Run ID: SRR11349186
Sample name:
Date: 02-04-2023 20:55:05
Number of reads: 3981696
Percentage reads mapped: 82.39
Strain: lineage4.3.3
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.3 | Euro-American (LAM) | mainly-LAM | None | 1.0 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761155 | p.Ser450Leu | missense_variant | 0.93 | rifampicin |
rpoC | 764841 | p.Ile491Thr | missense_variant | 0.84 | rifampicin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6727 | c.-575G>T | upstream_gene_variant | 0.12 |
gyrA | 6728 | c.-574C>T | upstream_gene_variant | 0.12 |
gyrA | 6760 | c.-542G>C | upstream_gene_variant | 0.13 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7475 | c.174A>G | synonymous_variant | 0.11 |
gyrA | 7484 | c.183T>C | synonymous_variant | 0.13 |
gyrA | 7490 | c.189C>G | synonymous_variant | 0.13 |
gyrA | 7496 | c.195C>G | synonymous_variant | 0.14 |
gyrA | 7499 | c.198G>C | synonymous_variant | 0.15 |
gyrA | 7523 | c.222C>G | synonymous_variant | 0.16 |
gyrA | 7526 | c.225G>C | synonymous_variant | 0.16 |
gyrA | 7532 | c.231T>G | synonymous_variant | 0.15 |
gyrA | 7559 | c.258G>A | synonymous_variant | 0.12 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 1.0 |
gyrA | 8990 | c.1689C>G | synonymous_variant | 0.12 |
gyrA | 8993 | c.1692C>T | synonymous_variant | 0.13 |
gyrA | 8996 | c.1695T>C | synonymous_variant | 0.13 |
gyrA | 8998 | p.Leu566Trp | missense_variant | 0.13 |
gyrA | 9018 | p.Gln573Lys | missense_variant | 0.15 |
gyrA | 9026 | c.1725G>C | synonymous_variant | 0.14 |
gyrA | 9029 | c.1728T>C | synonymous_variant | 0.13 |
gyrA | 9032 | c.1731T>C | synonymous_variant | 0.13 |
gyrA | 9035 | c.1734G>C | synonymous_variant | 0.13 |
gyrA | 9044 | c.1743C>G | synonymous_variant | 0.13 |
gyrA | 9051 | c.1750T>C | synonymous_variant | 0.13 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 575909 | p.Leu188Val | missense_variant | 1.0 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.35 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.13 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.12 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.14 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.14 |
rpoB | 760244 | c.438G>C | synonymous_variant | 0.14 |
rpoB | 761051 | c.1245G>T | synonymous_variant | 0.15 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.14 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.14 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.14 |
rpoB | 761063 | c.1257C>G | synonymous_variant | 0.15 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.16 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.13 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.13 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.12 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.12 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.12 |
rpoB | 761693 | c.1887G>C | synonymous_variant | 0.11 |
rpoB | 761955 | p.Ile717Val | missense_variant | 0.14 |
rpoB | 761969 | c.2163G>A | synonymous_variant | 0.18 |
rpoB | 761990 | c.2184G>C | synonymous_variant | 0.18 |
rpoB | 762008 | c.2202C>T | synonymous_variant | 0.16 |
rpoB | 762014 | c.2208C>G | synonymous_variant | 0.17 |
rpoB | 762038 | c.2232C>T | synonymous_variant | 0.13 |
rpoB | 762047 | c.2241G>A | synonymous_variant | 0.12 |
rpoB | 762065 | c.2259T>G | synonymous_variant | 0.14 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.11 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.11 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 0.14 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.15 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 0.16 |
rpoB | 762221 | c.2415G>A | synonymous_variant | 0.13 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.13 |
rpoB | 762236 | c.2430G>C | synonymous_variant | 0.13 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.13 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.12 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.12 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.17 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.16 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.2 |
rpoC | 762989 | c.-381G>A | upstream_gene_variant | 0.19 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.18 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 0.21 |
rpoC | 763034 | c.-336C>A | upstream_gene_variant | 0.2 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.21 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.24 |
rpoC | 763082 | c.-288C>T | upstream_gene_variant | 0.22 |
rpoC | 763085 | c.-285C>T | upstream_gene_variant | 0.22 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 0.21 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.21 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.2 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.2 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.18 |
rpoC | 763142 | c.-228C>G | upstream_gene_variant | 0.19 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.13 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.13 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.14 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.15 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.13 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.13 |
rpoC | 764713 | c.1344G>T | synonymous_variant | 0.15 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.17 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.16 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.18 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.18 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.15 |
rpoC | 764810 | p.Pro481Ala | missense_variant | 0.16 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.16 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.15 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.15 |
rpoC | 764869 | c.1500C>T | synonymous_variant | 0.13 |
rpoC | 764875 | c.1506C>A | synonymous_variant | 0.14 |
rpoC | 764878 | c.1509C>G | synonymous_variant | 0.13 |
rpoC | 764887 | c.1518G>C | synonymous_variant | 0.13 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.13 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 0.12 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.12 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.14 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.87 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpR5 | 778346 | c.-644G>A | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473129 | n.1284C>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473288 | n.1443C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473291 | n.1446G>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473815 | n.158T>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474263 | n.606G>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474282 | n.625G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474376 | n.719T>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474507 | n.850G>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474803 | n.1146G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475764 | n.2107A>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475765 | n.2108A>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476295 | n.2638C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476311 | n.2654G>A | non_coding_transcript_exon_variant | 0.22 |
