Run ID: SRR5341408
Sample name:
Date: 04-04-2023 10:19:52
Number of reads: 793132
Percentage reads mapped: 84.84
Strain: lineage3
Drug-resistance: Sensitive
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6362 | c.-940T>C | upstream_gene_variant | 0.16 |
gyrA | 6367 | c.-935C>T | upstream_gene_variant | 0.12 |
gyrA | 6379 | c.-923C>G | upstream_gene_variant | 0.12 |
gyrA | 6382 | c.-920A>G | upstream_gene_variant | 0.12 |
gyrA | 6388 | c.-914T>C | upstream_gene_variant | 0.12 |
gyrB | 6398 | p.Val387Ile | missense_variant | 0.11 |
gyrA | 6523 | c.-779G>C | upstream_gene_variant | 0.12 |
gyrA | 6526 | c.-776T>C | upstream_gene_variant | 0.12 |
gyrA | 6538 | c.-764C>G | upstream_gene_variant | 0.13 |
gyrA | 6547 | c.-755T>C | upstream_gene_variant | 0.14 |
gyrA | 6550 | c.-752A>G | upstream_gene_variant | 0.14 |
gyrA | 6551 | c.-751T>C | upstream_gene_variant | 0.14 |
gyrA | 6568 | c.-734C>G | upstream_gene_variant | 0.15 |
gyrA | 6571 | c.-731T>C | upstream_gene_variant | 0.15 |
gyrA | 6577 | c.-725T>C | upstream_gene_variant | 0.14 |
gyrA | 6583 | c.-719G>C | upstream_gene_variant | 0.13 |
gyrA | 6586 | c.-716T>C | upstream_gene_variant | 0.14 |
gyrA | 6589 | c.-713G>A | upstream_gene_variant | 0.14 |
gyrA | 6598 | c.-704C>G | upstream_gene_variant | 0.13 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7514 | c.213C>G | synonymous_variant | 0.13 |
gyrA | 7523 | c.222C>A | synonymous_variant | 0.13 |
gyrA | 7526 | c.225G>A | synonymous_variant | 0.13 |
gyrA | 7532 | c.231T>C | synonymous_variant | 0.12 |
gyrA | 7541 | c.240C>G | synonymous_variant | 0.12 |
gyrA | 7569 | p.Ala90Ser | missense_variant | 0.12 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8414 | c.1113C>T | synonymous_variant | 0.12 |
gyrA | 8420 | c.1119T>C | synonymous_variant | 0.12 |
gyrA | 8432 | c.1131C>G | synonymous_variant | 0.15 |
gyrA | 8453 | c.1152A>C | synonymous_variant | 0.16 |
gyrA | 8471 | c.1170T>C | synonymous_variant | 0.11 |
gyrA | 8579 | c.1278C>T | synonymous_variant | 0.12 |
gyrA | 8597 | c.1296C>G | synonymous_variant | 0.14 |
gyrA | 8603 | c.1302A>C | synonymous_variant | 0.14 |
gyrA | 8609 | c.1308G>C | synonymous_variant | 0.14 |
gyrA | 8612 | c.1311C>T | synonymous_variant | 0.15 |
gyrA | 8619 | c.1318T>C | synonymous_variant | 0.15 |
gyrA | 8624 | c.1323G>C | synonymous_variant | 0.2 |
gyrA | 8627 | c.1326C>G | synonymous_variant | 0.2 |
gyrA | 8630 | c.1329G>C | synonymous_variant | 0.2 |
gyrA | 8636 | c.1335A>C | synonymous_variant | 0.23 |
gyrA | 8642 | c.1341A>G | synonymous_variant | 0.23 |
gyrA | 8645 | c.1344C>T | synonymous_variant | 0.23 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491550 | c.768T>C | synonymous_variant | 0.11 |
fgd1 | 491569 | p.Asp263Asn | missense_variant | 0.11 |
fgd1 | 491577 | c.795G>C | synonymous_variant | 0.12 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 760181 | c.375T>G | synonymous_variant | 0.11 |
rpoB | 760454 | c.648C>G | synonymous_variant | 0.17 |
rpoB | 760463 | c.657C>T | synonymous_variant | 0.17 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.12 |
rpoB | 760478 | c.672C>T | synonymous_variant | 0.12 |
rpoB | 760481 | c.675G>T | synonymous_variant | 0.12 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.11 |
rpoB | 760487 | c.681G>C | synonymous_variant | 0.12 |
rpoB | 760508 | c.702G>A | synonymous_variant | 0.14 |
rpoB | 760532 | c.726T>C | synonymous_variant | 0.11 |
rpoB | 760535 | c.729C>G | synonymous_variant | 0.12 |
rpoB | 760634 | c.828T>C | synonymous_variant | 0.12 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.11 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.12 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.16 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.16 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.16 |
rpoB | 761051 | c.1245G>T | synonymous_variant | 0.14 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.14 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.14 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 0.14 |
rpoB | 761063 | c.1257C>G | synonymous_variant | 0.16 |
rpoB | 761066 | c.1260G>C | synonymous_variant | 0.16 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 0.12 |
rpoB | 761097 | c.1291_1292delAGinsTC | synonymous_variant | 0.12 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.12 |
rpoB | 761204 | c.1398C>G | synonymous_variant | 0.15 |
rpoB | 761217 | p.Pro471Ser | missense_variant | 0.14 |
rpoB | 761220 | c.1414_1416delTCGinsAGC | synonymous_variant | 0.15 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.15 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.25 |
rpoB | 761252 | c.1446C>G | synonymous_variant | 0.25 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.25 |
rpoB | 761258 | c.1452G>A | synonymous_variant | 0.22 |
rpoB | 761261 | c.1455G>C | synonymous_variant | 0.2 |
