Run ID: ERR3994115
Sample name:
Date: 01-04-2023 03:43:00
Number of reads: 3975547
Percentage reads mapped: 99.99
Strain: lineage2.2.1
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 1.0 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5753 | p.Arg172Trp | missense_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7607 | c.306C>A | synonymous_variant | 0.17 |
gyrA | 7671 | p.Pro124Ser | missense_variant | 0.13 |
gyrA | 9286 | p.Ala662Gly | missense_variant | 0.13 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491272 | p.Asp164His | missense_variant | 0.12 |
fgd1 | 491283 | p.Asp167Glu | missense_variant | 0.14 |
fgd1 | 491311 | p.Gly177Cys | missense_variant | 0.14 |
fgd1 | 491326 | p.Ala182Pro | missense_variant | 0.15 |
fgd1 | 491529 | p.Trp249Cys | missense_variant | 0.12 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575431 | c.84C>G | synonymous_variant | 0.12 |
mshA | 575720 | p.Leu125Met | missense_variant | 0.17 |
mshA | 575780 | p.Pro145Thr | missense_variant | 0.14 |
mshA | 575867 | p.Val174Leu | missense_variant | 0.13 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
mshA | 576119 | p.Ala258Ser | missense_variant | 0.22 |
mshA | 576151 | c.804G>T | synonymous_variant | 0.14 |
ccsA | 619713 | c.-178C>A | upstream_gene_variant | 0.18 |
ccsA | 619734 | c.-157C>A | upstream_gene_variant | 0.2 |
ccsA | 619886 | c.-5G>T | upstream_gene_variant | 0.15 |
ccsA | 620164 | p.Leu92Met | missense_variant | 0.15 |
ccsA | 620351 | p.Arg154Leu | missense_variant | 0.15 |
ccsA | 620505 | p.Glu205Asp | missense_variant | 0.18 |
ccsA | 620507 | p.Pro206Arg | missense_variant | 0.18 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 761257 | p.Glu484Val | missense_variant | 0.14 |
rpoB | 761525 | p.Met573Ile | missense_variant | 0.11 |
rpoB | 762562 | p.Arg919Pro | missense_variant | 0.13 |
rpoB | 762589 | p.Thr928Ser | missense_variant | 0.12 |
rpoB | 762761 | p.Cys985* | stop_gained | 0.17 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763939 | p.Lys190Asn | missense_variant | 0.12 |
rpoC | 764065 | p.Lys232Asn | missense_variant | 0.17 |
rpoC | 764596 | p.Lys409Asn | missense_variant | 0.13 |
rpoC | 764890 | p.Leu507Phe | missense_variant | 0.11 |
rpoC | 765157 | c.1788C>A | synonymous_variant | 0.14 |
rpoC | 765295 | c.1926G>A | synonymous_variant | 0.13 |
rpoC | 765342 | p.Pro658Arg | missense_variant | 0.12 |
rpoC | 765762 | p.Pro798Gln | missense_variant | 0.17 |
rpoC | 765822 | p.Ala818Asp | missense_variant | 0.14 |
rpoC | 765825 | p.Gly819Ala | missense_variant | 0.14 |
rpoC | 765833 | p.Gly822Cys | missense_variant | 0.14 |
rpoC | 766279 | c.2910C>G | synonymous_variant | 0.12 |
rpoC | 766364 | p.Ala999Pro | missense_variant | 0.13 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 776303 | c.2178G>C | synonymous_variant | 0.12 |
mmpL5 | 777709 | p.Leu258Phe | missense_variant | 0.13 |
mmpL5 | 777766 | p.Gly239Arg | missense_variant | 0.15 |
mmpL5 | 777890 | p.Gln197His | missense_variant | 0.14 |
mmpL5 | 778010 | p.Gln157His | missense_variant | 0.2 |
mmpL5 | 779472 | c.-992G>T | upstream_gene_variant | 0.14 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
Rv1258c | 1406111 | p.Asp410Glu | missense_variant | 0.18 |
Rv1258c | 1406693 | c.648G>T | synonymous_variant | 0.14 |
Rv1258c | 1406709 | p.Gly211Val | missense_variant | 0.14 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1407495 | c.-155C>A | upstream_gene_variant | 0.33 |
embR | 1416821 | p.Ala176Asp | missense_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472184 | n.339T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475859 | n.2202G>T | non_coding_transcript_exon_variant | 0.13 |
inhA | 1673766 | c.-436C>A | upstream_gene_variant | 0.14 |
inhA | 1674873 | p.Gln224His | missense_variant | 0.14 |
inhA | 1674925 | p.Val242Leu | missense_variant | 0.13 |
inhA | 1674932 | p.Ala244Gly | missense_variant | 0.12 |
rpsA | 1833409 | c.-133C>T | upstream_gene_variant | 1.0 |
rpsA | 1833420 | c.-122C>G | upstream_gene_variant | 0.12 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834980 | p.Ser480Ile | missense_variant | 0.14 |
tlyA | 1917769 | c.-171C>A | upstream_gene_variant | 0.17 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918674 | c.735G>C | synonymous_variant | 0.17 |
tlyA | 1918734 | p.Ser265Arg | missense_variant | 0.15 |
ndh | 2102139 | p.Arg302Gly | missense_variant | 0.17 |
ndh | 2102146 | c.897G>C | synonymous_variant | 0.17 |
ndh | 2102292 | p.Asp251Asn | missense_variant | 0.25 |
ndh | 2102358 | p.Gly229Arg | missense_variant | 0.17 |
ndh | 2102380 | c.663G>T | synonymous_variant | 0.14 |
ndh | 2102423 | p.Thr207Ser | missense_variant | 0.18 |
katG | 2153900 | p.Asp738Asn | missense_variant | 0.15 |
katG | 2154563 | p.Val517Leu | missense_variant | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155217 | p.Gly299Arg | missense_variant | 0.18 |
katG | 2155317 | c.795G>T | synonymous_variant | 0.18 |
katG | 2155477 | p.Gly212Asp | missense_variant | 0.18 |
katG | 2155693 | p.Ser140Ile | missense_variant | 0.14 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2169941 | c.672C>A | synonymous_variant | 0.18 |
PPE35 | 2170381 | p.Ala78Thr | missense_variant | 0.14 |
PPE35 | 2170472 | c.141G>C | synonymous_variant | 0.15 |
PPE35 | 2170623 | c.-11G>A | upstream_gene_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2290204 | c.-963G>T | upstream_gene_variant | 0.13 |
kasA | 2518737 | p.Ala208Glu | missense_variant | 0.15 |
kasA | 2519077 | c.963G>C | synonymous_variant | 0.22 |
eis | 2714248 | p.Gly362Ala | missense_variant | 0.22 |
eis | 2714955 | c.378C>T | synonymous_variant | 1.0 |
eis | 2715037 | p.Ala99Val | missense_variant | 0.13 |
eis | 2715433 | c.-101T>C | upstream_gene_variant | 0.11 |
folC | 2746317 | p.Asp428Asn | missense_variant | 0.17 |
folC | 2746366 | c.1233G>T | synonymous_variant | 0.18 |
folC | 2746511 | p.Ala363Glu | missense_variant | 0.2 |
folC | 2746648 | c.951G>T | synonymous_variant | 0.15 |
folC | 2746696 | p.Asn301Lys | missense_variant | 0.15 |
folC | 2746960 | c.639C>A | synonymous_variant | 0.18 |
folC | 2747775 | c.-177C>G | upstream_gene_variant | 0.17 |
pepQ | 2859759 | p.Ile220Met | missense_variant | 0.12 |
ribD | 2986669 | c.-170G>T | upstream_gene_variant | 0.17 |
ribD | 2987056 | p.Leu73Arg | missense_variant | 0.13 |
ribD | 2987120 | c.282C>T | synonymous_variant | 0.15 |
ribD | 2987132 | p.Met98Ile | missense_variant | 0.17 |
ribD | 2987184 | p.Gln116Lys | missense_variant | 0.17 |
ribD | 2987354 | c.516G>C | synonymous_variant | 0.15 |
ribD | 2987367 | p.Val177Leu | missense_variant | 0.18 |
ribD | 2987535 | p.Gln233Glu | missense_variant | 0.25 |
ribD | 2987582 | c.744C>G | synonymous_variant | 0.15 |
Rv2752c | 3066197 | c.-6C>T | upstream_gene_variant | 0.14 |
Rv2752c | 3066261 | c.-70G>C | upstream_gene_variant | 0.15 |
Rv2752c | 3066337 | c.-146G>T | upstream_gene_variant | 0.17 |
thyX | 3067907 | c.39C>G | synonymous_variant | 0.14 |
thyX | 3067948 | c.-3G>C | upstream_gene_variant | 0.15 |
thyA | 3074049 | p.Met141Ile | missense_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339139 | p.Gly8Arg | missense_variant | 0.4 |
fbiD | 3339630 | c.513C>T | synonymous_variant | 1.0 |
Rv3083 | 3449004 | p.Gln167His | missense_variant | 0.15 |
Rv3083 | 3449149 | p.Tyr216His | missense_variant | 0.13 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474049 | p.Ala15Pro | missense_variant | 0.12 |
Rv3236c | 3612007 | c.1110C>A | synonymous_variant | 0.2 |
Rv3236c | 3612025 | c.1092C>A | synonymous_variant | 0.2 |
Rv3236c | 3612070 | c.1047G>T | synonymous_variant | 0.15 |
Rv3236c | 3612083 | p.Gly345Ala | missense_variant | 0.17 |
Rv3236c | 3612152 | p.Gly322Val | missense_variant | 0.25 |
Rv3236c | 3612201 | p.Val306Leu | missense_variant | 0.14 |
Rv3236c | 3612346 | p.Asp257Glu | missense_variant | 0.18 |
Rv3236c | 3612617 | p.Pro167Gln | missense_variant | 0.15 |
Rv3236c | 3612692 | p.Arg142Gln | missense_variant | 0.17 |
Rv3236c | 3612715 | c.402G>T | synonymous_variant | 0.2 |
Rv3236c | 3612748 | c.369G>T | synonymous_variant | 0.22 |
Rv3236c | 3612783 | p.Gly112Trp | missense_variant | 0.2 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3640617 | c.-918G>T | upstream_gene_variant | 0.14 |
fbiA | 3641030 | p.Ser163Thr | missense_variant | 0.13 |
fbiA | 3641072 | p.Arg177Pro | missense_variant | 0.15 |
fbiB | 3641121 | c.-414C>G | upstream_gene_variant | 0.17 |
fbiA | 3641125 | p.Ala195Pro | missense_variant | 0.17 |
fbiA | 3641128 | p.Ala196Ser | missense_variant | 0.17 |
fbiA | 3641146 | p.Ala202Pro | missense_variant | 0.14 |
fbiA | 3641172 | p.Met210Ile | missense_variant | 0.14 |
fbiB | 3641858 | c.324G>T | synonymous_variant | 0.13 |
fbiB | 3642621 | p.Ala363Ser | missense_variant | 0.29 |
fbiB | 3642728 | p.Ile398Met | missense_variant | 0.33 |
fbiB | 3642872 | p.Ile446Met | missense_variant | 0.12 |
alr | 3841200 | p.Ala74Asp | missense_variant | 0.17 |
rpoA | 3877802 | p.Pro236Ala | missense_variant | 0.11 |
rpoA | 3878049 | c.459G>T | synonymous_variant | 0.13 |
rpoA | 3878078 | p.Arg144Ser | missense_variant | 0.18 |
rpoA | 3878090 | p.Val140Leu | missense_variant | 0.18 |
rpoA | 3878099 | p.Glu137* | stop_gained | 0.2 |
rpoA | 3878544 | c.-37C>G | upstream_gene_variant | 0.2 |
rpoA | 3878700 | c.-193C>G | upstream_gene_variant | 0.13 |
clpC1 | 4038227 | c.2478G>T | synonymous_variant | 0.14 |
clpC1 | 4039273 | p.Glu478Gln | missense_variant | 0.12 |
clpC1 | 4040265 | p.Gly147Ala | missense_variant | 0.12 |
panD | 4043918 | p.Ala122Pro | missense_variant | 0.11 |
panD | 4044391 | c.-111delG | upstream_gene_variant | 0.13 |
panD | 4044397 | c.-116G>C | upstream_gene_variant | 0.13 |
embC | 4239701 | c.-162C>A | upstream_gene_variant | 0.22 |
embC | 4239848 | c.-15G>C | upstream_gene_variant | 0.15 |
embC | 4240290 | p.Pro143Arg | missense_variant | 0.11 |
embC | 4240333 | p.Phe157Leu | missense_variant | 0.14 |
embC | 4240465 | p.Phe201Leu | missense_variant | 0.25 |
embC | 4240634 | p.Arg258Trp | missense_variant | 0.18 |
embC | 4240822 | c.960C>A | synonymous_variant | 0.13 |
embC | 4241327 | p.Arg489Ser | missense_variant | 0.33 |
embC | 4242223 | c.2361C>A | synonymous_variant | 0.15 |
embC | 4242286 | p.Phe808Leu | missense_variant | 0.15 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4243007 | p.Leu1049Ile | missense_variant | 0.17 |
embA | 4243255 | p.Arg8Pro | missense_variant | 0.15 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4243969 | p.Val246Ala | missense_variant | 0.13 |
embA | 4244222 | c.990G>T | synonymous_variant | 0.29 |
embA | 4244371 | p.Arg380Leu | missense_variant | 0.18 |
embA | 4244400 | p.Leu390Met | missense_variant | 0.22 |
embA | 4244419 | c.1189dupG | frameshift_variant | 0.22 |
embA | 4244501 | c.1269G>T | synonymous_variant | 0.29 |
embA | 4244660 | c.1428G>T | synonymous_variant | 0.15 |
embA | 4245473 | c.2241C>G | synonymous_variant | 0.15 |
embA | 4245513 | p.Asp761Asn | missense_variant | 0.14 |
embB | 4245527 | c.-987C>A | upstream_gene_variant | 0.14 |
embA | 4245975 | p.Asp915His | missense_variant | 0.13 |
embA | 4246007 | c.2776delC | frameshift_variant | 0.12 |
embA | 4246038 | p.Ala936Pro | missense_variant | 0.12 |
embA | 4246170 | p.Asp980Tyr | missense_variant | 0.15 |
embA | 4246289 | p.Asn1019Lys | missense_variant | 0.15 |
embA | 4246509 | p.Leu1093Ile | missense_variant | 0.14 |
embB | 4246767 | p.Cys85Phe | missense_variant | 0.13 |
embB | 4247001 | p.Gly163Val | missense_variant | 0.2 |
embB | 4248956 | p.Trp815Gly | missense_variant | 0.14 |
embB | 4248964 | c.2451G>C | synonymous_variant | 0.12 |
embB | 4249045 | p.Leu844Phe | missense_variant | 0.15 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4267708 | p.Gly377Arg | missense_variant | 0.2 |
aftB | 4267710 | p.Ser376Ile | missense_variant | 0.2 |
aftB | 4268127 | p.Pro237Gln | missense_variant | 0.14 |
aftB | 4268149 | p.Gly230Cys | missense_variant | 0.15 |
aftB | 4268176 | p.Pro221Ala | missense_variant | 0.17 |
aftB | 4268517 | p.Ala107Glu | missense_variant | 0.13 |
aftB | 4268695 | p.Val48Leu | missense_variant | 0.13 |
aftB | 4268701 | p.Gly46Arg | missense_variant | 0.13 |
aftB | 4268783 | c.54C>A | synonymous_variant | 0.13 |
ubiA | 4269120 | p.Phe238Leu | missense_variant | 0.25 |
aftB | 4269564 | c.-728G>C | upstream_gene_variant | 0.18 |
ethR | 4328026 | p.Gly160Ser | missense_variant | 0.14 |
ethR | 4328047 | p.Pro167Thr | missense_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |
gid | 4408215 | c.-13G>T | upstream_gene_variant | 0.17 |
gid | 4408465 | c.-263C>G | upstream_gene_variant | 0.12 |