Run ID: ERR2228817
Sample name:
Date: 31-03-2023 16:21:53
Number of reads: 371783
Percentage reads mapped: 99.38
Strain: lineage4
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5924 | p.Ala229Ser | missense_variant | 0.38 |
gyrB | 5996 | p.Tyr253Asn | missense_variant | 0.75 |
gyrB | 6100 | c.861G>T | synonymous_variant | 0.67 |
gyrA | 7353 | p.Val18Ile | missense_variant | 0.18 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7444 | p.Leu48Arg | missense_variant | 0.5 |
gyrA | 7539 | p.Thr80Pro | missense_variant | 0.23 |
gyrA | 7666 | p.Asp122Ala | missense_variant | 0.42 |
gyrA | 7704 | p.Thr135Pro | missense_variant | 0.22 |
gyrA | 8100 | p.Thr267Pro | missense_variant | 0.2 |
gyrA | 8992 | p.His564Arg | missense_variant | 0.27 |
fgd1 | 491181 | c.399T>G | synonymous_variant | 0.43 |
fgd1 | 491676 | c.894T>G | synonymous_variant | 0.4 |
rpoB | 759828 | p.Lys8* | stop_gained | 0.29 |
rpoB | 760804 | p.Val333Glu | missense_variant | 0.33 |
rpoB | 760822 | p.Leu339Gln | missense_variant | 0.33 |
rpoB | 761521 | p.Tyr572Cys | missense_variant | 0.15 |
rpoB | 762625 | p.Val940Gly | missense_variant | 0.25 |
rpoB | 763113 | p.Gly1103Cys | missense_variant | 0.25 |
rpoC | 763411 | c.42T>C | synonymous_variant | 0.29 |
rpoC | 764072 | p.Ile235Leu | missense_variant | 0.25 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.4 |
rpoC | 765465 | p.Asp699Ala | missense_variant | 0.18 |
rpoC | 765603 | p.Ile745Asn | missense_variant | 0.29 |
rpoC | 766038 | p.Asp890Ala | missense_variant | 0.29 |
rpoC | 766823 | p.Lys1152* | stop_gained | 0.33 |
rpoC | 766871 | p.Ile1168Val | missense_variant | 0.4 |
rpoC | 767100 | p.Lys1244Met | missense_variant | 0.25 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775643 | c.2838A>C | synonymous_variant | 0.29 |
mmpL5 | 777041 | c.1440G>T | synonymous_variant | 0.22 |
mmpL5 | 777219 | p.Leu421Gln | missense_variant | 0.25 |
mmpL5 | 777502 | p.Thr327Pro | missense_variant | 0.29 |
mmpL5 | 777691 | p.Asn264Tyr | missense_variant | 0.29 |
mmpR5 | 779150 | p.Glu54Val | missense_variant | 0.33 |
mmpS5 | 779678 | c.-773T>G | upstream_gene_variant | 0.22 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rplC | 800822 | p.Gly5Val | missense_variant | 0.22 |
rplC | 801035 | p.Asn76Thr | missense_variant | 0.33 |
fbiC | 1303525 | p.Ser199Ala | missense_variant | 0.33 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
Rv1258c | 1406135 | p.Glu402Asp | missense_variant | 0.4 |
Rv1258c | 1407092 | c.249T>G | synonymous_variant | 0.2 |
Rv1258c | 1407144 | p.Val66Gly | missense_variant | 0.22 |
Rv1258c | 1407236 | p.Leu35Phe | missense_variant | 0.25 |
embR | 1416215 | p.Phe378Tyr | missense_variant | 0.5 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471927 | n.82T>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474456 | n.799A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476183 | n.2526A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476219 | n.2562T>C | non_coding_transcript_exon_variant | 0.67 |
rpsA | 1833541 | c.-1T>A | upstream_gene_variant | 0.33 |
rpsA | 1833543 | c.2T>A | start_lost | 0.29 |
rpsA | 1834836 | p.Met432Lys | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918058 | p.Val40Gly | missense_variant | 0.25 |
ndh | 2102150 | p.Asp298Val | missense_variant | 0.33 |
ndh | 2102737 | p.Glu102Asp | missense_variant | 0.33 |
katG | 2154262 | p.Leu617Arg | missense_variant | 0.38 |
katG | 2154580 | p.Asp511Ala | missense_variant | 0.29 |
katG | 2154586 | p.Asp509Ala | missense_variant | 0.22 |
katG | 2155114 | p.Leu333His | missense_variant | 0.33 |
katG | 2155441 | p.Gln224Leu | missense_variant | 0.2 |
katG | 2155585 | p.Met176Lys | missense_variant | 0.25 |
katG | 2155756 | p.Arg119His | missense_variant | 0.25 |
katG | 2155850 | p.Gln88Lys | missense_variant | 0.4 |
PPE35 | 2168088 | p.Pro842Arg | missense_variant | 1.0 |
PPE35 | 2168600 | c.2013G>T | synonymous_variant | 0.29 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2168732 | c.1881T>A | synonymous_variant | 0.29 |
PPE35 | 2169269 | c.1344A>G | synonymous_variant | 0.3 |
PPE35 | 2169272 | c.1341C>G | synonymous_variant | 0.3 |
PPE35 | 2169278 | c.1335T>C | synonymous_variant | 0.2 |
PPE35 | 2169281 | c.1332T>G | synonymous_variant | 0.2 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.2 |
PPE35 | 2169293 | c.1320T>C | synonymous_variant | 0.2 |
PPE35 | 2169308 | c.1305C>T | synonymous_variant | 0.17 |
PPE35 | 2169510 | p.Asn368Thr | missense_variant | 0.5 |
Rv1979c | 2222687 | p.Lys160* | stop_gained | 0.33 |
Rv1979c | 2222705 | p.Phe154Ile | missense_variant | 0.29 |
Rv1979c | 2222733 | p.Phe144Leu | missense_variant | 0.33 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518722 | p.Glu203Ala | missense_variant | 0.22 |
kasA | 2519167 | c.1053T>G | synonymous_variant | 0.18 |
folC | 2747138 | p.Val154Gly | missense_variant | 0.4 |
folC | 2747457 | p.Thr48Pro | missense_variant | 0.3 |
folC | 2747673 | c.-75T>A | upstream_gene_variant | 0.67 |
folC | 2747794 | c.-196A>C | upstream_gene_variant | 0.25 |
pepQ | 2859842 | p.Ile193Phe | missense_variant | 0.29 |
pepQ | 2860249 | p.Asp57Ala | missense_variant | 0.3 |
ribD | 2987010 | p.Thr58Ala | missense_variant | 0.22 |
Rv2752c | 3066319 | c.-128T>G | upstream_gene_variant | 0.29 |
thyX | 3067414 | p.Ala178Ser | missense_variant | 0.22 |
thyX | 3067910 | c.36C>A | synonymous_variant | 0.67 |
thyX | 3068070 | c.-125T>A | upstream_gene_variant | 0.4 |
thyX | 3068096 | c.-151A>T | upstream_gene_variant | 0.33 |
thyX | 3068130 | c.-185A>T | upstream_gene_variant | 0.33 |
thyA | 3074220 | c.252A>T | synonymous_variant | 0.5 |
ald | 3087183 | p.Thr122Pro | missense_variant | 0.4 |
fbiD | 3339066 | c.-52C>A | upstream_gene_variant | 0.2 |
fbiD | 3339417 | p.Glu100Asp | missense_variant | 0.33 |
fbiD | 3339634 | p.Ser173Ala | missense_variant | 0.25 |
fprA | 3473906 | c.-101A>T | upstream_gene_variant | 0.3 |
Rv3236c | 3612135 | p.Thr328Ala | missense_variant | 0.33 |
Rv3236c | 3613046 | p.Val24Gly | missense_variant | 0.43 |
Rv3236c | 3613085 | p.Leu11Arg | missense_variant | 0.67 |
Rv3236c | 3613095 | p.Leu8Val | missense_variant | 0.67 |
fbiA | 3640763 | p.Asp74Ala | missense_variant | 0.4 |
fbiA | 3641001 | p.His153Gln | missense_variant | 0.25 |
alr | 3840908 | p.Gln171His | missense_variant | 0.33 |
rpoA | 3878066 | p.Pro148Thr | missense_variant | 0.4 |
ddn | 3986915 | c.72T>A | synonymous_variant | 0.33 |
clpC1 | 4039661 | c.1044T>G | synonymous_variant | 0.43 |
clpC1 | 4040209 | p.Ser166Ala | missense_variant | 0.25 |
clpC1 | 4040357 | c.348T>G | synonymous_variant | 0.22 |
clpC1 | 4040409 | p.Gly99Val | missense_variant | 0.14 |
embC | 4239868 | c.6T>G | synonymous_variant | 0.29 |
embC | 4240694 | p.Ile278Phe | missense_variant | 0.33 |
embC | 4241043 | p.Asn394Thr | missense_variant | 0.5 |
embC | 4241450 | p.Ser530Ala | missense_variant | 0.29 |
embC | 4241705 | p.Ser615Ala | missense_variant | 0.67 |
embC | 4241726 | p.Phe622Val | missense_variant | 0.75 |
embC | 4242062 | p.Trp734Arg | missense_variant | 0.22 |
embC | 4242204 | p.Leu781Gln | missense_variant | 0.33 |
embA | 4242565 | c.-668C>A | upstream_gene_variant | 0.29 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243051 | c.-182G>A | upstream_gene_variant | 0.17 |
embA | 4243193 | c.-40T>C | upstream_gene_variant | 0.25 |
embA | 4244508 | p.Leu426Val | missense_variant | 0.5 |
embA | 4245177 | p.Met649Leu | missense_variant | 0.22 |
embA | 4246210 | p.Phe993Tyr | missense_variant | 0.5 |
embB | 4246544 | p.Thr11Pro | missense_variant | 0.25 |
embB | 4247004 | p.Leu164Arg | missense_variant | 0.43 |
embB | 4247028 | p.Leu172Arg | missense_variant | 0.43 |
embB | 4247156 | p.Thr215Pro | missense_variant | 0.5 |
embB | 4247445 | p.Asp311Ala | missense_variant | 0.18 |
embB | 4247470 | c.957T>C | synonymous_variant | 0.17 |
embB | 4247472 | p.Phe320Tyr | missense_variant | 0.14 |
embB | 4247538 | p.His342Leu | missense_variant | 0.14 |
embB | 4247817 | p.Val435Ala | missense_variant | 0.22 |
embB | 4247862 | p.Ile450Ser | missense_variant | 0.22 |
embB | 4248431 | p.Trp640Gly | missense_variant | 0.27 |
embB | 4249298 | p.Trp929Gly | missense_variant | 0.25 |
embB | 4249443 | p.Tyr977Phe | missense_variant | 0.4 |
aftB | 4267161 | p.Val559Gly | missense_variant | 0.22 |
aftB | 4267206 | p.Val544Gly | missense_variant | 0.27 |
aftB | 4267467 | p.Tyr457Phe | missense_variant | 0.25 |
ubiA | 4269448 | p.Val129Gly | missense_variant | 0.4 |
ubiA | 4269754 | p.Val27Gly | missense_variant | 0.5 |
ubiA | 4269833 | c.1A>T | initiator_codon_variant | 0.5 |
ethA | 4326581 | p.Asn298Ile | missense_variant | 0.22 |
ethA | 4327194 | p.Ile94Phe | missense_variant | 0.22 |
ethR | 4327288 | c.-261T>A | upstream_gene_variant | 0.29 |
ethA | 4328234 | c.-761T>A | upstream_gene_variant | 0.23 |
whiB6 | 4338369 | c.153C>A | synonymous_variant | 0.25 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407652 | p.Val184Gly | missense_variant | 0.29 |