpoB | 760776 | p.Ser324Thr | missense_variant | 0.14 |
rpoB | 760805 | c.999G>C | synonymous_variant | 0.15 |
rpoB | 760859 | c.1053T>C | synonymous_variant | 0.13 |
rpoB | 760970 | c.1164G>C | synonymous_variant | 0.18 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.15 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.14 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.16 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.16 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.16 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.15 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.14 |
rpoB | 761171 | c.1365C>T | synonymous_variant | 0.14 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.14 |
rpoB | 761183 | c.1377T>G | synonymous_variant | 0.14 |
rpoB | 761222 | c.1416G>C | synonymous_variant | 0.15 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.19 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.18 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.18 |
rpoB | 761864 | c.2058G>C | synonymous_variant | 0.13 |
rpoB | 761873 | c.2067A>G | synonymous_variant | 0.18 |
rpoB | 761885 | c.2079T>C | synonymous_variant | 0.18 |
rpoB | 761891 | c.2085G>C | synonymous_variant | 0.17 |
rpoB | 761906 | c.2100C>G | synonymous_variant | 0.16 |
rpoB | 761909 | c.2103T>C | synonymous_variant | 0.16 |
rpoB | 761912 | c.2106T>C | synonymous_variant | 0.16 |
rpoB | 761915 | p.Asp703Glu | missense_variant | 0.15 |
rpoB | 761916 | p.Asp704Asn | missense_variant | 0.15 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.18 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 0.19 |
rpoB | 761999 | c.2193G>C | synonymous_variant | 0.2 |
rpoB | 762008 | c.2202C>G | synonymous_variant | 0.18 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.14 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.15 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.16 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.17 |
rpoC | 763076 | c.-294C>G | upstream_gene_variant | 0.15 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.15 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.15 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.17 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.17 |
rpoC | 763663 | c.294C>A | synonymous_variant | 0.97 |
rpoC | 763801 | c.432C>G | synonymous_variant | 0.15 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.18 |
rpoC | 763819 | c.450G>C | synonymous_variant | 0.17 |
rpoC | 763831 | c.462A>G | synonymous_variant | 0.18 |
rpoC | 763835 | p.Ala156Met | missense_variant | 0.16 |
rpoC | 763858 | c.489A>G | synonymous_variant | 0.17 |
rpoC | 763872 | p.Gly168Ala | missense_variant | 0.16 |
rpoC | 763876 | p.Glu169Asp | missense_variant | 0.16 |
rpoC | 763879 | c.510A>G | synonymous_variant | 0.16 |
rpoC | 763919 | c.550C>T | synonymous_variant | 0.17 |
rpoC | 763933 | c.564C>T | synonymous_variant | 0.22 |
rpoC | 763945 | c.576T>C | synonymous_variant | 0.17 |
rpoC | 763955 | p.Lys196Gln | missense_variant | 0.8 |
rpoC | 763960 | c.591T>C | synonymous_variant | 0.19 |
rpoC | 763967 | p.Gly200Ser | missense_variant | 0.19 |
rpoC | 763978 | c.609C>G | synonymous_variant | 0.19 |
rpoC | 763996 | c.627T>C | synonymous_variant | 0.19 |
rpoC | 764005 | c.636G>C | synonymous_variant | 0.19 |
rpoC | 764011 | c.642T>C | synonymous_variant | 0.16 |
rpoC | 764024 | c.655T>C | synonymous_variant | 0.18 |
rpoC | 764040 | p.Ser224Asn | missense_variant | 0.15 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.15 |
rpoC | 764059 | c.690G>C | synonymous_variant | 0.14 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.13 |
rpoC | 764644 | c.1275G>C | synonymous_variant | 0.14 |
rpoC | 764714 | c.1345C>T | synonymous_variant | 0.26 |
rpoC | 764720 | c.1351C>T | synonymous_variant | 0.25 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.26 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.26 |
rpoC | 764791 | c.1422C>G | synonymous_variant | 0.3 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.26 |
