Run ID: ERR3439277
Sample name:
Date: 01-04-2023 02:01:00
Number of reads: 53490
Percentage reads mapped: 2.28
Strain: lineage4.9
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.95 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.98 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
fbiC | 1304153 | p.Pro408Gln | missense_variant | 0.67 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475747 | n.2090A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475767 | n.2110G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475781 | n.2124T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475877 | n.2220C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475892 | n.2235A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476297 | n.2640C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476322 | n.2665C>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476359 | n.2702C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476368 | n.2711T>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476381 | n.2724G>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.53 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476428 | n.2771C>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 1.0 |
ndh | 2103173 | c.-132delG | upstream_gene_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155503 | c.609C>T | synonymous_variant | 1.0 |
Rv2752c | 3065472 | c.720C>T | synonymous_variant | 0.67 |
Rv3083 | 3448783 | p.Val94Ile | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embA | 4242970 | c.-263C>T | upstream_gene_variant | 1.0 |
embA | 4243693 | p.Gly154Asp | missense_variant | 0.5 |
aftB | 4267091 | c.1746C>A | synonymous_variant | 0.67 |
aftB | 4267167 | p.Gln557Pro | missense_variant | 0.4 |
aftB | 4269351 | c.-515C>T | upstream_gene_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |