Run ID: ERR4769408
Sample name:
Date: 01-04-2023 06:39:28
Number of reads: 579018
Percentage reads mapped: 27.9
Strain: La1.3
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
La1 | M.bovis | None | None | 1.0 |
La1.3 | M.bovis | None | None | 0.99 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
pncA | 2289073 | p.His57Asp | missense_variant | 1.0 | pyrazinamide |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrB | 5752 | c.513G>A | synonymous_variant | 1.0 |
gyrA | 6406 | c.-896C>T | upstream_gene_variant | 1.0 |
gyrB | 6446 | p.Ala403Ser | missense_variant | 1.0 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8285 | c.984C>T | synonymous_variant | 1.0 |
gyrA | 8762 | c.1461G>C | synonymous_variant | 0.14 |
gyrA | 8767 | p.Arg489Lys | missense_variant | 0.14 |
gyrA | 8769 | p.His490Tyr | missense_variant | 0.14 |
gyrA | 8783 | c.1482G>T | synonymous_variant | 0.2 |
gyrA | 8792 | c.1491G>C | synonymous_variant | 0.27 |
gyrA | 8801 | c.1500G>C | synonymous_variant | 0.25 |
gyrA | 8818 | p.Ser506Asn | missense_variant | 0.21 |
gyrA | 8829 | c.1528T>C | synonymous_variant | 0.2 |
gyrA | 8843 | c.1542G>A | synonymous_variant | 0.2 |
gyrA | 8852 | c.1551T>C | synonymous_variant | 0.2 |
gyrA | 8858 | c.1557T>G | synonymous_variant | 0.19 |
gyrA | 8867 | c.1566A>G | synonymous_variant | 0.16 |
gyrA | 8870 | c.1569G>C | synonymous_variant | 0.18 |
gyrA | 8873 | c.1572A>T | synonymous_variant | 0.17 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.14 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491214 | c.432C>T | synonymous_variant | 0.17 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 760121 | c.315T>A | synonymous_variant | 0.13 |
rpoB | 760130 | p.Asp108Glu | missense_variant | 0.13 |
rpoB | 760172 | c.366G>C | synonymous_variant | 0.2 |
rpoB | 760181 | c.375T>G | synonymous_variant | 0.17 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.17 |
rpoB | 760185 | c.379C>T | synonymous_variant | 0.16 |
rpoB | 760199 | c.393C>G | synonymous_variant | 0.14 |
rpoB | 760220 | c.414C>T | synonymous_variant | 0.13 |
rpoB | 760235 | c.429T>C | synonymous_variant | 0.13 |
rpoB | 761006 | c.1200C>G | synonymous_variant | 0.13 |
rpoB | 761063 | c.1257C>T | synonymous_variant | 0.15 |
rpoB | 761071 | p.Lys422Arg | missense_variant | 0.14 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.18 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.19 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.17 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.21 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.19 |
rpoB | 761138 | c.1332C>G | synonymous_variant | 0.17 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.19 |
rpoB | 761150 | c.1344A>T | synonymous_variant | 0.19 |
rpoB | 761156 | c.1350G>C | synonymous_variant | 0.16 |
rpoB | 761159 | c.1353G>C | synonymous_variant | 0.16 |
rpoB | 761162 | c.1356G>C | synonymous_variant | 0.16 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.15 |
rpoB | 761168 | c.1362C>G | synonymous_variant | 0.15 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.19 |
rpoB | 761189 | c.1383T>C | synonymous_variant | 0.2 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.23 |
rpoB | 761198 | c.1392G>C | synonymous_variant | 0.22 |
rpoB | 761204 | c.1398C>T | synonymous_variant | 0.21 |
rpoB | 761213 | c.1407G>T | synonymous_variant | 0.16 |
rpoB | 761234 | c.1428G>C | synonymous_variant | 0.15 |
rpoB | 761273 | c.1467T>C | synonymous_variant | 0.11 |
rpoB | 761969 | c.2163G>A | synonymous_variant | 0.18 |
rpoB | 761996 | c.2190C>T | synonymous_variant | 0.17 |
rpoB | 762002 | c.2196C>G | synonymous_variant | 0.16 |
rpoB | 762003 | p.Asn733Gln | missense_variant | 0.16 |
rpoB | 762008 | c.2202C>T | synonymous_variant | 0.17 |
rpoB | 762011 | c.2205G>C | synonymous_variant | 0.17 |
rpoB | 762014 | c.2208C>G | synonymous_variant | 0.17 |
rpoB | 762026 | c.2220G>C | synonymous_variant | 0.18 |
rpoB | 762029 | c.2223C>G | synonymous_variant | 0.18 |
rpoB | 762038 | c.2232C>T | synonymous_variant | 0.21 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.19 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.23 |
rpoB | 762080 | c.2274G>C | synonymous_variant | 0.21 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.2 |
rpoB | 762092 | c.2286G>A | synonymous_variant | 0.19 |
rpoB | 762098 | c.2292C>T | synonymous_variant | 0.2 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.17 |
rpoB | 762128 | c.2322G>C | synonymous_variant | 0.12 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.24 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.24 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.25 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.22 |
rpoB | 762161 | c.2355C>T | synonymous_variant | 0.22 |
rpoB | 762179 | c.2373C>T | synonymous_variant | 0.21 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.21 |
rpoB | 762189 | p.Ile795Val | missense_variant | 0.24 |
rpoB | 762200 | c.2394C>A | synonymous_variant | 0.21 |
rpoB | 762209 | c.2403C>G | synonymous_variant | 0.19 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.16 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.14 |
rpoB | 762236 | c.2430G>C | synonymous_variant | 0.13 |
rpoB | 762239 | c.2433G>A | synonymous_variant | 0.14 |
rpoB | 762245 | c.2439G>C | synonymous_variant | 0.14 |
rpoB | 762248 | c.2442G>C | synonymous_variant | 0.14 |
rpoB | 762251 | c.2445G>T | synonymous_variant | 0.14 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.14 |
rpoB | 762881 | p.Met1025Ile | missense_variant | 0.13 |
rpoC | 762894 | c.-476C>T | upstream_gene_variant | 0.14 |
rpoC | 762899 | c.-471G>C | upstream_gene_variant | 0.14 |
rpoC | 762917 | c.-453C>T | upstream_gene_variant | 0.17 |
rpoC | 762920 | c.-450C>T | upstream_gene_variant | 0.17 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.17 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.16 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 0.16 |
rpoC | 762956 | c.-414G>T | upstream_gene_variant | 0.17 |
rpoC | 762959 | c.-411G>C | upstream_gene_variant | 0.18 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.18 |
rpoC | 762971 | c.-399G>C | upstream_gene_variant | 0.19 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.16 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.13 |
rpoC | 763013 | c.-357C>G | upstream_gene_variant | 0.13 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.12 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763034 | c.-336C>T | upstream_gene_variant | 0.14 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.18 |
rpoC | 763049 | c.-321G>A | upstream_gene_variant | 0.17 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.17 |
rpoC | 763067 | c.-303C>T | upstream_gene_variant | 0.2 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.2 |
rpoB | 763074 | p.Thr1090Val | missense_variant | 0.17 |
rpoC | 763082 | c.-288C>T | upstream_gene_variant | 0.17 |
rpoC | 763085 | c.-285C>A | upstream_gene_variant | 0.17 |
rpoC | 763100 | c.-270G>A | upstream_gene_variant | 0.17 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.18 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.17 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.18 |
rpoC | 763130 | c.-240G>A | upstream_gene_variant | 0.15 |
rpoC | 763133 | c.-237G>C | upstream_gene_variant | 0.16 |
rpoC | 763456 | c.87A>G | synonymous_variant | 0.12 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.12 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.12 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.12 |
rpoC | 763507 | c.138G>C | synonymous_variant | 0.13 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.15 |
rpoC | 763531 | c.162G>C | synonymous_variant | 0.14 |
rpoC | 763537 | c.168C>G | synonymous_variant | 0.18 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.18 |
rpoC | 763558 | c.189C>T | synonymous_variant | 0.19 |
rpoC | 763570 | c.201G>T | synonymous_variant | 0.17 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.17 |
rpoC | 763618 | c.249C>T | synonymous_variant | 0.14 |
rpoC | 763630 | c.261G>T | synonymous_variant | 0.14 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.15 |
rpoC | 763648 | c.279C>T | synonymous_variant | 0.15 |
rpoC | 763657 | c.288G>A | synonymous_variant | 0.14 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.14 |
rpoC | 763666 | c.297G>A | synonymous_variant | 0.14 |
rpoC | 764341 | c.972G>T | synonymous_variant | 0.12 |
rpoC | 764353 | c.984G>T | synonymous_variant | 0.24 |
rpoC | 764365 | c.996C>T | synonymous_variant | 0.18 |
rpoC | 764368 | c.999C>A | synonymous_variant | 0.16 |
rpoC | 764371 | c.1002G>T | synonymous_variant | 0.17 |
rpoC | 764377 | c.1008C>G | synonymous_variant | 0.2 |
rpoC | 764387 | c.1018_1020delTTGinsCTC | synonymous_variant | 0.2 |
rpoC | 764405 | c.1036_1038delAGGinsCGC | synonymous_variant | 0.22 |
rpoC | 764410 | c.1041G>C | synonymous_variant | 0.22 |
rpoC | 764428 | c.1059G>C | synonymous_variant | 0.21 |
rpoC | 764431 | c.1062G>C | synonymous_variant | 0.24 |
rpoC | 764434 | c.1065A>G | synonymous_variant | 0.25 |
rpoC | 764435 | c.1066_1068delAGGinsCGA | synonymous_variant | 0.25 |
rpoC | 764446 | c.1077T>C | synonymous_variant | 0.25 |
rpoC | 764449 | c.1080G>C | synonymous_variant | 0.25 |
rpoC | 764455 | c.1086G>T | synonymous_variant | 0.27 |
rpoC | 764458 | c.1089G>C | synonymous_variant | 0.27 |
rpoC | 764461 | c.1092A>G | synonymous_variant | 0.27 |
rpoC | 764497 | c.1128A>G | synonymous_variant | 0.14 |
rpoC | 764500 | c.1131C>G | synonymous_variant | 0.14 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.14 |
rpoC | 764605 | c.1236G>C | synonymous_variant | 0.14 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.13 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.12 |
rpoC | 764647 | c.1278C>T | synonymous_variant | 0.13 |
rpoC | 764653 | c.1284G>C | synonymous_variant | 0.12 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.15 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.17 |
rpoC | 764671 | c.1302G>T | synonymous_variant | 0.17 |
rpoC | 764692 | c.1323C>T | synonymous_variant | 0.18 |
rpoC | 764713 | c.1344G>T | synonymous_variant | 0.22 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.23 |
rpoC | 764752 | c.1383G>C | synonymous_variant | 0.14 |
rpoC | 764755 | c.1386C>T | synonymous_variant | 0.14 |
rpoC | 764758 | c.1389C>G | synonymous_variant | 0.16 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.15 |
rpoC | 764781 | p.Ser471Thr | missense_variant | 0.14 |
rpoC | 764797 | c.1428G>C | synonymous_variant | 0.12 |
rpoC | 764804 | p.Gln479Lys | missense_variant | 0.17 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.12 |
rpoC | 767017 | c.3648C>G | synonymous_variant | 0.13 |
rpoC | 767020 | c.3651C>G | synonymous_variant | 0.13 |
rpoC | 767035 | c.3666G>C | synonymous_variant | 0.19 |
rpoC | 767041 | c.3672G>A | synonymous_variant | 0.19 |
rpoC | 767062 | c.3693C>T | synonymous_variant | 0.17 |
rpoC | 767065 | c.3696G>C | synonymous_variant | 0.18 |
rpoC | 767066 | c.3697C>T | synonymous_variant | 0.18 |
rpoC | 767074 | c.3705T>C | synonymous_variant | 0.19 |
rpoC | 767080 | c.3711G>T | synonymous_variant | 0.19 |
rpoC | 767093 | c.3724_3726delAGCinsTCG | synonymous_variant | 0.19 |
rpoC | 767098 | c.3729T>C | synonymous_variant | 0.19 |
rpoC | 767104 | c.3735C>G | synonymous_variant | 0.19 |
rpoC | 767106 | p.Asn1246Ile | missense_variant | 0.19 |
rpoC | 767122 | c.3753C>T | synonymous_variant | 0.18 |
rpoC | 767125 | c.3756G>C | synonymous_variant | 0.17 |
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 |
rplC | 800648 | c.-161A>G | upstream_gene_variant | 0.13 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.15 |
rplC | 800672 | c.-137G>C | upstream_gene_variant | 0.16 |
rplC | 800690 | c.-119C>T | upstream_gene_variant | 0.15 |
rplC | 800693 | c.-116A>T | upstream_gene_variant | 0.17 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.21 |
rplC | 800714 | c.-95C>T | upstream_gene_variant | 0.16 |
rplC | 800715 | c.-94A>C | upstream_gene_variant | 0.22 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.2 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.2 |
rplC | 800735 | c.-74C>G | upstream_gene_variant | 0.19 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
fbiC | 1304619 | c.1689G>A | synonymous_variant | 0.13 |
fbiC | 1304625 | c.1695C>T | synonymous_variant | 0.16 |
fbiC | 1304634 | c.1704C>G | synonymous_variant | 0.17 |
fbiC | 1304640 | c.1710A>C | synonymous_variant | 0.18 |
fbiC | 1304658 | c.1728C>G | synonymous_variant | 0.21 |
fbiC | 1304660 | p.Tyr577Phe | missense_variant | 0.21 |
fbiC | 1304662 | p.Ser578Thr | missense_variant | 0.21 |
fbiC | 1304671 | c.1742delT | frameshift_variant | 0.24 |
fbiC | 1304674 | p.Gly582Arg | missense_variant | 0.25 |
fbiC | 1304677 | c.1747_1748insC | frameshift_variant | 0.25 |
fbiC | 1304691 | c.1761G>T | synonymous_variant | 0.26 |
fbiC | 1304694 | c.1764A>G | synonymous_variant | 0.26 |
fbiC | 1304700 | c.1770G>A | synonymous_variant | 0.26 |
fbiC | 1304703 | c.1773C>G | synonymous_variant | 0.25 |
fbiC | 1304715 | c.1785G>C | synonymous_variant | 0.23 |
fbiC | 1304718 | c.1788C>A | synonymous_variant | 0.23 |
fbiC | 1304724 | c.1794A>G | synonymous_variant | 0.18 |
fbiC | 1304727 | c.1797A>G | synonymous_variant | 0.18 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471914 | n.69A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1471918 | n.73A>T | non_coding_transcript_exon_variant | 0.35 |
rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 0.35 |
rrs | 1471925 | n.81delC | non_coding_transcript_exon_variant | 0.35 |
rrs | 1471931 | n.87delA | non_coding_transcript_exon_variant | 0.36 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1471938 | n.93T>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1471943 | n.98T>C | non_coding_transcript_exon_variant | 0.41 |