rpsA | 1833604 | c.63C>T | synonymous_variant | 0.12 |
rpsA | 1833619 | c.78A>C | synonymous_variant | 0.13 |
rpsA | 1833625 | c.84A>G | synonymous_variant | 0.13 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.16 |
rpsA | 1833664 | c.123C>G | synonymous_variant | 0.15 |
rpsA | 1833685 | c.144G>C | synonymous_variant | 0.12 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.12 |
rpsA | 1833748 | c.207C>G | synonymous_variant | 0.12 |
rpsA | 1833760 | c.219C>T | synonymous_variant | 0.14 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.16 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.15 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.14 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 0.13 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 0.13 |
rpsA | 1833838 | c.297G>T | synonymous_variant | 0.14 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.14 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.13 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.14 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.14 |
rpsA | 1833874 | c.333T>G | synonymous_variant | 0.13 |
rpsA | 1833886 | c.345C>G | synonymous_variant | 0.13 |
rpsA | 1833892 | c.351G>A | synonymous_variant | 0.12 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.15 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.15 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.17 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.15 |
rpsA | 1833991 | c.450C>G | synonymous_variant | 0.15 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.15 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.11 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.12 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.12 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.12 |
rpsA | 1834297 | c.756C>T | synonymous_variant | 0.13 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.13 |
rpsA | 1834339 | c.798C>T | synonymous_variant | 0.12 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.12 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.12 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.11 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.15 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.17 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.18 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.17 |
rpsA | 1834480 | c.939C>G | synonymous_variant | 0.18 |
rpsA | 1834483 | c.942G>A | synonymous_variant | 0.18 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.19 |
rpsA | 1834498 | c.957C>T | synonymous_variant | 0.19 |
rpsA | 1834520 | p.Ala327Ser | missense_variant | 0.15 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.19 |
rpsA | 1834543 | c.1002C>G | synonymous_variant | 0.19 |
rpsA | 1834552 | c.1011G>T | synonymous_variant | 0.17 |
rpsA | 1834555 | c.1014T>G | synonymous_variant | 0.17 |
rpsA | 1834557 | p.Ala339Gly | missense_variant | 0.16 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 0.14 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.14 |
rpsA | 1834612 | c.1071G>C | synonymous_variant | 0.14 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 0.13 |
rpsA | 1834622 | c.1081_1083delTCGinsAGC | synonymous_variant | 0.13 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.14 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.14 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 0.99 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289208 | p.Asp12Tyr | missense_variant | 1.0 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 1.0 |
folC | 2747225 | p.Arg125Gln | missense_variant | 1.0 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3878160 | c.348C>G | synonymous_variant | 0.11 |
rpoA | 3878169 | c.339G>C | synonymous_variant | 0.11 |
rpoA | 3878184 | c.324C>T | synonymous_variant | 0.12 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.12 |
rpoA | 3878259 | c.249G>C | synonymous_variant | 0.12 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.14 |
rpoA | 3878301 | c.207C>G | synonymous_variant | 0.12 |
rpoA | 3878310 | c.198G>T | synonymous_variant | 0.12 |
rpoA | 3878313 | c.195G>C | synonymous_variant | 0.12 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.13 |
rpoA | 3878331 | c.177A>G | synonymous_variant | 0.13 |
rpoA | 3878334 | c.174T>C | synonymous_variant | 0.13 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.13 |
rpoA | 3878364 | c.144A>C | synonymous_variant | 0.12 |
rpoA | 3878618 | c.-111A>C | upstream_gene_variant | 0.25 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 1.0 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.14 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.14 |
clpC1 | 4039733 | c.972G>C | synonymous_variant | 0.13 |
clpC1 | 4039739 | c.966C>G | synonymous_variant | 0.13 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.17 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.18 |
clpC1 | 4039769 | c.936C>T | synonymous_variant | 0.17 |
clpC1 | 4039775 | c.930G>C | synonymous_variant | 0.17 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.17 |
clpC1 | 4039793 | c.912C>G | synonymous_variant | 0.17 |
clpC1 | 4039805 | c.900C>T | synonymous_variant | 0.18 |
clpC1 | 4039814 | c.891C>G | synonymous_variant | 0.17 |
clpC1 | 4039817 | c.888A>C | synonymous_variant | 0.18 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.18 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.17 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.16 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.14 |
clpC1 | 4039907 | c.798G>A | synonymous_variant | 0.14 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.12 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.12 |
clpC1 | 4039943 | c.762G>C | synonymous_variant | 0.13 |
clpC1 | 4039946 | c.759A>G | synonymous_variant | 0.13 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.13 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.13 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.13 |
clpC1 | 4039964 | c.741C>G | synonymous_variant | 0.15 |
clpC1 | 4039975 | p.Asp244Asn | missense_variant | 0.17 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.17 |
clpC1 | 4039982 | c.723G>A | synonymous_variant | 0.16 |
clpC1 | 4040000 | c.705C>T | synonymous_variant | 0.15 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.16 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.15 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.13 |
clpC1 | 4040042 | c.663C>T | synonymous_variant | 0.14 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338367 | p.Leu52Gln | missense_variant | 1.0 |
whiB6 | 4338593 | c.-73delT | upstream_gene_variant | 1.0 |
whiB6 | 4338596 | c.-75G>C | upstream_gene_variant | 1.0 |
gid | 4407986 | p.Gly73Arg | missense_variant | 1.0 |
gid | 4408156 | p.Leu16Arg | missense_variant | 1.0 |