Run ID: ERR702423
Sample name:
Date: 02-04-2023 03:53:58
Number of reads: 2859672
Percentage reads mapped: 66.75
Strain: lineage5.1.4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage5 | West-Africa 1 | AFRI_2;AFRI_3 | RD711 | 1.0 |
lineage5.1.4 | West-Africa 1 | AFRI_2;AFRI_3 | RD711 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5081 | c.-159G>C | upstream_gene_variant | 1.0 |
gyrB | 6446 | p.Ala403Ser | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9566 | c.2265C>T | synonymous_variant | 1.0 |
gyrA | 9771 | p.Asp824Asn | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775753 | c.2727delC | frameshift_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 0.98 |
rrs | 1472089 | n.244C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472210 | n.365A>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472213 | n.368G>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472215 | n.370A>G | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472234 | n.389T>C | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472236 | n.391C>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.11 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472518 | n.673G>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472544 | n.699C>G | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472570 | n.725G>A | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.49 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472779 | n.934G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472786 | n.941C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474790 | n.1133C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474798 | n.1141C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474804 | n.1147C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.51 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474844 | n.1187G>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474866 | n.1209C>A | non_coding_transcript_exon_variant | 0.51 |
rrl | 1474869 | n.1212G>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1474902 | n.1245T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.39 |
rrl | 1474913 | n.1256T>A | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474920 | n.1263G>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1474927 | n.1271delC | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474931 | n.1274G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475696 | n.2039T>C | non_coding_transcript_exon_variant | 0.11 |
rrl | 1475703 | n.2046A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475707 | n.2050T>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475843 | n.2186G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475849 | n.2192G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475853 | n.2196C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476512 | n.2855C>T | non_coding_transcript_exon_variant | 0.11 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476577 | n.2920T>G | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.24 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476614 | n.2957A>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476624 | n.2967T>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476637 | n.2980C>G | non_coding_transcript_exon_variant | 0.22 |
inhA | 1673338 | c.-864G>A | upstream_gene_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2101921 | c.1122G>A | synonymous_variant | 1.0 |
ndh | 2103112 | c.-70G>T | upstream_gene_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290062 | c.-821G>A | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
thyX | 3067976 | c.-31T>G | upstream_gene_variant | 1.0 |
ald | 3087084 | c.266delA | frameshift_variant | 1.0 |
ald | 3087184 | c.368_373delCCGACG | disruptive_inframe_deletion | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 0.98 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
alr | 3840932 | c.489C>T | synonymous_variant | 1.0 |
rpoA | 3878641 | c.-134C>G | upstream_gene_variant | 0.17 |
ddn | 3986987 | c.144G>T | synonymous_variant | 1.0 |
ddn | 3987180 | p.Asp113Asn | missense_variant | 1.0 |
clpC1 | 4038857 | c.1848C>A | synonymous_variant | 0.15 |
clpC1 | 4040824 | c.-120C>T | upstream_gene_variant | 1.0 |
embC | 4239843 | c.-20A>C | upstream_gene_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4244220 | c.988C>T | synonymous_variant | 0.96 |
embA | 4244635 | p.Val468Ala | missense_variant | 1.0 |
embA | 4245147 | p.Pro639Ser | missense_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ethR | 4326928 | c.-621G>A | upstream_gene_variant | 1.0 |
ethA | 4327103 | p.Gly124Asp | missense_variant | 1.0 |
whiB6 | 4338546 | c.-25G>A | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |