Run ID: SRR1140574
Sample name:
Date: 02-04-2023 20:56:13
Number of reads: 1045709
Percentage reads mapped: 40.54
Strain: lineage4.8;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 | 0.82 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 0.08 |
lineage4.3.3 | Euro-American (LAM) | LAM;T | RD115 | 0.87 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761110 | p.Asp435Val | missense_variant | 0.79 | rifampicin |
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.11 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 0.14 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.83 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.6 | kanamycin, capreomycin, aminoglycosides, amikacin |
katG | 2155168 | p.Ser315Thr | missense_variant | 0.71 | isoniazid |
embB | 4247729 | p.Gly406Ser | missense_variant | 0.75 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 0.81 |
gyrA | 8040 | p.Gly247Ser | missense_variant | 0.79 |
gyrA | 8444 | c.1143G>C | synonymous_variant | 0.12 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.7 |
mshA | 576467 | p.Val374Leu | missense_variant | 0.13 |
mshA | 576658 | c.1311G>A | synonymous_variant | 0.13 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.19 |
rpoB | 760997 | c.1191G>C | synonymous_variant | 0.18 |
rpoB | 761006 | c.1200C>G | synonymous_variant | 0.17 |
rpoB | 761013 | p.Val403Ile | missense_variant | 0.17 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.18 |
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 | 761046 | p.Ile414Val | missense_variant | 0.17 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.15 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.16 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.14 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.11 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.11 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.13 |
rpoB | 761345 | c.1539G>C | synonymous_variant | 0.2 |
rpoB | 761385 | p.Ala527Thr | missense_variant | 0.13 |
rpoB | 761534 | c.1728G>C | synonymous_variant | 0.18 |
rpoB | 761555 | c.1749G>C | synonymous_variant | 0.12 |
rpoB | 761558 | c.1752C>G | synonymous_variant | 0.12 |
rpoB | 761562 | p.Ala586Ser | missense_variant | 0.12 |
rpoB | 761565 | p.Met587Leu | missense_variant | 0.12 |
rpoB | 761568 | p.Ile588Val | missense_variant | 0.12 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.13 |
rpoB | 761588 | c.1782C>T | synonymous_variant | 0.14 |
rpoB | 761594 | c.1788C>G | synonymous_variant | 0.18 |
rpoB | 761595 | p.Asn597Gln | missense_variant | 0.17 |
rpoB | 761600 | c.1794T>C | synonymous_variant | 0.17 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.13 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.13 |
rpoB | 761880 | p.Ala692Thr | missense_variant | 1.0 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.35 |
rpoC | 762887 | c.-483G>C | upstream_gene_variant | 0.5 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.64 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.49 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.45 |
rpoC | 762983 | c.-387C>A | upstream_gene_variant | 0.34 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.24 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.15 |
rpoC | 763058 | c.-312C>G | upstream_gene_variant | 0.23 |
rpoB | 763075 | p.Thr1090Ile | missense_variant | 0.36 |
rpoB | 763077 | p.Val1091Leu | missense_variant | 0.36 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.43 |
rpoB | 763126 | p.Pro1107Gln | missense_variant | 0.36 |
rpoC | 763133 | c.-237G>C | upstream_gene_variant | 0.33 |
rpoC | 763142 | c.-228C>G | upstream_gene_variant | 0.31 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.13 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.11 |
rpoC | 763550 | p.Tyr61Ala | missense_variant | 0.12 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.17 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.17 |
rpoC | 763589 | p.Ile74Val | missense_variant | 0.21 |
rpoC | 763609 | c.240C>G | synonymous_variant | 0.18 |
rpoC | 763630 | c.261G>C | synonymous_variant | 0.12 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.21 |
rpoC | 763648 | c.279C>T | synonymous_variant | 0.29 |
rpoC | 763660 | c.291T>C | synonymous_variant | 0.33 |
rpoC | 763666 | c.297G>T | synonymous_variant | 0.39 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.42 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.38 |
rpoC | 763711 | c.342G>C | synonymous_variant | 0.37 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.37 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.41 |
rpoC | 763727 | p.Leu120Met | missense_variant | 0.41 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.32 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.23 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.23 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.22 |
rpoC | 763768 | c.399C>G | synonymous_variant | 0.14 |
rpoC | 764301 | p.Gly311Ala | missense_variant | 0.12 |
rpoC | 764316 | p.Ala316Val | missense_variant | 0.34 |
rpoC | 764344 | c.975C>T | synonymous_variant | 0.53 |
rpoC | 764353 | c.984G>C | synonymous_variant | 0.53 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.58 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.6 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.65 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.59 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.44 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.14 |
