Run ID: ERR4821578
Sample name:
Date: 01-04-2023 17:19:55
Number of reads: 1555803
Percentage reads mapped: 87.27
Strain: lineage4.1.2.1
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 | 0.99 |
lineage4.1.2 | Euro-American | T;H | None | 0.99 |
lineage4.1.2.1 | Euro-American (Haarlem) | T1;H1 | RD182 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7595 | c.294C>G | synonymous_variant | 0.15 |
gyrA | 7601 | c.300C>G | synonymous_variant | 0.15 |
gyrA | 7607 | c.306C>G | synonymous_variant | 0.15 |
gyrA | 7622 | c.321C>T | synonymous_variant | 0.14 |
gyrA | 7625 | c.324G>C | synonymous_variant | 0.14 |
gyrA | 7631 | c.330G>C | synonymous_variant | 0.13 |
gyrA | 7637 | c.336C>G | synonymous_variant | 0.13 |
gyrA | 7683 | c.382A>C | synonymous_variant | 0.12 |
gyrA | 8111 | c.810G>C | synonymous_variant | 0.17 |
gyrA | 8121 | c.820T>C | synonymous_variant | 0.16 |
gyrA | 8129 | c.828T>C | synonymous_variant | 0.13 |
gyrA | 8135 | c.834C>G | synonymous_variant | 0.14 |
gyrA | 8156 | c.855T>C | synonymous_variant | 0.15 |
gyrA | 8168 | c.867A>G | synonymous_variant | 0.15 |
gyrA | 8177 | c.876A>C | synonymous_variant | 0.14 |
gyrA | 8189 | c.888G>C | synonymous_variant | 0.15 |
gyrA | 8198 | c.897T>C | synonymous_variant | 0.14 |
gyrA | 8711 | c.1410A>C | synonymous_variant | 0.14 |
gyrA | 8829 | c.1528T>C | synonymous_variant | 0.13 |
gyrA | 8891 | c.1590G>A | synonymous_variant | 0.14 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491591 | p.Lys270Met | missense_variant | 0.91 |
mshA | 575679 | p.Asn111Ser | missense_variant | 0.97 |
rpoB | 760060 | p.Tyr85Leu | missense_variant | 0.13 |
rpoB | 760091 | c.285G>C | synonymous_variant | 0.16 |
rpoB | 760101 | c.295T>C | synonymous_variant | 0.14 |
rpoB | 760112 | c.306T>C | synonymous_variant | 0.14 |
rpoB | 760115 | c.309C>T | synonymous_variant | 0.86 |
rpoB | 760121 | c.315T>C | synonymous_variant | 0.15 |
rpoB | 760130 | p.Asp108Glu | missense_variant | 0.17 |
rpoB | 760139 | c.333A>G | synonymous_variant | 0.13 |
rpoB | 760142 | c.336C>G | synonymous_variant | 0.14 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.15 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.16 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.16 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.14 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.19 |
rpoB | 760412 | c.606C>G | synonymous_variant | 0.19 |
rpoB | 760424 | c.618C>G | synonymous_variant | 0.14 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.16 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.16 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.16 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.19 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.19 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.21 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.16 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.12 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.17 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.17 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.19 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.16 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.14 |
rpoB | 762317 | c.2511A>G | synonymous_variant | 0.17 |
rpoB | 762329 | c.2523G>C | synonymous_variant | 0.13 |
rpoB | 762338 | c.2532T>C | synonymous_variant | 0.22 |
rpoB | 762347 | c.2541T>C | synonymous_variant | 0.23 |
rpoB | 762362 | p.Glu852Asp | missense_variant | 0.19 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 0.23 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.16 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.19 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.2 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.17 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.19 |
rpoC | 763603 | c.234C>T | synonymous_variant | 0.15 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.16 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.15 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.16 |
rpoC | 763872 | p.Gly168Ala | missense_variant | 0.12 |
rpoC | 763876 | p.Glu169Asp | missense_variant | 0.13 |
rpoC | 763879 | c.510A>G | synonymous_variant | 0.19 |
rpoC | 763888 | c.519G>C | synonymous_variant | 0.21 |
rpoC | 763891 | c.522G>C | synonymous_variant | 0.29 |
rpoC | 763894 | c.525A>G | synonymous_variant | 0.21 |
rpoC | 763900 | c.531G>C | synonymous_variant | 0.22 |
rpoC | 763936 | c.567C>G | synonymous_variant | 0.21 |
rpoC | 763939 | c.570G>A | synonymous_variant | 0.21 |
rpoC | 763942 | c.573C>G | synonymous_variant | 0.21 |
rpoC | 763948 | c.579G>A | synonymous_variant | 0.24 |
rpoC | 763949 | c.580C>A | synonymous_variant | 0.22 |
rpoC | 763954 | c.585C>G | synonymous_variant | 0.22 |
rpoC | 763963 | c.594C>T | synonymous_variant | 0.25 |
rpoC | 763987 | c.618C>T | synonymous_variant | 0.26 |
rpoC | 763991 | p.Ile208Leu | missense_variant | 0.2 |
rpoC | 763996 | c.627T>C | synonymous_variant | 0.33 |
rpoC | 764002 | c.633C>G | synonymous_variant | 0.29 |
rpoC | 764005 | c.636G>C | synonymous_variant | 0.29 |
rpoC | 764024 | c.655_657delTTGinsCTC | synonymous_variant | 0.15 |
rpoC | 764032 | p.Asp221Glu | missense_variant | 0.17 |
rpoC | 764040 | p.Ser224Thr | missense_variant | 0.13 |
rpoC | 764059 | c.690G>T | synonymous_variant | 0.17 |
rpoC | 764098 | c.729A>G | synonymous_variant | 0.17 |
rpoC | 764101 | c.732C>G | synonymous_variant | 0.17 |
rpoC | 764102 | p.Val245Ile | missense_variant | 0.15 |
rpoC | 764112 | p.Tyr248Phe | missense_variant | 0.16 |
rpoC | 764116 | c.747C>T | synonymous_variant | 0.16 |
rpoC | 764131 | c.762T>C | synonymous_variant | 0.14 |
rpoC | 764140 | c.771C>T | synonymous_variant | 0.14 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.16 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.13 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.15 |
rpoC | 765150 | p.Gly594Glu | missense_variant | 1.0 |
rpoC | 765352 | c.1983G>C | synonymous_variant | 0.13 |
rpoC | 765383 | p.Met672Leu | missense_variant | 0.15 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.12 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.17 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.14 |
rpoC | 765580 | c.2211G>C | synonymous_variant | 0.17 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.14 |
rpoC | 765631 | p.Asp754Glu | missense_variant | 0.14 |
rpoC | 765700 | c.2331T>C | synonymous_variant | 0.26 |
rpoC | 765734 | c.2365T>C | synonymous_variant | 0.22 |
rpoC | 765739 | c.2370G>T | synonymous_variant | 0.22 |
rpoC | 765751 | c.2382C>G | synonymous_variant | 0.2 |
rpoC | 765753 | p.Asp795Ala | missense_variant | 0.19 |
rpoC | 765772 | c.2403C>G | synonymous_variant | 0.12 |
rpoC | 765784 | c.2415C>G | synonymous_variant | 0.12 |
rpoC | 765787 | c.2418C>T | synonymous_variant | 0.12 |
rpoC | 765793 | c.2424C>G | synonymous_variant | 0.13 |
rpoC | 765796 | c.2427C>T | synonymous_variant | 0.12 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.15 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.18 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.18 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.14 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.14 |
rpoC | 766357 | c.2988C>T | synonymous_variant | 0.13 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.21 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.21 |
rpoC | 766390 | c.3021C>T | synonymous_variant | 0.16 |
rpoC | 766408 | c.3039C>G | synonymous_variant | 0.18 |
rpoC | 766411 | c.3042C>G | synonymous_variant | 0.17 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.15 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.14 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.15 |
rpoC | 766801 | c.3432C>G | synonymous_variant | 0.17 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.17 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.14 |
rpoC | 766972 | c.3603G>C | synonymous_variant | 0.14 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.26 |
rpoC | 767009 | c.3640_3642delTCGinsAGC | synonymous_variant | 0.22 |
rpoC | 767014 | c.3645G>C | synonymous_variant | 0.21 |
rpoC | 767033 | c.3664_3666delTCGinsAGT | synonymous_variant | 0.17 |
rpoC | 767134 | c.3765C>A | synonymous_variant | 0.15 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775975 | c.2506T>C | synonymous_variant | 0.16 |
mmpL5 | 775981 | p.Leu834Met | missense_variant | 0.15 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781649 | c.90T>C | synonymous_variant | 0.12 |
rpsL | 781808 | c.249C>T | synonymous_variant | 0.17 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.17 |
rplC | 800771 | c.-38C>T | upstream_gene_variant | 0.22 |
rplC | 800794 | c.-15A>G | upstream_gene_variant | 0.13 |
rplC | 800796 | c.-13A>G | upstream_gene_variant | 0.13 |
rplC | 800798 | c.-10_-9delGG | upstream_gene_variant | 0.14 |
rplC | 800814 | c.6A>G | synonymous_variant | 0.15 |
rplC | 800817 | c.9A>T | synonymous_variant | 0.14 |
rplC | 800844 | c.36T>C | synonymous_variant | 0.15 |
rplC | 800934 | c.126C>G | synonymous_variant | 0.12 |
rplC | 800937 | c.129A>G | synonymous_variant | 0.12 |
rplC | 800946 | c.138T>G | synonymous_variant | 0.12 |
rplC | 801367 | p.Ala187Thr | missense_variant | 0.14 |
rplC | 801402 | c.594T>C | synonymous_variant | 0.15 |
rplC | 801405 | c.597T>C | synonymous_variant | 0.18 |
fbiC | 1304580 | c.1650T>C | synonymous_variant | 0.14 |
fbiC | 1304613 | c.1683T>C | synonymous_variant | 0.15 |
fbiC | 1304856 | c.1926C>G | synonymous_variant | 0.33 |
fbiC | 1304862 | c.1932G>A | synonymous_variant | 0.14 |
fbiC | 1304875 | p.Ile649Val | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471969 | n.124T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
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 | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472597 | n.752G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473002 | n.1157G>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473004 | n.1159T>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473008 | n.1163C>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473009 | n.1164T>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473038 | n.1193A>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473044 | n.1199C>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473053 | n.1208T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473068 | n.1223A>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473070 | n.1225G>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473071 | n.1226C>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475765 | n.2111delG | non_coding_transcript_exon_variant | 1.0 |
inhA | 1674756 | c.555T>C | synonymous_variant | 0.15 |
inhA | 1674780 | c.579T>G | synonymous_variant | 0.14 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.16 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.19 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.17 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.15 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.15 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.15 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.17 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.13 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.15 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.14 |
rpsA | 1834540 | c.999G>C | synonymous_variant | 0.13 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.17 |
rpsA | 1834555 | c.1014T>G | synonymous_variant | 0.15 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.23 |
rpsA | 1834618 | c.1077G>C | synonymous_variant | 0.23 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.22 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.19 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2517950 | c.-165C>G | upstream_gene_variant | 0.19 |
kasA | 2517989 | c.-126T>C | upstream_gene_variant | 0.16 |
kasA | 2517993 | c.-122G>T | upstream_gene_variant | 0.13 |
kasA | 2518019 | c.-96A>G | upstream_gene_variant | 0.16 |
kasA | 2518025 | c.-90G>C | upstream_gene_variant | 0.13 |
kasA | 2518076 | c.-39C>T | upstream_gene_variant | 1.0 |
thyA | 3074334 | c.138T>C | synonymous_variant | 0.12 |
thyA | 3074349 | c.123T>C | synonymous_variant | 0.13 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3877613 | p.Ile299Val | missense_variant | 0.15 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.19 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 0.23 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 0.24 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.24 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.27 |
rpoA | 3877791 | c.717C>G | synonymous_variant | 0.27 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.22 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.12 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.14 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.13 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.12 |
rpoA | 3878292 | c.216T>C | synonymous_variant | 0.17 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.19 |
rpoA | 3878304 | c.204G>C | synonymous_variant | 0.14 |
rpoA | 3878665 | c.-158A>G | upstream_gene_variant | 0.18 |
clpC1 | 4038320 | c.2385G>C | synonymous_variant | 0.13 |
clpC1 | 4038356 | c.2349T>C | synonymous_variant | 0.22 |
clpC1 | 4038359 | c.2346A>G | synonymous_variant | 0.21 |
clpC1 | 4038368 | c.2337T>C | synonymous_variant | 0.2 |
clpC1 | 4038388 | c.2317T>C | synonymous_variant | 0.24 |
clpC1 | 4038392 | c.2313C>T | synonymous_variant | 0.25 |
clpC1 | 4038398 | c.2307G>T | synonymous_variant | 0.19 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 0.18 |
clpC1 | 4038407 | c.2298G>C | synonymous_variant | 0.21 |
clpC1 | 4038419 | c.2286T>C | synonymous_variant | 0.19 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.19 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.32 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.2 |
clpC1 | 4038640 | p.Asp689Asn | missense_variant | 0.23 |
clpC1 | 4038653 | c.2052C>T | synonymous_variant | 0.2 |
clpC1 | 4038658 | p.Lys683Gln | missense_variant | 0.21 |
clpC1 | 4038661 | p.Ser682Thr | missense_variant | 0.21 |
clpC1 | 4038662 | c.2043T>C | synonymous_variant | 0.22 |
clpC1 | 4038671 | c.2034T>C | synonymous_variant | 0.28 |
clpC1 | 4038683 | c.2022T>C | synonymous_variant | 0.28 |
clpC1 | 4038695 | c.2010C>G | synonymous_variant | 0.2 |
clpC1 | 4038701 | c.2004G>C | synonymous_variant | 0.12 |
clpC1 | 4038704 | c.2001T>C | synonymous_variant | 0.12 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.13 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.17 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.17 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.15 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.15 |
clpC1 | 4039352 | c.1353C>G | synonymous_variant | 0.12 |
clpC1 | 4039391 | c.1314T>G | synonymous_variant | 0.17 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.13 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.13 |
clpC1 | 4039661 | c.1044T>G | synonymous_variant | 0.2 |
clpC1 | 4039664 | c.1041G>C | synonymous_variant | 0.25 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.27 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.27 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.21 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.17 |
clpC1 | 4039760 | c.945T>C | synonymous_variant | 0.17 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.17 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.16 |
clpC1 | 4039775 | c.930G>C | synonymous_variant | 0.14 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.14 |
clpC1 | 4039781 | c.924G>C | synonymous_variant | 0.13 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.12 |
clpC1 | 4039826 | c.879C>G | synonymous_variant | 0.16 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.15 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.14 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.18 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.18 |
clpC1 | 4039988 | c.717C>G | synonymous_variant | 0.2 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.2 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.28 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.15 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.28 |
clpC1 | 4040036 | c.669C>G | synonymous_variant | 0.27 |
clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 0.16 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.2 |
clpC1 | 4040105 | c.600C>G | synonymous_variant | 0.21 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.15 |
clpC1 | 4040171 | c.534C>G | synonymous_variant | 0.12 |
embC | 4240780 | c.918T>C | synonymous_variant | 0.13 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242803 | p.Val981Leu | missense_variant | 0.9 |
embA | 4245010 | p.Ala593Val | missense_variant | 1.0 |
embA | 4245044 | c.1812G>C | synonymous_variant | 0.12 |
embA | 4245060 | c.1828T>C | synonymous_variant | 0.13 |
embA | 4245083 | c.1851A>C | synonymous_variant | 0.2 |
embA | 4245089 | c.1857G>C | synonymous_variant | 0.2 |
embA | 4245092 | c.1860C>G | synonymous_variant | 0.2 |
embA | 4245101 | c.1869G>C | synonymous_variant | 0.19 |
embA | 4245137 | c.1905T>C | synonymous_variant | 0.12 |
embA | 4245182 | c.1950T>C | synonymous_variant | 0.14 |
embA | 4245198 | p.Leu656Ile | missense_variant | 0.13 |
embB | 4246184 | c.-330A>C | upstream_gene_variant | 0.19 |
embB | 4247893 | c.1380C>T | synonymous_variant | 0.16 |
embB | 4247899 | p.Met462Ile | missense_variant | 0.16 |
embB | 4247905 | c.1392G>C | synonymous_variant | 0.16 |
embB | 4247909 | c.1396T>C | synonymous_variant | 0.19 |
embB | 4247932 | c.1419C>G | synonymous_variant | 0.15 |
embB | 4247940 | p.Leu476Trp | missense_variant | 0.17 |
embB | 4247945 | c.1432T>C | synonymous_variant | 0.17 |
embB | 4248097 | c.1584C>G | synonymous_variant | 0.14 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407635 | p.Thr190Ala | missense_variant | 1.0 |