rpoB | 761264 | c.1458C>G | synonymous_variant | 0.2 |
rpoB | 761273 | c.1467T>C | synonymous_variant | 0.17 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.12 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.12 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.12 |
rpoB | 762158 | c.2352G>T | synonymous_variant | 0.12 |
rpoB | 762167 | c.2361T>C | synonymous_variant | 0.12 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoB | 762905 | p.Asp1033Glu | missense_variant | 0.11 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.12 |
rpoC | 762989 | c.-381G>A | upstream_gene_variant | 0.12 |
rpoC | 762995 | c.-375G>C | upstream_gene_variant | 0.14 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.13 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.25 |
rpoC | 763570 | c.201G>T | synonymous_variant | 0.25 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.25 |
rpoC | 763615 | c.246G>C | synonymous_variant | 0.18 |
rpoC | 763618 | c.249C>T | synonymous_variant | 0.18 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.12 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.17 |
rpoC | 763708 | c.339G>T | synonymous_variant | 0.17 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.18 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.19 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.21 |
rpoC | 763732 | c.363C>G | synonymous_variant | 0.21 |
rpoC | 763735 | c.366G>A | synonymous_variant | 0.21 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.19 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.18 |
rpoC | 763765 | c.396T>G | synonymous_variant | 0.2 |
rpoC | 763781 | p.Ser138Ala | missense_variant | 0.11 |
rpoC | 763801 | c.432C>G | synonymous_variant | 0.14 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.15 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.15 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.16 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.12 |
rpoC | 764791 | c.1422C>G | synonymous_variant | 0.15 |
rpoC | 764797 | c.1428G>C | synonymous_variant | 0.13 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.13 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.14 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.14 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.17 |
rpoC | 764844 | p.Ala492Gly | missense_variant | 0.13 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.12 |
rpoC | 765754 | p.Asp795Glu | missense_variant | 0.11 |
rpoC | 765802 | p.Phe811Leu | missense_variant | 0.11 |
rpoC | 765823 | c.2454C>G | synonymous_variant | 0.11 |
rpoC | 765826 | c.2457T>C | synonymous_variant | 0.12 |
rpoC | 765835 | c.2466C>T | synonymous_variant | 0.12 |
rpoC | 765875 | p.Val836Ile | missense_variant | 0.15 |
rpoC | 765886 | c.2517C>G | synonymous_variant | 0.15 |
rpoC | 765904 | c.2535C>G | synonymous_variant | 0.12 |
rpoC | 766345 | c.2976T>C | synonymous_variant | 0.2 |
rpoC | 766348 | c.2979A>G | synonymous_variant | 0.25 |
rpoC | 766351 | c.2982C>G | synonymous_variant | 0.22 |
rpoC | 766369 | c.3000C>G | synonymous_variant | 0.17 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.12 |
rpoC | 766393 | c.3024C>G | synonymous_variant | 0.11 |
rpoC | 767020 | c.3651C>G | synonymous_variant | 0.12 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.1 |
rpoC | 767167 | c.3798C>G | synonymous_variant | 0.14 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776030 | c.2451G>T | synonymous_variant | 0.22 |
mmpL5 | 776039 | c.2442C>G | synonymous_variant | 0.17 |
mmpL5 | 776075 | c.2406C>G | synonymous_variant | 0.17 |
mmpL5 | 776078 | c.2403C>T | synonymous_variant | 0.17 |
mmpL5 | 776087 | c.2394C>T | synonymous_variant | 0.15 |
mmpL5 | 776093 | c.2386_2388delCGCinsAGA | synonymous_variant | 0.15 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776107 | c.2374C>T | synonymous_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781718 | c.159C>G | synonymous_variant | 0.12 |
rpsL | 781724 | c.165G>C | synonymous_variant | 0.12 |
rpsL | 781728 | c.169T>C | synonymous_variant | 0.12 |
rpsL | 781733 | c.174G>C | synonymous_variant | 0.13 |
rpsL | 781736 | c.177T>C | synonymous_variant | 0.12 |
rpsL | 781742 | c.183C>T | synonymous_variant | 0.14 |
rplC | 800690 | c.-119C>T | upstream_gene_variant | 0.13 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.12 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.12 |
fbiC | 1303545 | c.615A>G | synonymous_variant | 0.14 |
fbiC | 1303581 | c.651G>C | synonymous_variant | 0.2 |
fbiC | 1303584 | c.654C>G | synonymous_variant | 0.22 |
fbiC | 1303590 | c.660A>G | synonymous_variant | 0.22 |
fbiC | 1303602 | c.672A>G | synonymous_variant | 0.15 |
fbiC | 1303611 | c.681G>T | synonymous_variant | 0.14 |
fbiC | 1303614 | c.684C>G | synonymous_variant | 0.14 |
fbiC | 1303632 | c.702T>G | synonymous_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.12 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472489 | n.644A>G | non_coding_transcript_exon_variant | 0.12 |
rrs | 1472973 | n.1128A>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473696 | n.39T>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473697 | n.40C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473728 | n.71A>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474057 | n.400G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474282 | n.625G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1474293 | n.637_647delCCTCTCCGGAG | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474306 | n.649A>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474552 | n.895C>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474629 | n.972G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474631 | n.974G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474639 | n.982G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475061 | n.1404C>T | non_coding_transcript_exon_variant | 0.23 |
rrl | 1475088 | n.1431A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475991 | n.2334T>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1475995 | n.2338G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476032 | n.2375C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476033 | n.2376T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476034 | n.2377C>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476088 | n.2431A>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 0.18 |
rrl | 1476105 | n.2448G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476106 | n.2449A>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476165 | n.2508T>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1476583 | n.2926G>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.13 |
rpsA | 1833616 | c.75A>C | synonymous_variant | 0.12 |
rpsA | 1833619 | c.78A>C | synonymous_variant | 0.12 |
rpsA | 1833628 | c.87G>C | synonymous_variant | 0.11 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.12 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.12 |
rpsA | 1833793 | c.252C>T | synonymous_variant | 0.12 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 0.1 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 0.14 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.13 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.13 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.13 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.11 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.12 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.14 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.11 |
rpsA | 1834520 | p.Ala327Ser | missense_variant | 0.12 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.12 |
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 |
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 | 2518249 | c.135A>C | synonymous_variant | 0.11 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
folC | 2746519 | c.1080T>C | synonymous_variant | 0.18 |
Rv2752c | 3067152 | c.-961G>A | upstream_gene_variant | 0.13 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087811 | p.Ala331Val | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fbiB | 3641463 | c.-72G>T | upstream_gene_variant | 0.13 |
rpoA | 3877734 | c.774G>T | synonymous_variant | 0.12 |
rpoA | 3877737 | c.771G>C | synonymous_variant | 0.12 |
rpoA | 3878358 | c.150C>G | synonymous_variant | 0.13 |
rpoA | 3878364 | c.144A>C | synonymous_variant | 0.13 |
rpoA | 3878388 | c.120C>G | synonymous_variant | 0.15 |
rpoA | 3878391 | c.117T>G | synonymous_variant | 0.17 |
rpoA | 3878394 | c.114G>T | synonymous_variant | 0.17 |
rpoA | 3878406 | c.102G>T | synonymous_variant | 0.17 |
rpoA | 3878415 | c.93C>T | synonymous_variant | 0.17 |
rpoA | 3878424 | c.84G>C | synonymous_variant | 0.17 |
clpC1 | 4039205 | c.1500C>T | synonymous_variant | 0.16 |
clpC1 | 4039241 | c.1464G>C | synonymous_variant | 0.12 |
clpC1 | 4039262 | c.1443C>T | synonymous_variant | 0.12 |
clpC1 | 4039271 | c.1434G>A | synonymous_variant | 0.11 |
clpC1 | 4039274 | c.1431G>C | synonymous_variant | 0.11 |
clpC1 | 4039280 | c.1425G>C | synonymous_variant | 0.11 |
clpC1 | 4039556 | c.1149G>C | synonymous_variant | 0.13 |
clpC1 | 4039559 | c.1146C>G | synonymous_variant | 0.13 |
clpC1 | 4039568 | p.Met379Ile | missense_variant | 0.13 |
clpC1 | 4039574 | p.Ala377Pro | missense_variant | 0.13 |
clpC1 | 4039592 | c.1113G>C | synonymous_variant | 0.13 |
clpC1 | 4039613 | c.1092C>T | synonymous_variant | 0.12 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.12 |
clpC1 | 4039622 | c.1083C>A | synonymous_variant | 0.12 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.11 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |