Run ID: SRR1140942
Sample name:
Date: 02-04-2023 20:59:24
Number of reads: 258511
Percentage reads mapped: 17.3
Strain:
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.97 | streptomycin |
tlyA | 1918388 | c.451delG | frameshift_variant | 0.25 | capreomycin |
pncA | 2288841 | c.400delG | frameshift_variant | 0.25 | pyrazinamide |
thyA | 3074246 | p.Gly76* | stop_gained | 0.29 | para-aminosalicylic_acid |
ethA | 4326707 | p.Trp256* | stop_gained | 0.25 | ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5072 | c.-168G>T | upstream_gene_variant | 0.25 |
gyrB | 5312 | p.Ala25Ser | missense_variant | 0.33 |
gyrB | 5555 | p.Gly106Ser | missense_variant | 1.0 |
gyrB | 5576 | p.Ala113Thr | missense_variant | 0.75 |
gyrB | 5830 | p.Met197Ile | missense_variant | 0.4 |
gyrB | 6001 | c.762G>T | synonymous_variant | 0.4 |
gyrA | 6397 | c.-905G>A | upstream_gene_variant | 0.29 |
gyrB | 6507 | p.Ala423Glu | missense_variant | 0.29 |
gyrA | 6901 | c.-401G>A | upstream_gene_variant | 0.33 |
gyrB | 7064 | c.1827delG | frameshift_variant | 0.33 |
gyrA | 7293 | c.-9G>A | upstream_gene_variant | 0.4 |
gyrA | 7324 | p.Pro8His | missense_variant | 0.4 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7427 | c.126G>A | synonymous_variant | 0.29 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 7805 | c.504C>T | synonymous_variant | 0.5 |
gyrA | 7909 | p.Trp203Leu | missense_variant | 0.67 |
gyrA | 8163 | p.Ala288Thr | missense_variant | 0.29 |
gyrA | 8244 | p.Val315Ile | missense_variant | 0.29 |
gyrA | 8535 | p.Glu412* | stop_gained | 0.4 |
gyrA | 8553 | p.Arg418Trp | missense_variant | 0.33 |
gyrA | 8872 | p.Gly524Val | missense_variant | 0.25 |
gyrA | 8937 | p.Gly546Arg | missense_variant | 0.29 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9380 | p.Met693Ile | missense_variant | 0.29 |
gyrA | 9468 | p.Leu723Met | missense_variant | 0.4 |
gyrA | 9509 | c.2208G>A | synonymous_variant | 0.5 |
gyrA | 9579 | p.Gly760Arg | missense_variant | 0.25 |
fgd1 | 491238 | c.456C>A | synonymous_variant | 0.25 |
fgd1 | 491279 | p.Pro166His | missense_variant | 0.33 |
fgd1 | 491641 | p.Ala287Ser | missense_variant | 0.67 |
fgd1 | 491671 | p.Val297Leu | missense_variant | 0.67 |
mshA | 575337 | c.-11T>A | upstream_gene_variant | 0.5 |
mshA | 575389 | c.42C>A | synonymous_variant | 0.25 |
mshA | 575419 | c.72C>T | synonymous_variant | 0.29 |
mshA | 575794 | c.447C>T | synonymous_variant | 0.4 |
mshA | 575801 | p.His152Asn | missense_variant | 0.4 |
mshA | 576162 | p.Gly272Glu | missense_variant | 0.67 |
mshA | 576203 | p.Ala286Pro | missense_variant | 1.0 |
mshA | 576217 | p.Leu290Phe | missense_variant | 1.0 |
mshA | 576342 | p.Ser332Tyr | missense_variant | 0.67 |
mshA | 576364 | c.1017G>A | synonymous_variant | 0.67 |
mshA | 576388 | c.1041G>A | synonymous_variant | 0.67 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
ccsA | 620644 | p.Glu252* | stop_gained | 1.0 |
ccsA | 620658 | c.768C>A | synonymous_variant | 1.0 |
rpoB | 760142 | c.336C>A | synonymous_variant | 0.4 |
rpoB | 760148 | p.Asp114Glu | missense_variant | 0.4 |
rpoB | 760268 | p.Met154Ile | missense_variant | 0.33 |
rpoB | 760408 | p.Ser201Ile | missense_variant | 0.25 |
rpoB | 760427 | c.621G>A | synonymous_variant | 0.29 |
rpoB | 760470 | p.Arg222Ser | missense_variant | 0.29 |
rpoB | 760580 | p.Lys258Asn | missense_variant | 0.44 |
rpoB | 760908 | p.Gly368Cys | missense_variant | 0.29 |
rpoB | 761015 | c.1209G>T | synonymous_variant | 0.5 |
rpoB | 761048 | c.1242C>T | synonymous_variant | 0.4 |
rpoB | 761486 | c.1680C>A | synonymous_variant | 0.67 |
rpoC | 762608 | c.-762C>A | upstream_gene_variant | 0.67 |
rpoC | 762665 | c.-705G>A | upstream_gene_variant | 0.5 |
rpoC | 762743 | c.-627G>T | upstream_gene_variant | 1.0 |
rpoB | 762841 | p.Pro1012Leu | missense_variant | 0.5 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763112 | p.Lys1102Asn | missense_variant | 0.22 |
rpoC | 763400 | p.Arg11Ser | missense_variant | 0.29 |
rpoC | 763446 | p.Gly26Asp | missense_variant | 0.33 |
rpoC | 763492 | c.123G>T | synonymous_variant | 0.29 |
rpoC | 764621 | p.Leu418Ile | missense_variant | 0.5 |
rpoC | 765668 | p.His767Asn | missense_variant | 0.33 |
rpoC | 765932 | p.Gly855Ser | missense_variant | 1.0 |
rpoC | 766123 | c.2754C>A | synonymous_variant | 0.5 |
rpoC | 766653 | p.Ser1095Tyr | missense_variant | 0.25 |
rpoC | 766692 | p.Gly1108Val | missense_variant | 0.25 |
rpoC | 766694 | p.Gln1109Lys | missense_variant | 0.25 |
rpoC | 766723 | c.3354G>T | synonymous_variant | 0.29 |
rpoC | 766748 | p.Pro1127Thr | missense_variant | 0.4 |
mmpL5 | 775717 | c.2764C>A | synonymous_variant | 1.0 |
mmpL5 | 775932 | p.Tyr850Phe | missense_variant | 0.22 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 0.8 |
mmpL5 | 776195 | c.2286G>T | synonymous_variant | 0.4 |
mmpL5 | 776390 | p.Asp697Glu | missense_variant | 0.25 |
mmpL5 | 776678 | c.1803G>A | synonymous_variant | 0.33 |
mmpL5 | 776696 | p.Pro595Gln | missense_variant | 0.29 |
mmpL5 | 776726 | c.1754delT | frameshift_variant | 0.33 |
mmpL5 | 776742 | c.1736_1738delGCC | disruptive_inframe_deletion | 0.33 |
mmpL5 | 777061 | p.Ala474Ser | missense_variant | 0.5 |
mmpL5 | 777245 | c.1236G>A | synonymous_variant | 0.67 |
mmpL5 | 777501 | p.Thr327Ile | missense_variant | 0.4 |
mmpL5 | 777661 | p.Ala274Thr | missense_variant | 0.4 |
mmpL5 | 777863 | c.618G>A | synonymous_variant | 0.4 |
mmpL5 | 777932 | p.Lys183Asn | missense_variant | 0.33 |
mmpR5 | 778211 | c.-779C>A | upstream_gene_variant | 0.67 |
mmpL5 | 778229 | p.Glu84Asp | missense_variant | 0.67 |
mmpS5 | 778927 | c.-22C>T | upstream_gene_variant | 0.33 |
mmpR5 | 779159 | p.Ala57Glu | missense_variant | 0.25 |
mmpR5 | 779167 | p.Leu60Val | missense_variant | 0.22 |
mmpL5 | 779364 | c.-884C>A | upstream_gene_variant | 0.67 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781554 | c.-6C>A | upstream_gene_variant | 0.25 |
rpsL | 781623 | p.Ala22Thr | missense_variant | 0.22 |
rpsL | 781636 | p.Gly26Val | missense_variant | 0.25 |
rpsL | 781806 | p.Arg83Gly | missense_variant | 0.33 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.4 |
rpsL | 781824 | p.Asp89Tyr | missense_variant | 0.33 |
rplC | 800671 | c.-138G>T | upstream_gene_variant | 0.67 |
rplC | 800768 | c.-41C>T | upstream_gene_variant | 0.29 |
rplC | 800803 | c.-6A>G | upstream_gene_variant | 0.25 |
rplC | 800823 | c.15C>A | synonymous_variant | 0.25 |
rplC | 800842 | p.Gly12Arg | missense_variant | 0.33 |
rplC | 801208 | p.Gly134Cys | missense_variant | 0.5 |
rplC | 801215 | p.Gly136Val | missense_variant | 0.4 |
rplC | 801245 | p.Arg146Leu | missense_variant | 0.29 |
rplC | 801301 | c.493C>A | synonymous_variant | 0.29 |
rplC | 801319 | p.Gly171Cys | missense_variant | 0.22 |
rplC | 801393 | p.Lys195Asn | missense_variant | 0.4 |
fbiC | 1302888 | c.-43G>T | upstream_gene_variant | 0.5 |
fbiC | 1303426 | p.Gly166Cys | missense_variant | 0.67 |
fbiC | 1304236 | p.Gln436Tyr | missense_variant | 1.0 |
fbiC | 1304291 | p.Asp454Gly | missense_variant | 0.5 |
fbiC | 1304714 | p.Gly595Val | missense_variant | 0.5 |
fbiC | 1304741 | p.Gly604Asp | missense_variant | 0.5 |
fbiC | 1304961 | c.2031C>A | synonymous_variant | 0.29 |
fbiC | 1304970 | c.2040G>T | synonymous_variant | 0.5 |
fbiC | 1304980 | p.Lys684Glu | missense_variant | 0.33 |
fbiC | 1305327 | p.Met799Ile | missense_variant | 0.33 |
fbiC | 1305416 | p.Thr829Ile | missense_variant | 0.5 |
Rv1258c | 1406090 | c.1251G>A | synonymous_variant | 0.22 |
Rv1258c | 1406099 | c.1242C>A | synonymous_variant | 0.25 |
Rv1258c | 1406268 | p.Ala358Val | missense_variant | 0.33 |
Rv1258c | 1406283 | p.Thr353Met | missense_variant | 0.5 |
Rv1258c | 1406440 | p.Ala301Thr | missense_variant | 0.5 |
Rv1258c | 1406722 | p.Gly207Trp | missense_variant | 0.67 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
Rv1258c | 1406817 | p.Trp175Ser | missense_variant | 0.67 |
Rv1258c | 1406855 | c.486C>A | synonymous_variant | 0.25 |
Rv1258c | 1406868 | p.Pro158Gln | missense_variant | 0.29 |
Rv1258c | 1406921 | c.420C>T | synonymous_variant | 0.4 |
Rv1258c | 1407214 | p.Gln43* | stop_gained | 0.4 |
Rv1258c | 1407217 | p.Gly42Trp | missense_variant | 0.4 |
Rv1258c | 1407371 | c.-31C>T | upstream_gene_variant | 0.22 |
Rv1258c | 1407376 | c.-36C>T | upstream_gene_variant | 0.22 |
Rv1258c | 1407476 | c.-136G>A | upstream_gene_variant | 0.67 |
embR | 1416195 | p.His385Tyr | missense_variant | 0.4 |
embR | 1416201 | p.Gly383Trp | missense_variant | 0.4 |
embR | 1416610 | c.738G>A | synonymous_variant | 0.67 |
embR | 1416737 | p.Arg204Leu | missense_variant | 0.2 |
embR | 1416739 | p.Tyr203* | stop_gained | 0.2 |
embR | 1416742 | c.606C>A | synonymous_variant | 0.18 |
embR | 1416789 | p.Ala187Thr | missense_variant | 0.22 |
embR | 1417387 | c.-40C>A | upstream_gene_variant | 0.4 |
embR | 1417442 | c.-95C>A | upstream_gene_variant | 0.29 |
atpE | 1460904 | c.-141C>A | upstream_gene_variant | 0.29 |
atpE | 1461188 | c.144G>T | synonymous_variant | 0.33 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471930 | n.88_89delGA | non_coding_transcript_exon_variant | 0.67 |
rrs | 1471946 | n.101C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472127 | n.282C>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472128 | n.283G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472129 | n.284G>C | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472130 | n.285G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472151 | n.306C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472203 | n.358G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472266 | n.421C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472378 | n.533G>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472380 | n.535G>C | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472396 | n.551A>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472498 | n.653C>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472579 | n.734G>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472670 | n.825G>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472677 | n.832C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472681 | n.837_838delTT | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472687 | n.842_843insC | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.96 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472827 | n.982G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472965 | n.1120C>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473053 | n.1208T>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473062 | n.1217T>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473068 | n.1223A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1473147 | n.1302G>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1473148 | n.1303G>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1473150 | n.1305T>G | non_coding_transcript_exon_variant | 0.58 |
rrs | 1473161 | n.1316A>C | non_coding_transcript_exon_variant | 0.64 |
rrs | 1473163 | n.1318C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473164 | n.1319C>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473177 | n.1332G>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473192 | n.1347A>G | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473199 | n.1356delA | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473205 | n.1360T>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473248 | n.1403G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473249 | n.1404T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473255 | n.1410A>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473259 | n.1414C>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1473260 | n.1415G>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473308 | n.1463G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473309 | n.1464G>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473327 | n.1482A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473328 | n.1483C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473352 | n.1507C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473364 | n.1519G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473455 | n.-203G>T | upstream_gene_variant | 0.67 |
rrl | 1473552 | n.-106G>T | upstream_gene_variant | 0.5 |
rrl | 1473989 | n.332C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474228 | n.571T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474234 | n.577G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474252 | n.595T>A | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474734 | n.1077G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474839 | n.1182C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474844 | n.1187G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474848 | n.1191G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474862 | n.1205C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474892 | n.1235G>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474902 | n.1245T>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474913 | n.1256T>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474920 | n.1263G>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475591 | n.1934G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475783 | n.2126T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475803 | n.2146T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475804 | n.2147G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475816 | n.2159C>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1475817 | n.2160A>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1475858 | n.2201T>C | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475866 | n.2209T>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476084 | n.2427G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476141 | n.2484A>G | non_coding_transcript_exon_variant | 0.27 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.96 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476580 | n.2923G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476655 | n.2998C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476684 | n.3027C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476706 | n.3049C>T | non_coding_transcript_exon_variant | 0.4 |
inhA | 1673559 | c.-643C>T | upstream_gene_variant | 0.5 |
inhA | 1673709 | c.-493C>A | upstream_gene_variant | 1.0 |
fabG1 | 1674170 | p.Gly244Asp | missense_variant | 0.67 |
inhA | 1674289 | p.Gln30Lys | missense_variant | 0.67 |
inhA | 1674470 | p.Gly90Val | missense_variant | 0.67 |
inhA | 1674551 | p.Ser117Tyr | missense_variant | 0.4 |
inhA | 1674621 | c.420C>A | synonymous_variant | 0.67 |
inhA | 1674738 | c.537C>A | synonymous_variant | 0.5 |
inhA | 1674741 | c.540C>A | synonymous_variant | 0.5 |
inhA | 1674817 | p.Ala206Ser | missense_variant | 0.4 |
rpsA | 1833522 | c.-20G>A | upstream_gene_variant | 0.5 |
rpsA | 1833886 | c.345C>T | synonymous_variant | 0.4 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834210 | c.669C>A | synonymous_variant | 0.4 |
rpsA | 1834612 | c.1071G>T | synonymous_variant | 0.33 |
rpsA | 1834943 | p.Ala468Ser | missense_variant | 0.4 |
rpsA | 1834946 | p.Gln469Glu | missense_variant | 0.4 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918336 | p.Arg133Trp | missense_variant | 0.33 |
tlyA | 1918651 | p.Glu238* | stop_gained | 0.4 |
ndh | 2101673 | p.Ala457Glu | missense_variant | 0.5 |
ndh | 2101698 | p.Ala449Ser | missense_variant | 0.67 |
ndh | 2101838 | p.Ala402Glu | missense_variant | 0.4 |
ndh | 2101913 | p.Ser377* | stop_gained | 0.4 |
ndh | 2101974 | p.Ala357Ser | missense_variant | 0.22 |
ndh | 2101997 | p.Ala349Val | missense_variant | 0.29 |
ndh | 2102014 | c.1029C>G | synonymous_variant | 0.4 |
ndh | 2102029 | p.Gln338His | missense_variant | 0.4 |
ndh | 2102241 | p.Arg268Ser | missense_variant | 0.67 |
ndh | 2102839 | c.204C>T | synonymous_variant | 0.29 |
katG | 2154072 | c.2040C>A | synonymous_variant | 1.0 |
katG | 2154432 | c.1680C>T | synonymous_variant | 0.5 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2154784 | p.Pro443His | missense_variant | 0.5 |
katG | 2154860 | c.1252C>A | synonymous_variant | 0.5 |
katG | 2154991 | p.Ser374Tyr | missense_variant | 0.4 |
katG | 2155496 | p.Gly206Ser | missense_variant | 0.4 |
katG | 2155701 | c.411C>T | synonymous_variant | 0.5 |
katG | 2156039 | p.His25Tyr | missense_variant | 0.5 |
katG | 2156200 | c.-89G>T | upstream_gene_variant | 0.67 |
katG | 2156223 | c.-112G>T | upstream_gene_variant | 1.0 |
katG | 2156521 | c.-410C>T | upstream_gene_variant | 0.29 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167985 | p.Met876Ile | missense_variant | 0.4 |
PPE35 | 2168086 | p.Glu843* | stop_gained | 0.33 |
PPE35 | 2168252 | c.2361G>A | synonymous_variant | 0.22 |
PPE35 | 2168672 | c.1941C>T | synonymous_variant | 0.33 |
PPE35 | 2168846 | c.1767G>T | synonymous_variant | 0.29 |
PPE35 | 2169503 | c.1110C>A | synonymous_variant | 0.25 |
PPE35 | 2170036 | p.Val193Met | missense_variant | 0.5 |
PPE35 | 2170156 | p.Ala153Ser | missense_variant | 0.67 |
PPE35 | 2170447 | c.165delG | frameshift_variant | 0.67 |
Rv1979c | 2221779 | p.Met462Ile | missense_variant | 0.67 |
Rv1979c | 2221801 | p.Thr455Arg | missense_variant | 0.67 |
Rv1979c | 2222172 | c.993G>T | synonymous_variant | 0.5 |
Rv1979c | 2222192 | p.Arg325Trp | missense_variant | 0.4 |
Rv1979c | 2222425 | p.Ala247Val | missense_variant | 0.4 |
Rv1979c | 2222445 | c.720C>T | synonymous_variant | 0.5 |
Rv1979c | 2222519 | p.Gly216Cys | missense_variant | 0.29 |
Rv1979c | 2222525 | p.Gly214Cys | missense_variant | 0.29 |
Rv1979c | 2222603 | p.Gln188* | stop_gained | 0.29 |
Rv1979c | 2222954 | p.Tyr71His | missense_variant | 0.25 |
Rv1979c | 2223077 | p.Ala30Ser | missense_variant | 0.33 |
Rv1979c | 2223080 | p.Gly29Arg | missense_variant | 0.33 |
Rv1979c | 2223088 | p.Ser26Leu | missense_variant | 0.4 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
Rv1979c | 2223341 | c.-177C>T | upstream_gene_variant | 0.4 |
pncA | 2289322 | c.-81C>T | upstream_gene_variant | 0.4 |
pncA | 2289401 | c.-160G>A | upstream_gene_variant | 0.4 |
pncA | 2289410 | c.-169G>A | upstream_gene_variant | 0.5 |
pncA | 2289445 | c.-204C>A | upstream_gene_variant | 0.5 |
pncA | 2289639 | c.-398C>A | upstream_gene_variant | 0.5 |
pncA | 2289660 | c.-419G>C | upstream_gene_variant | 0.67 |
pncA | 2289992 | c.-751G>T | upstream_gene_variant | 0.25 |
pncA | 2290037 | c.-796G>T | upstream_gene_variant | 0.25 |
pncA | 2290048 | c.-807C>T | upstream_gene_variant | 0.25 |
kasA | 2518141 | c.27C>T | synonymous_variant | 0.33 |
kasA | 2518142 | p.Gly10Cys | missense_variant | 0.33 |
kasA | 2518225 | p.Leu37Phe | missense_variant | 0.5 |
kasA | 2518286 | p.Val58Phe | missense_variant | 0.4 |
kasA | 2518470 | p.Ala119Val | missense_variant | 0.67 |
kasA | 2518788 | p.Arg225Gln | missense_variant | 0.29 |
kasA | 2518889 | p.Ala259Ser | missense_variant | 0.67 |
kasA | 2518960 | c.846C>T | synonymous_variant | 0.22 |
kasA | 2518983 | p.Ala290Glu | missense_variant | 0.5 |
kasA | 2519101 | c.987C>T | synonymous_variant | 0.5 |
kasA | 2519249 | p.Glu379Lys | missense_variant | 0.25 |
kasA | 2519270 | p.Ala386Pro | missense_variant | 0.25 |
eis | 2714220 | c.1113C>T | synonymous_variant | 0.4 |
eis | 2714260 | p.Ser358Ile | missense_variant | 0.5 |
eis | 2714385 | c.948G>A | synonymous_variant | 0.4 |
eis | 2714669 | p.Gly222Arg | missense_variant | 0.22 |
eis | 2714674 | p.Pro220His | missense_variant | 0.22 |
eis | 2714771 | p.Gly188Ser | missense_variant | 0.5 |
eis | 2715169 | p.Gly55Ala | missense_variant | 0.33 |
eis | 2715187 | p.Arg49His | missense_variant | 0.4 |
eis | 2715216 | c.117G>A | synonymous_variant | 0.33 |
