Run ID: SRR5341267
Sample name:
Date: 04-04-2023 10:11:59
Number of reads: 931098
Percentage reads mapped: 43.46
Strain: lineage3
Drug-resistance: Pre-XDR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage3 | East-African-Indian | CAS | RD750 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
gyrA | 7570 | p.Ala90Val | missense_variant | 1.0 | ofloxacin, moxifloxacin, levofloxacin, fluoroquinolones, ciprofloxacin |
rpoB | 761121 | p.Pro439Ser | missense_variant | 0.27 | rifampicin |
rpoB | 761155 | p.Ser450Phe | missense_variant | 0.58 | rifampicin |
rrs | 1472035 | n.190G>A | non_coding_transcript_exon_variant | 0.79 | streptomycin |
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.93 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
pncA | 2289252 | c.-11A>G | upstream_gene_variant | 1.0 | pyrazinamide |
embB | 4247431 | p.Met306Ile | missense_variant | 1.0 | ethambutol |
gid | 4407851 | c.351delG | frameshift_variant | 1.0 | streptomycin |
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 | 576201 | p.Arg285His | missense_variant | 0.12 |
rpoB | 759746 | c.-61C>T | upstream_gene_variant | 1.0 |
rpoB | 760290 | p.Ile162Val | missense_variant | 0.12 |
rpoB | 760310 | c.504G>C | synonymous_variant | 0.13 |
rpoB | 760318 | p.Ser171Thr | missense_variant | 0.14 |
rpoB | 760331 | c.525G>C | synonymous_variant | 0.14 |
rpoB | 760334 | c.528G>T | synonymous_variant | 0.15 |
rpoB | 760337 | c.531C>G | synonymous_variant | 0.14 |
rpoB | 760340 | c.534G>C | synonymous_variant | 0.14 |
rpoB | 760343 | c.537G>C | synonymous_variant | 0.14 |
rpoB | 761097 | c.1291_1292delAGinsTC | synonymous_variant | 0.12 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.12 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.33 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.33 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.4 |
rpoB | 761150 | c.1344A>T | synonymous_variant | 0.41 |
rpoB | 761159 | c.1353G>A | synonymous_variant | 0.43 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.43 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.44 |
rpoB | 761171 | c.1365C>T | synonymous_variant | 0.47 |
rpoB | 761178 | p.Ser458Thr | missense_variant | 0.44 |
rpoB | 761186 | p.Glu460Asp | missense_variant | 0.44 |
rpoB | 761192 | c.1386C>T | synonymous_variant | 0.47 |
rpoB | 761195 | c.1389G>T | synonymous_variant | 0.43 |
rpoB | 761198 | c.1392G>T | synonymous_variant | 0.42 |
rpoB | 761207 | c.1401C>A | synonymous_variant | 0.39 |
rpoB | 761213 | c.1407G>T | synonymous_variant | 0.38 |
rpoB | 761234 | c.1428G>T | synonymous_variant | 0.36 |
rpoB | 761243 | c.1437G>A | synonymous_variant | 0.33 |
rpoB | 761246 | c.1440C>T | synonymous_variant | 0.33 |
rpoB | 761249 | c.1443A>G | synonymous_variant | 0.34 |
rpoB | 761261 | c.1455G>T | synonymous_variant | 0.34 |
rpoB | 761264 | c.1458C>G | synonymous_variant | 0.35 |
rpoB | 761270 | c.1464C>T | synonymous_variant | 0.28 |
rpoB | 761279 | c.1473C>T | synonymous_variant | 0.2 |
rpoB | 761282 | c.1476C>T | synonymous_variant | 0.2 |
rpoB | 761948 | c.2142G>C | synonymous_variant | 0.2 |
rpoB | 761954 | c.2148C>A | synonymous_variant | 0.2 |
rpoB | 761955 | p.Ile717Phe | missense_variant | 0.23 |
rpoB | 761990 | c.2184G>C | synonymous_variant | 0.34 |
rpoB | 762000 | p.Ser732Asn | missense_variant | 0.36 |
rpoB | 762003 | p.Asn733Gln | missense_variant | 0.36 |
rpoB | 762009 | p.Leu735Met | missense_variant | 0.35 |
rpoB | 762014 | c.2208C>T | synonymous_variant | 0.35 |
rpoB | 762017 | c.2211A>G | synonymous_variant | 0.34 |
rpoB | 762020 | c.2214G>A | synonymous_variant | 0.35 |
rpoB | 762024 | p.Val740Ile | missense_variant | 0.34 |
rpoB | 762029 | c.2223C>G | synonymous_variant | 0.34 |
rpoB | 762038 | c.2232C>T | synonymous_variant | 0.35 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.37 |
rpoB | 762059 | c.2253C>T | synonymous_variant | 0.4 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.4 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.39 |
rpoB | 762084 | p.Ala760Pro | missense_variant | 0.33 |
rpoB | 762095 | c.2289C>T | synonymous_variant | 0.26 |
rpoB | 762101 | c.2295C>T | synonymous_variant | 0.21 |
rpoC | 762434 | c.-936T>G | upstream_gene_variant | 1.0 |
rpoC | 762776 | c.-594C>T | upstream_gene_variant | 0.15 |
rpoB | 762785 | p.Asp993Glu | missense_variant | 0.24 |
rpoB | 762795 | p.Asp997Asn | missense_variant | 0.31 |
rpoC | 762806 | c.-564C>T | upstream_gene_variant | 0.35 |
rpoB | 762814 | p.Met1003Thr | missense_variant | 0.36 |
rpoC | 762818 | c.-552C>G | upstream_gene_variant | 0.4 |
rpoC | 762827 | c.-543G>C | upstream_gene_variant | 0.35 |
rpoC | 762831 | c.-539_-537delAGCinsTCT | upstream_gene_variant | 0.37 |
rpoB | 762840 | p.Pro1012Lys | missense_variant | 0.36 |
rpoB | 762850 | p.Tyr1015Phe | missense_variant | 0.35 |
rpoC | 762857 | c.-513C>T | upstream_gene_variant | 0.34 |
rpoB | 762858 | p.Thr1018Ser | missense_variant | 0.34 |
rpoC | 762863 | c.-507T>G | upstream_gene_variant | 0.33 |
rpoB | 762878 | p.Ile1024Met | missense_variant | 0.33 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.34 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.44 |
rpoB | 762905 | p.Asp1033Glu | missense_variant | 0.47 |
rpoC | 762911 | c.-459C>T | upstream_gene_variant | 0.48 |
rpoC | 762917 | c.-453C>T | upstream_gene_variant | 0.48 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.49 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.56 |
rpoC | 762938 | c.-432G>C | upstream_gene_variant | 0.54 |
rpoC | 762944 | c.-426C>T | upstream_gene_variant | 0.53 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.58 |
rpoC | 762971 | c.-399G>T | upstream_gene_variant | 0.58 |
rpoC | 762983 | c.-387C>T | upstream_gene_variant | 0.61 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.61 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.62 |
rpoB | 763005 | p.Cys1067Val | missense_variant | 0.63 |
rpoC | 763013 | c.-357C>A | upstream_gene_variant | 0.66 |
rpoC | 763022 | c.-348C>A | upstream_gene_variant | 0.64 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.65 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 0.37 |
rpoC | 763053 | c.-317_-315delTTGinsCTC | upstream_gene_variant | 0.61 |
rpoB | 763074 | p.Thr1090Val | missense_variant | 0.5 |
rpoC | 763079 | c.-291C>T | upstream_gene_variant | 0.5 |
rpoC | 763094 | c.-276G>C | upstream_gene_variant | 0.47 |
rpoC | 763103 | c.-267G>A | upstream_gene_variant | 0.39 |
rpoC | 763109 | c.-261C>G | upstream_gene_variant | 0.37 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.34 |
rpoB | 763118 | p.Glu1104Asp | missense_variant | 0.34 |
rpoC | 763124 | c.-246C>T | upstream_gene_variant | 0.34 |
rpoB | 763130 | p.Glu1108Asp | missense_variant | 0.32 |
rpoC | 763136 | c.-234C>T | upstream_gene_variant | 0.34 |
rpoC | 763139 | c.-231C>T | upstream_gene_variant | 0.31 |
rpoC | 763142 | c.-228C>G | upstream_gene_variant | 0.32 |
rpoC | 763160 | c.-210G>T | upstream_gene_variant | 0.22 |
rpoC | 763163 | c.-207C>G | upstream_gene_variant | 0.21 |
rpoC | 763166 | c.-204A>G | upstream_gene_variant | 0.22 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.21 |
rpoC | 763462 | c.93G>C | synonymous_variant | 0.27 |
rpoC | 763471 | c.102C>T | synonymous_variant | 0.24 |
rpoC | 763480 | c.111C>T | synonymous_variant | 0.22 |
rpoC | 763486 | c.117T>G | synonymous_variant | 0.22 |
rpoC | 763495 | c.126G>A | synonymous_variant | 0.23 |
rpoC | 763501 | c.132C>T | synonymous_variant | 0.22 |
rpoC | 763507 | c.138G>T | synonymous_variant | 0.21 |
rpoC | 763513 | c.144C>T | synonymous_variant | 0.21 |
rpoC | 763517 | p.Lys50Arg | missense_variant | 0.21 |
rpoC | 763528 | c.159G>T | synonymous_variant | 0.22 |
rpoC | 763534 | c.165T>C | synonymous_variant | 0.22 |
rpoC | 763537 | c.168C>T | synonymous_variant | 0.21 |
rpoC | 763555 | c.186C>T | synonymous_variant | 0.19 |
rpoC | 763558 | c.189C>T | synonymous_variant | 0.2 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.22 |
rpoC | 763573 | c.204G>T | synonymous_variant | 0.22 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.19 |
rpoC | 763597 | c.228G>A | synonymous_variant | 0.17 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.2 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.25 |
rpoC | 763654 | c.285C>T | synonymous_variant | 0.26 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.26 |
rpoC | 763666 | c.297G>T | synonymous_variant | 0.26 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.26 |
rpoC | 763675 | c.306C>T | synonymous_variant | 0.29 |
rpoC | 763702 | c.333C>G | synonymous_variant | 0.3 |
rpoC | 763705 | c.336G>C | synonymous_variant | 0.27 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.27 |
rpoC | 763711 | c.342G>C | synonymous_variant | 0.26 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.26 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.31 |
rpoC | 763723 | c.354G>C | synonymous_variant | 0.31 |
