Run ID: ERR2228819
Sample name:
Date: 31-03-2023 16:22:01
Number of reads: 610402
Percentage reads mapped: 99.2
Strain: lineage4.8
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.8 | Euro-American (mainly T) | T1;T2;T3;T5 | RD219 | 0.98 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761136 | p.Thr444Pro | missense_variant | 0.2 | rifampicin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6210 | p.Leu324Gln | missense_variant | 0.22 |
gyrB | 6456 | p.Val406Asp | missense_variant | 0.25 |
gyrB | 6571 | p.Asp444Glu | missense_variant | 0.25 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 8060 | p.Met253Ile | missense_variant | 0.22 |
gyrA | 8749 | p.Leu483His | missense_variant | 0.25 |
fgd1 | 490590 | c.-193A>C | upstream_gene_variant | 0.35 |
fgd1 | 491610 | c.828A>T | synonymous_variant | 0.33 |
ccsA | 620090 | p.Gln67Leu | missense_variant | 0.17 |
ccsA | 620492 | p.Ser201Leu | missense_variant | 0.25 |
rpoB | 759898 | p.Asn31Thr | missense_variant | 0.5 |
rpoB | 760841 | c.1035T>G | synonymous_variant | 0.38 |
rpoB | 761914 | p.Asp703Ala | missense_variant | 0.18 |
rpoC | 763367 | c.-3T>A | upstream_gene_variant | 0.22 |
rpoC | 763592 | p.Cys75Ser | missense_variant | 0.27 |
rpoC | 764915 | p.Leu516Met | missense_variant | 0.22 |
rpoC | 765495 | p.Val709Gly | missense_variant | 0.29 |
rpoC | 766432 | c.3063T>A | synonymous_variant | 0.27 |
rpoC | 766686 | p.Glu1106Val | missense_variant | 0.29 |
mmpL5 | 775586 | c.2895A>C | stop_lost&splice_region_variant | 0.35 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 0.95 |
mmpL5 | 776569 | p.Met638Leu | missense_variant | 0.25 |
mmpL5 | 777250 | p.Tyr411Asp | missense_variant | 0.25 |
mmpL5 | 778144 | p.Ile113Leu | missense_variant | 0.3 |
mmpS5 | 778543 | p.Glu121Asp | missense_variant | 0.25 |
mmpL5 | 779100 | c.-620A>C | upstream_gene_variant | 0.22 |
mmpR5 | 779266 | p.Phe93Ile | missense_variant | 0.2 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781592 | c.33T>G | synonymous_variant | 0.5 |
rplC | 800822 | p.Gly5Asp | missense_variant | 0.17 |
rplC | 801068 | p.Asp87Ala | missense_variant | 0.22 |
fbiC | 1303747 | p.Thr273Ala | missense_variant | 1.0 |
fbiC | 1304011 | p.Thr361Pro | missense_variant | 0.31 |
fbiC | 1304646 | c.1716T>G | synonymous_variant | 0.25 |
Rv1258c | 1406255 | c.1086G>A | synonymous_variant | 0.27 |
Rv1258c | 1407039 | p.Val101Gly | missense_variant | 0.31 |
Rv1258c | 1407075 | p.Val89Gly | missense_variant | 0.27 |
embR | 1416323 | p.Asn342Thr | missense_variant | 0.27 |
embR | 1416372 | p.Ser326Arg | missense_variant | 0.27 |
embR | 1416949 | p.Gln133His | missense_variant | 0.33 |
atpE | 1461074 | c.30C>A | synonymous_variant | 0.4 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471750 | n.-96A>G | upstream_gene_variant | 0.25 |
rrs | 1471801 | n.-45A>T | upstream_gene_variant | 0.43 |
rrs | 1471881 | n.36A>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472549 | n.704G>T | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472974 | n.1129A>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1473563 | n.-95T>G | upstream_gene_variant | 0.33 |
rrl | 1473822 | n.165A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473826 | n.169A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1473844 | n.187C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474041 | n.384T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474161 | n.504A>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475628 | n.1971G>T | non_coding_transcript_exon_variant | 0.27 |
fabG1 | 1673154 | c.-286A>C | upstream_gene_variant | 0.25 |
rpsA | 1833543 | c.2T>A | start_lost | 0.25 |
rpsA | 1834026 | p.Gln162Pro | missense_variant | 0.38 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102559 | p.Ser162Gly | missense_variant | 0.25 |
PPE35 | 2167814 | c.2799C>T | synonymous_variant | 0.2 |
PPE35 | 2167846 | p.Ser923Cys | missense_variant | 0.22 |
PPE35 | 2168728 | p.Gly629Arg | missense_variant | 1.0 |
PPE35 | 2169013 | p.Val534Leu | missense_variant | 0.25 |
PPE35 | 2169226 | p.Pro463Ala | missense_variant | 0.12 |
PPE35 | 2169278 | c.1335T>G | synonymous_variant | 0.18 |
PPE35 | 2169329 | p.Asn428Lys | missense_variant | 0.21 |
PPE35 | 2169798 | p.Leu272Gln | missense_variant | 0.2 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv1979c | 2223320 | c.-156T>G | upstream_gene_variant | 0.27 |
pncA | 2289994 | c.-753A>T | upstream_gene_variant | 0.29 |
pncA | 2290023 | c.-782A>G | upstream_gene_variant | 0.67 |
kasA | 2518610 | p.Thr166Pro | missense_variant | 0.25 |
eis | 2715098 | p.Thr79Pro | missense_variant | 0.4 |
folC | 2747316 | p.Arg95* | stop_gained | 0.2 |
folC | 2747457 | p.Thr48Pro | missense_variant | 0.2 |
pepQ | 2859528 | c.891T>C | synonymous_variant | 0.23 |
pepQ | 2860114 | p.Val102Gly | missense_variant | 0.25 |
ribD | 2987069 | c.231T>A | synonymous_variant | 0.43 |
Rv2752c | 3064912 | p.Val427Asp | missense_variant | 0.29 |
Rv2752c | 3065098 | p.Asn365Thr | missense_variant | 0.22 |
thyX | 3067509 | p.Leu146Gln | missense_variant | 0.2 |
thyX | 3067651 | p.Phe99Leu | missense_variant | 0.17 |
thyX | 3067713 | p.Val78Ala | missense_variant | 0.15 |
thyA | 3073699 | p.Lys258Ile | missense_variant | 0.18 |
thyA | 3073828 | p.Gln215Arg | missense_variant | 0.1 |
thyA | 3074248 | p.His75Leu | missense_variant | 0.2 |
thyA | 3074365 | p.Tyr36Phe | missense_variant | 0.27 |
Rv3236c | 3612166 | c.951A>T | synonymous_variant | 0.29 |
Rv3236c | 3612377 | p.Val247Ala | missense_variant | 0.33 |
Rv3236c | 3613146 | c.-30T>G | upstream_gene_variant | 0.17 |
fbiA | 3640968 | p.Leu142Phe | missense_variant | 0.4 |
fbiB | 3642340 | p.Asp269Ala | missense_variant | 0.4 |
alr | 3840878 | p.Gln181His | missense_variant | 0.18 |
clpC1 | 4039691 | c.1014G>C | synonymous_variant | 0.21 |
clpC1 | 4040031 | p.Val225Gly | missense_variant | 0.14 |
clpC1 | 4040249 | p.Glu152Asp | missense_variant | 0.43 |
clpC1 | 4040574 | p.Val44Gly | missense_variant | 0.38 |
clpC1 | 4040593 | p.Ile38Val | missense_variant | 0.2 |
panD | 4043998 | p.Asp95Ala | missense_variant | 0.27 |
embC | 4242002 | p.Leu714Val | missense_variant | 0.29 |
embC | 4242069 | p.Val736Gly | missense_variant | 0.21 |
embC | 4242319 | p.Glu819Asp | missense_variant | 0.27 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242908 | p.Phe1016Val | missense_variant | 0.2 |
embA | 4243365 | p.Trp45Arg | missense_variant | 0.2 |
embA | 4243546 | p.Leu105Arg | missense_variant | 0.18 |
embA | 4245726 | p.Leu832Met | missense_variant | 0.5 |
embB | 4246743 | p.Val77Gly | missense_variant | 0.17 |
aftB | 4267596 | p.Tyr414Ser | missense_variant | 0.15 |
aftB | 4268034 | p.Val268Ala | missense_variant | 0.5 |
ethA | 4327176 | p.Phe100Leu | missense_variant | 0.4 |
ethR | 4327207 | c.-342C>A | upstream_gene_variant | 0.5 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407553 | p.Arg217Gln | missense_variant | 0.2 |
Rv3083 | 3448507 | c.5_*1408del | frameshift_variant&stop_lost&splice_region_variant | 1.0 |