rpoC | 764444 | p.Asp359Tyr | missense_variant | 0.14 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.4 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.4 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.4 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.21 |
rpoC | 764593 | c.1224C>A | synonymous_variant | 0.32 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.36 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.41 |
rpoC | 764611 | c.1242G>C | synonymous_variant | 0.46 |
rpoC | 764626 | c.1257C>A | synonymous_variant | 0.57 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.62 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.58 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.49 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.38 |
rpoC | 764722 | c.1353G>C | synonymous_variant | 0.33 |
rpoC | 764737 | c.1368G>C | synonymous_variant | 0.16 |
rpoC | 764740 | p.Met457Ile | missense_variant | 0.16 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.83 |
rpoC | 765671 | p.Asp768Tyr | missense_variant | 0.77 |
rpoC | 766058 | p.Ile897Phe | missense_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781793 | c.234G>C | synonymous_variant | 0.12 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.11 |
rpsL | 781805 | c.246G>C | synonymous_variant | 0.11 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.12 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.13 |
rplC | 801025 | p.Ala73Thr | missense_variant | 0.17 |
fbiC | 1303862 | p.Ile311Thr | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471878 | n.33C>T | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472068 | n.223T>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.19 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472333 | n.488G>A | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472496 | n.651T>G | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472507 | n.662C>T | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472571 | n.726G>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472606 | n.761C>G | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472623 | n.778A>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472645 | n.800G>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472660 | n.815T>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472666 | n.821G>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472686 | n.841G>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472694 | n.849C>A | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472714 | n.869A>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472982 | n.1137G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472993 | n.1148G>T | non_coding_transcript_exon_variant | 0.77 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473097 | n.1252G>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473122 | n.1277T>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473134 | n.1289T>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473147 | n.1302G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473164 | n.1319C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473269 | n.1424C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473291 | n.1446_1447insT | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473319 | n.1474C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1473320 | n.1475G>A | non_coding_transcript_exon_variant | 0.61 |
rrs | 1473324 | n.1479G>A | non_coding_transcript_exon_variant | 0.58 |
rrl | 1473828 | n.173_174delTG | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473844 | n.187C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473870 | n.213G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473871 | n.214T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473883 | n.226A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473887 | n.230T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473888 | n.231T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473890 | n.233T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473899 | n.242A>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473917 | n.260G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473922 | n.265A>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474166 | n.509G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474184 | n.527C>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474202 | n.545T>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474265 | n.608G>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474275 | n.618T>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474351 | n.694G>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1474359 | n.702C>G | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474452 | n.795C>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474466 | n.809G>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474476 | n.819C>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474496 | n.839C>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.74 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.77 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.77 |
rrl | 1474558 | n.901G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474583 | n.926C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474601 | n.944C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.63 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474770 | n.1113G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474783 | n.1126G>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474790 | n.1133C>T | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474794 | n.1137C>A | non_coding_transcript_exon_variant | 0.49 |
rrl | 1474800 | n.1143T>C | non_coding_transcript_exon_variant | 0.51 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.49 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1474830 | n.1173A>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.41 |
rrl | 1474920 | n.1263G>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474935 | n.1278A>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474938 | n.1281G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474988 | n.1331C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475104 | n.1447T>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475108 | n.1451C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475111 | n.1454G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475116 | n.1459G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475119 | n.1462C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475120 | n.1463G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475124 | n.1467A>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475129 | n.1472G>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1475493 | n.1836G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475508 | n.1851A>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475536 | n.1879C>A | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475538 | n.1881T>A | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475548 | n.1891C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475549 | n.1892T>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475550 | n.1893A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475692 | n.2035G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.87 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.81 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.81 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475963 | n.2306G>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.74 |
rrl | 1475997 | n.2340A>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1475998 | n.2341C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476025 | n.2368G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476032 | n.2375C>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476033 | n.2376T>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476034 | n.2377C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476045 | n.2388G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476046 | n.2389G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476047 | n.2390G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476076 | n.2419A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476079 | n.2422G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476080 | n.2423T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476081 | n.2424A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476082 | n.2425T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476087 | n.2430C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476095 | n.2438C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476104 | n.2448delG | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476165 | n.2508T>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476540 | n.2883C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476544 | n.2887T>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476566 | n.2909A>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476586 | n.2929C>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476613 | n.2956G>A | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.34 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476628 | n.2971T>G | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476630 | n.2973A>T | non_coding_transcript_exon_variant | 0.37 |
rpsA | 1833703 | c.162C>T | synonymous_variant | 0.13 |
rpsA | 1833704 | p.Ile55Val | missense_variant | 0.13 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.27 |
rpsA | 1833724 | c.183C>T | synonymous_variant | 0.29 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.29 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.29 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.3 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.31 |
rpsA | 1833748 | c.207C>G | synonymous_variant | 0.33 |
rpsA | 1833781 | c.240T>C | synonymous_variant | 0.38 |
rpsA | 1833782 | p.Ser81Ala | missense_variant | 0.38 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.36 |
rpsA | 1833794 | p.Glu85Gln | missense_variant | 0.36 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.27 |
rpsA | 1833811 | c.270G>T | synonymous_variant | 0.28 |
rpsA | 1833815 | p.Thr92Gln | missense_variant | 0.26 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 0.26 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 0.25 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.23 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.23 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.15 |
rpsA | 1834836 | p.Met432Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918526 | p.Gly196Glu | missense_variant | 0.71 |
katG | 2154459 | c.1653C>T | synonymous_variant | 1.0 |
PPE35 | 2168344 | p.Gly757Cys | missense_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289431 | c.-190G>T | upstream_gene_variant | 1.0 |
pncA | 2289877 | c.-636C>T | upstream_gene_variant | 0.2 |
kasA | 2518400 | p.Glu96Lys | missense_variant | 0.11 |
kasA | 2518919 | p.Gly269Ser | missense_variant | 0.92 |
eis | 2714424 | c.909C>A | synonymous_variant | 0.13 |
eis | 2714522 | p.Pro271Thr | missense_variant | 0.14 |
ahpC | 2726639 | c.447C>G | synonymous_variant | 0.15 |
folC | 2746716 | p.Gly295Ser | missense_variant | 0.17 |
Rv2752c | 3064965 | c.1227G>C | synonymous_variant | 0.12 |
thyX | 3067226 | c.719delA | frameshift_variant | 0.12 |
thyX | 3068105 | c.-160C>G | upstream_gene_variant | 0.12 |
thyA | 3073868 | p.Thr202Ala | missense_variant | 0.94 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.9 |
Rv3083 | 3449843 | p.Gly447Asp | missense_variant | 0.2 |
Rv3083 | 3449990 | c.1487G>T | stop_lost&splice_region_variant | 0.12 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 0.5 |
fbiB | 3642705 | p.Arg391Gly | missense_variant | 0.11 |
alr | 3841578 | c.-158G>C | upstream_gene_variant | 0.12 |
clpC1 | 4038287 | c.2418C>T | synonymous_variant | 0.68 |
clpC1 | 4038836 | c.1869G>C | synonymous_variant | 0.15 |
clpC1 | 4038839 | c.1866G>C | synonymous_variant | 0.15 |
clpC1 | 4038845 | c.1858_1860delTCGinsAGT | synonymous_variant | 0.14 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.15 |
clpC1 | 4039487 | c.1218G>C | synonymous_variant | 0.15 |
clpC1 | 4039508 | c.1197G>C | synonymous_variant | 0.12 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.13 |
clpC1 | 4039520 | c.1185G>C | synonymous_variant | 0.13 |
clpC1 | 4039526 | c.1179G>C | synonymous_variant | 0.13 |
clpC1 | 4039537 | p.Ile390Val | missense_variant | 0.25 |
clpC1 | 4039550 | c.1155G>C | synonymous_variant | 0.19 |
clpC1 | 4039554 | p.Thr384Asn | missense_variant | 0.14 |
clpC1 | 4039559 | c.1146C>G | synonymous_variant | 0.15 |
clpC1 | 4039568 | p.Met379Ile | missense_variant | 0.14 |
clpC1 | 4039574 | p.Ala377Gly | missense_variant | 0.13 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.12 |
clpC1 | 4039587 | p.Ser373Gln | missense_variant | 0.23 |
clpC1 | 4039593 | p.Arg371Lys | missense_variant | 0.21 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.25 |
clpC1 | 4039622 | c.1083C>G | synonymous_variant | 0.31 |
clpC1 | 4039634 | p.Glu357Asn | missense_variant | 0.14 |
clpC1 | 4039640 | p.Thr355Ala | missense_variant | 0.13 |
clpC1 | 4039647 | p.Glu353Pro | missense_variant | 0.13 |
clpC1 | 4039651 | p.Val352Leu | missense_variant | 0.12 |
clpC1 | 4039661 | p.Gly348Asn | missense_variant | 0.12 |
clpC1 | 4039691 | c.1014G>C | synonymous_variant | 0.3 |
clpC1 | 4039694 | c.1011G>A | synonymous_variant | 0.3 |
clpC1 | 4039711 | p.Ile332Phe | missense_variant | 0.22 |
clpC1 | 4039714 | p.Tyr331His | missense_variant | 0.22 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.33 |
clpC1 | 4039742 | c.963C>G | synonymous_variant | 0.29 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.24 |
clpC1 | 4039754 | c.951G>C | synonymous_variant | 0.26 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.25 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.15 |
clpC1 | 4039774 | p.Lys311Gln | missense_variant | 0.12 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.12 |
clpC1 | 4039781 | c.924G>C | synonymous_variant | 0.13 |
clpC1 | 4039787 | c.916_918delTCGinsAGC | synonymous_variant | 0.14 |
clpC1 | 4039793 | c.912C>G | synonymous_variant | 0.15 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 0.18 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.12 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.18 |
clpC1 | 4039929 | c.775_776delAGinsTC | synonymous_variant | 0.14 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.16 |
clpC1 | 4039937 | p.Val256Ile | missense_variant | 0.17 |
clpC1 | 4039940 | c.765G>C | synonymous_variant | 0.17 |
clpC1 | 4039946 | c.759A>C | synonymous_variant | 0.17 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.17 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.16 |
clpC1 | 4039955 | c.750G>C | synonymous_variant | 0.25 |
clpC1 | 4039960 | p.Thr249Ser | missense_variant | 0.25 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.42 |
clpC1 | 4039994 | p.Glu237Asp | missense_variant | 0.42 |
clpC1 | 4040000 | p.His235Lys | missense_variant | 0.38 |
clpC1 | 4040003 | c.702G>C | synonymous_variant | 0.38 |
clpC1 | 4040018 | c.687G>C | synonymous_variant | 0.52 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.52 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.44 |
clpC1 | 4040030 | c.675C>G | synonymous_variant | 0.12 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.52 |
clpC1 | 4040051 | c.654C>G | synonymous_variant | 0.12 |
clpC1 | 4040057 | c.648C>A | synonymous_variant | 0.61 |
clpC1 | 4040063 | p.Leu214Phe | missense_variant | 0.44 |
clpC1 | 4040066 | c.639G>C | synonymous_variant | 0.38 |
clpC1 | 4040069 | c.636G>C | synonymous_variant | 0.55 |
clpC1 | 4040083 | p.Thr208Ser | missense_variant | 0.18 |
clpC1 | 4040087 | c.618G>T | synonymous_variant | 0.21 |
clpC1 | 4040090 | c.615T>C | synonymous_variant | 0.21 |
clpC1 | 4040096 | p.Val203Ile | missense_variant | 0.23 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
ethA | 4328378 | c.-905G>C | upstream_gene_variant | 0.28 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407608 | p.Pro199Ser | missense_variant | 0.12 |
gid | 4407695 | p.Glu170Lys | missense_variant | 0.91 |
gid | 4407720 | c.483C>G | synonymous_variant | 0.95 |
gid | 4408156 | p.Leu16Arg | missense_variant | 0.91 |