Run ID: ERR6336807
Sample name:
Date: 02-04-2023 02:04:07
Number of reads: 800707
Percentage reads mapped: 99.01
Strain: lineage1.2.1.2.1
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage1 | Indo-Oceanic | EAI | RD239 | 1.0 |
lineage1.2.1 | Indo-Oceanic | EAI2 | RD239 | 0.99 |
lineage1.2.1.2 | Indo-Oceanic | NA | RD239 | 1.0 |
lineage1.2.1.2.1 | Indo-Oceanic | NA | RD239 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
katG | 2155405 | p.Asn236Thr | missense_variant | 0.12 | isoniazid |
pncA | 2289202 | p.Cys14Arg | missense_variant | 0.13 | pyrazinamide |
embB | 4247583 | p.Ala357Val | missense_variant | 0.25 | ethambutol |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5407 | c.168G>A | synonymous_variant | 0.12 |
gyrB | 6112 | p.Met291Ile | missense_variant | 1.0 |
gyrA | 6850 | c.-452C>T | upstream_gene_variant | 0.14 |
gyrB | 7164 | p.Ala642Gly | missense_variant | 0.11 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8243 | c.942C>T | synonymous_variant | 0.22 |
gyrA | 8452 | p.Ala384Val | missense_variant | 1.0 |
gyrA | 8730 | p.Gly477Arg | missense_variant | 0.12 |
gyrA | 9120 | p.Arg607Cys | missense_variant | 0.18 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9260 | c.1959G>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9331 | p.Asn677Ser | missense_variant | 0.14 |
fgd1 | 490691 | c.-92G>A | upstream_gene_variant | 0.17 |
fgd1 | 490740 | c.-42_-41delGC | upstream_gene_variant | 0.12 |
fgd1 | 490920 | c.138C>T | synonymous_variant | 0.12 |
fgd1 | 491213 | p.Ser144Asn | missense_variant | 0.17 |
fgd1 | 491443 | p.Ser221Ala | missense_variant | 0.14 |
fgd1 | 491533 | p.Pro251Ser | missense_variant | 0.14 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
fgd1 | 491764 | c.982C>T | synonymous_variant | 0.22 |
mshA | 575368 | c.21T>C | synonymous_variant | 1.0 |
mshA | 575956 | p.Glu203Asp | missense_variant | 0.33 |
mshA | 576108 | p.Ala254Gly | missense_variant | 0.43 |
mshA | 576435 | p.Gln363Pro | missense_variant | 0.25 |
mshA | 576437 | c.1091delC | frameshift_variant | 0.33 |
mshA | 576470 | p.Gly375Arg | missense_variant | 0.5 |
mshA | 576782 | p.Gly479Ser | missense_variant | 0.14 |
ccsA | 619882 | c.-9G>A | upstream_gene_variant | 0.12 |
ccsA | 620760 | c.870C>T | synonymous_variant | 0.12 |
ccsA | 620828 | p.Val313Gly | missense_variant | 0.15 |
rpoB | 759735 | c.-72G>A | upstream_gene_variant | 0.12 |
rpoB | 760042 | p.Gly79Asp | missense_variant | 0.12 |
rpoB | 760353 | p.Glu183Lys | missense_variant | 0.22 |
rpoB | 760878 | p.Pro358Ser | missense_variant | 0.5 |
rpoB | 761151 | p.Leu449Val | missense_variant | 0.5 |
rpoB | 762246 | c.2440C>T | synonymous_variant | 0.4 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763531 | c.162G>C | synonymous_variant | 1.0 |
rpoC | 763884 | p.Ala172Val | missense_variant | 1.0 |
rpoC | 763886 | c.517C>A | synonymous_variant | 1.0 |
rpoC | 764201 | p.Arg278Trp | missense_variant | 0.18 |
rpoC | 764207 | p.Val280Ile | missense_variant | 0.2 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 1.0 |
rpoC | 765004 | c.1635G>C | synonymous_variant | 0.18 |
rpoC | 765026 | p.Ala553Thr | missense_variant | 0.22 |
rpoC | 765103 | c.1734G>A | synonymous_variant | 1.0 |
rpoC | 765108 | p.Asp580Gly | missense_variant | 0.5 |
rpoC | 765114 | c.1746delG | frameshift_variant | 0.33 |
rpoC | 765486 | p.Met706Lys | missense_variant | 0.13 |
rpoC | 765777 | p.Val803Gly | missense_variant | 0.13 |
rpoC | 766027 | c.2658G>A | synonymous_variant | 0.15 |
rpoC | 766201 | c.2832G>A | synonymous_variant | 0.33 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775884 | p.Ile866Thr | missense_variant | 0.2 |
mmpL5 | 775970 | c.2511G>A | synonymous_variant | 0.13 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776282 | c.2199G>A | synonymous_variant | 0.17 |
mmpL5 | 776342 | c.2139G>A | synonymous_variant | 0.2 |
mmpL5 | 776564 | c.1917C>A | synonymous_variant | 0.2 |
mmpL5 | 776694 | p.Val596Ser | missense_variant | 0.15 |
mmpL5 | 776702 | c.1779C>T | synonymous_variant | 0.15 |
mmpL5 | 776726 | c.1755C>T | synonymous_variant | 0.29 |
mmpL5 | 776732 | c.1749C>T | synonymous_variant | 0.22 |
mmpL5 | 776735 | c.1746C>T | synonymous_variant | 0.22 |
mmpL5 | 776738 | c.1743C>T | synonymous_variant | 0.2 |
mmpL5 | 776741 | c.1740C>G | synonymous_variant | 0.2 |
mmpL5 | 776744 | c.1735_1737delCGCinsAGG | synonymous_variant | 0.17 |
mmpL5 | 777046 | p.Ser479Pro | missense_variant | 1.0 |
mmpL5 | 777466 | c.1015T>C | synonymous_variant | 0.22 |
mmpL5 | 778383 | p.Val33Ala | missense_variant | 0.15 |
mmpR5 | 778405 | c.-585T>G | upstream_gene_variant | 0.2 |
mmpL5 | 778891 | c.-411C>T | upstream_gene_variant | 0.14 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781913 | c.354C>A | synonymous_variant | 0.2 |
rplC | 800759 | c.-50C>T | upstream_gene_variant | 0.15 |
rplC | 800925 | c.117C>T | synonymous_variant | 0.18 |
rplC | 801195 | c.387G>T | synonymous_variant | 0.22 |
rplC | 801255 | c.447C>G | synonymous_variant | 0.18 |
fbiC | 1302821 | c.-110G>A | upstream_gene_variant | 1.0 |
fbiC | 1302936 | c.6G>A | synonymous_variant | 0.14 |
fbiC | 1303396 | p.Arg156Cys | missense_variant | 0.33 |
fbiC | 1303562 | p.Met211Lys | missense_variant | 0.2 |
fbiC | 1303658 | p.Arg243His | missense_variant | 0.29 |
fbiC | 1303788 | p.His286Gln | missense_variant | 0.25 |
fbiC | 1303851 | c.921C>A | synonymous_variant | 0.29 |
fbiC | 1303856 | c.926_927insA | frameshift_variant | 0.4 |
fbiC | 1303955 | p.Glu342Val | missense_variant | 0.2 |
fbiC | 1304618 | p.Arg563Pro | missense_variant | 0.17 |
fbiC | 1304624 | p.Cys565Ser | missense_variant | 0.2 |
fbiC | 1305003 | c.2073C>T | synonymous_variant | 0.29 |
Rv1258c | 1406312 | c.1029T>C | synonymous_variant | 1.0 |
Rv1258c | 1406329 | p.Thr338Ala | missense_variant | 0.2 |
Rv1258c | 1406563 | p.Leu260Val | missense_variant | 0.14 |
Rv1258c | 1407465 | c.-125G>A | upstream_gene_variant | 0.33 |
embR | 1416377 | p.Asn324Ser | missense_variant | 0.14 |
embR | 1416532 | c.816C>T | synonymous_variant | 0.25 |
embR | 1417019 | p.Cys110Tyr | missense_variant | 1.0 |
embR | 1417298 | p.Gly17Glu | missense_variant | 0.12 |
atpE | 1460907 | c.-138T>C | upstream_gene_variant | 1.0 |
atpE | 1461036 | c.-8delA | upstream_gene_variant | 0.14 |
atpE | 1461054 | p.Thr4Ser | missense_variant | 0.18 |
atpE | 1461166 | p.Arg41Pro | missense_variant | 0.12 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrl | 1473392 | n.-266C>T | upstream_gene_variant | 0.2 |
rrl | 1475510 | n.1853A>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475721 | n.2064C>T | non_coding_transcript_exon_variant | 0.33 |
fabG1 | 1673698 | p.Ser87Pro | missense_variant | 0.25 |
fabG1 | 1674088 | p.Val217Ile | missense_variant | 0.25 |
inhA | 1674162 | c.-40C>T | upstream_gene_variant | 1.0 |
inhA | 1674237 | c.36T>C | synonymous_variant | 0.1 |
inhA | 1674321 | c.120G>A | synonymous_variant | 0.12 |
inhA | 1674812 | p.Gly204Ala | missense_variant | 0.13 |
inhA | 1674966 | c.765T>G | synonymous_variant | 0.2 |
rpsA | 1833658 | c.118delG | frameshift_variant | 0.12 |
rpsA | 1833817 | c.278delA | frameshift_variant | 0.33 |
rpsA | 1834405 | c.864C>T | synonymous_variant | 0.12 |
rpsA | 1834421 | p.Gly294Arg | missense_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918187 | p.Gly83Asp | missense_variant | 0.18 |
tlyA | 1918294 | p.Ala119Thr | missense_variant | 0.13 |
tlyA | 1918745 | c.806A>G | stop_lost&splice_region_variant | 0.33 |
ndh | 2101766 | p.Arg426His | missense_variant | 0.15 |
ndh | 2101816 | c.1227C>G | synonymous_variant | 0.11 |
ndh | 2101950 | p.Phe365Ile | missense_variant | 0.17 |
ndh | 2102183 | p.Arg287Lys | missense_variant | 0.15 |
ndh | 2102296 | c.747C>T | synonymous_variant | 0.22 |
ndh | 2102358 | p.Gly229Ser | missense_variant | 0.18 |
katG | 2154296 | p.Ala606Thr | missense_variant | 0.15 |
katG | 2154298 | p.Pro605Gln | missense_variant | 0.15 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2154845 | p.Val423Leu | missense_variant | 0.14 |
katG | 2155428 | c.684C>T | synonymous_variant | 0.15 |
katG | 2155916 | p.Ala66Thr | missense_variant | 0.25 |
katG | 2156446 | c.-335C>T | upstream_gene_variant | 0.33 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168470 | p.Thr715Ala | missense_variant | 0.12 |
PPE35 | 2169488 | c.1125G>A | synonymous_variant | 0.17 |
PPE35 | 2169551 | c.1062C>T | synonymous_variant | 0.15 |
PPE35 | 2169969 | p.Gly215Asp | missense_variant | 0.12 |
Rv1979c | 2222167 | p.Ser333Asn | missense_variant | 0.14 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2222486 | p.Val227Ile | missense_variant | 0.15 |
Rv1979c | 2222697 | c.468C>T | synonymous_variant | 0.33 |
Rv1979c | 2222758 | p.Val136Glu | missense_variant | 0.18 |
Rv1979c | 2223242 | c.-78A>C | upstream_gene_variant | 0.22 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2288769 | p.Asp158Val | missense_variant | 0.13 |
pncA | 2288797 | p.Asn149Asp | missense_variant | 0.14 |
pncA | 2288934 | p.Tyr103Ala | missense_variant | 0.13 |
pncA | 2289116 | c.126T>C | synonymous_variant | 0.14 |
pncA | 2289215 | c.27G>C | synonymous_variant | 0.12 |
pncA | 2289561 | c.-320T>C | upstream_gene_variant | 0.2 |
pncA | 2289863 | c.-622G>A | upstream_gene_variant | 0.18 |
pncA | 2289901 | c.-660G>A | upstream_gene_variant | 0.14 |
pncA | 2289919 | c.-678C>T | upstream_gene_variant | 0.18 |
pncA | 2289988 | c.-747G>A | upstream_gene_variant | 0.33 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2518792 | c.678C>T | synonymous_variant | 0.15 |
