Run ID: SRR7535079
Sample name:
Date: 04-04-2023 19:44:15
Number of reads: 432404
Percentage reads mapped: 3.47
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 | 0.97 |
lineage4.6.1 | Euro-American (Uganda) | T2 | RD724 | 0.98 |
lineage4.6.1.1 | Euro-American | T2-Uganda | RD724 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
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 | 9304 | p.Gly668Asp | missense_variant | 1.0 |
rpoC | 762894 | c.-476C>T | upstream_gene_variant | 0.71 |
rpoB | 762911 | p.Ile1035Met | missense_variant | 0.79 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.77 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.73 |
rpoC | 762932 | c.-438G>T | upstream_gene_variant | 0.73 |
rpoB | 762939 | p.Met1045Leu | missense_variant | 0.71 |
rpoB | 762942 | p.Ile1046Val | missense_variant | 0.71 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 0.73 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.76 |
rpoC | 762989 | c.-381G>T | upstream_gene_variant | 0.64 |
rpoC | 762998 | c.-372G>A | upstream_gene_variant | 0.47 |
rpoB | 763002 | c.3197dupA | frameshift_variant | 0.25 |
rpoC | 764854 | c.1485G>C | synonymous_variant | 0.45 |
rpoC | 764858 | p.Leu497Met | missense_variant | 0.38 |
rpoC | 764869 | c.1500C>T | synonymous_variant | 0.36 |
rpoC | 764872 | c.1503A>G | synonymous_variant | 0.36 |
rpoC | 764875 | c.1506C>T | synonymous_variant | 0.36 |
rpoC | 764878 | c.1509C>G | synonymous_variant | 0.36 |
rpoC | 764887 | c.1518G>T | synonymous_variant | 0.5 |
rpoC | 764893 | c.1524T>C | synonymous_variant | 0.59 |
rpoC | 764905 | c.1536C>T | synonymous_variant | 0.66 |
rpoC | 764911 | c.1542A>C | synonymous_variant | 0.66 |
rpoC | 764914 | p.Met515Ile | missense_variant | 0.63 |
rpoC | 764918 | p.Val517Ile | missense_variant | 0.63 |
rpoC | 764939 | c.1570C>T | synonymous_variant | 0.61 |
rpoC | 764947 | c.1578G>C | synonymous_variant | 0.54 |
rpoC | 764948 | c.1579_1581delTTGinsCTC | synonymous_variant | 0.54 |
rpoC | 764953 | c.1584G>T | synonymous_variant | 0.52 |
rpoC | 764956 | c.1587T>C | synonymous_variant | 0.5 |
rpoC | 764958 | p.Glu530Ala | missense_variant | 0.56 |
rpoC | 764962 | c.1593G>C | synonymous_variant | 0.56 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.58 |
rpoC | 764995 | c.1626C>T | synonymous_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 777567 | p.Gly305Asp | missense_variant | 0.4 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303622 | p.Tyr231Cys | missense_variant | 0.92 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471876 | n.31G>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1471877 | n.32A>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1471878 | n.33C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1471892 | n.47G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1471896 | n.51T>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1471898 | n.53A>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1471930 | n.88_89delGA | non_coding_transcript_exon_variant | 0.36 |
rrs | 1471936 | n.91A>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1471938 | n.93_94insGA | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472153 | n.308G>A | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472210 | n.365A>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472214 | n.369C>G | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472235 | n.390G>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472240 | n.395G>C | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472242 | n.397C>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472251 | n.406G>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472252 | n.407G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472278 | n.433C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472279 | n.434T>G | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472333 | n.488G>T | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472390 | n.545T>A | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472391 | n.546C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472412 | n.567A>C | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472648 | n.803G>C | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472716 | n.871C>A | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472785 | n.940G>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472786 | n.941C>G | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472814 | n.969G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472824 | n.979T>C | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472887 | n.1042G>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473038 | n.1193A>C | non_coding_transcript_exon_variant | 0.27 |
rrs | 1473044 | n.1199C>G | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473139 | n.1294T>C | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473147 | n.1302G>C | non_coding_transcript_exon_variant | 0.79 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473164 | n.1319C>G | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473198 | n.1354delC | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473202 | n.1357C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473204 | n.1359C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1475783 | n.2126T>G | non_coding_transcript_exon_variant | 0.37 |
rrl | 1475787 | n.2130C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476411 | n.2754G>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476463 | n.2806C>A | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476470 | n.2813C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476483 | n.2826G>A | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476501 | n.2844C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.85 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
ald | 3087083 | c.264G>A | synonymous_variant | 0.13 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474162 | c.156G>T | synonymous_variant | 0.25 |
rpoA | 3878007 | p.Ile167Met | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243798 | p.Val189Gly | missense_variant | 0.25 |
ethA | 4328329 | c.-856C>G | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |