Run ID: SRR8692812
Sample name:
Date: 13-08-2023 19:22:55
Number of reads: NA
Percentage reads mapped: NA
Strain: lineage4.9
Drug-resistance: Other
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 |
---|---|---|---|---|---|
rplC | 801268 | p.Cys154Arg | missense_variant | 0.13 | linezolid |
pncA | 2289073 | p.His57Asp | missense_variant | 0.13 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7814 | c.513C>G | synonymous_variant | 0.11 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 0.2 |
rpoB | 760118 | c.312T>G | synonymous_variant | 0.1 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.11 |
rpoB | 760457 | c.651C>T | synonymous_variant | 0.14 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.14 |
rpoB | 760481 | c.675G>T | synonymous_variant | 0.12 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.12 |
rpoB | 760502 | c.696C>G | synonymous_variant | 0.14 |
rpoB | 760508 | c.702G>C | synonymous_variant | 0.14 |
rpoB | 760511 | c.705G>C | synonymous_variant | 0.14 |
rpoB | 760522 | p.Ser239Asn | missense_variant | 0.14 |
rpoB | 760567 | p.Ser254Trp | missense_variant | 0.11 |
rpoB | 760595 | c.789C>A | synonymous_variant | 0.12 |
rpoB | 761012 | p.Asp402Glu | missense_variant | 0.12 |
rpoB | 761217 | p.Pro471Thr | missense_variant | 0.13 |
rpoB | 761673 | p.Gly623Trp | missense_variant | 0.14 |
rpoB | 761990 | c.2184G>C | synonymous_variant | 0.3 |
rpoB | 761999 | c.2193G>C | synonymous_variant | 0.33 |
rpoB | 762002 | c.2196C>G | synonymous_variant | 0.33 |
rpoB | 762047 | c.2241G>A | synonymous_variant | 0.4 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.4 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.33 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.25 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.25 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.21 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.18 |
rpoB | 762122 | c.2316C>T | synonymous_variant | 0.14 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.1 |
rpoC | 763353 | c.-17A>G | upstream_gene_variant | 0.11 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.11 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.13 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.13 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.14 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.15 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.13 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.1 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.12 |
rpoC | 764719 | c.1350G>A | synonymous_variant | 0.14 |
rpoC | 764746 | c.1377G>T | synonymous_variant | 0.12 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.12 |
rpoC | 765952 | c.2583G>C | synonymous_variant | 0.11 |
mmpL5 | 776433 | p.Ser683* | stop_gained | 0.14 |
mmpL5 | 776878 | p.Gln535Lys | missense_variant | 0.13 |
mmpL5 | 778021 | p.Ala154Thr | missense_variant | 0.13 |
mmpS5 | 778820 | p.Arg29Leu | missense_variant | 0.14 |
mmpR5 | 779474 | p.Gly162Val | missense_variant | 0.12 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 0.12 |
rpsL | 781762 | p.Pro68Leu | missense_variant | 0.13 |
rpsL | 781857 | p.Gly100Cys | missense_variant | 0.13 |
rpsL | 781861 | p.Ser101* | stop_gained | 0.13 |
rplC | 801008 | p.Thr67Lys | missense_variant | 0.12 |
fbiC | 1305014 | p.Thr695Lys | missense_variant | 0.15 |
Rv1258c | 1406686 | p.Val219Ile | missense_variant | 0.87 |
Rv1258c | 1406699 | p.Glu214Asp | missense_variant | 0.13 |
atpE | 1460943 | c.-102C>T | upstream_gene_variant | 0.17 |
atpE | 1461099 | p.Gly19Cys | missense_variant | 0.17 |
atpE | 1461111 | p.Gly23Cys | missense_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471704 | n.-142C>A | upstream_gene_variant | 0.14 |
rrs | 1471774 | n.-72G>T | upstream_gene_variant | 0.17 |
rrs | 1471797 | n.-49G>T | upstream_gene_variant | 0.29 |
rrs | 1471817 | n.-29G>T | upstream_gene_variant | 0.4 |
rrs | 1471866 | n.21C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1471869 | n.24G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1471922 | n.78delT | non_coding_transcript_exon_variant | 0.67 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1471931 | n.87delA | non_coding_transcript_exon_variant | 0.67 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1471979 | n.134T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1471986 | n.141C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472019 | n.174G>A | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472023 | n.178G>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472029 | n.184C>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472030 | n.185G>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472033 | n.188A>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472035 | n.190G>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472040 | n.195T>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472043 | n.198T>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472324 | n.479G>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472337 | n.492C>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472380 | n.535G>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472624 | n.779T>C | non_coding_transcript_exon_variant | 0.15 |
rrs | 1472755 | n.910G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472762 | n.917C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472811 | n.966G>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472836 | n.991G>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472841 | n.996G>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472847 | n.1002G>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472848 | n.1003T>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472849 | n.1004C>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472850 | n.1005T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472857 | n.1012A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472858 | n.1013G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472859 | n.1014G>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472860 | n.1015C>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472970 | n.1125C>G | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472977 | n.1132G>C | non_coding_transcript_exon_variant | 0.6 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473072 | n.1227T>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.42 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1473668 | n.11C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473697 | n.40C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473717 | n.60G>A | non_coding_transcript_exon_variant | 0.54 |
rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473746 | n.89T>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1473814 | n.157A>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1473815 | n.158T>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1473816 | n.159C>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1473828 | n.171G>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1473829 | n.172G>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1473830 | n.173T>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1473831 | n.174G>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473887 | n.230T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473936 | n.279A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474199 | n.542G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474257 | n.600G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474412 | n.755G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474519 | n.862G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474753 | n.1096A>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474917 | n.1260G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475315 | n.1658A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475343 | n.1686A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475355 | n.1698C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475358 | n.1701T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475363 | n.1706C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475369 | n.1712G>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475380 | n.1723C>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475381 | n.1724G>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475382 | n.1725A>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475395 | n.1738T>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475396 | n.1739C>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475397 | n.1740G>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475402 | n.1745C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.8 |
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 | 1475647 | n.1990G>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475692 | n.2035G>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1475759 | n.2102C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1475764 | n.2107A>C | non_coding_transcript_exon_variant | 0.45 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1475775 | n.2118G>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475991 | n.2334T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475995 | n.2338G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476248 | n.2591G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476251 | n.2594T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476299 | n.2642C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476308 | n.2651G>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476384 | n.2727G>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476529 | n.2872A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476583 | n.2926G>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476674 | n.3017T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476679 | n.3022T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1476689 | n.3032A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476778 | n.3121G>A | non_coding_transcript_exon_variant | 0.25 |
fabG1 | 1674139 | p.Gly234Arg | missense_variant | 0.12 |
inhA | 1674165 | c.-37C>A | upstream_gene_variant | 0.12 |
rpsA | 1834096 | c.555G>C | synonymous_variant | 0.12 |
rpsA | 1834099 | c.558C>G | synonymous_variant | 0.12 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.12 |
rpsA | 1834108 | c.567C>G | synonymous_variant | 0.12 |
rpsA | 1834135 | c.594G>T | synonymous_variant | 0.17 |
rpsA | 1834150 | c.609G>C | synonymous_variant | 0.2 |
rpsA | 1834165 | c.624A>G | synonymous_variant | 0.2 |
rpsA | 1834168 | c.627C>T | synonymous_variant | 0.2 |
rpsA | 1834169 | p.Thr210Ala | missense_variant | 0.2 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.2 |
rpsA | 1834213 | c.672G>C | synonymous_variant | 0.38 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.2 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.19 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.17 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.19 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.17 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.16 |
rpsA | 1834279 | c.738C>T | synonymous_variant | 0.14 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 0.13 |
rpsA | 1834299 | p.Gln253Pro | missense_variant | 0.12 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.12 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.12 |
rpsA | 1834471 | p.Phe310Leu | missense_variant | 0.15 |
rpsA | 1834721 | p.Glu394Lys | missense_variant | 0.13 |
ndh | 2101694 | p.Ala450Asp | missense_variant | 0.13 |
ndh | 2101800 | p.Leu415Val | missense_variant | 0.15 |
ndh | 2102514 | p.Gly177Trp | missense_variant | 0.15 |
ndh | 2102942 | p.Lys34Arg | missense_variant | 0.17 |
PPE35 | 2170786 | c.-174G>T | upstream_gene_variant | 0.15 |
Rv1979c | 2222106 | c.1059C>T | synonymous_variant | 0.18 |
Rv1979c | 2222553 | c.612G>A | synonymous_variant | 0.12 |
Rv1979c | 2223088 | p.Ser26* | stop_gained | 0.13 |
pncA | 2289004 | p.Asp80Tyr | missense_variant | 0.12 |
pncA | 2289469 | c.-228C>A | upstream_gene_variant | 0.17 |
kasA | 2518045 | c.-70G>T | upstream_gene_variant | 0.13 |
kasA | 2518296 | p.Gly61Val | missense_variant | 0.17 |
kasA | 2519224 | c.1110C>G | synonymous_variant | 0.11 |
kasA | 2519227 | c.1113G>C | synonymous_variant | 0.12 |
kasA | 2519239 | c.1125A>C | synonymous_variant | 0.13 |
kasA | 2519248 | c.1134C>T | synonymous_variant | 0.14 |
kasA | 2519257 | c.1143C>T | synonymous_variant | 0.15 |
kasA | 2519260 | c.1146T>C | synonymous_variant | 0.14 |
kasA | 2519263 | c.1149C>T | synonymous_variant | 0.15 |
kasA | 2519266 | c.1152C>T | synonymous_variant | 0.14 |
kasA | 2519272 | c.1158C>G | synonymous_variant | 0.14 |
kasA | 2519275 | c.1161C>A | synonymous_variant | 0.14 |
kasA | 2519278 | c.1164A>G | synonymous_variant | 0.14 |
kasA | 2519281 | c.1167G>T | synonymous_variant | 0.14 |
kasA | 2519284 | c.1170C>G | synonymous_variant | 0.16 |
kasA | 2519287 | c.1173T>C | synonymous_variant | 0.16 |
kasA | 2519293 | c.1179T>C | synonymous_variant | 0.16 |
kasA | 2519298 | p.Arg395Gln | missense_variant | 0.17 |
kasA | 2519305 | c.1191A>C | synonymous_variant | 0.14 |
kasA | 2519306 | p.Val398Ile | missense_variant | 0.14 |
kasA | 2519323 | c.1209G>C | synonymous_variant | 0.12 |
pepQ | 2859464 | p.Gly319Cys | missense_variant | 0.18 |
Rv2752c | 3064944 | c.1248G>T | synonymous_variant | 0.12 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 0.14 |
Rv3083 | 3448627 | p.Gly42Ser | missense_variant | 0.14 |
Rv3083 | 3448847 | p.Arg115Leu | missense_variant | 0.17 |
whiB7 | 3568589 | p.Asp31Tyr | missense_variant | 0.13 |
whiB7 | 3568661 | p.Pro7Thr | missense_variant | 0.14 |
fbiA | 3641120 | p.Ser193Tyr | missense_variant | 0.15 |
rpoA | 3877584 | c.924C>G | synonymous_variant | 0.11 |
rpoA | 3877587 | c.921A>G | synonymous_variant | 0.1 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.17 |
rpoA | 3878360 | p.Ala50Ser | missense_variant | 0.12 |
clpC1 | 4039397 | c.1308A>G | synonymous_variant | 0.14 |
clpC1 | 4039409 | c.1296T>C | synonymous_variant | 0.16 |
clpC1 | 4039412 | c.1293T>G | synonymous_variant | 0.17 |
clpC1 | 4039415 | p.Glu430Asp | missense_variant | 0.17 |
clpC1 | 4039430 | c.1275T>C | synonymous_variant | 0.2 |
clpC1 | 4039442 | c.1263A>G | synonymous_variant | 0.2 |
clpC1 | 4039448 | c.1257A>G | synonymous_variant | 0.19 |
clpC1 | 4039454 | c.1251A>T | synonymous_variant | 0.19 |
clpC1 | 4039463 | c.1242C>G | synonymous_variant | 0.18 |
clpC1 | 4039466 | c.1239T>C | synonymous_variant | 0.2 |
clpC1 | 4039469 | c.1236T>C | synonymous_variant | 0.2 |
clpC1 | 4039472 | c.1233G>C | synonymous_variant | 0.21 |
clpC1 | 4039481 | c.1224T>C | synonymous_variant | 0.2 |
clpC1 | 4039484 | c.1221T>C | synonymous_variant | 0.19 |
clpC1 | 4039487 | c.1218G>C | synonymous_variant | 0.18 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.12 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.12 |
panD | 4043942 | p.Pro114Thr | missense_variant | 0.13 |
embC | 4240756 | c.894G>C | synonymous_variant | 0.12 |
embC | 4240774 | c.912C>G | synonymous_variant | 0.11 |
embC | 4240780 | c.918T>C | synonymous_variant | 0.1 |
embC | 4240783 | c.921G>C | synonymous_variant | 0.11 |
embC | 4240789 | c.927T>C | synonymous_variant | 0.1 |
embA | 4245173 | c.1941G>T | synonymous_variant | 0.17 |
ethA | 4326438 | p.Leu346Met | missense_variant | 0.18 |
ethA | 4327013 | p.Ser154* | stop_gained | 0.15 |