Run ID: SRR3675503
Sample name:
Date: 04-04-2023 05:30:56
Number of reads: 14842
Percentage reads mapped: 6.93
Strain: lineage4.9
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.99 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7442 | c.141G>C | synonymous_variant | 1.0 |
gyrA | 7451 | c.150C>G | synonymous_variant | 1.0 |
gyrA | 7457 | c.156T>C | synonymous_variant | 1.0 |
gyrA | 7475 | c.174A>G | synonymous_variant | 1.0 |
gyrA | 7480 | p.Phe60Tyr | missense_variant | 1.0 |
gyrA | 7484 | c.183T>C | synonymous_variant | 1.0 |
gyrA | 7490 | c.189C>G | synonymous_variant | 1.0 |
gyrA | 7523 | c.222C>G | synonymous_variant | 1.0 |
gyrA | 7532 | c.231T>G | synonymous_variant | 1.0 |
gyrA | 8987 | c.1686C>G | synonymous_variant | 1.0 |
gyrA | 8990 | c.1689C>G | synonymous_variant | 1.0 |
gyrA | 8996 | c.1695T>C | synonymous_variant | 1.0 |
gyrA | 8998 | p.Leu566Trp | missense_variant | 1.0 |
gyrA | 9017 | c.1716C>G | synonymous_variant | 1.0 |
gyrA | 9056 | c.1755C>G | synonymous_variant | 1.0 |
gyrA | 9062 | c.1761C>G | synonymous_variant | 1.0 |
gyrA | 9068 | c.1767G>C | synonymous_variant | 1.0 |
gyrA | 9071 | c.1770G>C | synonymous_variant | 1.0 |
gyrA | 9080 | c.1779G>T | synonymous_variant | 1.0 |
gyrA | 9089 | c.1788G>C | synonymous_variant | 1.0 |
gyrA | 9099 | c.1798_1800delTTAinsCTG | synonymous_variant | 1.0 |
gyrA | 9104 | c.1803C>G | synonymous_variant | 1.0 |
fgd1 | 491259 | c.477T>C | synonymous_variant | 1.0 |
fgd1 | 491283 | p.Asp167Glu | missense_variant | 1.0 |
fgd1 | 491286 | c.504G>C | synonymous_variant | 1.0 |
fgd1 | 491289 | c.507C>G | synonymous_variant | 1.0 |
fgd1 | 491292 | c.510G>C | synonymous_variant | 1.0 |
fgd1 | 491295 | c.513C>G | synonymous_variant | 1.0 |
fgd1 | 491296 | p.Val172Ile | missense_variant | 1.0 |
fgd1 | 491302 | p.Ile174Val | missense_variant | 1.0 |
fgd1 | 491307 | c.525C>G | synonymous_variant | 1.0 |
fgd1 | 491313 | c.531C>G | synonymous_variant | 1.0 |
fgd1 | 491319 | c.537G>C | synonymous_variant | 1.0 |
fgd1 | 491325 | c.543G>C | synonymous_variant | 1.0 |
fgd1 | 491337 | c.555C>G | synonymous_variant | 1.0 |
fgd1 | 491340 | c.558C>G | synonymous_variant | 1.0 |
fgd1 | 491349 | c.567T>C | synonymous_variant | 1.0 |
fgd1 | 491364 | c.582T>C | synonymous_variant | 1.0 |
fgd1 | 491367 | c.585G>C | synonymous_variant | 1.0 |
mshA | 575659 | c.312A>G | synonymous_variant | 1.0 |
mshA | 575662 | c.315C>G | synonymous_variant | 1.0 |
mshA | 575665 | c.318G>A | synonymous_variant | 1.0 |
mshA | 575674 | c.327G>C | synonymous_variant | 1.0 |
mshA | 575695 | c.348C>G | synonymous_variant | 1.0 |
mshA | 575701 | c.354G>A | synonymous_variant | 1.0 |
mshA | 575704 | c.357T>G | synonymous_variant | 1.0 |
mshA | 575705 | c.358T>C | synonymous_variant | 1.0 |
mshA | 575713 | c.366G>A | synonymous_variant | 1.0 |
mshA | 575719 | c.372C>T | synonymous_variant | 1.0 |
mshA | 575734 | c.387T>G | synonymous_variant | 1.0 |
mshA | 575737 | c.390T>C | synonymous_variant | 1.0 |
ccsA | 620295 | c.405G>T | synonymous_variant | 1.0 |
ccsA | 620298 | c.408G>C | synonymous_variant | 1.0 |
ccsA | 620310 | c.420C>T | synonymous_variant | 1.0 |
ccsA | 620317 | p.Val143Leu | missense_variant | 1.0 |
ccsA | 620340 | c.450C>G | synonymous_variant | 1.0 |
ccsA | 620346 | c.456C>G | synonymous_variant | 1.0 |
ccsA | 620362 | p.Ala158Thr | missense_variant | 1.0 |
ccsA | 620367 | c.477T>C | synonymous_variant | 1.0 |
ccsA | 620373 | c.483C>G | synonymous_variant | 1.0 |
ccsA | 620376 | c.486G>C | synonymous_variant | 1.0 |
ccsA | 620385 | c.495G>C | synonymous_variant | 1.0 |
ccsA | 620388 | c.498A>G | synonymous_variant | 1.0 |
ccsA | 620389 | c.499C>T | synonymous_variant | 1.0 |
ccsA | 620412 | c.522T>C | synonymous_variant | 1.0 |
ccsA | 620415 | c.525T>C | synonymous_variant | 1.0 |
ccsA | 620421 | c.531G>C | synonymous_variant | 1.0 |
rpoB | 760196 | c.390C>G | synonymous_variant | 1.0 |
rpoB | 760223 | c.417T>C | synonymous_variant | 1.0 |
rpoB | 760235 | c.429T>C | synonymous_variant | 1.0 |
rpoB | 760283 | c.477G>C | synonymous_variant | 1.0 |
rpoB | 760298 | c.492G>C | synonymous_variant | 1.0 |
rpoB | 760307 | c.501T>C | synonymous_variant | 1.0 |
rpoB | 760310 | c.504G>C | synonymous_variant | 1.0 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 1.0 |
rpoB | 761727 | p.Ser641Gly | missense_variant | 1.0 |
rpoB | 761728 | c.1923dupC | frameshift_variant | 1.0 |
rpoB | 761732 | c.1926C>G | synonymous_variant | 1.0 |
rpoB | 761735 | c.1929C>G | synonymous_variant | 1.0 |
rpoB | 761747 | c.1941G>C | synonymous_variant | 1.0 |
rpoB | 761750 | c.1944G>C | synonymous_variant | 1.0 |
rpoB | 761765 | c.1959T>C | synonymous_variant | 1.0 |
rpoB | 761772 | p.His656Ala | missense_variant | 1.0 |
rpoB | 761778 | p.Asn658Asp | missense_variant | 1.0 |
rpoB | 761791 | p.Arg662His | missense_variant | 1.0 |
rpoB | 762114 | p.Ile770Val | missense_variant | 1.0 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 1.0 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 1.0 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 1.0 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 1.0 |
rpoB | 762254 | c.2448T>G | synonymous_variant | 1.0 |
rpoC | 762398 | c.-972T>C | upstream_gene_variant | 1.0 |
rpoC | 763013 | c.-357C>G | upstream_gene_variant | 1.0 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 1.0 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 1.0 |
rpoC | 763034 | c.-336C>G | upstream_gene_variant | 1.0 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 1.0 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 1.0 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 1.0 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 1.0 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 1.0 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 1.0 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 1.0 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 1.0 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 1.0 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 1.0 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 1.0 |
rpoC | 765019 | c.1650A>G | synonymous_variant | 1.0 |
rpoC | 765034 | c.1665T>C | synonymous_variant | 1.0 |
rpoC | 765326 | p.His653Ala | missense_variant | 1.0 |
rpoC | 765330 | p.Ser654Asn | missense_variant | 1.0 |
rpoC | 765346 | c.1977C>G | synonymous_variant | 1.0 |
rpoC | 765349 | c.1980T>C | synonymous_variant | 1.0 |
rpoC | 765352 | c.1983G>C | synonymous_variant | 1.0 |
rpoC | 767059 | c.3690T>G | synonymous_variant | 1.0 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 1.0 |
rplC | 801309 | c.501C>G | synonymous_variant | 1.0 |
fbiC | 1303695 | c.765T>C | synonymous_variant | 1.0 |
fbiC | 1303704 | c.774T>C | synonymous_variant | 1.0 |
fbiC | 1303708 | c.778T>C | synonymous_variant | 1.0 |
fbiC | 1303728 | c.798G>A | synonymous_variant | 1.0 |
fbiC | 1303731 | c.801A>C | synonymous_variant | 1.0 |
fbiC | 1303732 | p.Ser268Ala | missense_variant | 1.0 |
fbiC | 1303736 | p.Glu269Val | missense_variant | 1.0 |
fbiC | 1303746 | c.816T>C | synonymous_variant | 1.0 |
fbiC | 1303749 | c.819G>C | synonymous_variant | 1.0 |
fbiC | 1303752 | c.822A>G | synonymous_variant | 1.0 |
fbiC | 1303755 | c.825T>C | synonymous_variant | 1.0 |
fbiC | 1303761 | c.831T>C | synonymous_variant | 1.0 |
fbiC | 1303785 | c.855G>C | synonymous_variant | 1.0 |
fbiC | 1303789 | p.Ile287Val | missense_variant | 1.0 |
fbiC | 1303797 | c.867A>G | synonymous_variant | 1.0 |
fbiC | 1303818 | c.888C>G | synonymous_variant | 1.0 |
fbiC | 1303827 | c.897A>G | synonymous_variant | 1.0 |
atpE | 1460852 | c.-193C>G | upstream_gene_variant | 1.0 |
atpE | 1460855 | c.-190T>C | upstream_gene_variant | 1.0 |
atpE | 1460858 | c.-187C>G | upstream_gene_variant | 1.0 |
atpE | 1460861 | c.-184C>G | upstream_gene_variant | 1.0 |
atpE | 1460882 | c.-163T>C | upstream_gene_variant | 1.0 |
atpE | 1460894 | c.-151A>G | upstream_gene_variant | 1.0 |
atpE | 1460897 | c.-148A>C | upstream_gene_variant | 1.0 |
atpE | 1460900 | c.-145T>C | upstream_gene_variant | 1.0 |
rrs | 1472518 | n.673G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472544 | n.699C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472557 | n.712G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472560 | n.715G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472579 | n.734G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472599 | n.754G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472647 | n.802C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472677 | n.833_834delTT | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472682 | n.837T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472683 | n.839_842delGGGA | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472690 | n.845C>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472726 | n.881G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472767 | n.922G>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474823 | n.1166C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476518 | n.2861G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 1.0 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 1.0 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 1.0 |
rpsA | 1834262 | c.721_723delTCGinsAGC | synonymous_variant | 1.0 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 1.0 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 1.0 |
kasA | 2518504 | c.390T>C | synonymous_variant | 1.0 |
kasA | 2518506 | p.Ala131Glu | missense_variant | 1.0 |
kasA | 2518519 | c.405G>C | synonymous_variant | 1.0 |
kasA | 2518528 | c.414C>G | synonymous_variant | 1.0 |
kasA | 2518540 | c.426T>C | synonymous_variant | 1.0 |
kasA | 2518561 | c.447T>C | synonymous_variant | 1.0 |
kasA | 2518567 | c.453G>C | synonymous_variant | 1.0 |
kasA | 2518570 | c.456G>C | synonymous_variant | 1.0 |
kasA | 2518573 | c.459G>C | synonymous_variant | 1.0 |
kasA | 2518574 | p.Ile154Val | missense_variant | 1.0 |
kasA | 2518579 | c.465T>C | synonymous_variant | 1.0 |
kasA | 2518588 | c.474T>C | synonymous_variant | 1.0 |
kasA | 2518591 | c.477G>C | synonymous_variant | 1.0 |
kasA | 2518609 | p.Met165Ile | missense_variant | 1.0 |
kasA | 2518624 | c.510C>G | synonymous_variant | 1.0 |
thyX | 3067391 | c.555G>C | synonymous_variant | 1.0 |
thyX | 3067394 | c.552G>C | synonymous_variant | 1.0 |
thyX | 3067439 | c.507A>G | synonymous_variant | 1.0 |
thyX | 3067445 | c.501C>G | synonymous_variant | 1.0 |
thyX | 3067457 | c.489C>G | synonymous_variant | 1.0 |
thyX | 3067462 | c.484C>T | synonymous_variant | 1.0 |
thyX | 3067465 | p.Ile161Val | missense_variant | 1.0 |
thyX | 3067466 | c.480G>C | synonymous_variant | 1.0 |
thyX | 3067475 | c.471A>G | synonymous_variant | 1.0 |
thyX | 3067490 | p.Ala152Glu | missense_variant | 1.0 |
thyX | 3067493 | c.453A>G | synonymous_variant | 1.0 |
thyX | 3067510 | c.436C>T | synonymous_variant | 1.0 |
thyX | 3067515 | p.Ser144Thr | missense_variant | 1.0 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 1.0 |
rpoA | 3877764 | c.744C>G | synonymous_variant | 1.0 |
rpoA | 3877770 | c.738A>G | synonymous_variant | 1.0 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 1.0 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 1.0 |
rpoA | 3877791 | c.717C>G | synonymous_variant | 1.0 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 1.0 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 1.0 |
rpoA | 3877848 | c.660C>T | synonymous_variant | 1.0 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 1.0 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 1.0 |
rpoA | 3878094 | c.414C>G | synonymous_variant | 1.0 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 1.0 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 1.0 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 1.0 |