rpoC | 763732 | c.363C>T | synonymous_variant | 0.31 |
rpoC | 763741 | c.372C>T | synonymous_variant | 0.3 |
rpoC | 763747 | c.378G>A | synonymous_variant | 0.3 |
rpoC | 763769 | p.Tyr134Asn | missense_variant | 0.25 |
rpoC | 763772 | p.Val135Ile | missense_variant | 0.25 |
rpoC | 764332 | c.963G>A | synonymous_variant | 0.17 |
rpoC | 764353 | c.984G>C | synonymous_variant | 0.45 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.46 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 0.42 |
rpoC | 764374 | c.1005C>T | synonymous_variant | 0.43 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 0.44 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 0.45 |
rpoC | 764398 | c.1029G>C | synonymous_variant | 0.45 |
rpoC | 764404 | c.1035C>T | synonymous_variant | 0.43 |
rpoC | 764405 | c.1036_1038delAGGinsCGT | synonymous_variant | 0.43 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 0.42 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.43 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.43 |
rpoC | 764435 | c.1066_1068delAGGinsCGC | synonymous_variant | 0.43 |
rpoC | 764438 | p.Leu357Met | missense_variant | 0.43 |
rpoC | 764443 | c.1074C>T | synonymous_variant | 0.42 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.41 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.4 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.4 |
rpoC | 764455 | c.1086G>T | synonymous_variant | 0.46 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.47 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 0.42 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 0.39 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.32 |
rpoC | 764503 | c.1134G>T | synonymous_variant | 0.15 |
rpoC | 764593 | c.1224C>T | synonymous_variant | 0.29 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.35 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.31 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.31 |
rpoC | 764623 | c.1254C>G | synonymous_variant | 0.29 |
rpoC | 764626 | c.1257C>T | synonymous_variant | 0.29 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 0.26 |
rpoC | 764644 | c.1275G>C | synonymous_variant | 0.26 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.26 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.27 |
rpoC | 764656 | c.1287C>T | synonymous_variant | 0.27 |
rpoC | 764659 | c.1290C>T | synonymous_variant | 0.29 |
rpoC | 764660 | p.Val431Ile | missense_variant | 0.28 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.32 |
rpoC | 764692 | c.1323C>T | synonymous_variant | 0.35 |
rpoC | 764701 | c.1332C>G | synonymous_variant | 0.34 |
rpoC | 764713 | c.1344G>T | synonymous_variant | 0.37 |
rpoC | 764716 | c.1347G>T | synonymous_variant | 0.35 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.16 |
rpoC | 764869 | c.1500C>T | synonymous_variant | 0.19 |
rpoC | 764875 | c.1506C>T | synonymous_variant | 0.19 |
rpoC | 764878 | c.1509C>G | synonymous_variant | 0.17 |
rpoC | 764887 | c.1518G>C | synonymous_variant | 0.16 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.16 |
rpoC | 764896 | c.1527C>T | synonymous_variant | 0.16 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.14 |
rpoC | 764912 | p.Met515Val | missense_variant | 0.13 |
rpoC | 764920 | c.1551G>T | synonymous_variant | 0.14 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 0.18 |
rpoC | 764926 | c.1557C>T | synonymous_variant | 0.16 |
rpoC | 764932 | c.1563C>T | synonymous_variant | 0.19 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.22 |
rpoC | 764952 | p.Val528Ala | missense_variant | 0.21 |
rpoC | 764959 | c.1590G>A | synonymous_variant | 0.2 |
rpoC | 764962 | c.1593G>T | synonymous_variant | 0.19 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.19 |
rpoC | 764995 | c.1626C>A | synonymous_variant | 0.14 |
rpoC | 764998 | c.1629G>C | synonymous_variant | 0.14 |
rpoC | 765038 | p.Ile557Val | missense_variant | 0.12 |
rpoC | 765041 | c.1672T>C | synonymous_variant | 0.12 |
rpoC | 765047 | c.1678T>C | synonymous_variant | 0.12 |
rpoC | 765055 | c.1686C>G | synonymous_variant | 0.11 |
rpoC | 766321 | c.2952C>A | synonymous_variant | 0.17 |
rpoC | 766345 | c.2976T>A | synonymous_variant | 0.16 |
rpoC | 766348 | c.2979A>G | synonymous_variant | 0.16 |
rpoC | 766351 | c.2982C>T | synonymous_variant | 0.16 |
rpoC | 766357 | c.2988C>T | synonymous_variant | 0.16 |
rpoC | 766360 | c.2991C>T | synonymous_variant | 0.17 |
rpoC | 766363 | c.2994G>C | synonymous_variant | 0.17 |
rpoC | 766369 | c.3000C>A | synonymous_variant | 0.16 |
rpoC | 766378 | c.3009C>T | synonymous_variant | 0.17 |
rpoC | 766381 | c.3012C>T | synonymous_variant | 0.18 |
rpoC | 766384 | c.3015A>G | synonymous_variant | 0.18 |
rpoC | 766387 | c.3018C>T | synonymous_variant | 0.18 |
rpoC | 766390 | c.3021C>T | synonymous_variant | 0.18 |
rpoC | 766408 | c.3039C>T | synonymous_variant | 0.19 |
rpoC | 766426 | c.3057C>T | synonymous_variant | 0.19 |
rpoC | 766434 | p.Glu1022Gly | missense_variant | 0.19 |
rpoC | 766441 | c.3072C>T | synonymous_variant | 0.19 |
rpoC | 766456 | c.3087C>G | synonymous_variant | 0.13 |
rpoC | 766459 | c.3090G>T | synonymous_variant | 0.13 |
rpoC | 766462 | c.3093G>C | synonymous_variant | 0.13 |
rpoC | 766466 | p.Glu1033Lys | missense_variant | 0.85 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781763 | c.204C>G | synonymous_variant | 0.11 |
rpsL | 781793 | c.234G>C | synonymous_variant | 0.22 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.19 |
rpsL | 781805 | c.246G>T | synonymous_variant | 0.2 |
rpsL | 781811 | c.252C>T | synonymous_variant | 0.19 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.19 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.19 |
rpsL | 781820 | c.261G>T | synonymous_variant | 0.2 |
rpsL | 781829 | c.270G>C | synonymous_variant | 0.21 |
rpsL | 781832 | c.273T>G | synonymous_variant | 0.21 |
rpsL | 781838 | c.279G>C | synonymous_variant | 0.21 |
rpsL | 781851 | p.Ile98Val | missense_variant | 0.16 |
fbiC | 1304146 | p.Ile406Val | missense_variant | 0.22 |
fbiC | 1304264 | p.Gly445Asp | missense_variant | 1.0 |
Rv1258c | 1406946 | p.Ala132Gly | missense_variant | 0.13 |
Rv1258c | 1406948 | c.391_392delGC | frameshift_variant | 0.14 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471858 | n.13A>G | non_coding_transcript_exon_variant | 0.28 |
rrs | 1471918 | n.73A>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1471922 | n.78delT | non_coding_transcript_exon_variant | 0.71 |
rrs | 1471932 | n.87A>G | non_coding_transcript_exon_variant | 0.69 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.69 |
rrs | 1471938 | n.93T>A | non_coding_transcript_exon_variant | 0.7 |
rrs | 1471972 | n.127T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472029 | n.184C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472030 | n.186_187insTGTG | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472036 | n.192_197delATGTCT | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472057 | n.212C>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472062 | n.217G>T | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.85 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472150 | n.305T>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472225 | n.380C>G | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472278 | n.433C>T | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472279 | n.434T>C | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472297 | n.454_457delTCCG | non_coding_transcript_exon_variant | 0.87 |
rrs | 1472304 | n.459G>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472307 | n.464_471delCTCGGATT | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472325 | n.480G>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472447 | n.602C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472450 | n.605A>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472451 | n.606C>G | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472461 | n.616G>C | non_coding_transcript_exon_variant | 0.78 |
rrs | 1472462 | n.617T>C | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.79 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472836 | n.991G>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472837 | n.992C>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472841 | n.996G>A | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472843 | n.998_999insT | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472847 | n.1003delT | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472850 | n.1005T>C | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472857 | n.1012A>G | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472859 | n.1014G>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472860 | n.1015C>G | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472861 | n.1016G>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1472874 | n.1029C>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472878 | n.1033G>A | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.77 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.89 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.89 |
rrs | 1473005 | n.1160C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1473053 | n.1208T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473089 | n.1244A>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473099 | n.1254T>G | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473100 | n.1255G>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473109 | n.1264T>G | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473110 | n.1265T>C | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473122 | n.1277T>G | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473123 | n.1278A>C | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473287 | n.1442C>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473292 | n.1447G>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473294 | n.1449A>G | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1473700 | n.43G>T | non_coding_transcript_exon_variant | 0.13 |
rrl | 1473718 | n.61G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1473731 | n.74T>G | non_coding_transcript_exon_variant | 0.19 |
rrl | 1473877 | n.220G>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474130 | n.473C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474180 | n.523T>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474181 | n.524C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474182 | n.525C>G | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474185 | n.529delA | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474263 | n.606G>A | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474289 | n.633_647delTTTTCCTCTCCGGAG | non_coding_transcript_exon_variant | 0.84 |
rrl | 1474306 | n.649A>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474351 | n.694G>C | non_coding_transcript_exon_variant | 0.77 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.74 |
rrl | 1474374 | n.717_718insTTG | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474384 | n.727C>T | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1474447 | n.790G>A | non_coding_transcript_exon_variant | 0.19 |
rrl | 1474451 | n.794T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474487 | n.830G>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474497 | n.840G>A | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474506 | n.849C>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474507 | n.850G>C | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474517 | n.860C>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474552 | n.895C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1474628 | n.971C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 0.16 |
rrl | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.72 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1474798 | n.1141C>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474825 | n.1168G>A | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474896 | n.1239A>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1474901 | n.1244A>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1474921 | n.1264C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1474952 | n.1296delC | non_coding_transcript_exon_variant | 0.32 |
rrl | 1474957 | n.1300C>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474958 | n.1301A>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474960 | n.1303C>A | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475120 | n.1463G>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1475171 | n.1514C>T | non_coding_transcript_exon_variant | 0.19 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 0.39 |
rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475480 | n.1823A>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475481 | n.1824C>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475483 | n.1826C>T | non_coding_transcript_exon_variant | 0.37 |
rrl | 1475485 | n.1828C>T | non_coding_transcript_exon_variant | 0.37 |
rrl | 1475499 | n.1842C>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475514 | n.1857G>A | non_coding_transcript_exon_variant | 0.36 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.39 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1475538 | n.1881T>A | non_coding_transcript_exon_variant | 0.39 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1475542 | n.1885A>G | non_coding_transcript_exon_variant | 0.39 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.39 |
rrl | 1475550 | n.1893A>G | non_coding_transcript_exon_variant | 0.37 |
rrl | 1475698 | n.2041G>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1475703 | n.2046A>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1475753 | n.2096C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475757 | n.2101_2104delACCC | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475765 | n.2108A>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475767 | n.2110G>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1475769 | n.2113_2114insGTCG | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.87 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.87 |
rrl | 1475902 | n.2245T>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.87 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.87 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476029 | n.2372A>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476035 | n.2378G>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476091 | n.2434_2435insC | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476100 | n.2443A>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476103 | n.2446C>G | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476113 | n.2456T>G | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476165 | n.2508T>A | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476267 | n.2610G>T | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476269 | n.2612C>G | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476274 | n.2617G>C | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476276 | n.2619C>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476300 | n.2643G>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476523 | n.2867delC | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476573 | n.2916A>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476600 | n.2943A>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476624 | n.2967T>A | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476665 | n.3008T>G | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476666 | n.3009C>T | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476675 | n.3018C>T | non_coding_transcript_exon_variant | 0.38 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.21 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.22 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.23 |
rpsA | 1833862 | c.321G>T | synonymous_variant | 0.26 |
rpsA | 1833893 | p.Ala118Gln | missense_variant | 0.26 |
rpsA | 1833907 | p.Lys122Asn | missense_variant | 0.24 |
rpsA | 1833914 | p.Ala125Pro | missense_variant | 0.24 |
rpsA | 1833919 | c.378C>T | synonymous_variant | 0.24 |
rpsA | 1833921 | p.Lys127Thr | missense_variant | 0.24 |
rpsA | 1833925 | c.384C>T | synonymous_variant | 0.25 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.29 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.37 |
rpsA | 1833967 | c.426C>T | synonymous_variant | 0.35 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.35 |
rpsA | 1833976 | c.435C>T | synonymous_variant | 0.33 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.33 |
rpsA | 1833988 | c.447C>G | synonymous_variant | 0.28 |
rpsA | 1833991 | c.450C>T | synonymous_variant | 0.28 |
rpsA | 1833994 | c.453G>C | synonymous_variant | 0.27 |
rpsA | 1833997 | c.456G>C | synonymous_variant | 0.27 |
rpsA | 1834000 | c.459G>T | synonymous_variant | 0.28 |
rpsA | 1834009 | c.468C>T | synonymous_variant | 0.28 |
rpsA | 1834012 | c.471G>T | synonymous_variant | 0.27 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.3 |
rpsA | 1834024 | c.483G>C | synonymous_variant | 0.3 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.3 |
rpsA | 1834040 | p.Lys167Gln | missense_variant | 0.3 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.29 |
rpsA | 1834090 | c.549G>C | synonymous_variant | 0.23 |
rpsA | 1834093 | c.552G>T | synonymous_variant | 0.2 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.13 |
rpsA | 1834189 | c.648G>T | synonymous_variant | 0.15 |
rpsA | 1834192 | c.651C>T | synonymous_variant | 0.15 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 0.17 |
rpsA | 1834213 | c.672G>A | synonymous_variant | 0.22 |
rpsA | 1834234 | c.693G>T | synonymous_variant | 0.19 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.19 |
rpsA | 1834246 | c.705G>T | synonymous_variant | 0.19 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.21 |
rpsA | 1834252 | c.711C>T | synonymous_variant | 0.21 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.23 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.23 |
rpsA | 1834294 | c.753G>T | synonymous_variant | 0.46 |
rpsA | 1834297 | c.756C>T | synonymous_variant | 0.46 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.48 |
rpsA | 1834318 | c.777C>T | synonymous_variant | 0.46 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.44 |
rpsA | 1834333 | p.Asp264Glu | missense_variant | 0.42 |
rpsA | 1834340 | p.Met267Leu | missense_variant | 0.39 |
rpsA | 1834343 | p.Asp268Asn | missense_variant | 0.39 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.38 |
rpsA | 1834354 | c.813G>C | synonymous_variant | 0.37 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.36 |
rpsA | 1834360 | c.819G>T | synonymous_variant | 0.35 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.35 |
rpsA | 1834366 | c.825A>C | synonymous_variant | 0.36 |
rpsA | 1834369 | c.828C>G | synonymous_variant | 0.36 |
rpsA | 1834375 | c.834G>T | synonymous_variant | 0.39 |
rpsA | 1834396 | c.855G>C | synonymous_variant | 0.44 |
rpsA | 1834397 | p.His286Val | missense_variant | 0.44 |
rpsA | 1834417 | c.876G>A | synonymous_variant | 0.4 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.38 |
rpsA | 1834429 | c.888C>T | synonymous_variant | 0.32 |
rpsA | 1834432 | c.891G>C | synonymous_variant | 0.31 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.22 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.22 |
rpsA | 1834483 | c.942G>A | synonymous_variant | 0.26 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.27 |
rpsA | 1834504 | c.963G>T | synonymous_variant | 0.27 |
rpsA | 1834683 | p.Ala381Gly | missense_variant | 0.14 |
rpsA | 1834688 | c.1147_1149delAGTinsTCC | synonymous_variant | 0.14 |
rpsA | 1834720 | c.1179C>G | synonymous_variant | 0.13 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289047 | c.195C>T | synonymous_variant | 1.0 |
pncA | 2289365 | c.-125delC | upstream_gene_variant | 1.0 |
kasA | 2518717 | c.603C>A | synonymous_variant | 0.13 |
ahpC | 2726105 | c.-88G>A | upstream_gene_variant | 1.0 |
ahpC | 2726341 | p.Val50Gly | missense_variant | 0.21 |
ald | 3086739 | c.-81G>A | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339559 | p.Thr148Ser | missense_variant | 0.15 |
fprA | 3473820 | c.-187C>A | upstream_gene_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.14 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.19 |
clpC1 | 4039769 | c.934_936delCTCinsTTG | synonymous_variant | 0.23 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.25 |
clpC1 | 4039784 | c.921C>T | synonymous_variant | 0.25 |
clpC1 | 4039793 | c.912C>G | synonymous_variant | 0.26 |
clpC1 | 4039799 | c.906C>T | synonymous_variant | 0.27 |
clpC1 | 4039802 | c.903G>A | synonymous_variant | 0.26 |
clpC1 | 4039811 | c.894C>A | synonymous_variant | 0.37 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 0.36 |
clpC1 | 4039820 | c.885T>C | synonymous_variant | 0.36 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.38 |
clpC1 | 4039832 | c.873C>G | synonymous_variant | 0.38 |
clpC1 | 4039838 | p.Leu289Ile | missense_variant | 0.4 |
clpC1 | 4039847 | c.858C>T | synonymous_variant | 0.47 |
clpC1 | 4039871 | p.Thr278Gln | missense_variant | 0.53 |
clpC1 | 4039877 | c.828C>T | synonymous_variant | 0.52 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.47 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.43 |
clpC1 | 4039925 | c.780C>T | synonymous_variant | 0.35 |
clpC1 | 4039929 | c.775_776delAGinsTC | synonymous_variant | 0.32 |
clpC1 | 4039937 | c.768G>C | synonymous_variant | 0.28 |
clpC1 | 4039946 | c.759A>C | synonymous_variant | 0.26 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.24 |
clpC1 | 4039955 | c.750G>T | synonymous_variant | 0.19 |
clpC1 | 4039958 | p.Thr249Ser | missense_variant | 0.17 |
clpC1 | 4039964 | c.741C>T | synonymous_variant | 0.16 |
clpC1 | 4039973 | c.732C>T | synonymous_variant | 0.17 |
clpC1 | 4039979 | c.726C>G | synonymous_variant | 0.18 |
clpC1 | 4039988 | c.717C>G | synonymous_variant | 0.15 |
embC | 4240009 | c.147G>A | synonymous_variant | 1.0 |
embC | 4242075 | p.Arg738Gln | missense_variant | 1.0 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243971 | p.Gly247* | stop_gained | 0.17 |
aftB | 4268100 | p.Ala246Val | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |