Run ID: ERR4769446
Sample name:
Date: 01-04-2023 06:40:54
Number of reads: 57373
Percentage reads mapped: 3.66
Strain: lineage4.9;La1.3
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
La1.3 | M.bovis | None | None | 0.06 |
lineage4 | Euro-American | LAM;T;S;X;H | None | 0.82 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 760982 | c.1176G>T | synonymous_variant | 1.0 |
rpoB | 760991 | c.1185G>A | synonymous_variant | 0.67 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.5 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.5 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.5 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.5 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.5 |
rpoB | 761051 | c.1245G>T | synonymous_variant | 0.5 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.5 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.5 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.5 |
rpoB | 761084 | c.1278C>G | synonymous_variant | 0.5 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.5 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 0.5 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.5 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.5 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.67 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.67 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.33 |
rpoC | 763031 | c.-339T>G | upstream_gene_variant | 1.0 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.43 |
rpoC | 763049 | c.-321G>A | upstream_gene_variant | 0.29 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.25 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.38 |
rpoB | 763074 | p.Thr1090Val | missense_variant | 0.25 |
rpoC | 763079 | c.-291C>G | upstream_gene_variant | 0.25 |
rpoC | 763085 | c.-285C>G | upstream_gene_variant | 0.38 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 0.25 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.25 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.33 |
rpoC | 763900 | c.531G>C | synonymous_variant | 1.0 |
rpoC | 763909 | c.540C>T | synonymous_variant | 1.0 |
rpoC | 763921 | c.552G>C | synonymous_variant | 1.0 |
rpoC | 763936 | c.567C>G | synonymous_variant | 1.0 |
rpoC | 763940 | p.Ala191Ser | missense_variant | 1.0 |
rpoC | 763947 | p.Ala193Val | missense_variant | 1.0 |
rpoC | 763951 | c.582G>C | synonymous_variant | 1.0 |
rpoC | 763960 | c.591T>C | synonymous_variant | 1.0 |
rpoC | 763961 | p.Arg198Lys | missense_variant | 1.0 |
rpoC | 763985 | p.Arg206Lys | missense_variant | 1.0 |
rpoC | 763991 | p.Ile208Leu | missense_variant | 0.67 |
rpoC | 763996 | c.627T>C | synonymous_variant | 0.67 |
rpoC | 764005 | c.636G>C | synonymous_variant | 0.67 |
rpoC | 764024 | c.655T>C | synonymous_variant | 0.67 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.67 |
rpoC | 764548 | c.1179G>C | synonymous_variant | 0.5 |
rpoC | 764554 | c.1185C>T | synonymous_variant | 0.5 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.5 |
rpoC | 764572 | c.1203G>C | synonymous_variant | 0.5 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.5 |
rpoC | 764576 | c.1207_1209delTCCinsAGT | synonymous_variant | 0.5 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.5 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.5 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.5 |
rpoC | 764644 | c.1275G>C | synonymous_variant | 0.5 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.5 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.5 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.5 |
rpoC | 764680 | c.1311G>A | synonymous_variant | 0.5 |
rpoC | 764731 | c.1362G>A | synonymous_variant | 0.67 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 1.0 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 1.0 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 1.0 |
rpoC | 765751 | c.2382C>T | synonymous_variant | 1.0 |
rpoC | 767023 | c.3654C>T | synonymous_variant | 0.4 |
rpoC | 767044 | c.3675G>C | synonymous_variant | 0.4 |
rpoC | 767059 | c.3690T>C | synonymous_variant | 0.4 |
rpoC | 767062 | c.3693C>A | synonymous_variant | 0.4 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.67 |
rpoC | 767106 | p.Asn1246Ile | missense_variant | 1.0 |
rpoC | 767110 | c.3741T>C | synonymous_variant | 1.0 |
rpsL | 781658 | c.99A>G | synonymous_variant | 0.67 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.8 |
rpsL | 781700 | c.141G>C | synonymous_variant | 0.8 |
rpsL | 781706 | c.147T>G | synonymous_variant | 0.8 |
rpsL | 781715 | c.156T>C | synonymous_variant | 0.8 |
rpsL | 781718 | c.159C>G | synonymous_variant | 0.8 |
rpsL | 781721 | c.162C>T | synonymous_variant | 0.8 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.8 |
rpsL | 781733 | c.174G>C | synonymous_variant | 0.8 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.8 |
rpsL | 781737 | p.Gln60Ala | missense_variant | 0.8 |
rpsL | 781754 | c.195G>T | synonymous_variant | 0.67 |
rpsL | 781763 | c.204C>G | synonymous_variant | 0.5 |
rpsL | 781766 | c.207C>T | synonymous_variant | 0.67 |
rpsL | 781769 | c.210G>A | synonymous_variant | 0.67 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.6 |
rplC | 800633 | c.-176T>C | upstream_gene_variant | 0.67 |
rplC | 800645 | c.-164C>T | upstream_gene_variant | 0.67 |
rplC | 800648 | c.-161A>G | upstream_gene_variant | 0.67 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.67 |
rplC | 800672 | c.-137G>C | upstream_gene_variant | 1.0 |
rplC | 800690 | c.-119C>T | upstream_gene_variant | 1.0 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 1.0 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 1.0 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.67 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.67 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.67 |
rplC | 800735 | c.-74C>G | upstream_gene_variant | 0.67 |
rplC | 800738 | c.-71T>G | upstream_gene_variant | 0.67 |
rplC | 800747 | c.-62C>T | upstream_gene_variant | 0.67 |
rplC | 800762 | c.-47T>G | upstream_gene_variant | 0.4 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472580 | n.735C>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472597 | n.752G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472836 | n.991G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472840 | n.995A>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472844 | n.999C>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472845 | n.1000G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472847 | n.1002G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472849 | n.1004C>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472850 | n.1005T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472855 | n.1011_1012insGT | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472873 | n.1028C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472875 | n.1030T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473291 | n.1446_1447insT | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475443 | n.1786G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475475 | n.1818C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475479 | n.1822C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475481 | n.1824C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475482 | n.1825A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475538 | n.1881T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475550 | n.1893A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475555 | n.1898T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475735 | n.2078T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475758 | n.2101A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475791 | n.2134A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475892 | n.2235A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476251 | n.2594T>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476300 | n.2643G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.5 |
rpsA | 1834261 | c.720A>C | synonymous_variant | 0.4 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.4 |
rpsA | 1834279 | c.738C>T | synonymous_variant | 0.4 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.4 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.4 |
rpsA | 1834307 | p.Asp256Asn | missense_variant | 0.4 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.5 |
rpsA | 1834375 | c.834G>C | synonymous_variant | 0.4 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.5 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.67 |
rpsA | 1834456 | c.915T>G | synonymous_variant | 0.67 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.67 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 1.0 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.67 |
rpsA | 1834534 | c.993C>G | synonymous_variant | 0.67 |
rpsA | 1834540 | c.999G>C | synonymous_variant | 0.67 |
rpsA | 1834543 | c.1002C>G | synonymous_variant | 0.67 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.67 |
rpsA | 1834552 | c.1011G>C | synonymous_variant | 0.67 |
rpsA | 1834555 | c.1014T>G | synonymous_variant | 0.67 |
rpsA | 1834557 | p.Ala339Val | missense_variant | 0.67 |
katG | 2155503 | c.609C>T | synonymous_variant | 1.0 |
katG | 2156465 | c.-354C>T | upstream_gene_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
ald | 3086728 | c.-92C>T | upstream_gene_variant | 1.0 |
ald | 3087084 | c.266delA | frameshift_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.5 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.5 |
clpC1 | 4038795 | p.Ser637Thr | missense_variant | 0.5 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.67 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.67 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.67 |
clpC1 | 4039472 | c.1233G>C | synonymous_variant | 0.67 |
clpC1 | 4039481 | c.1224T>C | synonymous_variant | 0.5 |
clpC1 | 4039484 | c.1221T>C | synonymous_variant | 0.5 |
clpC1 | 4039487 | c.1218G>C | synonymous_variant | 0.5 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.5 |
clpC1 | 4039556 | c.1149G>C | synonymous_variant | 0.5 |
clpC1 | 4039559 | c.1146C>G | synonymous_variant | 0.5 |
clpC1 | 4039570 | p.Met379Leu | missense_variant | 0.5 |
clpC1 | 4039571 | c.1134G>C | synonymous_variant | 0.5 |
clpC1 | 4039574 | p.Ala377Gly | missense_variant | 0.5 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.5 |
clpC1 | 4039586 | c.1119G>C | synonymous_variant | 0.6 |
clpC1 | 4039589 | c.1116G>C | synonymous_variant | 0.67 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.5 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.5 |
clpC1 | 4039622 | c.1083C>T | synonymous_variant | 0.43 |
clpC1 | 4039634 | p.Glu357Asn | missense_variant | 0.5 |
clpC1 | 4039649 | c.1056G>C | synonymous_variant | 0.5 |
clpC1 | 4039652 | c.1053G>C | synonymous_variant | 0.5 |
clpC1 | 4039661 | c.1044T>C | synonymous_variant | 0.6 |
clpC1 | 4039682 | c.1023C>G | synonymous_variant | 0.67 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.6 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.5 |
clpC1 | 4039733 | c.972G>T | synonymous_variant | 0.5 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.5 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.5 |
clpC1 | 4039760 | c.945T>G | synonymous_variant | 0.5 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.5 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.5 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.67 |
clpC1 | 4039793 | c.912C>T | synonymous_variant | 0.67 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.5 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.67 |
clpC1 | 4039887 | p.Leu273Pro | missense_variant | 0.67 |
clpC1 | 4040408 | c.297C>T | synonymous_variant | 0.67 |
clpC1 | 4040411 | c.294T>C | synonymous_variant | 0.75 |
clpC1 | 4040426 | c.279T>C | synonymous_variant | 1.0 |
clpC1 | 4040431 | c.274T>C | synonymous_variant | 1.0 |
clpC1 | 4040441 | c.264C>G | synonymous_variant | 1.0 |
clpC1 | 4040444 | c.261C>G | synonymous_variant | 1.0 |
clpC1 | 4040450 | c.255A>G | synonymous_variant | 1.0 |
clpC1 | 4040465 | c.240T>C | synonymous_variant | 1.0 |
clpC1 | 4040474 | c.231C>T | synonymous_variant | 1.0 |
clpC1 | 4040477 | c.228G>T | synonymous_variant | 1.0 |
clpC1 | 4040480 | c.225T>C | synonymous_variant | 1.0 |
clpC1 | 4040486 | c.219G>C | synonymous_variant | 1.0 |
clpC1 | 4040513 | c.192G>A | synonymous_variant | 1.0 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 1.0 |
clpC1 | 4040531 | c.174T>C | synonymous_variant | 1.0 |
clpC1 | 4040534 | c.171A>G | synonymous_variant | 1.0 |
clpC1 | 4040539 | c.166C>T | synonymous_variant | 0.67 |
clpC1 | 4040546 | c.159G>T | synonymous_variant | 1.0 |
clpC1 | 4040549 | c.154_156delTTGinsCTC | synonymous_variant | 1.0 |
clpC1 | 4040561 | c.144A>C | synonymous_variant | 1.0 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embA | 4242970 | c.-263C>T | upstream_gene_variant | 1.0 |
aftB | 4267858 | p.Ile327Val | missense_variant | 1.0 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 0.67 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4408304 | c.-102G>A | upstream_gene_variant | 0.29 |