Run ID: SRR1735596
Sample name:
Date: 03-04-2023 17:57:53
Number of reads: 90437
Percentage reads mapped: 2.63
Strain: lineage4.9
Drug-resistance: RR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage4 | Euro-American | LAM;T;S;X;H | None | 1.0 |
lineage4.9 | Euro-American (H37Rv-like) | T1 | None | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpoB | 761127 | p.Ser441Ala | missense_variant | 1.0 | rifampicin |
rpoB | 761196 | p.Leu464Met | missense_variant | 1.0 | rifampicin |
rrs | 1472733 | n.888G>A | non_coding_transcript_exon_variant | 0.53 | streptomycin |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
rpoB | 760997 | c.1191G>C | synonymous_variant | 1.0 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 1.0 |
rpoB | 761021 | c.1215G>C | synonymous_variant | 0.4 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 1.0 |
rpoB | 761030 | c.1224G>C | synonymous_variant | 0.71 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 1.0 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.8 |
rpoB | 761054 | c.1248G>C | synonymous_variant | 1.0 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.75 |
rpoB | 761060 | c.1254C>G | synonymous_variant | 1.0 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.44 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 1.0 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 1.0 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.36 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 1.0 |
rpoB | 761132 | c.1326G>T | synonymous_variant | 1.0 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 1.0 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 1.0 |
rpoB | 761154 | p.Ser450Asn | missense_variant | 0.59 |
rpoB | 761159 | c.1353G>C | synonymous_variant | 1.0 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 1.0 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 1.0 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 1.0 |
rpoB | 761193 | p.Gly463Ser | missense_variant | 0.84 |
rpoB | 761213 | c.1407G>C | synonymous_variant | 1.0 |
rpoB | 761217 | p.Pro471Thr | missense_variant | 0.81 |
rpoB | 761231 | c.1425C>G | synonymous_variant | 1.0 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 1.0 |
rpoB | 761243 | c.1437G>C | synonymous_variant | 0.62 |
rpoB | 761360 | c.1554T>C | synonymous_variant | 1.0 |
rpoB | 761362 | p.Ser519Thr | missense_variant | 1.0 |
rpoB | 761373 | p.Val523His | missense_variant | 1.0 |
rpoB | 761930 | c.2124G>C | synonymous_variant | 0.6 |
rpoB | 761937 | p.Lys711Gln | missense_variant | 0.71 |
rpoB | 761945 | c.2139G>C | synonymous_variant | 0.71 |
rpoB | 761951 | c.2145G>C | synonymous_variant | 0.88 |
rpoB | 761955 | p.Ile717Phe | missense_variant | 0.9 |
rpoB | 761961 | p.Pro719Thr | missense_variant | 0.89 |
rpoB | 761974 | p.His723Leu | missense_variant | 0.91 |
rpoB | 761990 | c.2184G>C | synonymous_variant | 0.83 |
rpoB | 761997 | p.Leu731Ile | missense_variant | 0.7 |
rpoB | 762003 | p.Asn733Gln | missense_variant | 0.75 |
rpoB | 762009 | p.Leu735Val | missense_variant | 0.82 |
rpoB | 762016 | p.Glu737Ala | missense_variant | 0.75 |
rpoB | 762024 | p.Val740Met | missense_variant | 0.83 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.92 |
rpoB | 762057 | p.Ile751Val | missense_variant | 0.92 |
rpoB | 762062 | c.2256T>C | synonymous_variant | 0.92 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.92 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.6 |
rpoB | 762085 | p.Ala760Asp | missense_variant | 0.38 |
rpoB | 762089 | c.2283G>A | synonymous_variant | 0.38 |
rpoB | 762110 | c.2304G>C | synonymous_variant | 0.8 |
rpoB | 762114 | p.Ile770Val | missense_variant | 1.0 |
rpoB | 762122 | p.Asp772Glu | missense_variant | 1.0 |
rpoB | 762125 | c.2319G>A | synonymous_variant | 1.0 |
rpoB | 762126 | p.Val774Ser | missense_variant | 1.0 |
rpoB | 762134 | c.2328C>T | synonymous_variant | 0.8 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 1.0 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 1.0 |
rpoB | 762156 | p.Val784Ile | missense_variant | 1.0 |
rpoB | 762173 | c.2367G>A | synonymous_variant | 0.5 |
rpoB | 762176 | c.2370T>C | synonymous_variant | 1.0 |
rpoB | 762177 | p.Arg791Thr | missense_variant | 0.67 |
rpoB | 762180 | p.Asp792Thr | missense_variant | 0.33 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 1.0 |