rpoC | 764812 | c.1443C>G | synonymous_variant | 0.26 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.26 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.33 |
rpoC | 764830 | c.1461C>G | synonymous_variant | 0.28 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.21 |
rpoC | 764872 | c.1503A>G | synonymous_variant | 0.21 |
rpoC | 764893 | c.1524T>C | synonymous_variant | 0.17 |
rpoC | 765383 | p.Met672Leu | missense_variant | 0.17 |
rpoC | 765404 | p.Leu679Val | missense_variant | 0.15 |
rpoC | 765409 | c.2040T>C | synonymous_variant | 0.19 |
rpoC | 765412 | c.2043T>C | synonymous_variant | 0.19 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.21 |
rpoC | 765451 | c.2082C>G | synonymous_variant | 0.18 |
rpoC | 765452 | p.Ala695Ser | missense_variant | 0.18 |
rpoC | 765478 | c.2109T>C | synonymous_variant | 0.24 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.26 |
rpoC | 765508 | c.2139C>G | synonymous_variant | 0.22 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.22 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.21 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.23 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.22 |
rpoC | 765578 | c.2209C>T | synonymous_variant | 0.18 |
rpoC | 765583 | c.2214G>T | synonymous_variant | 0.18 |
rpoC | 765613 | p.His748Gln | missense_variant | 0.18 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.18 |
rpoC | 765628 | c.2259G>C | synonymous_variant | 0.17 |
rpoC | 765631 | p.Asp754Glu | missense_variant | 0.17 |
rpoC | 765658 | c.2289C>T | synonymous_variant | 0.17 |
rpoC | 765682 | p.Asn771Lys | missense_variant | 0.87 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.15 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 0.15 |
rpoC | 766342 | c.2973C>A | synonymous_variant | 0.88 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 0.16 |
rpoC | 766522 | c.3153C>G | synonymous_variant | 0.16 |
rpoC | 766528 | c.3159T>C | synonymous_variant | 0.22 |
rpoC | 766531 | c.3162G>T | synonymous_variant | 0.19 |
rpoC | 766543 | c.3174C>T | synonymous_variant | 0.22 |
rpoC | 766549 | c.3180G>C | synonymous_variant | 0.22 |
rpoC | 766573 | c.3204T>C | synonymous_variant | 0.16 |
rpoC | 766583 | p.Gly1072Ser | missense_variant | 0.17 |
rpoC | 766588 | c.3219G>A | synonymous_variant | 0.17 |
rpoC | 766591 | c.3222A>G | synonymous_variant | 0.17 |
rpoC | 766594 | c.3225G>C | synonymous_variant | 0.17 |
rpoC | 766607 | p.Ile1080Leu | missense_variant | 0.2 |
rpoC | 766630 | c.3261G>C | synonymous_variant | 0.21 |
rpoC | 766645 | c.3276A>G | synonymous_variant | 0.22 |
rpoC | 766651 | c.3282T>C | synonymous_variant | 0.2 |
rpoC | 766657 | c.3288A>G | synonymous_variant | 0.22 |
rpoC | 766672 | c.3303T>C | synonymous_variant | 0.2 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.2 |
rpoC | 766738 | c.3369G>T | synonymous_variant | 0.18 |
rpoC | 766750 | c.3381C>G | synonymous_variant | 0.18 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.2 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.15 |
rpoC | 766801 | c.3432C>A | synonymous_variant | 0.17 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.17 |
rpoC | 766843 | c.3474T>C | synonymous_variant | 0.14 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.14 |
rpoC | 766894 | c.3525T>C | synonymous_variant | 0.18 |
rpoC | 766895 | c.3526T>C | synonymous_variant | 0.18 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.17 |
rpoC | 766933 | c.3564A>G | synonymous_variant | 0.19 |
rpoC | 766945 | c.3576A>G | synonymous_variant | 0.17 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.17 |
rpoC | 766978 | c.3609C>G | synonymous_variant | 0.21 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.19 |
rpoC | 767009 | c.3640_3642delTCGinsAGC | synonymous_variant | 0.19 |
rpoC | 767014 | c.3645G>C | synonymous_variant | 0.19 |
rpoC | 767033 | c.3664_3666delTCGinsAGT | synonymous_variant | 0.19 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.19 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.18 |
rpoC | 767074 | c.3705T>C | synonymous_variant | 0.21 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.19 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.2 |
rpoC | 767134 | c.3765C>G | synonymous_variant | 0.17 |
rpoC | 767158 | c.3789T>C | synonymous_variant | 0.15 |
rpoC | 767167 | c.3798C>G | synonymous_variant | 0.17 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.14 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.15 |
rpoC | 767206 | c.3837C>G | synonymous_variant | 0.15 |
rpoC | 767212 | c.3843G>C | synonymous_variant | 0.15 |
rpoC | 767221 | c.3852C>G | synonymous_variant | 0.12 |
rpsL | 781579 | p.Leu7Arg | missense_variant | 0.94 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.14 |
rplC | 801171 | c.363A>G | synonymous_variant | 0.17 |
rplC | 801174 | c.366T>C | synonymous_variant | 0.17 |
rplC | 801228 | c.420T>C | synonymous_variant | 0.14 |
rplC | 801267 | c.459A>C | synonymous_variant | 0.14 |
rplC | 801282 | c.474G>C | synonymous_variant | 0.16 |
rplC | 801301 | c.493C>A | synonymous_variant | 0.15 |
rplC | 801312 | c.504G>C | synonymous_variant | 0.16 |
rplC | 801324 | c.516T>C | synonymous_variant | 0.17 |
rplC | 801336 | c.528C>G | synonymous_variant | 0.18 |
rplC | 801339 | c.531T>C | synonymous_variant | 0.17 |
rplC | 801341 | p.Leu178Gln | missense_variant | 0.18 |
rplC | 801348 | c.540T>G | synonymous_variant | 0.18 |
rplC | 801357 | c.549T>C | synonymous_variant | 0.19 |
rplC | 801367 | p.Ala187Thr | missense_variant | 0.15 |
rplC | 801396 | c.588T>C | synonymous_variant | 0.14 |
rplC | 801402 | c.594T>C | synonymous_variant | 0.15 |
rplC | 801405 | c.597T>C | synonymous_variant | 0.14 |
rplC | 801423 | c.615G>C | synonymous_variant | 0.14 |
rplC | 801438 | c.630T>C | synonymous_variant | 0.17 |
fbiC | 1303995 | c.1065C>T | synonymous_variant | 0.13 |
fbiC | 1304580 | c.1650T>C | synonymous_variant | 0.18 |
fbiC | 1304628 | c.1698G>C | synonymous_variant | 0.18 |
fbiC | 1304634 | c.1704C>G | synonymous_variant | 0.17 |
fbiC | 1304640 | c.1710A>C | synonymous_variant | 0.17 |
fbiC | 1304646 | c.1716T>C | synonymous_variant | 0.18 |
fbiC | 1304658 | c.1728C>G | synonymous_variant | 0.18 |
fbiC | 1304670 | c.1740G>T | synonymous_variant | 0.17 |
fbiC | 1304671 | p.Val581Thr | missense_variant | 0.18 |
fbiC | 1304675 | p.Gly582Glu | missense_variant | 0.18 |
fbiC | 1304691 | c.1761G>C | synonymous_variant | 0.21 |
fbiC | 1304694 | c.1764A>C | synonymous_variant | 0.21 |
fbiC | 1304703 | c.1773C>G | synonymous_variant | 0.21 |
fbiC | 1304715 | c.1785G>C | synonymous_variant | 0.21 |
fbiC | 1304724 | c.1794A>G | synonymous_variant | 0.18 |
fbiC | 1304727 | c.1797A>G | synonymous_variant | 0.16 |
fbiC | 1304742 | c.1812T>C | synonymous_variant | 0.15 |
fbiC | 1304748 | c.1818T>C | synonymous_variant | 0.16 |
fbiC | 1304754 | c.1824G>A | synonymous_variant | 0.16 |
fbiC | 1304757 | c.1827A>G | synonymous_variant | 0.16 |
fbiC | 1304784 | c.1854T>C | synonymous_variant | 0.16 |
fbiC | 1304787 | c.1857T>C | synonymous_variant | 0.16 |
fbiC | 1304790 | c.1860C>G | synonymous_variant | 0.16 |
fbiC | 1304808 | c.1878C>G | synonymous_variant | 0.15 |
fbiC | 1304811 | c.1881C>G | synonymous_variant | 0.15 |
fbiC | 1304817 | c.1887T>C | synonymous_variant | 0.17 |
embR | 1416509 | p.Arg280Pro | missense_variant | 1.0 |
rrs | 1472101 | n.256G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472122 | n.277G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472230 | n.385C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472262 | n.417C>T | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472269 | n.424G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472271 | n.426T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472505 | n.660G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472596 | n.751G>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472614 | n.769G>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472665 | n.820G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472669 | n.824_825insTAGG | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473248 | n.1403G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473255 | n.1410A>G | non_coding_transcript_exon_variant | 0.41 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473260 | n.1415G>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.37 |
rrs | 1473281 | n.1436C>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473282 | n.1437C>G | non_coding_transcript_exon_variant | 0.37 |
rrs | 1473288 | n.1443C>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1473291 | n.1446G>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473296 | n.1451G>C | non_coding_transcript_exon_variant | 0.39 |
rrs | 1473297 | n.1452G>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473327 | n.1482A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473328 | n.1483C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473756 | n.99G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473839 | n.182G>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473899 | n.242A>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473937 | n.280C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473944 | n.287G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473945 | n.288T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474051 | n.394T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474054 | n.397T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474056 | n.399T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474104 | n.447G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474111 | n.454T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474112 | n.455T>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474164 | n.507C>A | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476215 | n.2558C>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476263 | n.2606C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476268 | n.2611A>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476275 | n.2618T>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476595 | n.2938C>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476596 | n.2939C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.14 |
inhA | 1674315 | c.114C>G | synonymous_variant | 1.0 |
inhA | 1674549 | c.348G>C | synonymous_variant | 0.14 |
inhA | 1674582 | c.381T>C | synonymous_variant | 0.15 |
inhA | 1674585 | c.384T>C | synonymous_variant | 0.15 |
inhA | 1674589 | p.Met130Leu | missense_variant | 0.14 |
inhA | 1674624 | c.423A>C | synonymous_variant | 0.13 |
inhA | 1674627 | c.426T>G | synonymous_variant | 0.14 |
inhA | 1674636 | c.435C>G | synonymous_variant | 0.19 |
inhA | 1674654 | c.453G>C | synonymous_variant | 0.17 |
inhA | 1674693 | c.492C>G | synonymous_variant | 0.14 |
inhA | 1674718 | c.517A>C | synonymous_variant | 0.14 |
inhA | 1674855 | c.654C>T | synonymous_variant | 0.12 |
rpsA | 1833667 | c.126C>G | synonymous_variant | 0.15 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.22 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.22 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.21 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.21 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.25 |
rpsA | 1833790 | c.249T>A | synonymous_variant | 0.23 |
rpsA | 1833799 | c.258C>G | synonymous_variant | 0.24 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 0.25 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.24 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.24 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.24 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.19 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.19 |
rpsA | 1834297 | c.756C>G | synonymous_variant | 0.17 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.21 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.17 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.18 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.14 |
rpsA | 1834375 | c.834G>A | synonymous_variant | 0.15 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.14 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.15 |
ndh | 2102009 | p.Ser345Asn | missense_variant | 0.15 |
ndh | 2102023 | c.1020G>C | synonymous_variant | 0.15 |
ndh | 2102026 | c.1017G>C | synonymous_variant | 0.15 |
ndh | 2102050 | c.993T>C | synonymous_variant | 0.15 |
ndh | 2102053 | c.990G>C | synonymous_variant | 0.15 |
ndh | 2102059 | c.984T>C | synonymous_variant | 0.14 |
ndh | 2102065 | c.978G>C | synonymous_variant | 0.15 |
ndh | 2102077 | c.966T>C | synonymous_variant | 0.14 |
ndh | 2102092 | c.951G>C | synonymous_variant | 0.15 |
ndh | 2102098 | c.945G>C | synonymous_variant | 0.18 |
ndh | 2102104 | c.939G>C | synonymous_variant | 0.13 |
ndh | 2102131 | p.Gln304Lys | missense_variant | 0.19 |
ndh | 2102140 | c.903C>G | synonymous_variant | 0.16 |
ndh | 2102149 | c.894C>T | synonymous_variant | 0.17 |
katG | 2154959 | c.1153C>A | synonymous_variant | 1.0 |
PPE35 | 2170236 | c.376_377insG | frameshift_variant | 1.0 |
pncA | 2290061 | c.-820C>T | upstream_gene_variant | 0.97 |
kasA | 2517947 | c.-168C>T | upstream_gene_variant | 0.21 |
kasA | 2518768 | c.654C>G | synonymous_variant | 0.13 |
kasA | 2518783 | c.669T>C | synonymous_variant | 0.15 |
kasA | 2518792 | c.678C>G | synonymous_variant | 0.15 |
kasA | 2518795 | c.681C>G | synonymous_variant | 0.16 |
kasA | 2518822 | c.708C>G | synonymous_variant | 0.17 |
kasA | 2518825 | c.711T>C | synonymous_variant | 0.17 |
kasA | 2518843 | c.729T>C | synonymous_variant | 0.15 |
kasA | 2518855 | c.741C>G | synonymous_variant | 0.15 |
folC | 2747798 | c.-200A>T | upstream_gene_variant | 1.0 |
pepQ | 2860252 | p.Thr56Ser | missense_variant | 1.0 |
Rv2752c | 3065651 | p.Arg181Gly | missense_variant | 1.0 |
thyA | 3074286 | c.186T>C | synonymous_variant | 0.17 |
thyA | 3074297 | c.175C>T | synonymous_variant | 0.2 |
thyA | 3074301 | c.171C>T | synonymous_variant | 0.18 |
thyA | 3074305 | p.Ala56Val | missense_variant | 0.19 |
thyA | 3074307 | c.165A>G | synonymous_variant | 0.19 |
thyA | 3074316 | p.Phe52Leu | missense_variant | 0.18 |
thyA | 3074322 | c.150C>G | synonymous_variant | 0.18 |
thyA | 3074325 | c.147A>G | synonymous_variant | 0.18 |
thyA | 3074334 | c.138T>C | synonymous_variant | 0.18 |
thyA | 3074339 | p.Leu45Ile | missense_variant | 0.17 |
thyA | 3074394 | c.78C>G | synonymous_variant | 0.14 |
thyA | 3074397 | c.75A>G | synonymous_variant | 0.15 |
thyA | 3074423 | p.Pro17Ala | missense_variant | 0.14 |
Rv3083 | 3448855 | p.Val118Ile | missense_variant | 1.0 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.14 |
rpoA | 3877638 | c.870T>C | synonymous_variant | 0.15 |
rpoA | 3877656 | c.852T>C | synonymous_variant | 0.15 |
rpoA | 3877679 | p.Ala277Thr | missense_variant | 0.14 |
rpoA | 3877765 | p.Ala248Gly | missense_variant | 0.94 |
ddn | 3986847 | c.4_5insA | frameshift_variant | 1.0 |
clpC1 | 4038462 | p.Ala748Glu | missense_variant | 0.15 |
clpC1 | 4038498 | p.Ser736Thr | missense_variant | 0.17 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.17 |
clpC1 | 4038536 | c.2169C>T | synonymous_variant | 0.16 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.17 |
clpC1 | 4038611 | c.2094C>T | synonymous_variant | 0.16 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.17 |
clpC1 | 4038640 | p.Asp689Asn | missense_variant | 0.14 |
clpC1 | 4038653 | c.2052C>T | synonymous_variant | 0.16 |
clpC1 | 4038658 | p.Lys683Gln | missense_variant | 0.18 |
clpC1 | 4038661 | p.Ser682Thr | missense_variant | 0.17 |
clpC1 | 4038662 | c.2043T>C | synonymous_variant | 0.16 |
clpC1 | 4038671 | c.2034T>C | synonymous_variant | 0.17 |
clpC1 | 4038683 | c.2022T>C | synonymous_variant | 0.16 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.15 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.16 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.16 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.14 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.17 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.15 |
clpC1 | 4039073 | c.1632C>G | synonymous_variant | 0.15 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.14 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.14 |
clpC1 | 4039187 | c.1518G>C | synonymous_variant | 0.15 |
clpC1 | 4039190 | c.1515C>G | synonymous_variant | 0.15 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.16 |
clpC1 | 4039793 | c.912C>G | synonymous_variant | 0.14 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 0.12 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.15 |
clpC1 | 4039832 | c.873C>G | synonymous_variant | 0.14 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.18 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.14 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.15 |
clpC1 | 4039929 | c.775_776delAGinsTC | synonymous_variant | 0.14 |
clpC1 | 4039946 | c.759A>T | synonymous_variant | 0.16 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.16 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.17 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.15 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 0.18 |
clpC1 | 4040363 | c.342A>C | synonymous_variant | 0.2 |
clpC1 | 4040369 | c.336C>G | synonymous_variant | 0.2 |
clpC1 | 4040380 | c.325T>C | synonymous_variant | 0.18 |
clpC1 | 4040387 | c.318A>G | synonymous_variant | 0.21 |
clpC1 | 4040393 | c.312G>C | synonymous_variant | 0.21 |
clpC1 | 4040411 | c.294T>C | synonymous_variant | 0.21 |
clpC1 | 4040423 | c.282A>G | synonymous_variant | 0.19 |
clpC1 | 4040426 | c.279T>C | synonymous_variant | 0.19 |
clpC1 | 4040431 | c.274T>C | synonymous_variant | 0.23 |
clpC1 | 4040441 | c.264C>G | synonymous_variant | 0.21 |
clpC1 | 4040444 | c.261C>G | synonymous_variant | 0.21 |
clpC1 | 4040450 | c.255A>G | synonymous_variant | 0.2 |
clpC1 | 4040459 | c.246C>G | synonymous_variant | 0.2 |
clpC1 | 4040465 | c.240T>C | synonymous_variant | 0.21 |
clpC1 | 4040471 | c.234T>C | synonymous_variant | 0.21 |
clpC1 | 4040477 | c.228G>A | synonymous_variant | 0.2 |
clpC1 | 4040480 | c.225T>C | synonymous_variant | 0.21 |
clpC1 | 4040528 | c.177G>C | synonymous_variant | 0.14 |
clpC1 | 4040531 | c.174T>C | synonymous_variant | 0.14 |
embC | 4240632 | p.Met257Thr | missense_variant | 0.14 |
embC | 4240642 | c.780G>C | synonymous_variant | 0.17 |
embC | 4240645 | c.783G>C | synonymous_variant | 0.17 |
embC | 4240657 | c.795G>C | synonymous_variant | 0.17 |
embC | 4240671 | p.Thr270Ile | missense_variant | 0.16 |
embC | 4240678 | c.816T>G | synonymous_variant | 0.16 |
embC | 4240685 | p.Thr275Ala | missense_variant | 0.16 |
embC | 4240693 | c.831T>C | synonymous_variant | 0.18 |
embC | 4240706 | p.Val282Thr | missense_variant | 0.15 |
embC | 4240726 | c.864G>C | synonymous_variant | 0.14 |
embC | 4240780 | c.918T>C | synonymous_variant | 0.19 |
embC | 4240783 | c.921G>C | synonymous_variant | 0.23 |
embC | 4240789 | c.927T>C | synonymous_variant | 0.23 |
embC | 4240819 | c.957A>G | synonymous_variant | 0.23 |
embC | 4240825 | c.963G>A | synonymous_variant | 0.22 |
embC | 4240831 | c.969T>G | synonymous_variant | 0.19 |
embC | 4240867 | c.1005T>G | synonymous_variant | 0.17 |
embC | 4240870 | c.1008T>C | synonymous_variant | 0.16 |
embC | 4240879 | c.1017G>C | synonymous_variant | 0.17 |
embC | 4240880 | p.Ala340Thr | missense_variant | 0.17 |
embC | 4240885 | c.1023T>C | synonymous_variant | 0.17 |
embC | 4240897 | c.1035C>G | synonymous_variant | 0.19 |
embC | 4240900 | c.1038A>G | synonymous_variant | 0.23 |
embC | 4240919 | c.1057_1059delCTCinsTTG | synonymous_variant | 0.18 |
embC | 4240945 | c.1083T>C | synonymous_variant | 0.16 |
embC | 4240951 | c.1089C>G | synonymous_variant | 0.15 |
embC | 4240957 | c.1095C>G | synonymous_variant | 0.16 |
embC | 4240979 | p.Thr373Gln | missense_variant | 0.16 |
embC | 4240983 | p.Ser374Asn | missense_variant | 0.16 |
embC | 4240990 | c.1128A>G | synonymous_variant | 0.16 |
embC | 4240996 | c.1134G>C | synonymous_variant | 0.16 |
embC | 4241017 | c.1155T>C | synonymous_variant | 0.15 |
embC | 4241026 | c.1164C>G | synonymous_variant | 0.15 |
embA | 4245137 | c.1905T>C | synonymous_variant | 0.15 |
embB | 4247059 | c.546C>G | synonymous_variant | 1.0 |
embB | 4247144 | p.Ser211Pro | missense_variant | 1.0 |
embB | 4249369 | c.2856T>C | synonymous_variant | 0.15 |
embB | 4249381 | c.2868A>G | synonymous_variant | 0.17 |
embB | 4249469 | p.Leu986Met | missense_variant | 0.14 |
embB | 4249483 | c.2970C>G | synonymous_variant | 0.15 |
embB | 4249486 | c.2973T>G | synonymous_variant | 0.14 |
ubiA | 4269553 | p.Ala94Gly | missense_variant | 1.0 |
gid | 4408259 | c.-57G>C | upstream_gene_variant | 1.0 |