kasA | 2519048 | p.Gly312Ser | missense_variant | 1.0 |
kasA | 2519146 | c.1032C>T | synonymous_variant | 0.14 |
kasA | 2519151 | p.Ser346Leu | missense_variant | 0.12 |
kasA | 2519267 | p.Val385Ile | missense_variant | 0.12 |
eis | 2714282 | p.Met351Val | missense_variant | 0.13 |
eis | 2714760 | c.573A>T | synonymous_variant | 0.13 |
eis | 2714934 | c.399C>A | synonymous_variant | 0.25 |
eis | 2714985 | c.348G>A | synonymous_variant | 0.25 |
eis | 2715338 | c.-6G>A | upstream_gene_variant | 0.15 |
ahpC | 2726051 | c.-142G>A | upstream_gene_variant | 1.0 |
ahpC | 2726211 | p.Gly7Arg | missense_variant | 0.13 |
folC | 2746926 | c.672dupC | frameshift_variant | 0.17 |
folC | 2747463 | p.Ser46Gly | missense_variant | 0.25 |
folC | 2747590 | c.9G>A | synonymous_variant | 0.13 |
pepQ | 2860436 | c.-18C>T | upstream_gene_variant | 0.13 |
ribD | 2986653 | c.-186T>A | upstream_gene_variant | 0.22 |
ribD | 2986820 | c.-19A>T | upstream_gene_variant | 0.13 |
ribD | 2987445 | p.Val203Ile | missense_variant | 0.22 |
Rv2752c | 3064548 | p.Gln548His | missense_variant | 0.4 |
Rv2752c | 3064692 | c.1500T>C | synonymous_variant | 0.67 |
Rv2752c | 3064763 | p.Val477Ile | missense_variant | 0.13 |
Rv2752c | 3065708 | p.Ala162Pro | missense_variant | 0.11 |
Rv2752c | 3065926 | p.Ala89Gly | missense_variant | 0.13 |
Rv2752c | 3066330 | c.-139G>A | upstream_gene_variant | 0.18 |
thyX | 3067297 | p.Arg217Cys | missense_variant | 0.5 |
thyX | 3067596 | p.Val117Gly | missense_variant | 0.11 |
thyA | 3073796 | p.Pro226Ala | missense_variant | 0.22 |
thyA | 3074113 | p.Arg120His | missense_variant | 0.17 |
thyA | 3074144 | p.Asp110His | missense_variant | 0.12 |
thyA | 3074386 | p.Leu29Arg | missense_variant | 0.18 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086975 | c.156G>A | synonymous_variant | 0.15 |
ald | 3087483 | p.Ala222Thr | missense_variant | 0.25 |
ald | 3087511 | p.Arg231His | missense_variant | 0.17 |
ald | 3087571 | p.Ser251Leu | missense_variant | 0.25 |
fbiD | 3339053 | c.-65G>A | upstream_gene_variant | 0.18 |
fbiD | 3339417 | c.300A>G | synonymous_variant | 1.0 |
fbiD | 3339547 | p.Leu144Phe | missense_variant | 0.25 |
fbiD | 3339661 | p.Trp182Gly | missense_variant | 0.22 |
Rv3083 | 3448318 | c.-186G>A | upstream_gene_variant | 0.4 |
Rv3083 | 3448692 | c.189C>T | synonymous_variant | 0.2 |
Rv3083 | 3448714 | p.Asp71His | missense_variant | 1.0 |
Rv3083 | 3448999 | p.Pro166Ser | missense_variant | 0.25 |
Rv3083 | 3449184 | c.681C>T | synonymous_variant | 0.29 |
Rv3083 | 3449203 | c.701delT | frameshift_variant | 0.25 |
fprA | 3473857 | c.-150G>A | upstream_gene_variant | 0.13 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474177 | c.171C>T | synonymous_variant | 0.14 |
fprA | 3474597 | c.591C>A | synonymous_variant | 1.0 |
fprA | 3474793 | p.Gly263Arg | missense_variant | 0.25 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
fprA | 3475230 | c.1224C>T | synonymous_variant | 0.14 |
whiB7 | 3568488 | c.191delG | frameshift_variant | 1.0 |
Rv3236c | 3612093 | p.Gly342Arg | missense_variant | 0.17 |
Rv3236c | 3612598 | c.519G>A | synonymous_variant | 0.12 |
Rv3236c | 3612668 | p.Ala150Val | missense_variant | 0.25 |
Rv3236c | 3613001 | p.Ala39Val | missense_variant | 0.13 |
fbiA | 3640484 | c.-59T>C | upstream_gene_variant | 0.33 |
fbiA | 3640513 | c.-30G>C | upstream_gene_variant | 1.0 |
fbiB | 3640557 | c.-978T>C | upstream_gene_variant | 1.0 |
fbiA | 3640718 | p.Cys59Tyr | missense_variant | 0.2 |
fbiB | 3640920 | c.-615A>T | upstream_gene_variant | 0.13 |
fbiA | 3641441 | p.Gly300Glu | missense_variant | 0.22 |
fbiB | 3641876 | c.342C>T | synonymous_variant | 0.14 |
fbiB | 3642286 | p.Leu251Gln | missense_variant | 0.29 |
fbiB | 3642473 | p.Met313Ile | missense_variant | 0.5 |
alr | 3840284 | p.Trp379* | stop_gained | 0.29 |
alr | 3840409 | p.Val338Met | missense_variant | 0.17 |
alr | 3840876 | p.Ala182Val | missense_variant | 0.18 |
alr | 3840899 | c.522C>T | synonymous_variant | 0.14 |
alr | 3840905 | c.516C>T | synonymous_variant | 0.13 |
alr | 3841261 | p.Glu54Lys | missense_variant | 0.17 |
alr | 3841365 | p.Gly19Asp | missense_variant | 0.12 |
alr | 3841368 | c.52_53insT | frameshift_variant | 0.14 |
alr | 3841372 | p.Gly17Arg | missense_variant | 0.13 |
alr | 3841378 | p.Thr15Ala | missense_variant | 0.13 |
alr | 3841398 | p.Val8Asp | missense_variant | 0.12 |
alr | 3841590 | c.-170G>C | upstream_gene_variant | 0.15 |
rpoA | 3877510 | p.Glu333Gly | missense_variant | 0.2 |
rpoA | 3877592 | c.916C>T | synonymous_variant | 0.22 |
rpoA | 3877868 | p.Thr214Ala | missense_variant | 0.12 |
rpoA | 3877957 | p.Glu184Gly | missense_variant | 0.13 |
rpoA | 3878081 | p.Gly143Ser | missense_variant | 0.18 |
rpoA | 3878316 | c.192C>T | synonymous_variant | 0.18 |
rpoA | 3878398 | p.Ser37Trp | missense_variant | 0.25 |
ddn | 3986906 | p.Met21Ile | missense_variant | 0.17 |
ddn | 3986940 | p.Asp33Asn | missense_variant | 0.18 |
ddn | 3986972 | c.130_131delAT | frameshift_variant | 0.17 |
ddn | 3986989 | p.Leu49Gln | missense_variant | 0.17 |
clpC1 | 4038654 | p.Gly684Asp | missense_variant | 0.22 |
clpC1 | 4038771 | p.Gly645Val | missense_variant | 0.25 |
clpC1 | 4038841 | p.Val622Met | missense_variant | 0.14 |
clpC1 | 4039071 | p.Pro545Leu | missense_variant | 0.14 |
clpC1 | 4039104 | p.Arg534Pro | missense_variant | 0.14 |
clpC1 | 4039108 | p.Arg533Trp | missense_variant | 0.12 |
clpC1 | 4039601 | c.1104G>A | synonymous_variant | 0.29 |
clpC1 | 4039813 | p.Ala298Thr | missense_variant | 0.14 |
clpC1 | 4039934 | c.771G>A | synonymous_variant | 0.17 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.18 |
clpC1 | 4040430 | p.Leu92Ser | missense_variant | 0.1 |
clpC1 | 4040517 | p.Val63Ala | missense_variant | 1.0 |
clpC1 | 4040807 | c.-103C>T | upstream_gene_variant | 0.18 |
panD | 4043889 | c.393G>T | synonymous_variant | 0.18 |
panD | 4044337 | c.-56G>A | upstream_gene_variant | 0.12 |
embC | 4239962 | p.Val34Met | missense_variant | 0.17 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241042 | p.Asn394Asp | missense_variant | 1.0 |
embC | 4241279 | p.Val473Met | missense_variant | 0.14 |
embC | 4241691 | p.Gly610Asp | missense_variant | 0.29 |
embC | 4241725 | c.1863G>A | synonymous_variant | 0.5 |
embC | 4242181 | c.2319G>A | synonymous_variant | 0.13 |
embC | 4242323 | p.Gly821Ser | missense_variant | 0.17 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embC | 4242650 | p.Arg930Cys | missense_variant | 0.15 |
embC | 4242669 | p.Ile936Thr | missense_variant | 0.18 |
embA | 4243580 | c.348G>A | synonymous_variant | 1.0 |
embA | 4244105 | c.873C>G | synonymous_variant | 0.25 |
embA | 4244365 | p.Gly378Asp | missense_variant | 0.15 |
embA | 4244383 | p.Leu384Pro | missense_variant | 0.2 |
embA | 4244420 | c.1188G>C | synonymous_variant | 1.0 |
embA | 4244773 | p.Ser514Leu | missense_variant | 0.15 |
embA | 4244953 | p.Phe574Ser | missense_variant | 0.12 |
embA | 4245069 | p.Val613Met | missense_variant | 0.17 |
embA | 4245141 | p.Ile637Phe | missense_variant | 0.13 |
embA | 4245183 | c.1951C>T | synonymous_variant | 0.12 |
embA | 4245741 | p.Thr837Ala | missense_variant | 0.33 |
embA | 4245808 | p.Leu859Ser | missense_variant | 0.2 |
embA | 4245969 | p.Pro913Ser | missense_variant | 1.0 |
embB | 4246563 | p.Leu17Trp | missense_variant | 0.25 |
embB | 4246567 | c.54G>T | synonymous_variant | 0.25 |
embB | 4246594 | c.81C>T | synonymous_variant | 0.18 |
embB | 4246807 | c.294G>C | synonymous_variant | 0.13 |
embB | 4247578 | c.1065G>A | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4248147 | p.Ile545Thr | missense_variant | 0.11 |
embB | 4248319 | c.1806A>T | synonymous_variant | 0.3 |
embB | 4248421 | c.1908G>T | synonymous_variant | 0.14 |
embB | 4248510 | p.Ile666Thr | missense_variant | 0.11 |
embB | 4249190 | c.2682delC | frameshift_variant | 0.2 |
embB | 4249398 | p.Ala962Val | missense_variant | 0.15 |
aftB | 4267088 | c.1749C>T | synonymous_variant | 0.17 |
aftB | 4267132 | p.Pro569Ser | missense_variant | 0.22 |
aftB | 4267288 | p.His517Asp | missense_variant | 0.18 |
aftB | 4268240 | p.Met199Ile | missense_variant | 0.15 |
aftB | 4268480 | c.357G>A | synonymous_variant | 0.25 |
aftB | 4268493 | p.Ala115Val | missense_variant | 0.14 |
aftB | 4268568 | p.Leu90Pro | missense_variant | 0.13 |
aftB | 4268976 | c.-140G>A | upstream_gene_variant | 0.17 |
aftB | 4268997 | c.-161G>A | upstream_gene_variant | 0.18 |
ubiA | 4269152 | p.Ala228Thr | missense_variant | 0.13 |
ubiA | 4269283 | p.Ser184Leu | missense_variant | 0.14 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
ubiA | 4269864 | c.-32delG | upstream_gene_variant | 1.0 |
ubiA | 4269878 | c.-45A>G | upstream_gene_variant | 0.15 |
ethA | 4326188 | p.Arg429Gln | missense_variant | 0.17 |
ethR | 4326661 | c.-888C>T | upstream_gene_variant | 0.33 |
ethA | 4327354 | p.Ser40Thr | missense_variant | 0.12 |
ethR | 4327737 | p.Phe63Leu | missense_variant | 0.17 |
ethR | 4327921 | p.Gln125* | stop_gained | 0.2 |
ethA | 4328265 | c.-792C>T | upstream_gene_variant | 0.25 |
ethA | 4328269 | c.-796C>T | upstream_gene_variant | 0.25 |
whiB6 | 4338361 | p.Arg54Gln | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338603 | c.-82C>T | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407873 | c.330G>T | synonymous_variant | 1.0 |
gid | 4407915 | c.288C>T | synonymous_variant | 0.18 |
gid | 4408282 | c.-80G>A | upstream_gene_variant | 0.15 |