Run ID: SRR4034769
Sample name:
Date: 04-04-2023 07:03:56
Number of reads: 964124
Percentage reads mapped: 27.65
Strain: lineage4.1.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.1 | Euro-American | T;X;H | None | 0.98 |
lineage4.1.1 | Euro-American (X-type) | X1;X2;X3 | None | 0.92 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.91 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5224 | c.-15_-14delGA | upstream_gene_variant | 0.25 |
gyrB | 7164 | p.Ala642Asp | missense_variant | 0.2 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7459 | p.Arg53Leu | missense_variant | 0.22 |
gyrA | 7499 | c.198G>A | synonymous_variant | 0.17 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7657 | p.Pro119Leu | missense_variant | 0.29 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9320 | c.2019G>C | synonymous_variant | 0.17 |
fgd1 | 491285 | p.Gly168Val | missense_variant | 0.29 |
fgd1 | 491342 | p.Arg187His | missense_variant | 0.8 |
rpoB | 759817 | p.Ser4Tyr | missense_variant | 0.17 |
rpoB | 760452 | p.Val216Ile | missense_variant | 0.15 |
rpoB | 761062 | p.Ala419Val | missense_variant | 0.67 |
rpoB | 761122 | p.Pro439Gln | missense_variant | 0.5 |
rpoB | 762120 | p.Asp772Asn | missense_variant | 0.22 |
rpoB | 762837 | p.Glu1011* | stop_gained | 0.22 |
rpoC | 763381 | c.12C>G | synonymous_variant | 0.17 |
rpoC | 763606 | c.237C>T | synonymous_variant | 0.18 |
rpoC | 764219 | p.Gly284Ser | missense_variant | 0.25 |
rpoC | 764331 | p.Pro321Gln | missense_variant | 0.25 |
rpoC | 764534 | p.Arg389Trp | missense_variant | 0.17 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.22 |
rpoC | 764620 | c.1251G>T | synonymous_variant | 0.29 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 0.83 |
rpoC | 765323 | p.Gly652Ser | missense_variant | 0.25 |
rpoC | 765580 | c.2211G>A | synonymous_variant | 0.33 |
rpoC | 765838 | c.2469G>A | synonymous_variant | 0.2 |
rpoC | 765885 | p.Ser839Tyr | missense_variant | 0.18 |
rpoC | 766625 | p.Leu1086Met | missense_variant | 0.4 |
rpoC | 766861 | c.3492G>A | synonymous_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776041 | p.Ala814Thr | missense_variant | 0.29 |
mmpL5 | 776345 | c.2136C>T | synonymous_variant | 0.2 |
mmpS5 | 778568 | p.Thr113Asn | missense_variant | 0.14 |
mmpR5 | 779375 | p.Pro129Leu | missense_variant | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781717 | p.Ala53Asp | missense_variant | 0.29 |
rpsL | 781927 | c.371delG | frameshift_variant | 0.29 |
rplC | 800717 | c.-92C>A | upstream_gene_variant | 0.14 |
fbiC | 1302757 | c.-173_-168delATCGCG | upstream_gene_variant | 0.2 |
fbiC | 1302891 | c.-40G>T | upstream_gene_variant | 0.25 |
fbiC | 1304067 | c.1137G>C | synonymous_variant | 0.15 |
Rv1258c | 1406143 | p.Leu400Met | missense_variant | 0.18 |
Rv1258c | 1407035 | p.Asn102Lys | missense_variant | 0.5 |
embR | 1416428 | p.Ala307Glu | missense_variant | 0.29 |
embR | 1416520 | c.828G>A | synonymous_variant | 0.25 |
embR | 1416688 | c.660G>A | synonymous_variant | 0.25 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471671 | n.-175G>T | upstream_gene_variant | 0.17 |
rrs | 1471776 | n.-70G>A | upstream_gene_variant | 0.14 |
rrs | 1471896 | n.51T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1471900 | n.55C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472078 | n.233C>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472079 | n.234C>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1473161 | n.1316A>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473164 | n.1319C>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1473172 | n.1327T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.41 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.48 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1473327 | n.1482A>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473328 | n.1483C>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1473533 | n.-125G>T | upstream_gene_variant | 0.18 |
rrl | 1474289 | n.636delT | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474302 | n.645G>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474789 | n.1132G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474839 | n.1182C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474844 | n.1187G>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474866 | n.1209C>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474869 | n.1212G>T | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474892 | n.1235G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1475672 | n.2015C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475673 | n.2016T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475687 | n.2030C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475688 | n.2031G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475692 | n.2035G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475695 | n.2038G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475704 | n.2047C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475707 | n.2050T>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475713 | n.2056C>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475716 | n.2059A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475783 | n.2126T>G | non_coding_transcript_exon_variant | 0.53 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.63 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.52 |
rrl | 1475866 | n.2209T>A | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475877 | n.2220C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476229 | n.2572C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476252 | n.2595T>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.94 |
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 | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476572 | n.2915G>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476577 | n.2920T>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.69 |
inhA | 1674859 | p.Glu220* | stop_gained | 0.25 |
rpsA | 1833438 | c.-104C>A | upstream_gene_variant | 0.4 |
rpsA | 1833633 | c.93_94dupGT | frameshift_variant | 0.22 |
rpsA | 1834110 | p.Trp190* | stop_gained | 0.2 |
rpsA | 1834379 | p.Gln280* | stop_gained | 0.25 |
rpsA | 1834444 | c.903C>A | synonymous_variant | 0.4 |
rpsA | 1834665 | p.Pro375Gln | missense_variant | 0.12 |
rpsA | 1834732 | p.Asp397Glu | missense_variant | 0.22 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918653 | c.714G>A | synonymous_variant | 0.14 |
ndh | 2102397 | p.Ala216Ser | missense_variant | 0.17 |
katG | 2154103 | p.Pro670His | missense_variant | 0.4 |
katG | 2154489 | c.1623C>T | synonymous_variant | 0.29 |
katG | 2154596 | p.Glu506* | stop_gained | 0.25 |
katG | 2155304 | p.His270Asn | missense_variant | 0.33 |
katG | 2155599 | c.513C>T | synonymous_variant | 0.25 |
katG | 2155706 | p.Pro136Ser | missense_variant | 0.25 |
PPE35 | 2168090 | c.2523C>A | synonymous_variant | 0.2 |
PPE35 | 2168504 | c.2109C>A | synonymous_variant | 0.14 |
PPE35 | 2169295 | p.Gly440Ser | missense_variant | 0.14 |
PPE35 | 2170553 | c.60C>A | synonymous_variant | 0.21 |
PPE35 | 2170617 | c.-5G>A | upstream_gene_variant | 0.13 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv1979c | 2223312 | c.-148C>A | upstream_gene_variant | 0.14 |
pncA | 2289161 | c.81G>T | synonymous_variant | 0.15 |
pncA | 2289897 | c.-656G>T | upstream_gene_variant | 0.18 |
pncA | 2289979 | c.-738G>T | upstream_gene_variant | 0.17 |
kasA | 2518719 | p.Ile202Asn | missense_variant | 0.4 |
eis | 2714871 | c.462G>T | synonymous_variant | 0.25 |
eis | 2715198 | c.135G>A | synonymous_variant | 0.5 |
eis | 2715209 | c.123dupC | frameshift_variant | 0.5 |
ahpC | 2725941 | c.-252C>T | upstream_gene_variant | 0.17 |
ahpC | 2726010 | c.-183G>A | upstream_gene_variant | 0.14 |
ahpC | 2726690 | c.498C>T | synonymous_variant | 0.25 |
folC | 2747327 | p.Arg91Leu | missense_variant | 0.22 |
folC | 2747789 | c.-191G>T | upstream_gene_variant | 0.25 |
pepQ | 2859883 | p.Leu179Pro | missense_variant | 0.33 |
ribD | 2986907 | c.69C>A | synonymous_variant | 1.0 |
ribD | 2987154 | c.316C>A | synonymous_variant | 0.33 |
Rv2752c | 3065433 | c.759G>T | synonymous_variant | 0.22 |
Rv2752c | 3065544 | p.Ser216Arg | missense_variant | 0.17 |
Rv2752c | 3065573 | p.Glu207* | stop_gained | 0.29 |
Rv2752c | 3066282 | c.-91G>A | upstream_gene_variant | 0.25 |
thyX | 3067588 | p.Pro120Thr | missense_variant | 0.29 |
thyX | 3067663 | p.Arg95Ser | missense_variant | 0.25 |
thyX | 3067831 | p.Ala39Ser | missense_variant | 0.2 |
thyA | 3074212 | p.Thr87Ile | missense_variant | 0.5 |
ald | 3086780 | c.-40T>A | upstream_gene_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087483 | p.Ala222Ser | missense_variant | 0.17 |
fbiD | 3338942 | c.-176G>T | upstream_gene_variant | 0.5 |
fbiD | 3339051 | c.-67C>A | upstream_gene_variant | 0.4 |
fbiD | 3339223 | p.Glu36* | stop_gained | 0.33 |
fbiD | 3339455 | p.Leu113Pro | missense_variant | 0.67 |
Rv3083 | 3449090 | p.Met196Thr | missense_variant | 0.22 |
Rv3083 | 3449418 | c.915G>A | synonymous_variant | 0.29 |
Rv3083 | 3449744 | p.Ala414Val | missense_variant | 0.29 |
Rv3083 | 3449790 | c.1287C>T | synonymous_variant | 0.2 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474039 | c.33C>A | synonymous_variant | 0.5 |
fprA | 3474598 | p.Gly198Trp | missense_variant | 0.25 |
fprA | 3474764 | p.Arg253His | missense_variant | 0.2 |
fprA | 3475167 | c.1161C>T | synonymous_variant | 1.0 |
Rv3236c | 3612390 | p.Gly243Cys | missense_variant | 0.18 |
Rv3236c | 3612688 | c.429C>A | synonymous_variant | 0.15 |
Rv3236c | 3612847 | c.270G>A | synonymous_variant | 0.29 |
Rv3236c | 3613150 | c.-34G>T | upstream_gene_variant | 0.33 |
fbiB | 3640578 | c.-957C>A | upstream_gene_variant | 0.2 |
fbiB | 3640728 | c.-807G>T | upstream_gene_variant | 0.2 |
fbiA | 3641093 | p.Ser184Ile | missense_variant | 0.29 |
fbiA | 3641447 | p.Thr302Met | missense_variant | 0.5 |
fbiB | 3641589 | p.Gly19Trp | missense_variant | 0.29 |
fbiB | 3641848 | p.Ala105Asp | missense_variant | 0.15 |
fbiB | 3642463 | p.Leu310Pro | missense_variant | 0.25 |
fbiB | 3642672 | c.1140delC | frameshift_variant | 0.25 |
alr | 3840370 | p.Gly351Cys | missense_variant | 0.22 |
alr | 3840628 | c.792delC | frameshift_variant | 0.22 |
alr | 3840728 | c.693G>T | synonymous_variant | 0.33 |
alr | 3840731 | p.Glu230Asp | missense_variant | 0.33 |
alr | 3840754 | p.Arg223Ser | missense_variant | 0.33 |
rpoA | 3877553 | p.Glu319Lys | missense_variant | 1.0 |
rpoA | 3877664 | p.Asp282Tyr | missense_variant | 0.22 |
rpoA | 3877737 | c.771G>A | synonymous_variant | 0.25 |
rpoA | 3877889 | p.Ala207Thr | missense_variant | 0.22 |
rpoA | 3878210 | p.Gln100* | stop_gained | 0.4 |
ddn | 3986699 | c.-145C>G | upstream_gene_variant | 0.22 |
clpC1 | 4038245 | c.2460C>T | synonymous_variant | 1.0 |
clpC1 | 4038416 | c.2289C>A | synonymous_variant | 0.5 |
clpC1 | 4038753 | p.Gln651Leu | missense_variant | 0.33 |
embC | 4239725 | c.-138G>T | upstream_gene_variant | 0.67 |
embC | 4240897 | c.1035C>G | synonymous_variant | 1.0 |
embC | 4241209 | c.1347G>A | synonymous_variant | 0.29 |
embC | 4241515 | c.1653G>A | synonymous_variant | 0.4 |
embC | 4241661 | c.1804delG | frameshift_variant | 0.29 |
embC | 4241725 | c.1863G>T | synonymous_variant | 0.15 |
embA | 4242544 | c.-689C>A | upstream_gene_variant | 0.4 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 0.88 |
embA | 4242895 | c.-338C>A | upstream_gene_variant | 0.5 |
embA | 4244362 | c.1132_1134delGGC | conservative_inframe_deletion | 0.2 |
embA | 4244707 | p.Thr492Asn | missense_variant | 1.0 |
embA | 4244977 | p.Gly582Glu | missense_variant | 0.67 |
embA | 4246404 | p.Glu1058* | stop_gained | 0.25 |
embA | 4246419 | p.Leu1063Met | missense_variant | 0.22 |
embB | 4249352 | p.Arg947Trp | missense_variant | 0.15 |
embB | 4249408 | c.2895G>A | synonymous_variant | 1.0 |
aftB | 4268191 | p.Ala216Thr | missense_variant | 0.67 |
aftB | 4268278 | p.Pro187Thr | missense_variant | 0.33 |
ubiA | 4269028 | p.Gly269Val | missense_variant | 0.25 |
aftB | 4269375 | c.-539G>A | upstream_gene_variant | 0.33 |
ethA | 4326654 | p.Glu274Lys | missense_variant | 0.22 |
ethA | 4327020 | p.Ala152Ser | missense_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338678 | c.-157G>C | upstream_gene_variant | 0.13 |
gid | 4408401 | c.-199T>C | upstream_gene_variant | 0.17 |