clpC1 | 4038356 | c.2349T>C | synonymous_variant | 1.0 |
clpC1 | 4038359 | c.2346A>G | synonymous_variant | 1.0 |
clpC1 | 4038368 | c.2337T>C | synonymous_variant | 1.0 |
clpC1 | 4038419 | c.2286T>C | synonymous_variant | 1.0 |
clpC1 | 4038433 | c.2272C>T | synonymous_variant | 1.0 |
clpC1 | 4038434 | c.2271G>A | synonymous_variant | 1.0 |
clpC1 | 4038444 | p.Ala754Lys | missense_variant | 1.0 |
clpC1 | 4038446 | c.2259T>C | synonymous_variant | 1.0 |
clpC1 | 4038456 | p.Val750Glu | missense_variant | 1.0 |
clpC1 | 4038460 | p.Leu749Met | missense_variant | 1.0 |
clpC1 | 4038486 | p.Gly740Asn | missense_variant | 1.0 |
clpC1 | 4038489 | p.Ala739Gly | missense_variant | 1.0 |
clpC1 | 4038494 | c.2211G>C | synonymous_variant | 1.0 |
clpC1 | 4038497 | p.Ser736Gln | missense_variant | 1.0 |
clpC1 | 4038509 | c.2196C>T | synonymous_variant | 1.0 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 1.0 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 1.0 |
clpC1 | 4039454 | c.1251A>G | synonymous_variant | 1.0 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 1.0 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 1.0 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 1.0 |
clpC1 | 4039481 | c.1224T>C | synonymous_variant | 1.0 |
clpC1 | 4039484 | c.1221T>C | synonymous_variant | 1.0 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 1.0 |
clpC1 | 4039556 | c.1149G>C | synonymous_variant | 1.0 |
clpC1 | 4039559 | c.1146C>G | synonymous_variant | 1.0 |
clpC1 | 4039562 | c.1143C>G | synonymous_variant | 1.0 |
clpC1 | 4039565 | c.1140G>C | synonymous_variant | 1.0 |
clpC1 | 4039570 | p.Met379Leu | missense_variant | 1.0 |
clpC1 | 4039576 | p.Ala377Pro | missense_variant | 1.0 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 1.0 |
clpC1 | 4039589 | c.1116G>C | synonymous_variant | 1.0 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 1.0 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 1.0 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 1.0 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 1.0 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 1.0 |
clpC1 | 4039760 | c.945T>C | synonymous_variant | 1.0 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 1.0 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 1.0 |
clpC1 | 4039775 | c.930G>C | synonymous_variant | 1.0 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 1.0 |
clpC1 | 4039781 | c.924G>C | synonymous_variant | 1.0 |
clpC1 | 4039790 | c.915C>G | synonymous_variant | 1.0 |
clpC1 | 4039817 | c.888A>C | synonymous_variant | 1.0 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 1.0 |
clpC1 | 4039826 | c.879C>G | synonymous_variant | 1.0 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 1.0 |
clpC1 | 4040369 | c.336C>G | synonymous_variant | 1.0 |
clpC1 | 4040380 | c.325T>C | synonymous_variant | 1.0 |
clpC1 | 4040381 | c.324T>C | synonymous_variant | 1.0 |
clpC1 | 4040387 | c.318A>G | synonymous_variant | 1.0 |
clpC1 | 4040393 | c.312G>C | synonymous_variant | 1.0 |
clpC1 | 4040411 | c.294T>C | synonymous_variant | 1.0 |
clpC1 | 4040418 | p.Leu96Pro | missense_variant | 0.67 |
clpC1 | 4040423 | c.282A>G | synonymous_variant | 1.0 |
clpC1 | 4040426 | c.279T>C | synonymous_variant | 1.0 |
clpC1 | 4040431 | c.274T>C | synonymous_variant | 1.0 |
clpC1 | 4040444 | c.261C>T | synonymous_variant | 1.0 |
clpC1 | 4040450 | c.255A>G | synonymous_variant | 1.0 |
clpC1 | 4040459 | c.246C>G | synonymous_variant | 1.0 |
clpC1 | 4040465 | c.240T>C | synonymous_variant | 1.0 |
clpC1 | 4040471 | c.234T>C | synonymous_variant | 1.0 |
clpC1 | 4040477 | c.228G>C | synonymous_variant | 1.0 |
clpC1 | 4040480 | c.225T>G | synonymous_variant | 1.0 |
embB | 4247951 | p.Ser480Ala | missense_variant | 1.0 |
embB | 4247956 | c.1443G>C | synonymous_variant | 1.0 |
embB | 4247974 | c.1461C>G | synonymous_variant | 1.0 |