rpoB | 762191 | c.2385C>T | synonymous_variant | 0.44 |
rpoB | 762194 | c.2388G>C | synonymous_variant | 1.0 |
rpoB | 762206 | c.2400C>G | synonymous_variant | 0.33 |
rpoB | 762212 | c.2406G>C | synonymous_variant | 0.44 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.67 |
rpoB | 762239 | c.2433G>A | synonymous_variant | 0.57 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 1.0 |
rpoB | 762248 | c.2442G>C | synonymous_variant | 0.43 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 1.0 |
rpoB | 762266 | c.2460T>C | synonymous_variant | 1.0 |
rpoB | 762287 | c.2481C>T | synonymous_variant | 1.0 |
rpoB | 762293 | c.2487T>C | synonymous_variant | 1.0 |
rpoB | 762881 | p.Met1025Ile | missense_variant | 1.0 |
rpoC | 762887 | c.-483G>C | upstream_gene_variant | 1.0 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.86 |
rpoC | 762926 | c.-444C>G | upstream_gene_variant | 0.91 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 1.0 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 0.94 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 1.0 |
rpoC | 762980 | c.-390T>C | upstream_gene_variant | 0.95 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 1.0 |
rpoC | 762995 | c.-375G>C | upstream_gene_variant | 1.0 |
rpoB | 763005 | p.Cys1067Val | missense_variant | 1.0 |
rpoB | 763014 | p.Met1070Leu | missense_variant | 1.0 |
rpoB | 763017 | p.Gln1071Glu | missense_variant | 1.0 |
rpoC | 763022 | c.-348C>T | upstream_gene_variant | 0.31 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.58 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoB | 763038 | p.Thr1078Ala | missense_variant | 1.0 |
rpoC | 763043 | c.-327G>C | upstream_gene_variant | 1.0 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 1.0 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 1.0 |
rpoB | 763077 | p.Val1091Thr | missense_variant | 1.0 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 1.0 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 1.0 |
rpoB | 763119 | p.Asn1105Asp | missense_variant | 1.0 |
rpoC | 763442 | p.Tyr25His | missense_variant | 1.0 |
rpoC | 763456 | c.87A>G | synonymous_variant | 1.0 |
rpoC | 763462 | c.93G>C | synonymous_variant | 1.0 |
rpoC | 763468 | c.99G>C | synonymous_variant | 1.0 |
rpoC | 763483 | c.114G>C | synonymous_variant | 1.0 |
rpoC | 763486 | c.117T>C | synonymous_variant | 1.0 |
rpoC | 763492 | c.123G>C | synonymous_variant | 1.0 |
rpoC | 763507 | c.138G>C | synonymous_variant | 1.0 |
rpoC | 763528 | c.159G>C | synonymous_variant | 1.0 |
rpoC | 763531 | c.162G>C | synonymous_variant | 1.0 |
rpoC | 763534 | c.165T>C | synonymous_variant | 1.0 |
rpoC | 763537 | c.168C>G | synonymous_variant | 1.0 |
rpoC | 763546 | c.177A>G | synonymous_variant | 1.0 |
rpoC | 763550 | p.Tyr61Ala | missense_variant | 1.0 |
rpoC | 763570 | c.201G>C | synonymous_variant | 1.0 |
rpoC | 763578 | p.Phe70Tyr | missense_variant | 1.0 |
rpoC | 763585 | c.216C>G | synonymous_variant | 1.0 |
rpoC | 763589 | p.Ile74Val | missense_variant | 1.0 |
rpoC | 763606 | c.237C>A | synonymous_variant | 1.0 |
rpoC | 763615 | c.246G>C | synonymous_variant | 1.0 |
rpoC | 763618 | c.249C>T | synonymous_variant | 1.0 |
rpoC | 763622 | p.Ala85Ser | missense_variant | 1.0 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.97 |
rpoC | 763642 | c.273G>C | synonymous_variant | 1.0 |
rpoC | 763647 | p.Gly93Ala | missense_variant | 0.91 |
rpoC | 763655 | p.Glu96Lys | missense_variant | 0.9 |
rpoC | 763660 | c.291T>C | synonymous_variant | 1.0 |
rpoC | 763669 | c.300C>G | synonymous_variant | 0.89 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.89 |
rpoC | 763708 | c.339G>C | synonymous_variant | 1.0 |
rpoC | 763714 | c.345G>C | synonymous_variant | 1.0 |
rpoC | 763717 | c.348T>C | synonymous_variant | 1.0 |
rpoC | 763723 | c.354G>C | synonymous_variant | 1.0 |
rpoC | 763724 | p.Asp119Asn | missense_variant | 1.0 |
rpoC | 763729 | c.360G>C | synonymous_variant | 1.0 |
rpoC | 763732 | c.363C>G | synonymous_variant | 1.0 |
rpoC | 763735 | c.366G>C | synonymous_variant | 1.0 |
rpoC | 763751 | p.Ile128Val | missense_variant | 1.0 |
rpoC | 763765 | c.396T>G | synonymous_variant | 0.8 |
rpoC | 763772 | p.Val135Met | missense_variant | 1.0 |
rpoC | 763775 | p.Ile136Val | missense_variant | 0.4 |
rpoC | 763781 | p.Ser138Glu | missense_variant | 1.0 |
rpoC | 764347 | c.978G>C | synonymous_variant | 0.67 |
rpoC | 764353 | c.984G>T | synonymous_variant | 0.67 |
rpoC | 764359 | c.990C>G | synonymous_variant | 1.0 |
rpoC | 764371 | c.1002G>C | synonymous_variant | 1.0 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 1.0 |
rpoC | 764380 | c.1011G>C | synonymous_variant | 1.0 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 1.0 |
rpoC | 764404 | c.1035C>T | synonymous_variant | 0.5 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 1.0 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 1.0 |
rpoC | 764424 | p.Asn352Thr | missense_variant | 1.0 |
rpoC | 764428 | c.1059G>A | synonymous_variant | 1.0 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 1.0 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 1.0 |
rpoC | 764435 | c.1066_1068delAGGinsCGA | synonymous_variant | 1.0 |
rpoC | 764441 | p.Ile358Leu | missense_variant | 1.0 |
rpoC | 764446 | p.Asp359Glu | missense_variant | 1.0 |
rpoC | 764452 | c.1083T>C | synonymous_variant | 0.6 |
rpoC | 764455 | c.1086G>C | synonymous_variant | 1.0 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 1.0 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 1.0 |
rpoC | 764485 | c.1116G>C | synonymous_variant | 1.0 |
rpoC | 764491 | c.1122G>T | synonymous_variant | 1.0 |
rpoC | 764497 | p.Glu376Asp | missense_variant | 0.69 |
rpoC | 764498 | p.Ser377Ala | missense_variant | 0.57 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 1.0 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 1.0 |
rpoC | 764512 | c.1143G>C | synonymous_variant | 0.43 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 1.0 |
rpoC | 764536 | c.1167G>C | synonymous_variant | 1.0 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.6 |
rpoC | 764543 | p.Thr392Ala | missense_variant | 0.42 |
rpoC | 764548 | c.1179G>C | synonymous_variant | 1.0 |
rpoC | 764549 | p.Pro394Val | missense_variant | 0.56 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.72 |
rpoC | 764572 | c.1203G>C | synonymous_variant | 0.55 |
rpoC | 764573 | p.Leu402Met | missense_variant | 0.45 |
rpoC | 764578 | c.1209C>G | synonymous_variant | 0.43 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 1.0 |
rpoC | 764582 | p.Leu405Met | missense_variant | 1.0 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.43 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 1.0 |
rpoC | 764611 | c.1242G>C | synonymous_variant | 1.0 |
rpoC | 764620 | c.1251G>C | synonymous_variant | 0.57 |
rpoC | 764623 | c.1254C>G | synonymous_variant | 0.56 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 1.0 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 0.52 |
rpoC | 764644 | c.1275G>C | synonymous_variant | 0.66 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.34 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 1.0 |
rpoC | 764651 | c.1282_1284delTCGinsAGC | synonymous_variant | 0.65 |
rpoC | 764656 | c.1287C>T | synonymous_variant | 0.34 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.97 |
rpoC | 764671 | c.1302G>C | synonymous_variant | 0.5 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.5 |
rpoC | 764678 | p.Lys437Gln | missense_variant | 0.5 |
rpoC | 764683 | c.1314G>C | synonymous_variant | 0.62 |
rpoC | 764703 | p.Lys445Ser | missense_variant | 0.54 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 1.0 |
rpoC | 764713 | c.1344G>C | synonymous_variant | 1.0 |
rpoC | 764731 | c.1362G>C | synonymous_variant | 1.0 |
rpoC | 764737 | c.1368G>C | synonymous_variant | 1.0 |
rpoC | 764749 | c.1380G>C | synonymous_variant | 0.75 |
rpoC | 764755 | p.Asp462Glu | missense_variant | 1.0 |
rpoC | 764774 | p.Ile469Val | missense_variant | 1.0 |
rpoC | 764780 | p.Ser471Ala | missense_variant | 1.0 |
rpoC | 764797 | c.1428G>C | synonymous_variant | 1.0 |
rpoC | 765888 | p.Phe840Tyr | missense_variant | 1.0 |
rpoC | 765903 | p.Thr845Ser | missense_variant | 1.0 |
rpoC | 765907 | c.2538G>C | synonymous_variant | 1.0 |
rpoC | 765923 | p.Asn852Ala | missense_variant | 1.0 |
rpoC | 765937 | c.2568T>C | synonymous_variant | 1.0 |
rpoC | 765940 | c.2571A>T | synonymous_variant | 1.0 |
rpoC | 765947 | c.2578T>C | synonymous_variant | 1.0 |
rpoC | 765958 | c.2589C>G | synonymous_variant | 1.0 |
rpoC | 765962 | c.2593T>C | synonymous_variant | 1.0 |
rpoC | 765967 | c.2598C>T | synonymous_variant | 1.0 |
rpoC | 765988 | c.2619G>C | synonymous_variant | 1.0 |
rpoC | 765991 | c.2622C>G | synonymous_variant | 1.0 |
rpoC | 765994 | c.2625A>T | synonymous_variant | 1.0 |
rpoC | 766003 | c.2634G>C | synonymous_variant | 1.0 |
rpoC | 766009 | c.2640G>C | synonymous_variant | 1.0 |
rpoC | 766021 | c.2652G>C | synonymous_variant | 1.0 |
rpoC | 766027 | c.2658G>C | synonymous_variant | 1.0 |
rpoC | 766034 | p.His889Glu | missense_variant | 1.0 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 1.0 |
rplC | 800618 | c.-191T>C | upstream_gene_variant | 1.0 |
rplC | 800632 | c.-177_-176delATinsTC | upstream_gene_variant | 1.0 |
rplC | 800639 | c.-170C>G | upstream_gene_variant | 1.0 |
rplC | 800645 | c.-164C>G | upstream_gene_variant | 1.0 |
rplC | 800648 | c.-161A>G | upstream_gene_variant | 1.0 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 1.0 |
rplC | 800667 | c.-142_-140delTCGinsAGC | upstream_gene_variant | 1.0 |
rplC | 800672 | c.-137G>C | upstream_gene_variant | 1.0 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 1.0 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 1.0 |
rplC | 800715 | c.-94A>G | upstream_gene_variant | 1.0 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 1.0 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 1.0 |
rplC | 800729 | c.-80G>C | upstream_gene_variant | 1.0 |
rplC | 800733 | c.-76A>G | upstream_gene_variant | 1.0 |
rplC | 800738 | c.-71T>C | upstream_gene_variant | 1.0 |
rplC | 800742 | c.-67G>T | upstream_gene_variant | 1.0 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472122 | n.277G>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472123 | n.278A>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472124 | n.279C>T | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472151 | n.306C>A | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472155 | n.310C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472160 | n.315C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472258 | n.413A>G | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472259 | n.414C>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472484 | n.639A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472496 | n.651T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472507 | n.662C>G | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472513 | n.668T>C | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472517 | n.672T>A | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472518 | n.673G>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472537 | n.692C>T | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472544 | n.699C>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472545 | n.700A>T | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472549 | n.704G>A | non_coding_transcript_exon_variant | 0.3 |
rrs | 1472566 | n.721G>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472571 | n.726G>C | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472579 | n.734G>C | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472580 | n.735C>T | non_coding_transcript_exon_variant | 0.39 |
rrs | 1472581 | n.736A>T | non_coding_transcript_exon_variant | 0.98 |
rrs | 1472598 | n.753A>C | non_coding_transcript_exon_variant | 0.59 |
rrs | 1472599 | n.754G>T | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472616 | n.771G>A | non_coding_transcript_exon_variant | 0.52 |
rrs | 1472655 | n.810G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472658 | n.813G>A | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472690 | n.845C>A | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472697 | n.852T>C | non_coding_transcript_exon_variant | 0.31 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472716 | n.871C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472742 | n.897C>T | non_coding_transcript_exon_variant | 0.51 |
rrs | 1472744 | n.899A>G | non_coding_transcript_exon_variant | 0.55 |
rrs | 1472781 | n.936C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1472958 | n.1113A>G | non_coding_transcript_exon_variant | 0.61 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472974 | n.1129A>G | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472988 | n.1143T>C | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.9 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473080 | n.1235C>T | non_coding_transcript_exon_variant | 0.32 |
