Run ID: SRR1181251
Sample name:
Date: 03-04-2023 04:41:47
Number of reads: 3510673
Percentage reads mapped: 79.04
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 | 0.98 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
embB | 4247448 | p.His312Arg | missense_variant | 0.14 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6307 | c.-995T>G | upstream_gene_variant | 0.15 |
gyrA | 6730 | c.-572A>G | upstream_gene_variant | 0.14 |
gyrA | 6745 | c.-557T>C | upstream_gene_variant | 0.14 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7541 | c.240C>G | synonymous_variant | 0.14 |
gyrA | 7547 | c.246C>T | synonymous_variant | 0.15 |
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 | 7799 | c.498A>G | synonymous_variant | 0.14 |
gyrA | 8603 | c.1302A>G | synonymous_variant | 0.14 |
gyrA | 8609 | c.1308G>C | synonymous_variant | 0.16 |
gyrA | 8619 | c.1318T>C | synonymous_variant | 0.16 |
gyrA | 8645 | c.1344C>T | synonymous_variant | 0.14 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491106 | c.324T>C | synonymous_variant | 0.17 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.99 |
mshA | 575907 | p.Ala187Val | missense_variant | 0.9 |
ccsA | 620415 | c.525T>C | synonymous_variant | 0.15 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.14 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.15 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.14 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.14 |
rpoB | 761537 | c.1731C>G | synonymous_variant | 0.14 |
rpoB | 761561 | c.1755C>G | synonymous_variant | 0.15 |
rpoB | 761564 | c.1758G>C | synonymous_variant | 0.15 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.15 |
rpoB | 761612 | c.1806G>T | synonymous_variant | 0.15 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.16 |
rpoB | 761636 | c.1830G>T | synonymous_variant | 0.16 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.15 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.15 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.17 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.14 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 1.0 |
rpoC | 762395 | c.-975G>C | upstream_gene_variant | 0.15 |
rpoC | 762404 | c.-966T>C | upstream_gene_variant | 0.14 |
rpoC | 762410 | c.-960T>C | upstream_gene_variant | 0.17 |
rpoC | 762416 | c.-954A>G | upstream_gene_variant | 0.18 |
rpoC | 762470 | c.-900G>C | upstream_gene_variant | 0.15 |
rpoC | 762857 | c.-513C>G | upstream_gene_variant | 0.15 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.19 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 0.2 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.2 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.2 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.2 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.17 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.19 |
rpoC | 763169 | c.-201A>G | upstream_gene_variant | 0.22 |
rpoC | 763202 | c.-168A>G | upstream_gene_variant | 0.16 |
rpoC | 763206 | c.-164_-163delAGinsTC | upstream_gene_variant | 0.15 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.14 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.14 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.16 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.18 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.21 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.21 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.19 |
rpoC | 763781 | p.Ser138Ala | missense_variant | 0.18 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.14 |
rpoC | 764024 | c.655T>C | synonymous_variant | 0.14 |
rpoC | 764083 | c.714A>G | synonymous_variant | 0.22 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.15 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.24 |
rpoC | 764284 | c.915G>C | synonymous_variant | 0.17 |
rpoC | 764317 | c.948C>G | synonymous_variant | 0.2 |
rpoC | 764320 | c.951C>T | synonymous_variant | 0.16 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.18 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.14 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.14 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.2 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.16 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.15 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.17 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.24 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.16 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.2 |
rpoC | 764755 | c.1386C>T | synonymous_variant | 0.14 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.18 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 0.17 |
rpoC | 764932 | c.1563C>G | synonymous_variant | 0.14 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.14 |
rpoC | 765547 | c.2178C>A | synonymous_variant | 0.16 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.18 |
rpoC | 765562 | c.2193G>C | synonymous_variant | 0.18 |
rpoC | 765583 | c.2214G>T | synonymous_variant | 0.17 |
rpoC | 765628 | c.2259G>C | synonymous_variant | 0.14 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.16 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 0.18 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.15 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.15 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.16 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.15 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.14 |
rpoC | 765979 | c.2610C>G | synonymous_variant | 0.15 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.14 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 0.18 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.21 |
rpoC | 766486 | c.3117A>G | synonymous_variant | 0.17 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.21 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.22 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.21 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.18 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.15 |
rpoC | 766972 | c.3603G>C | synonymous_variant | 0.23 |
rpoC | 766975 | c.3606C>T | synonymous_variant | 0.16 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.28 |
rpoC | 767002 | c.3633G>C | synonymous_variant | 0.27 |
rpoC | 767033 | c.3664_3666delTCGinsAGT | synonymous_variant | 0.27 |
rpoC | 767044 | c.3675G>A | synonymous_variant | 0.14 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.23 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.26 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.18 |
rpoC | 767221 | c.3852C>G | synonymous_variant | 0.15 |
rpoC | 767233 | c.3864T>C | synonymous_variant | 0.15 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
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 | 0.98 |
rpsL | 781649 | c.90T>C | synonymous_variant | 0.14 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.15 |
rpsL | 781709 | c.150G>C | synonymous_variant | 0.14 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.15 |
rpsL | 781718 | c.159C>G | synonymous_variant | 0.15 |
rpsL | 781721 | c.162C>G | synonymous_variant | 0.14 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.2 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.25 |
rpsL | 781808 | c.249C>T | synonymous_variant | 0.16 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.14 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.13 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.15 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.14 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.16 |
rpsL | 781929 | p.Gly124Ser | missense_variant | 0.15 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.19 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.2 |
rplC | 800648 | c.-161A>C | upstream_gene_variant | 0.19 |
rplC | 800693 | c.-116A>C | upstream_gene_variant | 0.19 |
rplC | 800759 | c.-50C>T | upstream_gene_variant | 0.13 |
rplC | 800865 | c.57A>G | synonymous_variant | 0.14 |
rplC | 800922 | c.114C>G | synonymous_variant | 0.14 |
rplC | 800934 | c.126C>G | synonymous_variant | 0.13 |
rplC | 801210 | c.402T>C | synonymous_variant | 0.16 |
rplC | 801297 | c.489C>T | synonymous_variant | 0.15 |
rplC | 801312 | c.504G>C | synonymous_variant | 0.17 |
rplC | 801339 | c.531T>G | synonymous_variant | 0.14 |
rplC | 801341 | p.Leu178His | missense_variant | 0.13 |
fbiC | 1303545 | c.615A>G | synonymous_variant | 0.15 |
fbiC | 1304832 | c.1902C>T | synonymous_variant | 0.15 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
atpE | 1461161 | c.117C>T | synonymous_variant | 0.13 |
atpE | 1461219 | c.175T>C | synonymous_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471935 | n.90T>C | non_coding_transcript_exon_variant | 0.16 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473887 | n.230T>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474034 | n.377G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474083 | n.426C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474717 | n.1060A>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474794 | n.1137C>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475638 | n.1981C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476035 | n.2378G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476580 | n.2923G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476732 | n.3075T>C | non_coding_transcript_exon_variant | 0.13 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.14 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.99 |
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 |
kasA | 2517941 | c.-174C>G | upstream_gene_variant | 0.17 |
kasA | 2517956 | c.-159G>A | upstream_gene_variant | 0.15 |
kasA | 2518561 | c.447T>C | synonymous_variant | 0.15 |
kasA | 2518567 | c.453G>T | synonymous_variant | 0.16 |
kasA | 2518588 | c.474T>C | synonymous_variant | 0.16 |
kasA | 2518591 | c.477G>C | synonymous_variant | 0.15 |
kasA | 2518642 | c.528A>G | synonymous_variant | 0.16 |
kasA | 2518648 | c.534C>T | synonymous_variant | 0.13 |
kasA | 2518672 | c.558G>C | synonymous_variant | 0.22 |
kasA | 2518681 | c.567C>T | synonymous_variant | 0.16 |
kasA | 2518684 | c.570C>A | synonymous_variant | 0.16 |
kasA | 2518711 | c.597A>G | synonymous_variant | 0.22 |
kasA | 2518714 | c.600A>T | synonymous_variant | 0.14 |
kasA | 2518747 | c.633C>G | synonymous_variant | 0.18 |
kasA | 2518864 | c.750G>C | synonymous_variant | 0.14 |
kasA | 2518885 | c.771T>C | synonymous_variant | 0.18 |
kasA | 2518939 | c.825T>C | synonymous_variant | 0.15 |
kasA | 2518942 | c.828T>C | synonymous_variant | 0.16 |
kasA | 2518951 | c.837G>A | synonymous_variant | 0.16 |
kasA | 2518960 | c.846C>G | synonymous_variant | 0.16 |
kasA | 2518963 | c.849T>C | synonymous_variant | 0.15 |
pepQ | 2860448 | c.-30C>A | upstream_gene_variant | 0.14 |
thyX | 3067316 | c.630A>G | synonymous_variant | 0.17 |
thyX | 3067325 | c.621A>G | synonymous_variant | 0.17 |
thyX | 3067373 | c.573C>G | synonymous_variant | 0.18 |
thyX | 3067874 | c.72C>G | synonymous_variant | 0.14 |
thyA | 3073932 | c.540C>T | synonymous_variant | 0.18 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.14 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.13 |
thyA | 3074031 | c.441T>C | synonymous_variant | 0.15 |
thyA | 3074037 | c.435C>G | synonymous_variant | 0.14 |
thyA | 3074053 | p.Arg140Gln | missense_variant | 0.15 |
thyA | 3074056 | p.Glu139Pro | missense_variant | 0.15 |
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 | 3877613 | p.Ile299Val | missense_variant | 0.14 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.19 |
rpoA | 3877680 | c.828G>C | synonymous_variant | 0.16 |
rpoA | 3877692 | c.816G>C | synonymous_variant | 0.19 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.14 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.14 |
rpoA | 3878157 | c.351C>G | synonymous_variant | 0.18 |
rpoA | 3878163 | c.345C>T | synonymous_variant | 0.17 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.2 |
rpoA | 3878217 | c.291A>G | synonymous_variant | 0.24 |
rpoA | 3878247 | c.261G>C | synonymous_variant | 0.26 |
rpoA | 3878256 | c.252G>C | synonymous_variant | 0.28 |
rpoA | 3878262 | c.246C>T | synonymous_variant | 0.27 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.24 |
rpoA | 3878283 | p.Glu75Asp | missense_variant | 0.24 |
rpoA | 3878295 | c.213A>G | synonymous_variant | 0.18 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.18 |
rpoA | 3878331 | c.177A>G | synonymous_variant | 0.19 |
rpoA | 3878334 | c.174T>C | synonymous_variant | 0.19 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.2 |
clpC1 | 4038519 | p.Arg729Gln | missense_variant | 0.2 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.21 |
clpC1 | 4038536 | c.2169C>T | synonymous_variant | 0.2 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.14 |
clpC1 | 4038713 | c.1992T>C | synonymous_variant | 0.14 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.14 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.15 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.16 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.17 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.14 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 0.13 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.15 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.16 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.14 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.15 |
clpC1 | 4039574 | c.1131G>C | synonymous_variant | 0.14 |
clpC1 | 4039589 | c.1116G>T | synonymous_variant | 0.14 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.19 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.18 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.16 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.15 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.13 |
clpC1 | 4040444 | c.261C>T | synonymous_variant | 0.17 |
clpC1 | 4040459 | c.246C>G | synonymous_variant | 0.18 |
clpC1 | 4040471 | c.234T>C | synonymous_variant | 0.18 |
clpC1 | 4040480 | c.225T>C | synonymous_variant | 0.21 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.15 |
clpC1 | 4040528 | c.177G>C | synonymous_variant | 0.13 |
embC | 4240486 | c.624G>A | synonymous_variant | 0.16 |
embC | 4240489 | c.627A>G | synonymous_variant | 0.16 |
embC | 4240495 | c.633T>C | synonymous_variant | 0.17 |
embC | 4241140 | c.1278A>G | synonymous_variant | 0.15 |
embA | 4242391 | c.-842G>T | upstream_gene_variant | 0.15 |
embA | 4242400 | c.-833C>G | upstream_gene_variant | 0.15 |
embC | 4242402 | p.Arg847His | missense_variant | 0.15 |
embA | 4242406 | c.-827A>T | upstream_gene_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embB | 4246567 | c.54G>T | synonymous_variant | 1.0 |
embB | 4247470 | c.957T>C | synonymous_variant | 0.17 |
embB | 4247497 | c.984T>C | synonymous_variant | 0.16 |
embB | 4247500 | c.987C>G | synonymous_variant | 0.16 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.17 |
embB | 4247554 | c.1041T>C | synonymous_variant | 0.15 |
embB | 4247590 | c.1077A>G | synonymous_variant | 0.16 |
embB | 4248070 | c.1557T>C | synonymous_variant | 0.13 |
embB | 4248277 | c.1764G>C | synonymous_variant | 0.15 |
aftB | 4267535 | c.1302A>G | synonymous_variant | 0.13 |
aftB | 4267556 | c.1281G>C | synonymous_variant | 0.14 |
aftB | 4267622 | p.Ser405Thr | missense_variant | 0.14 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 0.87 |
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 |