Run ID: SRR3601585
Sample name:
Date: 04-04-2023 05:20:33
Number of reads: 1039512
Percentage reads mapped: 39.78
Strain: lineage2.2
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 0.99 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7582 | p.Asp94Ala | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761127 | p.Ser441Ala | missense_variant | 0.47 | rifampicin |
rpoB | 761140 | p.His445Arg | missense_variant | 0.58 | rifampicin |
rpsL | 781687 | p.Lys43Arg | missense_variant | 0.9 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.88 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.78 | kanamycin, capreomycin, aminoglycosides, amikacin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2288844 | p.Ile133Thr | missense_variant | 1.0 | pyrazinamide |
folC | 2747151 | p.Ser150Gly | missense_variant | 1.0 | para-aminosalicylic_acid |
embB | 4247431 | p.Met306Ile | missense_variant | 1.0 | ethambutol |
embB | 4247730 | p.Gly406Asp | missense_variant | 1.0 | ethambutol |
ethA | 4326008 | c.1465delG | frameshift_variant | 0.15 | ethionamide, ethionamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 760916 | c.1110C>T | synonymous_variant | 0.33 |
rpoB | 760920 | p.Leu372Ile | missense_variant | 0.29 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.29 |
rpoB | 760926 | p.Thr374Ala | missense_variant | 0.25 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.42 |
rpoB | 760953 | p.Ile383Val | missense_variant | 0.42 |
rpoB | 760955 | c.1151_1152insCACG | frameshift_variant | 0.45 |
rpoB | 760961 | c.1156_1159delGGCA | frameshift_variant | 0.56 |
rpoB | 760973 | c.1167G>C | synonymous_variant | 0.42 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.56 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.62 |
rpoB | 760988 | c.1182C>G | synonymous_variant | 0.56 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.56 |
rpoB | 760997 | c.1191G>C | synonymous_variant | 0.56 |
rpoB | 761003 | c.1197C>G | synonymous_variant | 0.56 |
rpoB | 761006 | c.1200C>G | synonymous_variant | 0.42 |
rpoB | 761009 | c.1203G>A | synonymous_variant | 0.42 |
rpoB | 761013 | p.Val403Ile | missense_variant | 0.42 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.46 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.43 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.43 |
rpoB | 761046 | p.Ile414Val | missense_variant | 0.43 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.43 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 0.47 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.5 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.47 |
rpoB | 761088 | c.1282_1284delAGCinsTCG | synonymous_variant | 0.44 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.5 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.47 |
rpoB | 761126 | c.1320G>C | synonymous_variant | 0.47 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 0.44 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.33 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.33 |
rpoB | 761153 | c.1347G>C | synonymous_variant | 0.33 |
rpoB | 761162 | c.1356G>C | synonymous_variant | 0.36 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.38 |
rpoB | 761171 | c.1365C>T | synonymous_variant | 0.36 |
rpoB | 761177 | c.1371G>C | synonymous_variant | 0.36 |
rpoB | 761180 | c.1374A>G | synonymous_variant | 0.31 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.33 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.33 |
rpoB | 761196 | p.Leu464Val | missense_variant | 0.27 |
rpoB | 761204 | c.1398C>T | synonymous_variant | 0.3 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.36 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 0.36 |
rpoB | 761219 | c.1413G>C | synonymous_variant | 0.36 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.33 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.3 |
rpoB | 761255 | c.1449T>G | synonymous_variant | 0.33 |
rpoB | 761258 | c.1452G>A | synonymous_variant | 0.25 |
rpoB | 761261 | c.1455G>C | synonymous_variant | 0.25 |
rpoB | 761264 | c.1458C>G | synonymous_variant | 0.25 |
rpoB | 761273 | c.1467T>C | synonymous_variant | 0.29 |
rpoB | 761282 | c.1476C>T | synonymous_variant | 0.22 |
rpoB | 761283 | p.Ser493Ala | missense_variant | 0.22 |
rpoB | 761288 | c.1482G>C | synonymous_variant | 0.2 |
rpoB | 761289 | p.Ser495Ala | missense_variant | 0.2 |
rpoB | 761292 | p.Val496Ser | missense_variant | 0.18 |
rpoB | 761296 | p.Tyr497Phe | missense_variant | 0.18 |
rpoB | 761303 | c.1497G>C | synonymous_variant | 0.22 |
rpoB | 761304 | p.Val500Ile | missense_variant | 0.22 |
rpoB | 761310 | p.Pro502Ser | missense_variant | 0.22 |
rpoB | 761318 | c.1512G>C | synonymous_variant | 0.2 |
rpoB | 761327 | c.1521A>G | synonymous_variant | 0.22 |
rpoB | 761330 | c.1524G>C | synonymous_variant | 0.25 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.38 |
rpoC | 762896 | c.-474G>C | upstream_gene_variant | 0.43 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.43 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.44 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.44 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.46 |
rpoC | 762926 | c.-444C>G | upstream_gene_variant | 0.44 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.5 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 0.47 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.5 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.58 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.6 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.55 |
rpoB | 763005 | p.Cys1067Val | missense_variant | 0.53 |
rpoC | 763013 | c.-357C>A | upstream_gene_variant | 0.5 |
rpoB | 763014 | p.Met1070Leu | missense_variant | 0.5 |
rpoB | 763017 | p.Gln1071Glu | missense_variant | 0.5 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763038 | p.Thr1078Ala | missense_variant | 0.52 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.55 |
rpoC | 763058 | c.-312C>G | upstream_gene_variant | 0.55 |
rpoB | 763059 | p.Ile1085Val | missense_variant | 0.57 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.53 |
rpoB | 763075 | p.Thr1090Ile | missense_variant | 0.55 |
rpoB | 763077 | p.Val1091Leu | missense_variant | 0.57 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.55 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.52 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.48 |
rpoC | 763133 | c.-237G>C | upstream_gene_variant | 0.45 |
rpoC | 763148 | c.-222G>C | upstream_gene_variant | 0.35 |
rpoC | 763160 | c.-210G>C | upstream_gene_variant | 0.21 |
rpoB | 763161 | p.Leu1119Ile | missense_variant | 0.21 |
rpoC | 763169 | c.-201A>G | upstream_gene_variant | 0.21 |
rpoB | 763170 | p.Leu1122Met | missense_variant | 0.21 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.28 |
rpoC | 763462 | c.93G>C | synonymous_variant | 0.32 |
rpoC | 763465 | c.96G>A | synonymous_variant | 0.35 |
rpoC | 763483 | c.114G>C | synonymous_variant | 0.37 |
rpoC | 763486 | c.117T>G | synonymous_variant | 0.38 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.38 |
rpoC | 763504 | c.135C>T | synonymous_variant | 0.36 |
rpoC | 763511 | p.Cys48Gly | missense_variant | 0.33 |
rpoC | 763517 | p.Lys50Gln | missense_variant | 0.33 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.32 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.32 |
rpoC | 763532 | p.Thr55Ser | missense_variant | 0.32 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.32 |
rpoC | 763550 | p.Tyr61Ala | missense_variant | 0.35 |
rpoC | 763555 | c.186C>T | synonymous_variant | 0.35 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.45 |
rpoC | 763589 | p.Ile74Val | missense_variant | 0.44 |
rpoC | 763609 | c.240C>G | synonymous_variant | 0.48 |
rpoC | 763614 | c.246_251delGACCCG | disruptive_inframe_deletion | 0.5 |
rpoC | 763622 | p.Ala85Thr | missense_variant | 0.5 |
rpoC | 763627 | c.258_259insTCCTCC | conservative_inframe_insertion | 0.5 |
rpoC | 763630 | c.261G>C | synonymous_variant | 0.52 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.52 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.57 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.57 |
rpoC | 763660 | c.291T>C | synonymous_variant | 0.55 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.53 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.53 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.44 |
rpoC | 763709 | c.340C>T | synonymous_variant | 0.4 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.33 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.33 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.33 |
rpoC | 763727 | p.Leu120Met | missense_variant | 0.33 |
rpoC | 763732 | c.363C>A | synonymous_variant | 0.33 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.36 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.27 |
rpoC | 764387 | c.1018T>C | synonymous_variant | 0.14 |
rpoC | 764405 | c.1036A>C | synonymous_variant | 0.15 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.15 |
rpoC | 764435 | c.1066A>C | synonymous_variant | 0.16 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.16 |
rpoC | 764455 | c.1086G>C | synonymous_variant | 0.18 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.17 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.19 |
rpoC | 764479 | c.1110G>A | synonymous_variant | 0.33 |
rpoC | 764494 | c.1125G>A | synonymous_variant | 0.31 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.31 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.31 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.4 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.34 |
rpoC | 764545 | c.1176C>G | synonymous_variant | 0.28 |
rpoC | 764548 | c.1179G>C | synonymous_variant | 0.35 |
rpoC | 764549 | p.Pro394Thr | missense_variant | 0.29 |
rpoC | 764560 | c.1191T>G | synonymous_variant | 0.3 |
rpoC | 764561 | p.Pro398Ala | missense_variant | 0.3 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.39 |
rpoC | 764572 | c.1203G>C | synonymous_variant | 0.31 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.4 |
rpoC | 764576 | c.1207_1208delTCinsAG | synonymous_variant | 0.34 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.4 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.41 |
rpoC | 764593 | c.1224C>A | synonymous_variant | 0.36 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.35 |
rpoC | 764611 | c.1242G>C | synonymous_variant | 0.39 |
rpoC | 764623 | c.1254C>G | synonymous_variant | 0.14 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.46 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 0.33 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.44 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.41 |
rpoC | 764665 | c.1296C>G | synonymous_variant | 0.41 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.33 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.39 |
rpoC | 764683 | c.1314G>C | synonymous_variant | 0.3 |
rpoC | 764692 | c.1323C>T | synonymous_variant | 0.26 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.32 |
rpoC | 764713 | c.1344G>T | synonymous_variant | 0.22 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.17 |
rpoC | 765050 | p.Ser561Pro | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 778345 | p.Leu46Ile | missense_variant | 0.2 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781754 | c.195G>C | synonymous_variant | 0.31 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.38 |
rpsL | 781766 | c.207C>T | synonymous_variant | 0.41 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.55 |
rpsL | 781805 | c.246G>C | synonymous_variant | 0.55 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.5 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.48 |
rpsL | 781829 | c.270G>C | synonymous_variant | 0.43 |
rpsL | 781832 | c.273T>C | synonymous_variant | 0.43 |
rpsL | 781851 | p.Ile98Val | missense_variant | 0.33 |
rpsL | 781859 | c.300T>C | synonymous_variant | 0.32 |
rpsL | 781860 | p.Ser101Ala | missense_variant | 0.32 |
rpsL | 781865 | c.306G>C | synonymous_variant | 0.29 |
rpsL | 781868 | c.309T>C | synonymous_variant | 0.29 |
rpsL | 781876 | p.Gly106Ala | missense_variant | 0.26 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.25 |
rpsL | 781898 | c.339A>C | synonymous_variant | 0.25 |
rpsL | 781901 | c.342C>T | synonymous_variant | 0.25 |
rpsL | 781907 | c.348T>C | synonymous_variant | 0.26 |
rpsL | 781916 | c.357T>G | synonymous_variant | 0.26 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1472078 | n.233C>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472094 | n.249T>A | non_coding_transcript_exon_variant | 0.28 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472240 | n.395G>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472284 | n.439C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472293 | n.448C>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472333 | n.488G>A | non_coding_transcript_exon_variant | 0.37 |
rrs | 1472338 | n.493A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472349 | n.504A>T | non_coding_transcript_exon_variant | 0.18 |
rrs | 1472379 | n.534T>C | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472434 | n.589_590insC | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472437 | n.592T>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472438 | n.594delC | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472450 | n.605A>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472451 | n.606C>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472456 | n.611T>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472460 | n.615T>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472461 | n.616G>T | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472462 | n.617T>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472467 | n.622G>C | non_coding_transcript_exon_variant | 0.53 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472473 | n.628G>T | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472474 | n.629C>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472476 | n.631A>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472485 | n.640G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472496 | n.651T>G | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472507 | n.662C>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472571 | n.726G>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472581 | n.736A>C | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472606 | n.761C>G | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472623 | n.778A>C | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472645 | n.800G>C | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472660 | n.815T>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472666 | n.821G>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472673 | n.828T>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472675 | n.830T>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472677 | n.832C>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472686 | n.841G>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472687 | n.842A>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472694 | n.849C>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472697 | n.852T>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472714 | n.869A>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472734 | n.889C>T | non_coding_transcript_exon_variant | 0.16 |
rrs | 1472741 | n.896G>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472767 | n.922G>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472793 | n.948A>T | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472803 | n.958T>A | non_coding_transcript_exon_variant | 0.24 |
rrs | 1472812 | n.967A>C | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472887 | n.1042G>C | non_coding_transcript_exon_variant | 0.13 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472982 | n.1137G>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472993 | n.1148G>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1473038 | n.1193A>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1473044 | n.1199C>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473097 | n.1252G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473105 | n.1260G>A | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473122 | n.1277T>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473134 | n.1289T>C | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473147 | n.1302G>A | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473164 | n.1319C>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473226 | n.1381C>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1473269 | n.1424C>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.87 |
rrs | 1473283 | n.1438T>C | non_coding_transcript_exon_variant | 0.87 |
rrs | 1473290 | n.1445C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473291 | n.1446_1447insT | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1473319 | n.1474C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473320 | n.1475G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473324 | n.1479G>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1473698 | n.41G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473707 | n.50T>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473717 | n.60G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473719 | n.62G>C | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473721 | n.64G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473722 | n.65G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473740 | n.83G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1473746 | n.89T>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473747 | n.90C>T | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473750 | n.93C>G | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473752 | n.95G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473844 | n.187C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1473870 | n.213G>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473871 | n.214T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.39 |
rrl | 1473887 | n.230T>C | non_coding_transcript_exon_variant | 0.37 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474177 | n.520T>C | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474184 | n.527C>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474202 | n.545T>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474265 | n.608G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474275 | n.618T>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474280 | n.623C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474281 | n.624A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474286 | n.629C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474287 | n.630T>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474292 | n.635T>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474293 | n.636T>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474295 | n.638C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474296 | n.639T>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474298 | n.642_654delCCGGAGGAGGGTG | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474316 | n.659T>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1474317 | n.660G>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474351 | n.694G>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474359 | n.702C>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474374 | n.717T>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474376 | n.719T>A | non_coding_transcript_exon_variant | 0.76 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1474414 | n.757C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474415 | n.758C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474416 | n.761_784delCACGCGCATACGCGCGTGTGAATA | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474444 | n.787G>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474447 | n.790G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474451 | n.794T>C | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474466 | n.809G>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474476 | n.819C>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474488 | n.831G>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474496 | n.839C>A | non_coding_transcript_exon_variant | 0.76 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.77 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474516 | n.859C>G | non_coding_transcript_exon_variant | 0.81 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474558 | n.901G>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474583 | n.926C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474601 | n.944C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.77 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.77 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.79 |
rrl | 1474709 | n.1053_1056delTGGT | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474717 | n.1060_1061insGTGAG | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474723 | n.1066G>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474770 | n.1113G>A | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474783 | n.1126G>A | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474790 | n.1133C>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474800 | n.1143T>C | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474830 | n.1173A>C | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474831 | n.1174A>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474920 | n.1263G>A | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474935 | n.1278A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474938 | n.1281G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475060 | n.1404delC | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475065 | n.1408G>A | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475067 | n.1410A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475068 | n.1411A>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475073 | n.1416G>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475076 | n.1419C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475078 | n.1421T>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475079 | n.1422T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475081 | n.1424C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475084 | n.1427G>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475104 | n.1447T>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475108 | n.1451C>T | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475111 | n.1454G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475116 | n.1459G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475119 | n.1462C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475120 | n.1463G>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475124 | n.1467A>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1475129 | n.1472G>A | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475171 | n.1514C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475172 | n.1515A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1475508 | n.1851A>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.92 |
rrl | 1475536 | n.1879C>A | non_coding_transcript_exon_variant | 0.92 |
rrl | 1475538 | n.1881T>A | non_coding_transcript_exon_variant | 0.92 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475548 | n.1891C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475549 | n.1892T>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475550 | n.1893A>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475652 | n.1995C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1475659 | n.2002G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475692 | n.2035G>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475751 | n.2094C>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475752 | n.2095C>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.79 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1475776 | n.2119G>C | non_coding_transcript_exon_variant | 0.79 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.87 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.87 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.87 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 0.87 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.87 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475963 | n.2306G>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.68 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475997 | n.2340A>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1475998 | n.2341C>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476025 | n.2368G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476045 | n.2388G>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476046 | n.2389G>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476076 | n.2419A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476079 | n.2422G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476080 | n.2423T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476081 | n.2424A>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476082 | n.2425T>C | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476087 | n.2430C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476095 | n.2438C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476104 | n.2448delG | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476119 | n.2462G>A | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476165 | n.2508T>A | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476442 | n.2785T>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476443 | n.2786G>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476537 | n.2880A>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476540 | n.2883C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476544 | n.2887T>A | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476566 | n.2909A>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476596 | n.2939C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476601 | n.2944G>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476628 | n.2971T>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476630 | n.2973A>T | non_coding_transcript_exon_variant | 0.31 |
inhA | 1674218 | p.Asp6Gly | missense_variant | 0.13 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 0.71 |
rpsA | 1833959 | p.Leu140Val | missense_variant | 0.71 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.71 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.69 |
rpsA | 1833985 | c.444G>C | synonymous_variant | 0.69 |
rpsA | 1834061 | p.Ile174Leu | missense_variant | 0.3 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.3 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834210 | c.669C>T | synonymous_variant | 0.2 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2153970 | p.Asp714Glu | missense_variant | 0.17 |
katG | 2154212 | p.Leu634Ile | missense_variant | 0.13 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.15 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.15 |
PPE35 | 2170066 | p.Ala183Thr | missense_variant | 0.2 |
PPE35 | 2170294 | p.Pro107Ser | missense_variant | 1.0 |
Rv1979c | 2222874 | c.291C>A | synonymous_variant | 0.4 |
Rv1979c | 2223215 | c.-51T>C | upstream_gene_variant | 0.12 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289919 | c.-678C>A | upstream_gene_variant | 0.14 |
kasA | 2518509 | p.Gly132Asp | missense_variant | 1.0 |
folC | 2746764 | c.835C>T | synonymous_variant | 0.13 |
thyA | 3074368 | p.Arg35Leu | missense_variant | 0.29 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474829 | p.Pro275Thr | missense_variant | 0.13 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3642356 | c.822C>T | synonymous_variant | 0.14 |
fbiB | 3642757 | p.Val408Asp | missense_variant | 0.25 |
alr | 3841288 | p.Ile45Val | missense_variant | 0.13 |
clpC1 | 4038866 | p.Lys613Asn | missense_variant | 0.25 |
clpC1 | 4040069 | c.636G>C | synonymous_variant | 0.13 |
clpC1 | 4040123 | c.582G>A | synonymous_variant | 0.13 |
clpC1 | 4040129 | c.576C>G | synonymous_variant | 0.14 |
embC | 4240835 | c.975_985delCTGGTACTACG | frameshift_variant | 0.14 |
embC | 4241484 | p.Val541Ala | missense_variant | 0.18 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4245115 | p.Gly628Val | missense_variant | 0.13 |
embB | 4246593 | p.Arg27His | missense_variant | 0.14 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
ubiA | 4269707 | p.Gly43Cys | missense_variant | 0.15 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407795 | c.408A>G | synonymous_variant | 0.17 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |
gid | 4407980 | p.Pro75Thr | missense_variant | 0.17 |