rrs | 1473081 | n.1236C>T | non_coding_transcript_exon_variant | 0.34 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.98 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.99 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.33 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.97 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473130 | n.1285G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473148 | n.1303G>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1473163 | n.1318C>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.56 |
rrs | 1473172 | n.1327T>G | non_coding_transcript_exon_variant | 0.41 |
rrs | 1473173 | n.1328C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473221 | n.1376C>T | non_coding_transcript_exon_variant | 0.74 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1473276 | n.1431A>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473277 | n.1432G>A | non_coding_transcript_exon_variant | 0.35 |
rrs | 1473300 | n.1455C>T | non_coding_transcript_exon_variant | 0.29 |
rrs | 1473301 | n.1456T>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473314 | n.1469A>G | non_coding_transcript_exon_variant | 0.34 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1473319 | n.1474C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474181 | n.524C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474197 | n.540C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474199 | n.542G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474200 | n.545delT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474272 | n.615C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474275 | n.618T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474280 | n.623C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474281 | n.624A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474284 | n.631_633delCCT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474293 | n.637_651delCCTCTCCGGAGGAGG | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474316 | n.659T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474317 | n.660G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474355 | n.698A>G | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474393 | n.736A>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474402 | n.745T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474448 | n.791T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474467 | n.810A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474498 | n.841G>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1474505 | n.848C>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.84 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474527 | n.870T>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474542 | n.885A>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.59 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474634 | n.977T>G | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474636 | n.979A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474640 | n.983C>T | non_coding_transcript_exon_variant | 0.4 |
rrl | 1474658 | n.1001A>G | non_coding_transcript_exon_variant | 0.43 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1474677 | n.1020A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474692 | n.1035G>A | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474709 | n.1052G>A | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474734 | n.1077G>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474780 | n.1123C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.66 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474802 | n.1145T>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474831 | n.1174A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474832 | n.1175A>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474901 | n.1244A>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474933 | n.1276A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474934 | n.1277C>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475026 | n.1369G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475031 | n.1374G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475059 | n.1403_1404insTA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475062 | n.1405A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475065 | n.1409_1411delCAA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475080 | n.1425_1426delCC | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475104 | n.1447T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475124 | n.1467A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475171 | n.1514C>T | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475172 | n.1515A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475672 | n.2015C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475673 | n.2016T>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475686 | n.2029C>G | non_coding_transcript_exon_variant | 0.53 |
rrl | 1475696 | n.2039T>C | non_coding_transcript_exon_variant | 0.61 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475703 | n.2046A>G | non_coding_transcript_exon_variant | 0.63 |
rrl | 1475715 | n.2058G>C | non_coding_transcript_exon_variant | 0.52 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475751 | n.2094C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475752 | n.2095C>T | non_coding_transcript_exon_variant | 0.31 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1475777 | n.2120A>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.53 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.54 |
rrl | 1475898 | n.2241A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475906 | n.2249C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475937 | n.2280A>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475945 | n.2288C>A | non_coding_transcript_exon_variant | 0.76 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475993 | n.2336C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475995 | n.2338G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475998 | n.2341C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476000 | n.2343G>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476032 | n.2375C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476040 | n.2383C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476047 | n.2390G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476135 | n.2478T>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476141 | n.2484A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476153 | n.2496T>C | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476164 | n.2507A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476165 | n.2508T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476195 | n.2538C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476196 | n.2539C>A | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476204 | n.2547C>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1476207 | n.2550T>C | non_coding_transcript_exon_variant | 0.28 |
rrl | 1476210 | n.2553G>T | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476211 | n.2554G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476212 | n.2555T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476215 | n.2558C>A | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.31 |
rrl | 1476225 | n.2568T>G | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476227 | n.2570C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476229 | n.2572C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476251 | n.2594T>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.52 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476280 | n.2623A>C | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476293 | n.2636C>T | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476294 | n.2637A>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476295 | n.2638C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476296 | n.2639C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476297 | n.2640C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476301 | n.2644A>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1476302 | n.2645G>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476313 | n.2656G>A | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476332 | n.2675G>C | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476338 | n.2681C>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476353 | n.2696G>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476369 | n.2712C>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476383 | n.2726T>A | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476425 | n.2768G>T | non_coding_transcript_exon_variant | 0.54 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.87 |
rrl | 1476429 | n.2772A>C | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476481 | n.2824T>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.99 |
rrl | 1476513 | n.2856G>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1476514 | n.2857C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476517 | n.2860C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476519 | n.2862C>G | non_coding_transcript_exon_variant | 0.3 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476542 | n.2885T>C | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476567 | n.2910C>T | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476594 | n.2937C>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476600 | n.2943A>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476603 | n.2946G>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1476607 | n.2950C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476608 | n.2951C>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1833688 | c.147C>T | synonymous_variant | 1.0 |
rpsA | 1833694 | c.153G>C | synonymous_variant | 1.0 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 1.0 |
rpsA | 1833732 | p.Pro64Leu | missense_variant | 1.0 |
rpsA | 1833736 | c.195C>T | synonymous_variant | 1.0 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 1.0 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 1.0 |
rpsA | 1833886 | c.345C>T | synonymous_variant | 1.0 |
rpsA | 1833905 | p.Lys122Glu | missense_variant | 1.0 |
rpsA | 1833912 | p.Glu124Gly | missense_variant | 1.0 |
rpsA | 1833915 | p.Ala125Val | missense_variant | 1.0 |
rpsA | 1833921 | p.Lys127Thr | missense_variant | 1.0 |
rpsA | 1833926 | p.Thr129Ser | missense_variant | 1.0 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.86 |
rpsA | 1833952 | c.411C>T | synonymous_variant | 0.77 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 0.89 |
rpsA | 1833961 | c.420C>G | synonymous_variant | 0.71 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 1.0 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 1.0 |
rpsA | 1833994 | c.453G>C | synonymous_variant | 1.0 |
rpsA | 1834009 | c.468C>T | synonymous_variant | 0.91 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 1.0 |
rpsA | 1834015 | c.474G>T | synonymous_variant | 1.0 |
rpsA | 1834024 | c.483G>C | synonymous_variant | 1.0 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 0.73 |
rpsA | 1834040 | p.Lys167Arg | missense_variant | 1.0 |
rpsA | 1834046 | p.Ile169Leu | missense_variant | 0.73 |
rpsA | 1834054 | c.513C>G | synonymous_variant | 1.0 |
rpsA | 1834063 | c.522C>T | synonymous_variant | 0.73 |
rpsA | 1834093 | c.552G>C | synonymous_variant | 1.0 |
rpsA | 1834096 | c.555G>C | synonymous_variant | 0.82 |
rpsA | 1834114 | c.573G>C | synonymous_variant | 1.0 |
rpsA | 1834135 | c.594G>C | synonymous_variant | 1.0 |
rpsA | 1834140 | p.Ser200Thr | missense_variant | 1.0 |
rpsA | 1834195 | c.654G>C | synonymous_variant | 1.0 |
rpsA | 1834210 | c.669C>T | synonymous_variant | 0.67 |
rpsA | 1834213 | c.672G>C | synonymous_variant | 0.67 |
rpsA | 1834219 | c.678C>G | synonymous_variant | 0.67 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.67 |
rpsA | 1834225 | c.684C>G | synonymous_variant | 0.67 |
rpsA | 1834228 | c.687C>T | synonymous_variant | 0.83 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.83 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 1.0 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.31 |
rpsA | 1834246 | c.705G>C | synonymous_variant | 0.92 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 1.0 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 1.0 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 1.0 |
rpsA | 1834285 | c.744G>C | synonymous_variant | 0.68 |
rpsA | 1834294 | c.753G>C | synonymous_variant | 1.0 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 1.0 |
