Run ID: SRR1140723
Sample name:
Date: 02-04-2023 20:57:59
Number of reads: 470100
Percentage reads mapped: 18.28
Strain: lineage4.6.1.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.6 | Euro-American | T;LAM | None | 1.0 |
lineage4.6.1 | Euro-American (Uganda) | T2 | RD724 | 0.99 |
lineage4.6.1.1 | Euro-American | T2-Uganda | RD724 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5315 | p.Val26Ile | missense_variant | 0.22 |
gyrA | 7352 | c.51G>T | synonymous_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7539 | p.Thr80Ala | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8857 | p.Thr519Ile | missense_variant | 0.14 |
gyrA | 8865 | p.Glu522* | stop_gained | 0.13 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
mshA | 575426 | p.Ser27Pro | missense_variant | 0.25 |
ccsA | 620354 | p.Trp155Leu | missense_variant | 0.22 |
ccsA | 620675 | c.789delC | frameshift_variant | 0.2 |
rpoB | 762837 | p.Glu1011Lys | missense_variant | 0.33 |
rpoC | 762887 | c.-483G>C | upstream_gene_variant | 0.56 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.67 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.6 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.6 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.6 |
rpoB | 762925 | p.Thr1040Ile | missense_variant | 0.6 |
rpoB | 762934 | c.3129_3130insAGCC | frameshift_variant | 0.56 |
rpoB | 762938 | c.3133_3136delATGA | frameshift_variant | 0.56 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.38 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.36 |
rpoC | 764198 | p.Leu277Val | missense_variant | 0.2 |
rpoC | 764512 | c.1143G>A | synonymous_variant | 0.15 |
rpoC | 764557 | p.Asn396Lys | missense_variant | 0.17 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.36 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.47 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.5 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.47 |
rpoC | 764587 | c.1218C>G | synonymous_variant | 0.56 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.55 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.57 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.59 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.67 |
rpoC | 764641 | c.1272C>T | synonymous_variant | 0.65 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.71 |
rpoC | 764663 | p.Val432Thr | missense_variant | 0.5 |
rpoC | 764672 | p.Gln435Glu | missense_variant | 0.64 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.42 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.3 |
rpoC | 766889 | p.Glu1174* | stop_gained | 0.18 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775936 | p.Asp849Tyr | missense_variant | 0.22 |
mmpR5 | 778127 | c.-863G>C | upstream_gene_variant | 0.15 |
mmpR5 | 778457 | c.-533C>T | upstream_gene_variant | 0.17 |
mmpL5 | 778663 | c.-183C>A | upstream_gene_variant | 0.29 |
mmpL5 | 779118 | c.-638C>A | upstream_gene_variant | 0.2 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303875 | c.945G>C | synonymous_variant | 0.5 |
fbiC | 1304117 | p.Pro396His | missense_variant | 0.12 |
fbiC | 1304812 | p.Met628Leu | missense_variant | 0.13 |
fbiC | 1304920 | p.Ile664Phe | missense_variant | 0.25 |
embR | 1417256 | p.Gly31Asp | missense_variant | 0.33 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471876 | n.31G>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1471892 | n.47G>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1471896 | n.51T>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472153 | n.308G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472242 | n.397C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472264 | n.419T>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472266 | n.421C>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472277 | n.432C>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472298 | n.453G>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472333 | n.488G>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472338 | n.493A>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472349 | n.504A>C | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472374 | n.529T>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472379 | n.534T>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472382 | n.537G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472386 | n.541G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472391 | n.546C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472412 | n.567A>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472415 | n.570T>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472598 | n.753A>T | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472694 | n.849C>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472714 | n.869A>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472715 | n.870C>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472770 | n.925C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472812 | n.967A>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472826 | n.981G>C | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472887 | n.1042G>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473223 | n.1378G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473352 | n.1507C>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473353 | n.1508C>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473358 | n.1513G>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473359 | n.1514G>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1473461 | n.-197T>A | upstream_gene_variant | 0.29 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474869 | n.1212G>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474875 | n.1218G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474876 | n.1219T>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474883 | n.1226T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475499 | n.1842C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475526 | n.1869C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475707 | n.2050T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475713 | n.2056C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475716 | n.2059A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475735 | n.2078T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475736 | n.2079G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475790 | n.2133C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475791 | n.2134A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.72 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475892 | n.2235A>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476232 | n.2575G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476336 | n.2679C>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476357 | n.2700T>A | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476368 | n.2711T>C | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476470 | n.2813C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476491 | n.2834T>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476501 | n.2844C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476739 | n.3082T>A | non_coding_transcript_exon_variant | 0.18 |
rpsA | 1834723 | p.Glu394Asp | missense_variant | 0.29 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101865 | p.Trp393Ser | missense_variant | 0.14 |
katG | 2154140 | p.Phe658Leu | missense_variant | 0.25 |
katG | 2154187 | p.Pro642Gln | missense_variant | 0.2 |
PPE35 | 2168636 | c.1977G>A | synonymous_variant | 0.18 |
PPE35 | 2168762 | c.1850delC | frameshift_variant | 0.18 |
PPE35 | 2170791 | c.-179A>G | upstream_gene_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
eis | 2714422 | p.Ala304Glu | missense_variant | 0.33 |
eis | 2714460 | c.873G>A | synonymous_variant | 0.33 |
Rv2752c | 3065364 | c.828G>C | synonymous_variant | 0.29 |
thyX | 3067472 | c.474C>G | synonymous_variant | 0.18 |
thyX | 3067634 | c.312C>T | synonymous_variant | 0.25 |
fbiD | 3339267 | c.150G>A | synonymous_variant | 0.18 |
Rv3083 | 3448532 | p.Ile10Thr | missense_variant | 0.22 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474314 | p.Ala103Val | missense_variant | 0.25 |
fprA | 3474477 | p.Asn157Lys | missense_variant | 0.29 |
fprA | 3474489 | p.Asp161Glu | missense_variant | 0.2 |
whiB7 | 3568523 | c.157T>C | synonymous_variant | 0.33 |
whiB7 | 3568735 | c.-56G>A | upstream_gene_variant | 0.2 |
whiB7 | 3568806 | c.-127G>T | upstream_gene_variant | 0.15 |
fbiB | 3642411 | c.877C>A | synonymous_variant | 0.18 |
clpC1 | 4039496 | p.Ile403Met | missense_variant | 0.18 |
clpC1 | 4039520 | c.1185G>C | synonymous_variant | 0.22 |
clpC1 | 4039526 | c.1179G>C | synonymous_variant | 0.22 |
clpC1 | 4039533 | p.Asn391Thr | missense_variant | 0.2 |
clpC1 | 4039546 | p.Asp387Asn | missense_variant | 0.2 |
clpC1 | 4039739 | c.966C>G | synonymous_variant | 0.29 |
clpC1 | 4040269 | p.Gln146Lys | missense_variant | 0.13 |
clpC1 | 4040308 | c.397C>A | synonymous_variant | 0.18 |
clpC1 | 4040503 | p.Gly68Cys | missense_variant | 0.18 |
embC | 4240702 | c.840G>T | synonymous_variant | 0.33 |
embC | 4241985 | p.Leu708Ser | missense_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4245352 | p.Lys707Arg | missense_variant | 0.15 |
aftB | 4267095 | p.Pro581Gln | missense_variant | 0.22 |
ethA | 4327995 | c.-522C>T | upstream_gene_variant | 0.15 |
ethA | 4328329 | c.-856C>G | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |