Run ID: ERR3797074
Sample name:
Date: 01-04-2023 03:04:38
Number of reads: 20668
Percentage reads mapped: 13.29
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 | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.67 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.67 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.67 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.67 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.67 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.67 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.5 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 1.0 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 1.0 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.67 |
rpoC | 764507 | p.Ala380Ser | missense_variant | 0.67 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 1.0 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 1.0 |
rpoC | 764542 | c.1173C>G | synonymous_variant | 0.67 |
rpoC | 764548 | c.1179G>C | synonymous_variant | 1.0 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.67 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.67 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.67 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 1.0 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 1.0 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 1.0 |
rpoC | 764749 | c.1380G>C | synonymous_variant | 1.0 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 1.0 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 1.0 |
rpoC | 764780 | c.1411_1412delAGinsTC | synonymous_variant | 1.0 |
rpoC | 764804 | p.Gln479Phe | missense_variant | 1.0 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 1.0 |
rpoC | 764812 | c.1443C>G | synonymous_variant | 1.0 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 1.0 |
rpoC | 764818 | c.1449G>C | synonymous_variant | 1.0 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 1.0 |
rpoC | 764833 | c.1464A>G | synonymous_variant | 1.0 |
rpoC | 764843 | p.Ala492Thr | missense_variant | 1.0 |
rpoC | 764857 | c.1488G>C | synonymous_variant | 1.0 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 1.0 |
rpoC | 764872 | c.1503A>C | synonymous_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
fbiC | 1304613 | c.1683T>C | synonymous_variant | 1.0 |
fbiC | 1304634 | c.1704C>G | synonymous_variant | 1.0 |
fbiC | 1304640 | c.1710A>C | synonymous_variant | 1.0 |
fbiC | 1304646 | c.1716T>C | synonymous_variant | 1.0 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472085 | n.240C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472086 | n.241T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472089 | n.244C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472223 | n.378C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472228 | n.383G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472253 | n.408G>T | non_coding_transcript_exon_variant | 0.97 |
rrs | 1472277 | n.432C>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472282 | n.437T>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472378 | n.533G>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472379 | n.534T>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472396 | n.551A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472496 | n.651T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472498 | n.653C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472505 | n.660G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472518 | n.673G>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 | 1472541 | n.696T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472544 | n.699C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472573 | n.728C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472579 | n.734G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472659 | n.814G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472678 | n.834_840delTCCTTGG | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472687 | n.842_843insCC | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472690 | n.845C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472698 | n.853A>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472715 | n.870C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472778 | n.933C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472779 | n.934G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474747 | n.1090C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474758 | n.1101G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474790 | n.1133C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474794 | n.1137C>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474798 | n.1141C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474801 | n.1144G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474802 | n.1145T>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474804 | n.1147C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474825 | n.1168G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474828 | n.1171G>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474830 | n.1173A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474839 | n.1182C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474844 | n.1187G>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474869 | n.1212G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475713 | n.2056C>T | non_coding_transcript_exon_variant | 1.0 |
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 | 1475843 | n.2186G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475853 | n.2196C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475874 | n.2217C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476229 | n.2572C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476238 | n.2581T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476248 | n.2591G>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476252 | n.2595T>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476259 | n.2602C>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476298 | n.2642_2644delCGA | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476306 | n.2649A>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476572 | n.2915G>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476573 | n.2916A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476608 | n.2951C>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476614 | n.2957A>G | non_coding_transcript_exon_variant | 0.75 |
rpsA | 1834859 | p.Ala440Thr | missense_variant | 1.0 |