rpsA | 1834303 | c.762T>C | synonymous_variant | 0.68 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 1.0 |
rpsA | 1834307 | p.Asp256Lys | missense_variant | 1.0 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.32 |
rpsA | 1834318 | c.777C>G | synonymous_variant | 0.68 |
rpsA | 1834327 | c.786G>C | synonymous_variant | 1.0 |
rpsA | 1834330 | c.789C>G | synonymous_variant | 0.62 |
rpsA | 1834340 | p.Met267Phe | missense_variant | 0.67 |
rpsA | 1834345 | c.804C>T | synonymous_variant | 0.33 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 1.0 |
rpsA | 1834354 | c.813G>C | synonymous_variant | 1.0 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 1.0 |
rpsA | 1834360 | c.819G>C | synonymous_variant | 1.0 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 1.0 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 1.0 |
rpsA | 1834375 | c.834G>C | synonymous_variant | 0.29 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 1.0 |
rpsA | 1834384 | c.843A>G | synonymous_variant | 0.71 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.31 |
rpsA | 1834395 | p.Arg285Gln | missense_variant | 1.0 |
rpsA | 1834397 | p.His286Ala | missense_variant | 1.0 |
rpsA | 1834408 | c.867C>G | synonymous_variant | 0.57 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 1.0 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.8 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 1.0 |
rpsA | 1834427 | p.Ile296Val | missense_variant | 1.0 |
rpsA | 1834432 | c.891G>T | synonymous_variant | 0.75 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 1.0 |
rpsA | 1834451 | c.910_912delTTGinsCTC | synonymous_variant | 1.0 |
rpsA | 1834456 | c.915T>C | synonymous_variant | 0.8 |
rpsA | 1834459 | c.918G>C | synonymous_variant | 1.0 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 1.0 |
rpsA | 1834468 | c.927A>C | synonymous_variant | 1.0 |
rpsA | 1834474 | c.933C>G | synonymous_variant | 0.83 |
rpsA | 1834477 | c.936C>T | synonymous_variant | 0.83 |
rpsA | 1834486 | p.Glu315Asp | missense_variant | 1.0 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 1.0 |
rpsA | 1834504 | c.963G>C | synonymous_variant | 1.0 |
rpsA | 1834513 | c.972C>T | synonymous_variant | 0.92 |
rpsA | 1834522 | c.981C>G | synonymous_variant | 1.0 |
rpsA | 1834523 | p.Glu328Gln | missense_variant | 1.0 |
rpsA | 1834540 | c.999G>C | synonymous_variant | 1.0 |
rpsA | 1834546 | p.Asp335Glu | missense_variant | 1.0 |
rpsA | 1834552 | c.1013_1015delTTG | disruptive_inframe_deletion | 1.0 |
rpsA | 1834558 | c.1017_1018insAAG | conservative_inframe_insertion | 1.0 |
rpsA | 1834570 | p.Asp343Glu | missense_variant | 1.0 |
rpsA | 1834572 | p.Ala344Val | missense_variant | 1.0 |
rpsA | 1834574 | p.Met345Phe | missense_variant | 1.0 |
rpsA | 1834612 | c.1071G>C | synonymous_variant | 1.0 |
rpsA | 1834618 | c.1077G>C | synonymous_variant | 1.0 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 1.0 |
rpsA | 1834627 | c.1086C>G | synonymous_variant | 1.0 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 1.0 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 1.0 |
clpC1 | 4039982 | c.723G>C | synonymous_variant | 1.0 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 1.0 |
clpC1 | 4039994 | p.Glu237Asp | missense_variant | 1.0 |
clpC1 | 4040003 | c.702G>C | synonymous_variant | 1.0 |
clpC1 | 4040015 | p.Ala230Ser | missense_variant | 1.0 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 1.0 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 1.0 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 1.0 |
clpC1 | 4040045 | c.660C>G | synonymous_variant | 1.0 |
clpC1 | 4040051 | c.654C>G | synonymous_variant | 1.0 |
clpC1 | 4040057 | c.648C>G | synonymous_variant | 1.0 |
clpC1 | 4040063 | c.642G>C | synonymous_variant | 1.0 |
clpC1 | 4040066 | c.639G>C | synonymous_variant | 1.0 |
clpC1 | 4040069 | c.636G>C | synonymous_variant | 1.0 |
clpC1 | 4040090 | c.615T>C | synonymous_variant | 1.0 |
clpC1 | 4040096 | c.609G>C | synonymous_variant | 1.0 |
clpC1 | 4040110 | c.595C>A | synonymous_variant | 1.0 |
clpC1 | 4040114 | p.Ile197Met | missense_variant | 1.0 |
clpC1 | 4040117 | c.588A>G | synonymous_variant | 1.0 |
clpC1 | 4040125 | p.Glu194Lys | missense_variant | 1.0 |
clpC1 | 4040147 | c.558A>G | synonymous_variant | 1.0 |