Run ID: SRR13861372
Sample name:
Date: 03-04-2023 09:30:06
Number of reads: 186704
Percentage reads mapped: 9.34
Strain: lineage4.9
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.86 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6715 | c.-587C>T | upstream_gene_variant | 1.0 |
gyrA | 7838 | c.537C>G | synonymous_variant | 0.29 |
gyrA | 8156 | c.855T>C | synonymous_variant | 0.4 |
gyrA | 8204 | c.903C>T | synonymous_variant | 0.33 |
gyrA | 8207 | c.906T>C | synonymous_variant | 0.33 |
gyrA | 8216 | c.915G>A | synonymous_variant | 0.33 |
gyrA | 8219 | c.918T>C | synonymous_variant | 0.33 |
gyrA | 8225 | c.924T>C | synonymous_variant | 0.33 |
gyrA | 8234 | c.933T>G | synonymous_variant | 0.33 |
gyrA | 8235 | c.934_936delTTAinsCTG | synonymous_variant | 0.33 |
gyrA | 8253 | p.Ile318Leu | missense_variant | 0.33 |
gyrA | 8693 | c.1392T>C | synonymous_variant | 0.2 |
gyrA | 8699 | c.1398A>G | synonymous_variant | 0.18 |
gyrA | 8711 | c.1410A>C | synonymous_variant | 0.22 |
gyrA | 8714 | c.1413A>G | synonymous_variant | 0.22 |
gyrA | 8717 | c.1416C>G | synonymous_variant | 0.22 |
gyrA | 8720 | c.1419G>A | synonymous_variant | 0.22 |
gyrA | 8729 | c.1428T>C | synonymous_variant | 0.22 |
gyrA | 8732 | c.1431G>C | synonymous_variant | 0.22 |
gyrA | 8747 | c.1446A>G | synonymous_variant | 0.29 |
gyrA | 8756 | c.1455A>G | synonymous_variant | 0.4 |
gyrA | 8762 | c.1461G>C | synonymous_variant | 0.4 |
gyrA | 8765 | p.Asp488Glu | missense_variant | 0.4 |
gyrA | 8767 | p.Arg489Lys | missense_variant | 0.4 |
gyrA | 8779 | p.Asp493Ala | missense_variant | 0.4 |
gyrA | 8786 | c.1485T>C | synonymous_variant | 0.4 |
gyrA | 8796 | p.Ile499Val | missense_variant | 0.5 |
gyrA | 8801 | c.1500G>C | synonymous_variant | 0.5 |
gyrA | 8810 | c.1509A>C | synonymous_variant | 0.5 |
gyrA | 8816 | c.1515C>T | synonymous_variant | 0.5 |
gyrA | 8852 | c.1551T>C | synonymous_variant | 0.4 |
gyrA | 8858 | c.1557T>C | synonymous_variant | 0.4 |
gyrA | 8867 | c.1566A>G | synonymous_variant | 0.4 |
gyrA | 8870 | c.1569G>C | synonymous_variant | 0.4 |
gyrA | 8873 | c.1572A>C | synonymous_variant | 0.4 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.43 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 0.43 |
gyrA | 8915 | c.1614A>G | synonymous_variant | 0.43 |
gyrA | 8939 | c.1638T>C | synonymous_variant | 0.38 |
gyrA | 8942 | c.1641G>C | synonymous_variant | 0.38 |
gyrA | 8945 | c.1644G>C | synonymous_variant | 0.43 |
gyrA | 8946 | c.1645_1647delTTGinsCTC | synonymous_variant | 0.43 |
gyrA | 8951 | p.Lys550Asn | missense_variant | 0.43 |
gyrA | 8966 | c.1665C>G | synonymous_variant | 0.5 |
gyrA | 8967 | p.Ala556Arg | missense_variant | 0.43 |
gyrA | 8987 | c.1686C>G | synonymous_variant | 0.5 |
gyrA | 8990 | c.1689C>G | synonymous_variant | 0.5 |
gyrA | 8996 | c.1695T>C | synonymous_variant | 0.4 |
gyrA | 8998 | p.Leu566Trp | missense_variant | 0.4 |
gyrA | 9023 | c.1722A>C | synonymous_variant | 0.33 |
gyrA | 9029 | c.1728T>C | synonymous_variant | 0.33 |
gyrA | 9032 | c.1731T>C | synonymous_variant | 0.33 |
gyrA | 9062 | c.1761C>G | synonymous_variant | 0.4 |
gyrA | 9153 | p.Thr618Ala | missense_variant | 0.5 |
gyrA | 9252 | p.Val651Ile | missense_variant | 0.33 |
fgd1 | 490948 | p.Ser56Ala | missense_variant | 0.2 |
fgd1 | 490962 | c.180T>C | synonymous_variant | 0.22 |
fgd1 | 490988 | p.Leu69Pro | missense_variant | 0.25 |
fgd1 | 491514 | p.Asn244Lys | missense_variant | 0.17 |
fgd1 | 491547 | c.765A>C | synonymous_variant | 0.17 |
fgd1 | 491550 | c.768T>C | synonymous_variant | 0.15 |
fgd1 | 491583 | c.801G>A | synonymous_variant | 0.17 |
fgd1 | 491595 | c.813C>G | synonymous_variant | 0.17 |
fgd1 | 491601 | c.819T>C | synonymous_variant | 0.18 |
mshA | 575693 | p.Pro116Ala | missense_variant | 1.0 |
rpoB | 760399 | p.Val198Ala | missense_variant | 1.0 |
rpoB | 763150 | p.Phe1115Tyr | missense_variant | 1.0 |
rpoC | 764516 | p.Asp383Asn | missense_variant | 1.0 |
rpoC | 765499 | c.2130C>G | synonymous_variant | 0.18 |
rpoC | 765508 | c.2139C>G | synonymous_variant | 0.18 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.33 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.33 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.33 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.33 |
rpoC | 765578 | c.2209C>T | synonymous_variant | 0.4 |
rpoC | 765583 | c.2214G>T | synonymous_variant | 0.33 |
rpoC | 765613 | p.His748Gln | missense_variant | 0.4 |
rpoC | 765625 | c.2256C>G | synonymous_variant | 0.29 |
rpoC | 766103 | p.Arg912Gly | missense_variant | 1.0 |
rpoC | 766726 | c.3357T>C | synonymous_variant | 0.22 |
rpoC | 766738 | c.3369G>T | synonymous_variant | 0.22 |
rpoC | 766750 | c.3381C>G | synonymous_variant | 0.22 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.22 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.22 |
rpoC | 766801 | c.3432C>A | synonymous_variant | 0.2 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.2 |
rpoC | 766843 | c.3474T>C | synonymous_variant | 0.22 |
rpoC | 766894 | c.3525T>C | synonymous_variant | 0.22 |
rpoC | 766895 | c.3526T>C | synonymous_variant | 0.22 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.22 |
rpoC | 766933 | c.3564A>G | synonymous_variant | 0.22 |
rpoC | 766945 | c.3576A>G | synonymous_variant | 0.22 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.3 |
rpoC | 766978 | c.3609C>G | synonymous_variant | 0.3 |
rpoC | 766996 | c.3627C>T | synonymous_variant | 0.22 |
rpoC | 767009 | c.3640_3642delTCGinsAGC | synonymous_variant | 0.25 |
rpoC | 767014 | c.3645G>C | synonymous_variant | 0.29 |
rpoC | 767119 | c.3750A>G | synonymous_variant | 0.4 |
rpoC | 767134 | c.3765C>G | synonymous_variant | 0.33 |
rpoC | 767158 | c.3789T>C | synonymous_variant | 0.33 |
rpoC | 767167 | c.3798C>G | synonymous_variant | 0.33 |
rpoC | 767180 | p.Ala1271Gln | missense_variant | 0.33 |
rpoC | 767191 | c.3822C>G | synonymous_variant | 0.33 |
rpoC | 767206 | c.3837C>G | synonymous_variant | 0.33 |
rpoC | 767209 | c.3840T>C | synonymous_variant | 0.4 |
rpoC | 767212 | c.3843G>C | synonymous_variant | 0.4 |
rpoC | 767221 | c.3852C>G | synonymous_variant | 0.25 |
rpoC | 767230 | c.3861G>C | synonymous_variant | 0.29 |
rpoC | 767233 | c.3864T>C | synonymous_variant | 0.29 |
mmpL5 | 775975 | c.2506T>C | synonymous_variant | 0.22 |
mmpL5 | 775981 | p.Leu834Met | missense_variant | 0.22 |
mmpL5 | 775997 | c.2484T>C | synonymous_variant | 0.2 |
mmpL5 | 777066 | p.Ile472Ser | missense_variant | 1.0 |
rplC | 801127 | p.Ala107Thr | missense_variant | 0.18 |
rplC | 801147 | c.339T>C | synonymous_variant | 0.17 |
rplC | 801150 | c.342G>C | synonymous_variant | 0.17 |
rplC | 801153 | c.345G>C | synonymous_variant | 0.17 |
rplC | 801156 | c.348T>A | synonymous_variant | 0.15 |
rplC | 801171 | c.363A>G | synonymous_variant | 0.2 |
rplC | 801174 | c.366T>C | synonymous_variant | 0.2 |
rplC | 801222 | c.414T>C | synonymous_variant | 0.18 |
rplC | 801228 | c.420T>C | synonymous_variant | 0.18 |
rplC | 801246 | c.438C>G | synonymous_variant | 0.18 |
rplC | 801249 | c.441T>G | synonymous_variant | 0.18 |
rplC | 801255 | c.447C>T | synonymous_variant | 0.2 |
rplC | 801267 | c.459A>C | synonymous_variant | 0.23 |
rplC | 801270 | c.462T>C | synonymous_variant | 0.17 |
rplC | 801276 | c.468G>C | synonymous_variant | 0.17 |
rplC | 801279 | c.471G>C | synonymous_variant | 0.17 |
rplC | 801282 | c.474G>C | synonymous_variant | 0.17 |
rplC | 801301 | c.493C>A | synonymous_variant | 0.2 |
rplC | 801312 | c.504G>C | synonymous_variant | 0.22 |
rplC | 801324 | c.516T>C | synonymous_variant | 0.22 |
rplC | 801336 | c.528C>G | synonymous_variant | 0.2 |
rplC | 801339 | c.531T>C | synonymous_variant | 0.2 |
rplC | 801341 | p.Leu178Gln | missense_variant | 0.2 |
rplC | 801348 | c.540T>G | synonymous_variant | 0.22 |
rplC | 801357 | c.549T>C | synonymous_variant | 0.2 |
rplC | 801367 | p.Ala187Thr | missense_variant | 0.22 |
rrs | 1471969 | n.124T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1471970 | n.125G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472028 | n.183A>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472030 | n.185G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472031 | n.186G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472034 | n.189T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472044 | n.199G>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472101 | n.256G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472122 | n.277G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472164 | n.319G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472177 | n.332C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472230 | n.385C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472262 | n.417C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472269 | n.424G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472271 | n.426T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472277 | n.432C>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472505 | n.660G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472596 | n.751G>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472614 | n.769G>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472665 | n.820G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472669 | n.824_825insTAGG | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472695 | n.850C>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1473248 | n.1403G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473255 | n.1410A>G | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473260 | n.1415G>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473281 | n.1436C>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473282 | n.1437C>G | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473288 | n.1443C>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473291 | n.1446G>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473296 | n.1451G>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473297 | n.1452G>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473327 | n.1482A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473328 | n.1483C>T | non_coding_transcript_exon_variant | 0.59 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474104 | n.447G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474823 | n.1166C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475638 | n.1981C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475642 | n.1985T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475659 | n.2002G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476179 | n.2522C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476195 | n.2538C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476196 | n.2539C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476204 | n.2547C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476215 | n.2558C>A | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476263 | n.2606C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476268 | n.2611A>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476275 | n.2618T>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476279 | n.2622G>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476301 | n.2644A>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476572 | n.2915G>A | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476595 | n.2938C>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476596 | n.2939C>T | non_coding_transcript_exon_variant | 0.43 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.5 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.5 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.5 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.5 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.67 |
rpsA | 1833790 | c.249T>A | synonymous_variant | 0.67 |
rpsA | 1833799 | c.258C>G | synonymous_variant | 0.67 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 0.62 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.57 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.57 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.5 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.44 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.38 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.33 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.43 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.38 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.29 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.29 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.33 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.33 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.33 |
ndh | 2103185 | c.-143A>C | upstream_gene_variant | 1.0 |
PPE35 | 2168894 | c.1718dupG | frameshift_variant | 1.0 |
PPE35 | 2170039 | p.Ala192Thr | missense_variant | 1.0 |
Rv1979c | 2221777 | p.Ala463Val | missense_variant | 1.0 |
pncA | 2289958 | c.-717T>C | upstream_gene_variant | 0.33 |
pncA | 2289991 | c.-750G>C | upstream_gene_variant | 0.25 |
pncA | 2289994 | c.-753A>G | upstream_gene_variant | 0.29 |
pncA | 2289997 | c.-756G>C | upstream_gene_variant | 0.29 |
pncA | 2290006 | c.-765T>C | upstream_gene_variant | 0.33 |
pncA | 2290009 | c.-768A>G | upstream_gene_variant | 0.29 |
pncA | 2290015 | c.-774A>C | upstream_gene_variant | 0.29 |
pncA | 2290027 | c.-786G>A | upstream_gene_variant | 0.33 |
pncA | 2290030 | c.-791_-789delAATinsCAC | upstream_gene_variant | 0.33 |
pncA | 2290033 | c.-792C>G | upstream_gene_variant | 0.33 |
pncA | 2290038 | c.-797G>T | upstream_gene_variant | 0.33 |
pncA | 2290042 | c.-801T>C | upstream_gene_variant | 0.33 |
pncA | 2290071 | c.-830A>G | upstream_gene_variant | 0.29 |
pncA | 2290072 | c.-831T>C | upstream_gene_variant | 0.29 |
pncA | 2290087 | c.-846T>C | upstream_gene_variant | 0.29 |
kasA | 2518793 | p.Ser227Thr | missense_variant | 0.8 |
ahpC | 2726300 | c.108C>A | synonymous_variant | 1.0 |
folC | 2747094 | p.Asp169His | missense_variant | 1.0 |
Rv2752c | 3064936 | p.Ser419* | stop_gained | 1.0 |
Rv2752c | 3065523 | c.669C>T | synonymous_variant | 1.0 |
Rv2752c | 3066039 | c.153C>T | synonymous_variant | 0.8 |
alr | 3841286 | c.135T>A | synonymous_variant | 1.0 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.25 |
clpC1 | 4039368 | p.Lys446Thr | missense_variant | 0.83 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.43 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.43 |
clpC1 | 4039448 | c.1257A>G | synonymous_variant | 0.43 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 0.43 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.3 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.3 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.3 |
clpC1 | 4039481 | c.1224T>G | synonymous_variant | 0.3 |
clpC1 | 4039484 | c.1221T>G | synonymous_variant | 0.3 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.22 |
clpC1 | 4039524 | p.Phe394Tyr | missense_variant | 0.22 |
clpC1 | 4039547 | c.1158C>G | synonymous_variant | 0.31 |
clpC1 | 4039553 | c.1152C>G | synonymous_variant | 0.31 |
clpC1 | 4039562 | c.1143C>G | synonymous_variant | 0.25 |
clpC1 | 4039565 | c.1140G>C | synonymous_variant | 0.25 |
clpC1 | 4039576 | p.Ala377Ser | missense_variant | 0.18 |
clpC1 | 4039586 | c.1119G>C | synonymous_variant | 0.31 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.36 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.4 |
clpC1 | 4039622 | c.1083C>G | synonymous_variant | 0.33 |
clpC1 | 4039682 | c.1023C>G | synonymous_variant | 0.25 |
clpC1 | 4039685 | c.1020C>T | synonymous_variant | 0.25 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.25 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.27 |
clpC1 | 4040441 | c.264C>G | synonymous_variant | 0.29 |
panD | 4044138 | c.144T>C | synonymous_variant | 0.33 |
panD | 4044150 | c.132A>G | synonymous_variant | 0.29 |
panD | 4044162 | c.120A>G | synonymous_variant | 0.33 |
panD | 4044165 | c.117G>C | synonymous_variant | 0.33 |
panD | 4044188 | c.94T>C | synonymous_variant | 0.4 |
panD | 4044195 | c.87T>C | synonymous_variant | 0.4 |
panD | 4044213 | c.69C>G | synonymous_variant | 0.33 |
embC | 4241777 | p.Gly639Ser | missense_variant | 1.0 |
embA | 4245355 | p.Ala708Gly | missense_variant | 0.5 |
embA | 4245368 | c.2136T>C | synonymous_variant | 0.4 |
embB | 4247824 | c.1311C>G | synonymous_variant | 0.25 |
embB | 4247830 | c.1317A>C | synonymous_variant | 0.25 |
embB | 4247836 | c.1323A>G | synonymous_variant | 0.25 |
embB | 4247842 | c.1329T>C | synonymous_variant | 0.22 |
embB | 4247876 | c.1363C>T | synonymous_variant | 0.38 |
embB | 4247881 | c.1368G>C | synonymous_variant | 0.38 |
embB | 4247887 | c.1374C>T | synonymous_variant | 0.43 |
embB | 4247890 | c.1377C>T | synonymous_variant | 0.43 |
embB | 4247899 | p.Met462Ile | missense_variant | 0.5 |
embB | 4247905 | c.1392G>C | synonymous_variant | 0.4 |
embB | 4247909 | c.1396T>C | synonymous_variant | 0.4 |
embB | 4247914 | c.1401G>C | synonymous_variant | 0.4 |
embB | 4247920 | c.1407T>G | synonymous_variant | 0.4 |
embB | 4247923 | c.1410T>C | synonymous_variant | 0.4 |
embB | 4247926 | c.1413C>G | synonymous_variant | 0.4 |
embB | 4247927 | p.Leu472Val | missense_variant | 0.4 |
embB | 4247932 | c.1419C>G | synonymous_variant | 0.33 |
embB | 4247938 | c.1425G>C | synonymous_variant | 0.4 |
embB | 4247940 | p.Leu476Trp | missense_variant | 0.4 |
embB | 4247945 | c.1432T>C | synonymous_variant | 0.4 |
embB | 4247951 | p.Ser480Ala | missense_variant | 0.43 |
embB | 4247956 | c.1443G>C | synonymous_variant | 0.38 |
embB | 4247974 | c.1461C>G | synonymous_variant | 0.33 |
embB | 4247977 | c.1464C>G | synonymous_variant | 0.33 |
embB | 4247986 | c.1473C>G | synonymous_variant | 0.29 |
embB | 4248007 | c.1494C>G | synonymous_variant | 0.33 |
embB | 4248011 | p.Ser500Ala | missense_variant | 0.29 |
embB | 4248035 | p.Val508Ile | missense_variant | 0.29 |
embB | 4248041 | p.Ala510Thr | missense_variant | 0.29 |
embB | 4248044 | p.Lys511Ala | missense_variant | 0.29 |
embB | 4248052 | c.1539G>A | synonymous_variant | 0.29 |
embB | 4248055 | c.1542G>C | synonymous_variant | 0.29 |
embB | 4248064 | c.1551G>C | synonymous_variant | 0.29 |
embB | 4248070 | c.1557T>C | synonymous_variant | 0.25 |
embB | 4248085 | c.1572T>C | synonymous_variant | 0.33 |
embB | 4248097 | c.1584C>G | synonymous_variant | 0.38 |
embB | 4248118 | c.1605T>C | synonymous_variant | 0.25 |
embB | 4248127 | c.1614G>C | synonymous_variant | 0.25 |
embB | 4248133 | c.1620C>G | synonymous_variant | 0.25 |
embB | 4248142 | c.1629T>C | synonymous_variant | 0.25 |
embB | 4248143 | c.1630T>C | synonymous_variant | 0.25 |
embB | 4249369 | c.2856T>C | synonymous_variant | 0.2 |
embB | 4249381 | c.2868A>G | synonymous_variant | 0.22 |
embB | 4249456 | c.2943G>C | synonymous_variant | 0.25 |
embB | 4249469 | p.Leu986Met | missense_variant | 0.25 |
embB | 4249483 | c.2970C>G | synonymous_variant | 0.25 |
embB | 4249486 | c.2973T>G | synonymous_variant | 0.25 |
embB | 4249487 | c.2974T>C | synonymous_variant | 0.25 |
ubiA | 4269888 | c.-55C>A | upstream_gene_variant | 1.0 |