Run ID: ERR1023302
Sample name:
Date: 31-03-2023 09:16:45
Number of reads: 3929746
Percentage reads mapped: 87.07
Strain: lineage3;La3
Drug-resistance: MDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
La3 | M.orygis | None | None | 0.05 |
lineage3 | East-African-Indian | CAS | RD750 | 0.97 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761140 | p.His445Leu | missense_variant | 0.86 | rifampicin |
rrs | 1472307 | n.462C>T | non_coding_transcript_exon_variant | 0.14 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 0.98 | isoniazid |
gid | 4408087 | c.115delC | frameshift_variant | 1.0 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 6289 | c.1050C>T | synonymous_variant | 0.13 |
gyrA | 6319 | c.-983G>C | upstream_gene_variant | 0.14 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8225 | c.924T>C | synonymous_variant | 0.14 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9596 | c.2295G>T | synonymous_variant | 0.99 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 760142 | c.336C>G | synonymous_variant | 0.14 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.17 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.17 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.17 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.15 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.15 |
rpoB | 760283 | c.477G>C | synonymous_variant | 0.16 |
rpoB | 760298 | c.492G>C | synonymous_variant | 0.15 |
rpoB | 760328 | c.522G>C | synonymous_variant | 0.15 |
rpoB | 760331 | c.525G>C | synonymous_variant | 0.15 |
rpoB | 760340 | c.534G>T | synonymous_variant | 0.16 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.17 |
rpoB | 760370 | c.564C>G | synonymous_variant | 0.15 |
rpoB | 760406 | c.600G>C | synonymous_variant | 0.14 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.17 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.16 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.17 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.16 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.15 |
rpoB | 761129 | c.1323G>C | synonymous_variant | 0.15 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.14 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.15 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.15 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.14 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.15 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.15 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.19 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.19 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.18 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.15 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.15 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.16 |
rpoB | 761306 | c.1500C>G | synonymous_variant | 0.16 |
rpoB | 761570 | c.1764T>C | synonymous_variant | 0.16 |
rpoB | 761573 | c.1767C>G | synonymous_variant | 0.17 |
rpoB | 761579 | c.1773G>C | synonymous_variant | 0.18 |
rpoB | 761588 | c.1782C>T | synonymous_variant | 0.18 |
rpoB | 761606 | c.1800C>G | synonymous_variant | 0.17 |
rpoB | 761612 | c.1806G>C | synonymous_variant | 0.17 |
rpoB | 761615 | c.1809A>C | synonymous_variant | 0.16 |
rpoB | 761645 | c.1839C>G | synonymous_variant | 0.13 |
rpoB | 761648 | c.1842T>C | synonymous_variant | 0.13 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.14 |
rpoB | 762008 | c.2202C>T | synonymous_variant | 0.14 |
rpoB | 762206 | c.2400C>G | synonymous_variant | 0.14 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.15 |
rpoB | 762254 | c.2448T>G | synonymous_variant | 0.14 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.14 |
rpoB | 762369 | c.2563T>C | synonymous_variant | 0.14 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 762467 | c.-903C>T | upstream_gene_variant | 0.14 |
rpoC | 762827 | c.-543G>C | upstream_gene_variant | 0.14 |
rpoC | 762857 | c.-513C>G | upstream_gene_variant | 0.15 |
rpoC | 762860 | c.-510G>C | upstream_gene_variant | 0.15 |
rpoC | 762863 | c.-507T>C | upstream_gene_variant | 0.15 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.2 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763190 | c.-180C>T | upstream_gene_variant | 0.13 |
rpoC | 763441 | c.72C>T | synonymous_variant | 0.18 |
rpoC | 763444 | c.75T>C | synonymous_variant | 0.18 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.18 |
rpoC | 763486 | c.117T>G | synonymous_variant | 0.16 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.15 |
rpoC | 763528 | c.159G>A | synonymous_variant | 0.16 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.18 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.18 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.2 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.2 |
rpoC | 763603 | c.234C>T | synonymous_variant | 0.22 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.18 |
rpoC | 763657 | c.288G>A | synonymous_variant | 0.19 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.18 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.17 |
rpoC | 763765 | c.396T>C | synonymous_variant | 0.14 |
rpoC | 763774 | c.405G>C | synonymous_variant | 0.14 |
rpoC | 763835 | p.Ala156Met | missense_variant | 0.14 |
rpoC | 763853 | p.Val162Ile | missense_variant | 0.15 |
rpoC | 763858 | c.489A>G | synonymous_variant | 0.15 |
rpoC | 763861 | c.492C>T | synonymous_variant | 0.15 |
rpoC | 763945 | c.576T>C | synonymous_variant | 0.13 |
rpoC | 763951 | c.582G>C | synonymous_variant | 0.13 |
rpoC | 764020 | c.651C>T | synonymous_variant | 0.15 |
rpoC | 764024 | c.655_657delTTGinsCTC | synonymous_variant | 0.15 |
rpoC | 764032 | p.Asp221Glu | missense_variant | 0.16 |
rpoC | 764040 | p.Ser224Thr | missense_variant | 0.15 |
rpoC | 764044 | c.675T>C | synonymous_variant | 0.15 |
rpoC | 764059 | c.690G>T | synonymous_variant | 0.14 |
rpoC | 764181 | p.Asp271Gly | missense_variant | 0.9 |
rpoC | 765529 | c.2160C>T | synonymous_variant | 0.17 |
rpoC | 765541 | c.2172C>G | synonymous_variant | 0.16 |
rpoC | 765553 | c.2184C>T | synonymous_variant | 0.17 |
rpoC | 765556 | c.2187G>C | synonymous_variant | 0.17 |
rpoC | 765559 | c.2190G>C | synonymous_variant | 0.16 |
rpoC | 765580 | c.2211G>C | synonymous_variant | 0.14 |
rpoC | 765734 | p.Leu789Ala | missense_variant | 1.0 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 0.13 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.16 |
rpoC | 765883 | c.2514C>G | synonymous_variant | 0.15 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.15 |
rpoC | 765892 | c.2523T>C | synonymous_variant | 0.16 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 0.15 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 0.15 |
rpoC | 765982 | c.2613C>G | synonymous_variant | 0.15 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 0.14 |
rpoC | 766021 | c.2652G>C | synonymous_variant | 0.15 |
rpoC | 766027 | c.2658G>C | synonymous_variant | 0.16 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.15 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.16 |
rpoC | 766801 | c.3432C>G | synonymous_variant | 0.14 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.17 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781703 | c.144G>T | synonymous_variant | 0.14 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.16 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.17 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.16 |
rpsL | 781742 | c.183C>T | synonymous_variant | 0.18 |
rpsL | 781748 | c.189C>G | synonymous_variant | 0.17 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.17 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.14 |
rpsL | 781772 | c.213C>A | synonymous_variant | 0.13 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.14 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.14 |
rplC | 800627 | c.-182C>T | upstream_gene_variant | 0.13 |
rplC | 800648 | c.-161A>T | upstream_gene_variant | 0.19 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.18 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.15 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.18 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.16 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.15 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.16 |
rplC | 800747 | c.-62C>G | upstream_gene_variant | 0.15 |
fbiC | 1304553 | c.1623C>T | synonymous_variant | 0.13 |
fbiC | 1304875 | p.Ile649Val | missense_variant | 0.13 |
fbiC | 1304893 | p.Gly655Ser | missense_variant | 0.13 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473877 | n.220G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473943 | n.286G>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473945 | n.288T>A | non_coding_transcript_exon_variant | 0.16 |
rrl | 1473946 | n.289A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473986 | n.329T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473987 | n.330G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474093 | n.436G>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474099 | n.442G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474639 | n.982G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474904 | n.1247G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475199 | n.1542G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475206 | n.1549C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475209 | n.1552G>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475213 | n.1556C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475249 | n.1592T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475252 | n.1595C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475266 | n.1609T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475267 | n.1610G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475275 | n.1618C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475276 | n.1619T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475291 | n.1634A>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1475313 | n.1656G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475402 | n.1745C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475608 | n.1951T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475765 | n.2111delG | non_coding_transcript_exon_variant | 0.16 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476214 | n.2557G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476583 | n.2926G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.16 |
inhA | 1674846 | p.Ile215Met | missense_variant | 0.14 |
inhA | 1674864 | c.663C>T | synonymous_variant | 0.14 |
inhA | 1674870 | c.669T>C | synonymous_variant | 0.14 |
inhA | 1674879 | c.678T>C | synonymous_variant | 0.15 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.17 |
rpsA | 1833971 | c.430C>T | synonymous_variant | 0.2 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.17 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.19 |
rpsA | 1834021 | c.480C>T | synonymous_variant | 0.18 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.15 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.16 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.16 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.16 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.16 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.17 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.15 |
rpsA | 1834609 | c.1068T>C | synonymous_variant | 0.15 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.16 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.15 |
rpsA | 1834654 | p.Glu371Asp | missense_variant | 0.15 |
rpsA | 1834684 | c.1143C>T | synonymous_variant | 0.15 |
rpsA | 1834690 | c.1149T>C | synonymous_variant | 0.17 |
rpsA | 1834732 | c.1191T>C | synonymous_variant | 0.15 |
rpsA | 1834733 | p.Ala398Ser | missense_variant | 0.15 |
rpsA | 1834738 | c.1197A>G | synonymous_variant | 0.15 |
rpsA | 1834765 | p.Glu408Asp | missense_variant | 0.15 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170769 | c.-157C>T | upstream_gene_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
kasA | 2518220 | c.106C>T | synonymous_variant | 0.14 |
kasA | 2518528 | c.414C>G | synonymous_variant | 0.16 |
kasA | 2518540 | c.426T>C | synonymous_variant | 0.16 |
kasA | 2518561 | c.447T>C | synonymous_variant | 0.14 |
kasA | 2518825 | c.711T>C | synonymous_variant | 0.15 |
kasA | 2518864 | c.750G>C | synonymous_variant | 0.16 |
kasA | 2518879 | c.765A>G | synonymous_variant | 0.18 |
kasA | 2518885 | c.771T>C | synonymous_variant | 0.16 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
thyX | 3067602 | p.Arg115Gln | missense_variant | 0.13 |
thyX | 3067611 | p.Lys112Thr | missense_variant | 0.14 |
thyX | 3067652 | c.294T>C | synonymous_variant | 0.14 |
thyX | 3067761 | p.Arg62Gln | missense_variant | 0.14 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.16 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.14 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.15 |
rpoA | 3877791 | c.717C>G | synonymous_variant | 0.15 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.17 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.18 |
rpoA | 3877848 | c.660C>T | synonymous_variant | 0.19 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.21 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.21 |
rpoA | 3877875 | c.633T>G | synonymous_variant | 0.17 |
rpoA | 3877878 | c.630G>C | synonymous_variant | 0.17 |
rpoA | 3877890 | c.618C>T | synonymous_variant | 0.16 |
rpoA | 3877896 | c.612G>C | synonymous_variant | 0.15 |
rpoA | 3877900 | p.Ser203Asn | missense_variant | 0.14 |
rpoA | 3877909 | p.Asn200Ser | missense_variant | 0.14 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.15 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.18 |
rpoA | 3878028 | c.480G>C | synonymous_variant | 0.17 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.16 |
rpoA | 3878040 | c.468T>C | synonymous_variant | 0.17 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.17 |
rpoA | 3878058 | c.450G>T | synonymous_variant | 0.16 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.16 |
rpoA | 3878067 | c.441C>G | synonymous_variant | 0.15 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.15 |
rpoA | 3878076 | c.432C>T | synonymous_variant | 0.14 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.14 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.14 |
clpC1 | 4038640 | p.Asp689Asn | missense_variant | 0.13 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.14 |
clpC1 | 4038845 | c.1860G>C | synonymous_variant | 0.19 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.17 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.16 |
clpC1 | 4038905 | c.1800A>G | synonymous_variant | 0.15 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.14 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.15 |
clpC1 | 4038923 | c.1780_1782delCTAinsTTG | synonymous_variant | 0.14 |
clpC1 | 4039064 | c.1641C>T | synonymous_variant | 0.16 |
clpC1 | 4039097 | c.1608G>C | synonymous_variant | 0.15 |
clpC1 | 4039103 | c.1602T>C | synonymous_variant | 0.14 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.14 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.14 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.14 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.14 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.16 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.16 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.17 |
clpC1 | 4039183 | c.1522T>C | synonymous_variant | 0.16 |
clpC1 | 4039186 | c.1519C>T | synonymous_variant | 0.15 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.15 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.18 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.15 |
clpC1 | 4039988 | c.717C>G | synonymous_variant | 0.14 |
embC | 4240828 | c.966G>A | synonymous_variant | 0.15 |
embC | 4240831 | c.969T>G | synonymous_variant | 0.14 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 0.98 |
embA | 4245137 | c.1905T>C | synonymous_variant | 0.14 |
embA | 4245146 | c.1914G>A | synonymous_variant | 0.14 |
embA | 4245149 | c.1917C>G | synonymous_variant | 0.15 |
embA | 4245153 | p.Ile641Val | missense_variant | 0.15 |
embA | 4245182 | c.1950T>C | synonymous_variant | 0.15 |
embA | 4245189 | c.1957C>T | synonymous_variant | 0.17 |
embA | 4245198 | p.Leu656Ile | missense_variant | 0.16 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |