Run ID: SRR13861699
Sample name:
Date: 03-04-2023 09:38:23
Number of reads: 327479
Percentage reads mapped: 32.78
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 | 1.0 |
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 |
---|---|---|---|---|
gyrB | 5532 | c.295dupG | frameshift_variant | 1.0 |
gyrB | 5832 | p.Ala198Gly | missense_variant | 1.0 |
gyrB | 6209 | c.970C>T | synonymous_variant | 0.15 |
gyrB | 6214 | c.975G>C | synonymous_variant | 0.15 |
gyrB | 6217 | c.978G>C | synonymous_variant | 0.15 |
gyrB | 6223 | c.984G>C | synonymous_variant | 0.17 |
gyrB | 6242 | p.Arg335Lys | missense_variant | 0.18 |
gyrB | 6250 | c.1011A>G | synonymous_variant | 0.18 |
gyrB | 6253 | c.1014G>C | synonymous_variant | 0.17 |
gyrB | 6280 | c.1041T>C | synonymous_variant | 0.13 |
gyrB | 6286 | c.1047T>C | synonymous_variant | 0.15 |
gyrB | 6292 | c.1053G>C | synonymous_variant | 0.15 |
gyrA | 6976 | c.-326A>G | upstream_gene_variant | 1.0 |
gyrA | 8069 | c.768T>C | synonymous_variant | 0.22 |
gyrA | 8078 | c.777A>G | synonymous_variant | 0.22 |
gyrA | 8090 | c.789C>G | synonymous_variant | 0.2 |
gyrA | 8096 | c.795T>C | synonymous_variant | 0.2 |
gyrA | 8099 | c.798T>C | synonymous_variant | 0.2 |
gyrA | 8111 | c.810G>C | synonymous_variant | 0.22 |
gyrA | 8156 | c.855T>C | synonymous_variant | 0.29 |
gyrA | 8168 | c.867A>G | synonymous_variant | 0.29 |
gyrA | 8174 | c.873C>G | synonymous_variant | 0.29 |
gyrA | 8177 | c.876A>C | synonymous_variant | 0.29 |
gyrA | 8198 | c.897T>C | synonymous_variant | 0.38 |
gyrA | 8204 | c.903C>T | synonymous_variant | 0.38 |
gyrA | 8207 | c.906T>C | synonymous_variant | 0.38 |
gyrA | 8216 | c.915G>A | synonymous_variant | 0.29 |
gyrA | 8219 | c.918T>C | synonymous_variant | 0.29 |
gyrA | 8225 | c.924T>C | synonymous_variant | 0.29 |
gyrA | 8234 | c.933T>G | synonymous_variant | 0.25 |
gyrA | 8235 | c.934_936delTTAinsCTG | synonymous_variant | 0.25 |
gyrA | 8253 | p.Ile318Leu | missense_variant | 0.29 |
gyrA | 8264 | c.963T>C | synonymous_variant | 0.25 |
gyrA | 8267 | c.966G>C | synonymous_variant | 0.25 |
gyrA | 8270 | c.969G>C | synonymous_variant | 0.25 |
gyrA | 8283 | p.Ile328Leu | missense_variant | 0.29 |
gyrA | 8288 | c.987T>C | synonymous_variant | 0.33 |
gyrA | 8294 | c.993T>C | synonymous_variant | 0.33 |
gyrA | 8324 | c.1023T>C | synonymous_variant | 0.33 |
ccsA | 619735 | c.-156G>C | upstream_gene_variant | 1.0 |
ccsA | 620100 | c.210G>T | synonymous_variant | 1.0 |
ccsA | 620245 | c.355T>C | synonymous_variant | 0.14 |
ccsA | 620249 | p.Ser120Cys | missense_variant | 0.14 |
ccsA | 620254 | c.364_366delCTCinsTTG | synonymous_variant | 0.14 |
ccsA | 620265 | c.375C>G | synonymous_variant | 0.17 |
ccsA | 620269 | p.Val127Ile | missense_variant | 0.15 |
ccsA | 620275 | c.385C>T | synonymous_variant | 0.15 |
ccsA | 620283 | c.393T>C | synonymous_variant | 0.14 |
ccsA | 620284 | p.Ala132Pro | missense_variant | 0.14 |
ccsA | 620288 | p.Arg133Gln | missense_variant | 0.14 |
ccsA | 620307 | c.417C>G | synonymous_variant | 0.15 |
ccsA | 620317 | p.Val143Leu | missense_variant | 0.15 |
ccsA | 620331 | c.441C>T | synonymous_variant | 0.13 |
ccsA | 620340 | c.450C>G | synonymous_variant | 0.15 |
rpoB | 759609 | c.-198C>A | upstream_gene_variant | 0.86 |
rpoB | 759644 | c.-163T>A | upstream_gene_variant | 0.18 |
rpoB | 759647 | c.-160T>C | upstream_gene_variant | 0.18 |
rpoB | 759655 | c.-151delA | upstream_gene_variant | 0.17 |
rpoB | 759659 | c.-148_-147insGA | upstream_gene_variant | 0.18 |
rpoB | 759662 | c.-145C>T | upstream_gene_variant | 0.18 |
rpoB | 759667 | c.-140C>T | upstream_gene_variant | 0.2 |
rpoB | 759670 | c.-137C>T | upstream_gene_variant | 0.2 |
rpoB | 759671 | c.-136G>T | upstream_gene_variant | 0.18 |
rpoB | 759672 | c.-135G>C | upstream_gene_variant | 0.18 |
rpoB | 759683 | c.-124T>C | upstream_gene_variant | 0.15 |
rpoB | 759701 | c.-106A>T | upstream_gene_variant | 0.14 |
rpoB | 760611 | c.805T>C | synonymous_variant | 0.13 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.13 |
rpoB | 760661 | c.855A>C | synonymous_variant | 0.12 |
rpoB | 760793 | c.987A>G | synonymous_variant | 0.17 |
rpoB | 760805 | c.999G>C | synonymous_variant | 0.17 |
rpoB | 760817 | c.1011A>G | synonymous_variant | 0.2 |
rpoB | 760820 | c.1014T>C | synonymous_variant | 0.19 |
rpoB | 760826 | c.1020C>G | synonymous_variant | 0.19 |
rpoB | 760830 | c.1024T>C | synonymous_variant | 0.13 |
rpoB | 760845 | p.Thr347Pro | missense_variant | 0.13 |
rpoB | 760859 | c.1053T>C | synonymous_variant | 0.2 |
rpoB | 760869 | p.Val355Ile | missense_variant | 0.18 |
rpoB | 760886 | c.1080A>G | synonymous_variant | 0.17 |
rpoB | 760919 | c.1113C>G | synonymous_variant | 0.17 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.17 |
rpoB | 761133 | c.1327_1329delTTGinsCTC | synonymous_variant | 0.15 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.15 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.17 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.15 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.14 |
rpoB | 761847 | p.Cys681Ser | missense_variant | 0.12 |
rpoB | 761852 | c.2046C>G | synonymous_variant | 0.14 |
rpoB | 761858 | c.2052G>C | synonymous_variant | 0.14 |
rpoB | 761864 | c.2058G>C | synonymous_variant | 0.14 |
rpoB | 761873 | c.2067A>G | synonymous_variant | 0.17 |
rpoB | 761885 | c.2079T>C | synonymous_variant | 0.17 |
rpoB | 761891 | c.2085G>C | synonymous_variant | 0.18 |
rpoB | 761906 | c.2100C>G | synonymous_variant | 0.2 |
rpoB | 761909 | c.2103T>C | synonymous_variant | 0.2 |
rpoB | 761912 | c.2106T>C | synonymous_variant | 0.18 |
rpoB | 761915 | p.Asp703Glu | missense_variant | 0.18 |
rpoB | 761916 | p.Asp704Asn | missense_variant | 0.17 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.17 |
rpoB | 761954 | c.2148C>G | synonymous_variant | 0.17 |
rpoB | 762014 | c.2208C>T | synonymous_variant | 0.2 |
rpoC | 762860 | c.-510G>C | upstream_gene_variant | 0.18 |
rpoC | 762863 | c.-507T>C | upstream_gene_variant | 0.18 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.22 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.17 |
rpoC | 763050 | c.-320C>T | upstream_gene_variant | 1.0 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.18 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.21 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 0.15 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.23 |
rpoC | 764455 | c.1086G>T | synonymous_variant | 0.14 |
rpoC | 764461 | p.Glu364Asp | missense_variant | 0.17 |
rpoC | 764470 | c.1101C>G | synonymous_variant | 0.15 |
rpoC | 764471 | p.Asn368Arg | missense_variant | 0.15 |
rpoC | 764479 | c.1110G>A | synonymous_variant | 0.15 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.15 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.15 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.17 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.2 |
rpoC | 764513 | p.Phe382Leu | missense_variant | 0.2 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.22 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.14 |
rpoC | 764872 | c.1503A>G | synonymous_variant | 0.13 |
rpoC | 764893 | c.1524T>C | synonymous_variant | 0.12 |
rpoC | 764932 | c.1563C>A | synonymous_variant | 0.18 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.19 |
rpoC | 764995 | c.1626C>G | synonymous_variant | 0.2 |
rpoC | 765007 | c.1638T>G | synonymous_variant | 0.2 |
rpoC | 765019 | c.1650A>G | synonymous_variant | 0.2 |
rpoC | 765022 | c.1653G>C | synonymous_variant | 0.14 |
rpoC | 765034 | c.1665T>C | synonymous_variant | 0.17 |
rpoC | 766447 | c.3078T>C | synonymous_variant | 0.22 |
rpoC | 766549 | c.3180G>C | synonymous_variant | 0.2 |
rpoC | 766583 | p.Gly1072Ser | missense_variant | 0.18 |
rpoC | 766750 | c.3381C>G | synonymous_variant | 0.2 |
rpoC | 766765 | c.3396A>C | synonymous_variant | 0.17 |
rpoC | 766774 | c.3405T>C | synonymous_variant | 0.18 |
rpoC | 766801 | c.3432C>A | synonymous_variant | 0.18 |
rpoC | 766804 | c.3435A>G | synonymous_variant | 0.18 |
mmpL5 | 776796 | p.Val562Ala | missense_variant | 1.0 |
mmpS5 | 778642 | p.Trp88* | stop_gained | 1.0 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.17 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 0.17 |
rplC | 800648 | c.-161A>C | upstream_gene_variant | 0.14 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.14 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.14 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.14 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.14 |
rplC | 801127 | p.Ala107Thr | missense_variant | 0.2 |
rplC | 801132 | c.324T>C | synonymous_variant | 0.2 |
rplC | 801147 | c.339T>C | synonymous_variant | 0.33 |
rplC | 801150 | c.342G>C | synonymous_variant | 0.33 |
rplC | 801153 | c.345G>C | synonymous_variant | 0.33 |
rplC | 801156 | c.348T>A | synonymous_variant | 0.29 |
rplC | 801171 | c.363A>G | synonymous_variant | 0.25 |
rplC | 801174 | c.366T>C | synonymous_variant | 0.29 |
fbiC | 1303632 | c.702T>G | synonymous_variant | 0.14 |
fbiC | 1303818 | c.888C>G | synonymous_variant | 0.29 |
fbiC | 1303836 | c.906G>C | synonymous_variant | 0.25 |
fbiC | 1303845 | c.915C>G | synonymous_variant | 0.25 |
fbiC | 1303846 | p.Phe306Val | missense_variant | 0.22 |
fbiC | 1303854 | c.924T>C | synonymous_variant | 0.25 |
fbiC | 1303860 | c.930A>C | synonymous_variant | 0.25 |
fbiC | 1303881 | c.951G>C | synonymous_variant | 0.33 |
fbiC | 1303884 | c.954T>G | synonymous_variant | 0.33 |
fbiC | 1303911 | c.981G>C | synonymous_variant | 0.5 |
fbiC | 1303914 | c.984C>G | synonymous_variant | 0.5 |
fbiC | 1303920 | c.990C>G | synonymous_variant | 0.4 |
fbiC | 1303923 | c.993C>T | synonymous_variant | 0.33 |
fbiC | 1303929 | c.999G>C | synonymous_variant | 0.33 |
fbiC | 1303947 | c.1017T>C | synonymous_variant | 0.33 |
fbiC | 1303948 | p.Gly340Arg | missense_variant | 0.33 |
fbiC | 1303969 | p.Val347Ile | missense_variant | 0.33 |
fbiC | 1303973 | p.Gly348Ala | missense_variant | 0.33 |
fbiC | 1303995 | c.1065C>T | synonymous_variant | 0.57 |
fbiC | 1304001 | c.1071C>G | synonymous_variant | 0.67 |
fbiC | 1304008 | c.1078T>C | synonymous_variant | 0.67 |
fbiC | 1304034 | c.1104A>G | synonymous_variant | 0.5 |
fbiC | 1304040 | c.1110C>G | synonymous_variant | 0.5 |
fbiC | 1304046 | c.1116C>G | synonymous_variant | 0.5 |
fbiC | 1304049 | c.1119T>G | synonymous_variant | 0.5 |
fbiC | 1304058 | c.1128G>A | synonymous_variant | 0.5 |
fbiC | 1304059 | c.1129C>T | synonymous_variant | 0.5 |
fbiC | 1304064 | c.1134G>C | synonymous_variant | 0.5 |
fbiC | 1304067 | c.1137G>C | synonymous_variant | 0.5 |
fbiC | 1304073 | c.1143C>T | synonymous_variant | 0.67 |
fbiC | 1304080 | p.Ala384Ser | missense_variant | 0.57 |
fbiC | 1304091 | p.Asp387Glu | missense_variant | 0.43 |
fbiC | 1304092 | p.Met388Leu | missense_variant | 0.43 |
fbiC | 1304097 | c.1167G>C | synonymous_variant | 0.43 |
fbiC | 1304115 | c.1185A>G | synonymous_variant | 0.5 |
fbiC | 1304127 | c.1197A>G | synonymous_variant | 0.5 |
fbiC | 1304136 | c.1206C>T | synonymous_variant | 0.43 |
fbiC | 1304142 | c.1212G>C | synonymous_variant | 0.29 |
fbiC | 1304161 | p.Arg411Ser | missense_variant | 0.33 |
fbiC | 1304166 | c.1236A>G | synonymous_variant | 0.33 |
fbiC | 1304172 | c.1242G>C | synonymous_variant | 0.5 |
fbiC | 1304173 | p.Val415Arg | missense_variant | 0.33 |
fbiC | 1304184 | c.1254G>C | synonymous_variant | 0.33 |
fbiC | 1304192 | p.Ala421Val | missense_variant | 0.33 |
fbiC | 1304199 | c.1269C>T | synonymous_variant | 0.33 |
fbiC | 1304628 | c.1698G>C | synonymous_variant | 0.15 |
fbiC | 1304634 | c.1704C>G | synonymous_variant | 0.15 |
fbiC | 1304640 | c.1710A>C | synonymous_variant | 0.15 |
Rv1258c | 1407009 | p.Ala111Asp | missense_variant | 1.0 |
rrl | 1473944 | n.287G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473945 | n.288T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473995 | n.338G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474001 | n.344C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474009 | n.352A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474012 | n.355C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474051 | n.394T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474054 | n.397T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474056 | n.399T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474103 | n.446A>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474104 | n.447G>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474111 | n.454T>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474112 | n.455T>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474376 | n.719T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474823 | n.1166C>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1475199 | n.1542G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476336 | n.2679C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476356 | n.2699C>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476357 | n.2700T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476383 | n.2726T>G | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476408 | n.2751G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476411 | n.2754G>A | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476425 | n.2768G>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476443 | n.2786G>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476455 | n.2798C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476456 | n.2799A>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476463 | n.2806C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.47 |
inhA | 1674582 | c.381T>C | synonymous_variant | 0.14 |
inhA | 1674585 | c.384T>C | synonymous_variant | 0.14 |
inhA | 1674589 | p.Met130Leu | missense_variant | 0.15 |
inhA | 1674654 | c.453G>C | synonymous_variant | 0.13 |
inhA | 1674703 | c.502T>C | synonymous_variant | 0.14 |
inhA | 1674891 | p.Trp230Cys | missense_variant | 1.0 |
rpsA | 1833568 | c.27G>C | synonymous_variant | 0.14 |
rpsA | 1833589 | c.48A>T | synonymous_variant | 0.14 |
rpsA | 1833595 | c.54T>C | synonymous_variant | 0.14 |
rpsA | 1833619 | c.78A>C | synonymous_variant | 0.14 |
rpsA | 1833661 | c.120A>G | synonymous_variant | 0.25 |
rpsA | 1833667 | c.126C>G | synonymous_variant | 0.2 |
rpsA | 1833724 | c.183C>G | synonymous_variant | 0.22 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.24 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.27 |
rpsA | 1833745 | c.204G>C | synonymous_variant | 0.27 |
rpsA | 1833787 | c.246C>G | synonymous_variant | 0.27 |
rpsA | 1833790 | c.249T>A | synonymous_variant | 0.29 |
rpsA | 1833799 | c.258C>G | synonymous_variant | 0.23 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 0.15 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.17 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.18 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.17 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.31 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.2 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.18 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.18 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.17 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.17 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.17 |
tlyA | 1918625 | p.Pro229Leu | missense_variant | 1.0 |
ndh | 2101906 | c.1137G>C | synonymous_variant | 0.17 |
ndh | 2101924 | c.1119T>G | synonymous_variant | 0.17 |
Rv1979c | 2222721 | c.444G>C | synonymous_variant | 1.0 |
ahpC | 2726345 | p.Phe51Leu | missense_variant | 1.0 |
ahpC | 2726591 | c.399C>G | synonymous_variant | 0.2 |
ahpC | 2726593 | p.Val134Ala | missense_variant | 0.2 |
ahpC | 2726600 | c.408T>C | synonymous_variant | 0.2 |
ahpC | 2726612 | c.420C>G | synonymous_variant | 0.22 |
ahpC | 2726638 | p.Ala149Val | missense_variant | 0.22 |
ahpC | 2726645 | c.453C>G | synonymous_variant | 0.22 |
ahpC | 2726657 | c.465A>C | synonymous_variant | 0.2 |
ahpC | 2726669 | p.Asp159Glu | missense_variant | 0.18 |
ahpC | 2726672 | c.480G>A | synonymous_variant | 0.18 |
ahpC | 2726675 | c.483A>G | synonymous_variant | 0.18 |
ahpC | 2726681 | c.489A>G | synonymous_variant | 0.18 |
ahpC | 2726687 | c.495C>G | synonymous_variant | 0.18 |
ahpC | 2726690 | c.498C>T | synonymous_variant | 0.18 |
ahpC | 2726693 | c.501C>G | synonymous_variant | 0.2 |
ahpC | 2726696 | c.504C>G | synonymous_variant | 0.2 |
ahpC | 2726717 | c.525A>G | synonymous_variant | 0.15 |
ribD | 2987230 | p.Ala131Val | missense_variant | 0.25 |
Rv2752c | 3065166 | c.1026C>G | synonymous_variant | 0.22 |
Rv2752c | 3065997 | c.195C>G | synonymous_variant | 0.13 |
Rv2752c | 3066002 | p.Met64Leu | missense_variant | 0.15 |
Rv2752c | 3066024 | c.168T>C | synonymous_variant | 0.17 |
Rv2752c | 3066040 | p.Gly51Thr | missense_variant | 0.33 |
Rv2752c | 3066042 | c.150T>C | synonymous_variant | 0.22 |
Rv2752c | 3066050 | p.Leu48Met | missense_variant | 0.22 |
Rv2752c | 3066054 | c.138T>G | synonymous_variant | 0.22 |
Rv2752c | 3066066 | c.126T>C | synonymous_variant | 0.18 |
Rv2752c | 3066075 | c.117A>G | synonymous_variant | 0.18 |
Rv2752c | 3066087 | c.105A>G | synonymous_variant | 0.17 |
Rv2752c | 3066118 | p.Asn25Ser | missense_variant | 0.17 |
Rv2752c | 3067095 | c.-904G>C | upstream_gene_variant | 1.0 |
thyX | 3067220 | c.726G>C | synonymous_variant | 0.29 |
thyX | 3067223 | c.723G>C | synonymous_variant | 0.29 |
thyX | 3067244 | c.702C>G | synonymous_variant | 0.29 |
thyX | 3067249 | p.Thr233Ala | missense_variant | 0.33 |
thyX | 3067250 | p.Val232Ile | missense_variant | 0.33 |
thyX | 3067277 | c.669C>G | synonymous_variant | 0.22 |
thyX | 3067280 | c.666G>C | synonymous_variant | 0.22 |
thyX | 3067284 | p.Ala221Asp | missense_variant | 0.22 |
thyX | 3067286 | c.660C>G | synonymous_variant | 0.22 |
thyX | 3067289 | c.657C>G | synonymous_variant | 0.2 |
thyX | 3067293 | p.Gln218Arg | missense_variant | 0.2 |
thyX | 3067304 | c.642A>G | synonymous_variant | 0.18 |
thyX | 3067316 | c.630A>G | synonymous_variant | 0.2 |
thyX | 3067325 | c.621A>G | synonymous_variant | 0.22 |
thyX | 3067355 | c.591A>C | synonymous_variant | 0.25 |
thyX | 3067493 | c.453A>G | synonymous_variant | 0.14 |
thyX | 3067500 | p.Lys149Arg | missense_variant | 0.14 |
thyA | 3073794 | c.678A>C | synonymous_variant | 0.25 |
thyA | 3073827 | c.645A>G | synonymous_variant | 0.2 |
thyA | 3073839 | c.633T>C | synonymous_variant | 0.2 |
thyA | 3073872 | p.Ile200Val | missense_variant | 0.2 |
thyA | 3073878 | c.594G>A | synonymous_variant | 0.22 |
thyA | 3073892 | c.580T>C | synonymous_variant | 0.22 |
thyA | 3073893 | c.579C>G | synonymous_variant | 0.22 |
thyA | 3073925 | c.547T>C | synonymous_variant | 0.33 |
thyA | 3073926 | c.546G>C | synonymous_variant | 0.33 |
thyA | 3073929 | c.543T>C | synonymous_variant | 0.33 |
thyA | 3073953 | c.519T>C | synonymous_variant | 0.3 |
thyA | 3073977 | c.495A>G | synonymous_variant | 0.18 |
thyA | 3073989 | c.483T>C | synonymous_variant | 0.18 |
thyA | 3074001 | c.471C>G | synonymous_variant | 0.18 |
thyA | 3074004 | c.468T>C | synonymous_variant | 0.18 |
thyA | 3074010 | c.462C>G | synonymous_variant | 0.23 |
thyA | 3074031 | c.441T>C | synonymous_variant | 0.2 |
thyA | 3074037 | c.435C>G | synonymous_variant | 0.2 |
thyA | 3074056 | p.Glu139Pro | missense_variant | 0.18 |
thyA | 3074061 | c.411A>G | synonymous_variant | 0.18 |
thyA | 3074076 | c.396C>G | synonymous_variant | 0.17 |
Rv3083 | 3448912 | p.Ile137Phe | missense_variant | 1.0 |
fprA | 3474133 | p.Pro43Thr | missense_variant | 1.0 |
whiB7 | 3568676 | p.Ser2Ala | missense_variant | 1.0 |
fbiB | 3642677 | c.1143A>G | synonymous_variant | 0.27 |
fbiB | 3642696 | c.1162C>T | synonymous_variant | 0.22 |
fbiB | 3642701 | c.1167C>G | synonymous_variant | 0.25 |
alr | 3840783 | c.637_638insT | frameshift_variant | 1.0 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.18 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.25 |
rpoA | 3877857 | c.651G>A | synonymous_variant | 0.3 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.27 |
rpoA | 3877872 | c.636C>T | synonymous_variant | 0.25 |
rpoA | 3877875 | c.633T>G | synonymous_variant | 0.25 |
rpoA | 3877899 | p.Ser203Thr | missense_variant | 0.17 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.15 |
rpoA | 3877908 | p.Asn200Ser | missense_variant | 0.15 |
rpoA | 3877953 | c.555G>A | synonymous_variant | 0.2 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.23 |
rpoA | 3877986 | c.522G>C | synonymous_variant | 0.14 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.14 |
rpoA | 3878022 | c.486T>C | synonymous_variant | 0.17 |
rpoA | 3878025 | c.483C>T | synonymous_variant | 0.17 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.15 |
rpoA | 3878040 | c.468T>C | synonymous_variant | 0.15 |
rpoA | 3878046 | c.462T>C | synonymous_variant | 0.14 |
rpoA | 3878049 | c.459G>C | synonymous_variant | 0.15 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.15 |
ddn | 3986648 | c.-196C>G | upstream_gene_variant | 0.25 |
ddn | 3986655 | c.-189A>T | upstream_gene_variant | 0.27 |
ddn | 3986660 | c.-184C>T | upstream_gene_variant | 0.21 |
ddn | 3986665 | c.-179G>C | upstream_gene_variant | 0.21 |
ddn | 3986667 | c.-177_-176delCTinsAC | upstream_gene_variant | 0.21 |
ddn | 3986681 | c.-163C>G | upstream_gene_variant | 0.2 |
ddn | 3986690 | c.-154C>G | upstream_gene_variant | 0.2 |
ddn | 3986696 | c.-148G>T | upstream_gene_variant | 0.19 |
ddn | 3986699 | c.-145C>G | upstream_gene_variant | 0.2 |
clpC1 | 4038271 | p.Pro812Ala | missense_variant | 0.25 |
clpC1 | 4038272 | p.Gly811Ser | missense_variant | 0.25 |
clpC1 | 4038278 | c.2427T>C | synonymous_variant | 0.25 |
clpC1 | 4038293 | c.2412G>C | synonymous_variant | 0.2 |
clpC1 | 4038302 | c.2403C>G | synonymous_variant | 0.2 |
clpC1 | 4038308 | p.Val799Ile | missense_variant | 0.25 |
clpC1 | 4038317 | c.2388G>C | synonymous_variant | 0.18 |
clpC1 | 4038326 | p.Glu793Asp | missense_variant | 0.83 |
clpC1 | 4038359 | c.2346A>G | synonymous_variant | 0.14 |
clpC1 | 4038368 | c.2337T>C | synonymous_variant | 0.15 |
clpC1 | 4038388 | c.2317T>C | synonymous_variant | 0.17 |
clpC1 | 4038398 | c.2307G>T | synonymous_variant | 0.17 |
clpC1 | 4038498 | p.Ser736Thr | missense_variant | 0.14 |
clpC1 | 4038530 | p.Glu725Asp | missense_variant | 0.13 |
clpC1 | 4038536 | c.2169C>T | synonymous_variant | 0.13 |
clpC1 | 4038596 | c.2109A>G | synonymous_variant | 0.2 |
clpC1 | 4038611 | c.2094C>T | synonymous_variant | 0.2 |
clpC1 | 4038623 | c.2082A>G | synonymous_variant | 0.25 |
clpC1 | 4038640 | p.Asp689Asn | missense_variant | 0.27 |
clpC1 | 4038653 | c.2052C>T | synonymous_variant | 0.22 |
clpC1 | 4038658 | p.Lys683Gln | missense_variant | 0.22 |
clpC1 | 4038740 | c.1965G>C | synonymous_variant | 0.2 |
clpC1 | 4038748 | p.Arg653Cys | missense_variant | 0.2 |
clpC1 | 4038755 | c.1950G>C | synonymous_variant | 0.2 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.25 |
clpC1 | 4038782 | c.1923G>C | synonymous_variant | 0.18 |
clpC1 | 4038790 | c.1915C>T | synonymous_variant | 0.2 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.17 |
clpC1 | 4038815 | c.1890G>T | synonymous_variant | 0.17 |
clpC1 | 4038851 | c.1854G>A | synonymous_variant | 0.18 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.3 |
clpC1 | 4038908 | c.1797C>G | synonymous_variant | 0.27 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.27 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.2 |
clpC1 | 4038932 | c.1773G>C | synonymous_variant | 0.22 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.2 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.2 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.2 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.2 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.2 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.2 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.17 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.17 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.17 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.17 |
clpC1 | 4040036 | c.669C>G | synonymous_variant | 0.18 |
clpC1 | 4040090 | c.613_615delTCTinsAGC | synonymous_variant | 0.25 |
clpC1 | 4040093 | c.612C>G | synonymous_variant | 0.25 |
clpC1 | 4040105 | c.600C>G | synonymous_variant | 0.29 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 0.43 |
clpC1 | 4040201 | c.504C>G | synonymous_variant | 0.5 |
clpC1 | 4040207 | c.498T>C | synonymous_variant | 0.5 |
clpC1 | 4040213 | c.490_492delTCTinsAGC | synonymous_variant | 0.5 |
clpC1 | 4040225 | c.480A>C | synonymous_variant | 0.5 |
clpC1 | 4040228 | c.477G>C | synonymous_variant | 0.5 |
clpC1 | 4040234 | c.471C>G | synonymous_variant | 0.5 |
clpC1 | 4040237 | c.468C>T | synonymous_variant | 0.5 |
clpC1 | 4040249 | c.456A>G | synonymous_variant | 0.43 |
clpC1 | 4040273 | c.432T>C | synonymous_variant | 0.5 |
clpC1 | 4040411 | c.294T>C | synonymous_variant | 0.25 |
clpC1 | 4040423 | c.282A>G | synonymous_variant | 0.22 |
clpC1 | 4040426 | c.279T>C | synonymous_variant | 0.22 |
clpC1 | 4040441 | c.264C>G | synonymous_variant | 0.2 |
clpC1 | 4040444 | c.261C>G | synonymous_variant | 0.18 |
clpC1 | 4040450 | c.255A>G | synonymous_variant | 0.18 |
clpC1 | 4040459 | c.246C>G | synonymous_variant | 0.18 |
clpC1 | 4040465 | c.240T>C | synonymous_variant | 0.17 |
clpC1 | 4040471 | c.234T>C | synonymous_variant | 0.14 |
clpC1 | 4040477 | c.228G>A | synonymous_variant | 0.15 |
clpC1 | 4040480 | c.225T>C | synonymous_variant | 0.15 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.15 |
clpC1 | 4040531 | c.174T>C | synonymous_variant | 0.14 |
clpC1 | 4040534 | c.171A>G | synonymous_variant | 0.14 |
clpC1 | 4040546 | c.159G>C | synonymous_variant | 0.13 |
embC | 4241026 | c.1164C>G | synonymous_variant | 1.0 |
embA | 4242250 | c.-983C>G | upstream_gene_variant | 1.0 |
embA | 4242760 | c.-473G>C | upstream_gene_variant | 0.18 |
embA | 4245077 | c.1845G>C | synonymous_variant | 0.15 |
embA | 4245083 | c.1851A>C | synonymous_variant | 0.17 |
embA | 4245089 | c.1857G>C | synonymous_variant | 0.17 |
embA | 4245092 | c.1860C>G | synonymous_variant | 0.17 |
embA | 4245101 | c.1869G>C | synonymous_variant | 0.18 |
embA | 4245137 | c.1905T>C | synonymous_variant | 0.25 |
embA | 4245149 | c.1917C>G | synonymous_variant | 0.25 |
embA | 4245182 | c.1950T>C | synonymous_variant | 0.29 |
embB | 4247398 | c.885G>T | synonymous_variant | 0.91 |
embB | 4249328 | p.Met939Leu | missense_variant | 1.0 |
aftB | 4267490 | c.1347G>C | synonymous_variant | 1.0 |
ethA | 4326203 | p.Ser424* | stop_gained | 1.0 |