Run ID: SRR6785527
Sample name:
Date: 04-04-2023 16:02:14
Number of reads: 2855538
Percentage reads mapped: 83.2
Strain: lineage2.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.97 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 0.98 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 0.98 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6670 | c.-632G>C | upstream_gene_variant | 0.14 |
gyrA | 6673 | c.-629A>C | upstream_gene_variant | 0.14 |
gyrA | 6676 | c.-626T>G | upstream_gene_variant | 0.14 |
gyrA | 6700 | c.-602T>C | upstream_gene_variant | 0.14 |
gyrA | 6703 | c.-599G>C | upstream_gene_variant | 0.14 |
gyrA | 6709 | c.-593A>G | upstream_gene_variant | 0.16 |
gyrA | 6712 | c.-590G>C | upstream_gene_variant | 0.15 |
gyrA | 6728 | c.-574_-572delCTAinsTTG | upstream_gene_variant | 0.15 |
gyrA | 6742 | c.-560A>G | upstream_gene_variant | 0.14 |
gyrA | 6745 | c.-557T>G | upstream_gene_variant | 0.14 |
gyrA | 6751 | c.-551G>C | upstream_gene_variant | 0.13 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7427 | c.126G>C | synonymous_variant | 0.14 |
gyrA | 7442 | c.141G>C | synonymous_variant | 0.15 |
gyrA | 7451 | c.150C>G | synonymous_variant | 0.16 |
gyrA | 7457 | c.156T>C | synonymous_variant | 0.16 |
gyrA | 7475 | c.174A>G | synonymous_variant | 0.13 |
gyrA | 7480 | p.Phe60Tyr | missense_variant | 0.13 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8372 | c.1071G>C | synonymous_variant | 0.13 |
gyrA | 8375 | c.1074G>C | synonymous_variant | 0.13 |
gyrA | 8382 | p.Leu361Met | missense_variant | 0.14 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 0.95 |
mshA | 575770 | c.423G>A | synonymous_variant | 0.14 |
mshA | 575771 | p.Val142Ser | missense_variant | 0.14 |
mshA | 575779 | c.432A>G | synonymous_variant | 0.16 |
mshA | 575782 | c.435G>C | synonymous_variant | 0.16 |
mshA | 575821 | c.474G>C | synonymous_variant | 0.16 |
mshA | 575824 | c.477T>G | synonymous_variant | 0.19 |
mshA | 575830 | c.483C>G | synonymous_variant | 0.17 |
mshA | 575833 | c.486C>G | synonymous_variant | 0.18 |
mshA | 575845 | c.498C>T | synonymous_variant | 0.18 |
mshA | 575884 | c.537G>C | synonymous_variant | 0.14 |
mshA | 575887 | c.540G>C | synonymous_variant | 0.14 |
mshA | 575907 | p.Ala187Val | missense_variant | 0.89 |
ccsA | 620625 | p.Ile245Met | missense_variant | 0.99 |
rpoB | 760340 | c.534G>T | synonymous_variant | 0.13 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.14 |
rpoB | 760370 | c.564C>G | synonymous_variant | 0.14 |
rpoB | 760381 | p.Thr192Met | missense_variant | 0.14 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.14 |
rpoB | 760412 | c.606C>G | synonymous_variant | 0.14 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.15 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.16 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.13 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.16 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.16 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.16 |
rpoB | 761006 | c.1200C>G | synonymous_variant | 0.17 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.14 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.15 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.17 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.17 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.17 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.18 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.14 |
rpoB | 761306 | c.1500C>G | synonymous_variant | 0.17 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.95 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.17 |
rpoC | 763486 | c.117T>G | synonymous_variant | 0.19 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.23 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.22 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.17 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.17 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.16 |
rpoC | 763603 | c.234C>T | synonymous_variant | 0.14 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.15 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.19 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.18 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.2 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.2 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.23 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.24 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.25 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.25 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.26 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.23 |
rpoC | 763774 | c.405G>C | synonymous_variant | 0.24 |
rpoC | 763807 | c.438T>C | synonymous_variant | 0.22 |
rpoC | 763816 | c.447C>G | synonymous_variant | 0.2 |
rpoC | 763835 | p.Ala156Met | missense_variant | 0.17 |
rpoC | 763853 | p.Val162Ile | missense_variant | 0.16 |
rpoC | 763858 | c.489A>G | synonymous_variant | 0.16 |
rpoC | 763872 | p.Gly168Ala | missense_variant | 0.15 |
rpoC | 763876 | p.Glu169Asp | missense_variant | 0.14 |
rpoC | 763879 | c.510A>G | synonymous_variant | 0.14 |
rpoC | 763900 | c.531G>C | synonymous_variant | 0.14 |
rpoC | 763991 | p.Ile208Leu | missense_variant | 0.15 |
rpoC | 763996 | c.627T>C | synonymous_variant | 0.14 |
rpoC | 764002 | c.633C>G | synonymous_variant | 0.15 |
rpoC | 764005 | c.636G>C | synonymous_variant | 0.15 |
rpoC | 764026 | p.Leu219Phe | missense_variant | 0.14 |
rpoC | 764112 | p.Tyr248Phe | missense_variant | 0.14 |
rpoC | 764116 | c.747C>T | synonymous_variant | 0.14 |
rpoC | 764215 | c.846A>G | synonymous_variant | 0.16 |
rpoC | 764236 | c.867G>A | synonymous_variant | 0.14 |
rpoC | 764338 | c.969G>A | synonymous_variant | 0.16 |
rpoC | 764353 | c.984G>C | synonymous_variant | 0.16 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.15 |
rpoC | 764381 | p.Ser338Thr | missense_variant | 0.12 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.14 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.19 |
rpoC | 764872 | c.1503A>G | synonymous_variant | 0.2 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.23 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.19 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 0.19 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 0.19 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.18 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.17 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.15 |
rpoC | 765319 | c.1950A>G | synonymous_variant | 0.13 |
rpoC | 765421 | c.2052C>G | synonymous_variant | 0.14 |
rpoC | 765529 | c.2160C>T | synonymous_variant | 0.13 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.2 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 0.18 |
rpoC | 765739 | c.2370G>T | synonymous_variant | 0.16 |
rpoC | 765751 | c.2382C>G | synonymous_variant | 0.15 |
rpoC | 765753 | p.Asp795Ala | missense_variant | 0.14 |
rpoC | 765772 | c.2403C>G | synonymous_variant | 0.15 |
rpoC | 765784 | c.2415C>G | synonymous_variant | 0.16 |
rpoC | 765787 | c.2418C>T | synonymous_variant | 0.16 |
rpoC | 765793 | c.2424C>G | synonymous_variant | 0.13 |
rpoC | 765796 | c.2427C>T | synonymous_variant | 0.14 |
rpoC | 765811 | c.2442T>C | synonymous_variant | 0.15 |
rpoC | 765814 | c.2445A>G | synonymous_variant | 0.15 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 0.16 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.15 |
rpoC | 765850 | c.2481G>C | synonymous_variant | 0.15 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.17 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.17 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.17 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.13 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.13 |
rpoC | 765982 | c.2613C>G | synonymous_variant | 0.15 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.13 |
rpoC | 766010 | p.Ser881Thr | missense_variant | 0.13 |
rpoC | 766027 | c.2658G>C | synonymous_variant | 0.13 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.15 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.16 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.19 |
rpoC | 766801 | c.3432C>G | synonymous_variant | 0.19 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.2 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.17 |
rpoC | 766864 | c.3495G>C | synonymous_variant | 0.15 |
rpoC | 766894 | c.3525T>C | synonymous_variant | 0.14 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.14 |
rpoC | 766972 | c.3603G>C | synonymous_variant | 0.14 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.23 |
rpoC | 767009 | c.3640_3642delTCGinsAGC | synonymous_variant | 0.23 |
rpoC | 767014 | c.3645G>C | synonymous_variant | 0.23 |
rpoC | 767033 | c.3664_3666delTCGinsAGT | synonymous_variant | 0.24 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 0.2 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.22 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.21 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.19 |
rpoC | 767134 | c.3765C>A | synonymous_variant | 0.16 |
rpoC | 767158 | c.3789T>C | synonymous_variant | 0.16 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.15 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.16 |
rpoC | 767206 | c.3837C>G | synonymous_variant | 0.16 |
rpoC | 767209 | c.3840T>C | synonymous_variant | 0.14 |
rpoC | 767212 | c.3843G>C | synonymous_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 0.96 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 0.95 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 0.98 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.15 |
rpsL | 781838 | c.279G>C | synonymous_variant | 0.16 |
rpsL | 781841 | c.282C>G | synonymous_variant | 0.15 |
rpsL | 781865 | c.306G>C | synonymous_variant | 0.15 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.15 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.15 |
rpsL | 781877 | c.318T>C | synonymous_variant | 0.16 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.15 |
rpsL | 781898 | c.339A>T | synonymous_variant | 0.15 |
rpsL | 781916 | c.357T>C | synonymous_variant | 0.15 |
rplC | 801367 | p.Ala187Thr | missense_variant | 0.13 |
rplC | 801402 | c.594T>C | synonymous_variant | 0.17 |
rplC | 801405 | c.597T>C | synonymous_variant | 0.17 |
rplC | 801423 | c.615G>C | synonymous_variant | 0.15 |
rplC | 801426 | c.618C>G | synonymous_variant | 0.15 |
rplC | 801427 | p.Met207Val | missense_variant | 0.15 |
rplC | 801438 | c.630T>C | synonymous_variant | 0.15 |
rplC | 801442 | p.Ile212Val | missense_variant | 0.17 |
fbiC | 1303860 | c.930A>C | synonymous_variant | 0.13 |
fbiC | 1303884 | c.954T>G | synonymous_variant | 0.18 |
fbiC | 1303905 | c.975G>C | synonymous_variant | 0.17 |
fbiC | 1303914 | c.984C>G | synonymous_variant | 0.19 |
fbiC | 1303920 | c.990C>T | synonymous_variant | 0.17 |
fbiC | 1303971 | c.1041T>C | synonymous_variant | 0.15 |
fbiC | 1303980 | c.1050G>A | synonymous_variant | 0.17 |
fbiC | 1303998 | c.1068T>G | synonymous_variant | 0.17 |
fbiC | 1304004 | c.1074A>G | synonymous_variant | 0.15 |
fbiC | 1304174 | p.Val415Ala | missense_variant | 0.13 |
fbiC | 1304184 | c.1254G>C | synonymous_variant | 0.14 |
fbiC | 1304187 | c.1257T>C | synonymous_variant | 0.14 |
fbiC | 1304208 | c.1278C>T | synonymous_variant | 0.14 |
fbiC | 1304893 | p.Gly655Ser | missense_variant | 0.13 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475088 | n.1431A>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475199 | n.1542G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475313 | n.1656G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475402 | n.1745C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475638 | n.1981C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475659 | n.2002G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.17 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.13 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.19 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.2 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.24 |
rpsA | 1833886 | c.345C>G | synonymous_variant | 0.31 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.28 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.26 |
rpsA | 1833971 | c.430C>T | synonymous_variant | 0.18 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.2 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.19 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.16 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.14 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 0.97 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.17 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.18 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv2752c | 3065109 | c.1081_1083delAGAinsCGC | synonymous_variant | 0.14 |
Rv2752c | 3065115 | c.1077C>A | synonymous_variant | 0.14 |
Rv2752c | 3065142 | c.1050A>C | synonymous_variant | 0.14 |
Rv2752c | 3065146 | p.Phe349Tyr | missense_variant | 0.13 |
Rv2752c | 3065151 | c.1041G>C | synonymous_variant | 0.15 |
thyX | 3067391 | c.555G>C | synonymous_variant | 0.13 |
thyX | 3067394 | c.552G>C | synonymous_variant | 0.13 |
thyX | 3067439 | c.507A>G | synonymous_variant | 0.16 |
thyX | 3067445 | c.501C>G | synonymous_variant | 0.16 |
thyX | 3067457 | c.489C>G | synonymous_variant | 0.18 |
thyX | 3067465 | p.Ile161Val | missense_variant | 0.2 |
thyX | 3067475 | c.471A>G | synonymous_variant | 0.19 |
thyX | 3067490 | c.456C>G | synonymous_variant | 0.16 |
thyX | 3067493 | c.453A>G | synonymous_variant | 0.17 |
thyX | 3067515 | p.Ser144Thr | missense_variant | 0.17 |
thyX | 3067530 | p.Ala139Ser | missense_variant | 0.17 |
thyX | 3067545 | p.Glu134Ala | missense_variant | 0.17 |
thyX | 3067549 | p.Thr133Ala | missense_variant | 0.16 |
thyX | 3067559 | c.387C>G | synonymous_variant | 0.13 |
thyX | 3067781 | c.165C>A | synonymous_variant | 0.16 |
thyX | 3067793 | c.153T>C | synonymous_variant | 0.16 |
thyX | 3067799 | c.147G>A | synonymous_variant | 0.17 |
thyX | 3067802 | c.144C>G | synonymous_variant | 0.19 |
thyX | 3067814 | c.132T>C | synonymous_variant | 0.2 |
thyX | 3067850 | c.96A>C | synonymous_variant | 0.17 |
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 | 1.0 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.13 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.14 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.13 |
clpC1 | 4040267 | c.438A>G | synonymous_variant | 0.16 |
clpC1 | 4040273 | c.432T>C | synonymous_variant | 0.16 |
clpC1 | 4040277 | c.427_428delTCinsAG | synonymous_variant | 0.16 |
clpC1 | 4040279 | c.426C>G | synonymous_variant | 0.17 |
clpC1 | 4040291 | c.414G>C | synonymous_variant | 0.19 |
clpC1 | 4040318 | c.387C>G | synonymous_variant | 0.18 |
clpC1 | 4040330 | c.375C>G | synonymous_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 0.99 |
embA | 4244582 | c.1350T>C | synonymous_variant | 0.14 |
embB | 4246548 | p.Pro12Gln | missense_variant | 0.12 |
embB | 4246555 | c.42G>C | synonymous_variant | 0.15 |
embB | 4246556 | p.Ala15Pro | missense_variant | 0.15 |
embB | 4247491 | c.978G>C | synonymous_variant | 0.14 |
embB | 4247497 | c.984T>C | synonymous_variant | 0.15 |
embB | 4247512 | c.999T>C | synonymous_variant | 0.16 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 0.96 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |
gid | 4408107 | p.Glu32Asp | missense_variant | 0.95 |