eis | 2715320 | p.Leu5Met | missense_variant | 0.5 |
eis | 2715326 | p.Val3Met | missense_variant | 0.5 |
eis | 2715412 | c.-80C>A | upstream_gene_variant | 0.5 |
ahpC | 2725934 | c.-259G>A | upstream_gene_variant | 1.0 |
ahpC | 2725999 | c.-194C>A | upstream_gene_variant | 0.4 |
ahpC | 2726057 | c.-136C>T | upstream_gene_variant | 0.25 |
ahpC | 2726084 | c.-109C>A | upstream_gene_variant | 0.18 |
ahpC | 2726139 | c.-54C>A | upstream_gene_variant | 0.22 |
ahpC | 2726158 | c.-35C>A | upstream_gene_variant | 0.33 |
ahpC | 2726384 | p.Glu64Asp | missense_variant | 0.25 |
ahpC | 2726774 | c.582G>T | synonymous_variant | 0.4 |
ahpC | 2726776 | p.Ala195Val | missense_variant | 0.4 |
folC | 2746227 | p.Gly458Trp | missense_variant | 0.67 |
folC | 2746246 | c.1353C>T | synonymous_variant | 0.67 |
folC | 2746370 | p.Arg410Leu | missense_variant | 0.67 |
folC | 2746531 | c.1068G>A | synonymous_variant | 0.29 |
folC | 2746555 | c.1044G>A | synonymous_variant | 0.29 |
folC | 2746778 | p.Gly274Asp | missense_variant | 0.5 |
folC | 2746827 | p.Arg258Trp | missense_variant | 0.25 |
folC | 2746833 | p.Val256Leu | missense_variant | 0.25 |
folC | 2746926 | c.672delC | frameshift_variant | 1.0 |
folC | 2746946 | p.Gly218Val | missense_variant | 1.0 |
folC | 2747026 | c.573C>A | synonymous_variant | 0.4 |
folC | 2747215 | p.Glu128Asp | missense_variant | 0.29 |
folC | 2747245 | c.354G>A | synonymous_variant | 0.5 |
folC | 2747252 | p.Ser116Ile | missense_variant | 0.5 |
folC | 2747456 | p.Thr48Ile | missense_variant | 0.67 |
folC | 2747493 | p.Gln36Lys | missense_variant | 0.33 |
folC | 2747532 | p.Glu23Lys | missense_variant | 0.29 |
folC | 2747569 | c.30C>T | synonymous_variant | 0.33 |
folC | 2747579 | p.Gly7Val | missense_variant | 0.33 |
pepQ | 2859617 | p.Ala268Thr | missense_variant | 0.4 |
pepQ | 2859644 | p.Ala259Ser | missense_variant | 0.33 |
pepQ | 2859657 | c.762C>T | synonymous_variant | 0.4 |
pepQ | 2860407 | c.12C>T | synonymous_variant | 0.29 |
pepQ | 2860473 | c.-55C>A | upstream_gene_variant | 0.33 |
pepQ | 2860487 | c.-69G>A | upstream_gene_variant | 0.4 |
pepQ | 2860515 | c.-99_-97delCTGinsATA | upstream_gene_variant | 0.4 |
pepQ | 2860519 | c.-101C>A | upstream_gene_variant | 0.4 |
ribD | 2986654 | c.-185C>T | upstream_gene_variant | 0.5 |
Rv2752c | 3064758 | c.1434G>C | synonymous_variant | 1.0 |
Rv2752c | 3064957 | p.Ser412Asn | missense_variant | 0.29 |
Rv2752c | 3065250 | c.942G>A | synonymous_variant | 0.29 |
Rv2752c | 3065407 | p.Val262Ala | missense_variant | 0.33 |
Rv2752c | 3065411 | p.Phe261Leu | missense_variant | 0.4 |
Rv2752c | 3065412 | p.Ser260Thr | missense_variant | 0.4 |
Rv2752c | 3065416 | p.Val259Thr | missense_variant | 0.4 |
Rv2752c | 3065421 | c.771G>A | synonymous_variant | 0.4 |
Rv2752c | 3065440 | p.Ala251Asp | missense_variant | 0.33 |
Rv2752c | 3065467 | p.Val242Ala | missense_variant | 0.4 |
Rv2752c | 3066110 | p.Gly28Cys | missense_variant | 0.4 |
Rv2752c | 3066112 | c.79delA | frameshift_variant | 0.5 |
Rv2752c | 3066355 | c.-165delG | upstream_gene_variant | 0.29 |
Rv2752c | 3067084 | c.-893C>T | upstream_gene_variant | 0.67 |
Rv2752c | 3067111 | c.-920G>T | upstream_gene_variant | 0.4 |
thyX | 3067261 | p.Asp229Asn | missense_variant | 0.5 |
thyX | 3067589 | c.357G>A | synonymous_variant | 0.25 |
thyX | 3067601 | c.345G>T | synonymous_variant | 0.22 |
thyX | 3067657 | p.Arg97Trp | missense_variant | 0.33 |
thyA | 3073867 | p.Thr202Ile | missense_variant | 0.5 |
thyA | 3074197 | p.Pro92Leu | missense_variant | 0.33 |
thyA | 3074202 | c.270C>T | synonymous_variant | 0.29 |
thyA | 3074554 | c.-83G>T | upstream_gene_variant | 0.29 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3086942 | p.Glu41Asp | missense_variant | 1.0 |
ald | 3087659 | c.840G>A | synonymous_variant | 0.5 |
ald | 3087746 | c.927G>T | synonymous_variant | 0.29 |
ald | 3087767 | c.948G>T | synonymous_variant | 0.29 |
ald | 3087862 | p.Gly348Val | missense_variant | 0.33 |
fbiD | 3339270 | c.153G>T | synonymous_variant | 0.4 |
fbiD | 3339360 | c.243C>A | synonymous_variant | 0.67 |
fbiD | 3339517 | p.His134Tyr | missense_variant | 0.33 |
Rv3083 | 3449367 | c.864G>T | synonymous_variant | 0.67 |
Rv3083 | 3449401 | p.Val300Met | missense_variant | 0.22 |
Rv3083 | 3449448 | c.945G>A | synonymous_variant | 0.29 |
Rv3083 | 3449487 | c.984C>A | synonymous_variant | 0.4 |
Rv3083 | 3449493 | c.990G>A | synonymous_variant | 0.4 |
Rv3083 | 3449676 | c.1173C>T | synonymous_variant | 1.0 |
Rv3083 | 3449827 | p.Gly442Ser | missense_variant | 1.0 |
fprA | 3473890 | c.-117C>A | upstream_gene_variant | 0.5 |
fprA | 3473970 | c.-37C>A | upstream_gene_variant | 0.5 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474719 | p.Ala238Val | missense_variant | 0.67 |
fprA | 3474774 | c.768G>A | synonymous_variant | 0.33 |
whiB7 | 3568692 | c.-13G>T | upstream_gene_variant | 1.0 |
whiB7 | 3568855 | c.-176G>A | upstream_gene_variant | 0.67 |
Rv3236c | 3612196 | c.921C>T | synonymous_variant | 0.5 |
Rv3236c | 3612427 | c.690G>T | synonymous_variant | 0.4 |
Rv3236c | 3612446 | p.Gly224Val | missense_variant | 0.33 |
Rv3236c | 3612448 | c.669G>T | synonymous_variant | 0.29 |
Rv3236c | 3612456 | p.Arg221Trp | missense_variant | 0.29 |
Rv3236c | 3612680 | p.Arg146Leu | missense_variant | 0.22 |
Rv3236c | 3612692 | p.Arg142Leu | missense_variant | 0.29 |
Rv3236c | 3612709 | c.408G>T | synonymous_variant | 0.33 |
Rv3236c | 3612929 | p.Pro63His | missense_variant | 0.4 |
Rv3236c | 3612978 | p.Gly47Cys | missense_variant | 0.4 |
Rv3236c | 3613024 | c.93G>A | synonymous_variant | 0.4 |
Rv3236c | 3613291 | c.-175G>T | upstream_gene_variant | 0.29 |
fbiA | 3640356 | c.-187G>T | upstream_gene_variant | 0.29 |
fbiB | 3640722 | c.-813G>A | upstream_gene_variant | 0.33 |
fbiA | 3640896 | p.Met118Ile | missense_variant | 0.29 |
fbiA | 3640903 | p.Ala121Ser | missense_variant | 0.29 |
fbiA | 3640975 | p.Ala145Thr | missense_variant | 0.5 |
fbiA | 3640987 | p.Arg149Ser | missense_variant | 0.33 |
fbiA | 3641062 | p.Val174Met | missense_variant | 0.4 |
fbiA | 3641236 | p.Ala232Ser | missense_variant | 0.67 |
fbiB | 3641917 | p.Ser128Ile | missense_variant | 0.33 |
fbiB | 3641960 | c.426C>T | synonymous_variant | 0.25 |
fbiB | 3642413 | c.879G>T | synonymous_variant | 0.33 |
alr | 3840494 | c.927G>A | synonymous_variant | 0.4 |
alr | 3840534 | p.Gly296Glu | missense_variant | 0.33 |
alr | 3840551 | c.870G>T | synonymous_variant | 0.5 |
alr | 3840625 | p.Leu266Ile | missense_variant | 0.67 |
alr | 3840885 | c.534_535delGT | frameshift_variant | 0.5 |
alr | 3841036 | p.Gln129* | stop_gained | 0.33 |
alr | 3841324 | p.Gly33Ser | missense_variant | 0.4 |
alr | 3841368 | p.Arg18Leu | missense_variant | 0.25 |
alr | 3841370 | p.Gly17Val | missense_variant | 0.25 |
rpoA | 3877794 | c.714G>T | synonymous_variant | 0.67 |
rpoA | 3878367 | c.141C>A | synonymous_variant | 0.4 |
ddn | 3986673 | c.-171C>T | upstream_gene_variant | 1.0 |
clpC1 | 4038563 | c.2142C>T | synonymous_variant | 1.0 |
clpC1 | 4038655 | p.Gly684Cys | missense_variant | 0.29 |
clpC1 | 4038678 | p.Pro676Gln | missense_variant | 0.29 |
clpC1 | 4038991 | p.Gly572Ser | missense_variant | 0.33 |
clpC1 | 4039155 | p.Arg517Gln | missense_variant | 0.4 |
clpC1 | 4039165 | p.Leu514Met | missense_variant | 0.33 |
clpC1 | 4039346 | c.1359G>T | synonymous_variant | 0.5 |
clpC1 | 4039564 | p.Ala381Ser | missense_variant | 1.0 |
clpC1 | 4039803 | p.Ala301Val | missense_variant | 0.5 |
clpC1 | 4039844 | c.861C>T | synonymous_variant | 0.33 |
clpC1 | 4039934 | c.771G>A | synonymous_variant | 0.33 |
clpC1 | 4040296 | p.Gln137* | stop_gained | 0.67 |
clpC1 | 4040660 | c.45G>T | synonymous_variant | 0.5 |
embC | 4239942 | p.Arg27Leu | missense_variant | 0.5 |
embC | 4240044 | p.Trp61Leu | missense_variant | 0.4 |
embC | 4240048 | c.186C>A | synonymous_variant | 0.4 |
embC | 4240089 | p.Gly76Val | missense_variant | 0.5 |
embC | 4240319 | p.Gln153* | stop_gained | 0.22 |
embC | 4241028 | p.Trp389* | stop_gained | 0.4 |
embC | 4241074 | c.1212G>T | synonymous_variant | 0.22 |
embC | 4241102 | p.Glu414* | stop_gained | 0.25 |
embC | 4241105 | p.Arg415Trp | missense_variant | 0.25 |
embC | 4241416 | c.1554C>A | synonymous_variant | 0.67 |
embC | 4241553 | p.Pro564Gln | missense_variant | 0.4 |
embC | 4241641 | c.1779C>T | synonymous_variant | 0.4 |
embC | 4241644 | c.1782G>T | synonymous_variant | 0.4 |
embC | 4241703 | p.Arg614Leu | missense_variant | 0.4 |
embC | 4241925 | p.Arg688Leu | missense_variant | 0.67 |
embC | 4241928 | p.Arg689Leu | missense_variant | 0.67 |
embC | 4242255 | p.Pro798Gln | missense_variant | 1.0 |
embA | 4243141 | c.-92C>T | upstream_gene_variant | 0.33 |
embA | 4243201 | c.-32G>T | upstream_gene_variant | 0.5 |
embA | 4243273 | p.Arg14His | missense_variant | 0.33 |
embA | 4243287 | p.Val19Ile | missense_variant | 0.33 |
embA | 4243522 | p.Gly97Val | missense_variant | 1.0 |
embA | 4244093 | c.861C>A | synonymous_variant | 0.67 |
embA | 4244269 | p.Arg346Leu | missense_variant | 0.4 |
embA | 4244304 | c.1072C>A | synonymous_variant | 1.0 |
embA | 4244721 | p.Gln497* | stop_gained | 0.67 |
embA | 4244798 | c.1566G>T | synonymous_variant | 0.5 |
embA | 4245437 | p.Met735Ile | missense_variant | 0.33 |
embA | 4245460 | p.Pro743Leu | missense_variant | 0.25 |
embA | 4245663 | p.Gly811Cys | missense_variant | 0.67 |
embA | 4246271 | p.Gln1013His | missense_variant | 0.67 |
embA | 4246294 | p.Trp1021Ser | missense_variant | 0.4 |
embB | 4246618 | c.105G>T | synonymous_variant | 1.0 |
embB | 4246692 | p.Gln60Arg | missense_variant | 0.67 |
embB | 4246877 | p.Arg122Cys | missense_variant | 0.4 |
embB | 4247186 | p.Ala225Leu | missense_variant | 0.67 |
embB | 4247442 | p.Ala310Asp | missense_variant | 0.33 |
embB | 4247854 | c.1341C>T | synonymous_variant | 0.4 |
embB | 4248171 | p.Ala553Val | missense_variant | 0.33 |
embB | 4248382 | c.1869C>A | synonymous_variant | 0.67 |
embB | 4248506 | p.Gly665Arg | missense_variant | 0.29 |
embB | 4248553 | c.2040C>T | synonymous_variant | 0.67 |
embB | 4248846 | p.Gly778Val | missense_variant | 0.67 |
embB | 4249121 | p.Asp870His | missense_variant | 0.2 |
embB | 4249144 | c.2631G>A | synonymous_variant | 0.2 |
embB | 4249147 | c.2634C>T | synonymous_variant | 0.22 |
embB | 4249152 | p.Ala880Val | missense_variant | 0.22 |
embB | 4249154 | p.Gly881Cys | missense_variant | 0.22 |
embB | 4249196 | p.Gly895Arg | missense_variant | 0.29 |
embB | 4249220 | p.Ala903Ser | missense_variant | 0.4 |
embB | 4249471 | c.2958G>A | synonymous_variant | 0.29 |
embB | 4249785 | p.Pro1091Leu | missense_variant | 0.22 |
aftB | 4266996 | p.Gly614Val | missense_variant | 0.25 |
aftB | 4267560 | p.Ala426Val | missense_variant | 0.5 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4267695 | p.Gly381Glu | missense_variant | 0.29 |
aftB | 4268357 | p.Gln160His | missense_variant | 0.4 |
aftB | 4268747 | c.90C>T | synonymous_variant | 0.4 |
aftB | 4269366 | c.-530G>A | upstream_gene_variant | 0.5 |
aftB | 4269681 | c.-845G>T | upstream_gene_variant | 0.4 |
ubiA | 4269713 | p.Gly41Cys | missense_variant | 0.33 |
ubiA | 4269787 | p.Gly16Val | missense_variant | 0.33 |
aftB | 4269804 | c.-968G>T | upstream_gene_variant | 0.4 |
aftB | 4269819 | c.-983G>T | upstream_gene_variant | 0.4 |
ethA | 4326285 | p.Leu397Met | missense_variant | 0.4 |
ethA | 4326472 | c.1002G>T | synonymous_variant | 0.25 |
ethA | 4326538 | c.936G>T | synonymous_variant | 0.2 |
ethA | 4327028 | p.Pro149Arg | missense_variant | 0.5 |
ethR | 4328014 | p.Glu156* | stop_gained | 0.33 |
ethR | 4328044 | p.Leu166Met | missense_variant | 0.5 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407620 | p.Tyr195His | missense_variant | 1.0 |
gid | 4407747 | c.456G>A | synonymous_variant | 0.33 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |
gid | 4408439 | c.-237G>A | upstream_gene_variant | 0.33 |