rrs | 1472023 | n.178G>T | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472028 | n.183A>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472030 | n.185G>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472031 | n.186G>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472032 | n.187G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472033 | n.188A>T | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472034 | n.189T>C | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472040 | n.195T>G | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472041 | n.196C>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472042 | n.197T>G | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472043 | n.198T>G | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472057 | n.212C>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472062 | n.217G>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472068 | n.223T>C | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472069 | n.224G>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472137 | n.292G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.62 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.54 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.26 |
rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.23 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472414 | n.569C>T | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 0.42 |
rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472449 | n.604C>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472450 | n.605A>G | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472456 | n.611T>C | non_coding_transcript_exon_variant | 0.46 |
rrs | 1472462 | n.617T>C | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472463 | n.618G>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.47 |
rrs | 1472467 | n.622G>T | non_coding_transcript_exon_variant | 0.48 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.56 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472599 | n.754G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.65 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472686 | n.841G>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.66 |
rrs | 1472836 | n.991G>A | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472837 | n.992C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472840 | n.995A>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472856 | n.1012_1015delAGGC | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472873 | n.1028C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472875 | n.1030T>G | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472878 | n.1033G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472951 | n.1106T>C | non_coding_transcript_exon_variant | 0.63 |
rrs | 1472953 | n.1108G>A | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472957 | n.1112C>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1472989 | n.1144G>A | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473082 | n.1237G>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.73 |
rrs | 1473099 | n.1254T>G | non_coding_transcript_exon_variant | 0.7 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.69 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.65 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473129 | n.1284C>T | non_coding_transcript_exon_variant | 0.68 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1473282 | n.1437C>T | non_coding_transcript_exon_variant | 0.6 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1473717 | n.60G>A | non_coding_transcript_exon_variant | 0.24 |
rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 0.26 |
rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1473757 | n.100T>G | non_coding_transcript_exon_variant | 0.42 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1473814 | n.157A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1473815 | n.158T>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1473830 | n.173T>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1473833 | n.176_177insT | non_coding_transcript_exon_variant | 0.76 |
rrl | 1473844 | n.187C>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1473870 | n.213G>A | non_coding_transcript_exon_variant | 0.61 |
rrl | 1473871 | n.214T>C | non_coding_transcript_exon_variant | 0.61 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.61 |
rrl | 1473887 | n.230T>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1473888 | n.231T>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 0.52 |
rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 0.41 |
rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1474116 | n.459G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474124 | n.467G>C | non_coding_transcript_exon_variant | 0.42 |
rrl | 1474135 | n.478G>A | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474142 | n.485C>G | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474153 | n.496C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474166 | n.509G>A | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474186 | n.529A>G | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474249 | n.592G>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474266 | n.609T>C | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474288 | n.631C>T | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474289 | n.633_644delTTTTCCTCTCCG | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474305 | n.648G>C | non_coding_transcript_exon_variant | 0.36 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474353 | n.696A>G | non_coding_transcript_exon_variant | 0.59 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.61 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1474402 | n.745T>C | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474414 | n.757C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474447 | n.790G>A | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474450 | n.793T>C | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1474496 | n.839C>A | non_coding_transcript_exon_variant | 0.63 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.68 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 0.69 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474552 | n.895C>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474638 | n.981C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474662 | n.1005C>T | non_coding_transcript_exon_variant | 0.18 |
rrl | 1474664 | n.1007G>T | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474666 | n.1009T>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474670 | n.1013C>G | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474673 | n.1016T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474679 | n.1022G>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474684 | n.1027T>C | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474687 | n.1030C>A | non_coding_transcript_exon_variant | 0.12 |
rrl | 1474688 | n.1031G>A | non_coding_transcript_exon_variant | 0.13 |
rrl | 1474708 | n.1052dupG | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474711 | n.1054_1055insA | non_coding_transcript_exon_variant | 0.15 |
rrl | 1474714 | n.1058delT | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474717 | n.1060A>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 0.25 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474740 | n.1083G>C | non_coding_transcript_exon_variant | 0.38 |
rrl | 1474747 | n.1090C>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.35 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.39 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474790 | n.1133C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.52 |
rrl | 1474803 | n.1146G>A | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.65 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474903 | n.1246T>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.61 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.61 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474938 | n.1281G>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474946 | n.1289C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1474953 | n.1296C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475060 | n.1404delC | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475065 | n.1408G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475067 | n.1410A>G | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475076 | n.1419C>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475079 | n.1422T>C | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475081 | n.1424C>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 0.29 |
rrl | 1475113 | n.1456C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475116 | n.1459G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475144 | n.1487G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475163 | n.1506T>C | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475414 | n.1757G>C | non_coding_transcript_exon_variant | 0.27 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475422 | n.1765A>G | non_coding_transcript_exon_variant | 0.28 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1475443 | n.1786G>A | non_coding_transcript_exon_variant | 0.44 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475481 | n.1824C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475482 | n.1825A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.53 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.55 |
rrl | 1475538 | n.1881T>A | non_coding_transcript_exon_variant | 0.59 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 0.57 |
rrl | 1475599 | n.1942A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1475761 | n.2104C>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475762 | n.2105G>T | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475764 | n.2107A>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1475765 | n.2108A>G | non_coding_transcript_exon_variant | 0.46 |
rrl | 1475767 | n.2110G>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1475769 | n.2112T>C | non_coding_transcript_exon_variant | 0.49 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.51 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.63 |
rrl | 1475896 | n.2239A>G | non_coding_transcript_exon_variant | 0.63 |
rrl | 1475916 | n.2259C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.68 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476032 | n.2375C>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476033 | n.2376T>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476034 | n.2377C>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476045 | n.2388G>A | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476046 | n.2389G>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476047 | n.2390G>C | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476080 | n.2423T>A | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476088 | n.2431A>C | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476103 | n.2446C>A | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476110 | n.2453G>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1476300 | n.2643G>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476358 | n.2701T>C | non_coding_transcript_exon_variant | 0.16 |
rrl | 1476372 | n.2715T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476382 | n.2725A>G | non_coding_transcript_exon_variant | 0.13 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.46 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476665 | n.3008T>G | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476666 | n.3009C>T | non_coding_transcript_exon_variant | 0.42 |
rrl | 1476675 | n.3018C>G | non_coding_transcript_exon_variant | 0.37 |
rrl | 1476689 | n.3032A>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476728 | n.3071T>C | non_coding_transcript_exon_variant | 1.0 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 0.13 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.14 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.14 |
rpsA | 1833850 | c.309C>G | synonymous_variant | 0.14 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.19 |
rpsA | 1833949 | c.408T>C | synonymous_variant | 0.27 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 0.26 |
rpsA | 1833961 | c.420C>T | synonymous_variant | 0.21 |
rpsA | 1833970 | c.429G>T | synonymous_variant | 0.21 |
rpsA | 1833973 | c.432G>T | synonymous_variant | 0.21 |
rpsA | 1833976 | c.435C>T | synonymous_variant | 0.21 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.2 |
rpsA | 1833985 | c.444G>C | synonymous_variant | 0.19 |
rpsA | 1833991 | c.450C>T | synonymous_variant | 0.19 |
rpsA | 1833997 | c.456G>C | synonymous_variant | 0.17 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.17 |
rpsA | 1834003 | c.462G>A | synonymous_variant | 0.17 |
rpsA | 1834009 | c.468C>T | synonymous_variant | 0.16 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.16 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.16 |
rpsA | 1834024 | c.483G>C | synonymous_variant | 0.17 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.18 |
rpsA | 1834034 | p.Ile165Val | missense_variant | 0.18 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.13 |
rpsA | 1834399 | p.His286Gln | missense_variant | 0.13 |
rpsA | 1834411 | c.870T>G | synonymous_variant | 0.19 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.19 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.22 |
rpsA | 1834447 | c.906C>G | synonymous_variant | 0.26 |
rpsA | 1834451 | c.910T>C | synonymous_variant | 0.25 |
rpsA | 1834474 | c.933C>G | synonymous_variant | 0.25 |
rpsA | 1834483 | c.942G>A | synonymous_variant | 0.3 |
rpsA | 1834489 | c.948T>A | synonymous_variant | 0.31 |
rpsA | 1834495 | c.954G>A | synonymous_variant | 0.32 |
rpsA | 1834501 | c.960G>C | synonymous_variant | 0.3 |
rpsA | 1834504 | c.963G>T | synonymous_variant | 0.32 |
rpsA | 1834513 | c.972C>G | synonymous_variant | 0.37 |
rpsA | 1834519 | c.978G>C | synonymous_variant | 0.28 |
rpsA | 1834522 | c.981C>T | synonymous_variant | 0.25 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.29 |
rpsA | 1834540 | c.999G>T | synonymous_variant | 0.27 |
rpsA | 1834543 | c.1002C>G | synonymous_variant | 0.23 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.22 |
rpsA | 1834552 | c.1011G>T | synonymous_variant | 0.2 |
rpsA | 1834555 | c.1014T>C | synonymous_variant | 0.21 |
rpsA | 1834557 | p.Ala339Gly | missense_variant | 0.21 |
rpsA | 1834570 | c.1029C>T | synonymous_variant | 0.24 |
rpsA | 1834573 | c.1032G>A | synonymous_variant | 0.24 |
rpsA | 1834574 | p.Met345Leu | missense_variant | 0.24 |
rpsA | 1834600 | c.1059G>C | synonymous_variant | 0.23 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 0.21 |
rpsA | 1834612 | c.1071G>T | synonymous_variant | 0.29 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 0.25 |
rpsA | 1834627 | c.1086C>G | synonymous_variant | 0.25 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.26 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.23 |
rpsA | 1834645 | c.1104C>T | synonymous_variant | 0.23 |
rpsA | 1834650 | p.Thr370Asn | missense_variant | 0.23 |
rpsA | 1834653 | p.Glu371Ala | missense_variant | 0.24 |
rpsA | 1834663 | c.1122C>T | synonymous_variant | 0.22 |
rpsA | 1834667 | p.Ala376Ser | missense_variant | 0.23 |
rpsA | 1834688 | c.1147_1149delAGTinsTCG | synonymous_variant | 0.24 |
rpsA | 1834733 | p.Ala398Pro | missense_variant | 0.29 |
rpsA | 1834738 | c.1197A>G | synonymous_variant | 0.29 |
rpsA | 1834753 | c.1212T>C | synonymous_variant | 0.29 |
rpsA | 1834759 | c.1218A>C | synonymous_variant | 0.17 |
rpsA | 1834859 | p.Ala440Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2103173 | c.-132delG | upstream_gene_variant | 1.0 |
katG | 2154166 | p.Ala649Val | missense_variant | 0.23 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155503 | c.609C>T | synonymous_variant | 1.0 |
katG | 2156025 | c.87C>A | synonymous_variant | 1.0 |
katG | 2156465 | c.-354C>T | upstream_gene_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168011 | p.Ser868Arg | missense_variant | 1.0 |
PPE35 | 2168814 | c.1798dupA | frameshift_variant | 1.0 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
kasA | 2519305 | c.1191A>G | synonymous_variant | 0.13 |
ahpC | 2726579 | c.387T>C | synonymous_variant | 0.11 |
ald | 3086728 | c.-92C>T | upstream_gene_variant | 1.0 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
ald | 3087084 | c.266delA | frameshift_variant | 1.0 |
Rv3083 | 3448783 | p.Val94Ile | missense_variant | 1.0 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
fprA | 3474427 | p.Val141Ile | missense_variant | 1.0 |
fprA | 3475159 | p.Asn385Asp | missense_variant | 1.0 |
rpoA | 3878166 | c.342C>A | synonymous_variant | 0.14 |
rpoA | 3878172 | c.336G>C | synonymous_variant | 0.14 |
rpoA | 3878187 | c.321C>A | synonymous_variant | 0.14 |
rpoA | 3878190 | c.318C>T | synonymous_variant | 0.15 |
rpoA | 3878196 | p.Glu104Ala | missense_variant | 0.14 |
rpoA | 3878199 | c.309T>C | synonymous_variant | 0.14 |
rpoA | 3878202 | c.306G>C | synonymous_variant | 0.14 |
rpoA | 3878205 | c.303T>C | synonymous_variant | 0.14 |
rpoA | 3878217 | p.Leu97Val | missense_variant | 0.14 |
rpoA | 3878630 | c.-124delC | upstream_gene_variant | 1.0 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
clpC1 | 4038795 | p.Ser637Thr | missense_variant | 0.19 |
clpC1 | 4038812 | c.1893T>C | synonymous_variant | 0.18 |
clpC1 | 4038815 | c.1890G>A | synonymous_variant | 0.18 |
clpC1 | 4038842 | c.1863G>C | synonymous_variant | 0.15 |
clpC1 | 4038845 | p.Ser620Cys | missense_variant | 0.19 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.14 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.15 |
clpC1 | 4038884 | c.1821C>T | synonymous_variant | 0.16 |
clpC1 | 4038890 | c.1815G>A | synonymous_variant | 0.16 |
clpC1 | 4038896 | c.1809C>A | synonymous_variant | 0.17 |
clpC1 | 4038905 | c.1800A>G | synonymous_variant | 0.17 |
clpC1 | 4038911 | c.1794G>T | synonymous_variant | 0.14 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.13 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.14 |
clpC1 | 4038926 | c.1779G>C | synonymous_variant | 0.14 |
clpC1 | 4038932 | c.1773G>T | synonymous_variant | 0.13 |
clpC1 | 4038941 | c.1764G>C | synonymous_variant | 0.14 |
clpC1 | 4039526 | c.1179G>C | synonymous_variant | 0.12 |
clpC1 | 4039575 | p.Ala377Gly | missense_variant | 0.11 |
clpC1 | 4039586 | c.1119G>C | synonymous_variant | 0.12 |
clpC1 | 4039601 | c.1104G>T | synonymous_variant | 0.21 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.18 |
clpC1 | 4039616 | c.1089G>T | synonymous_variant | 0.18 |
clpC1 | 4039619 | c.1086G>T | synonymous_variant | 0.18 |
clpC1 | 4039622 | c.1083C>T | synonymous_variant | 0.22 |
clpC1 | 4039649 | c.1056G>C | synonymous_variant | 0.2 |
clpC1 | 4039652 | c.1053G>C | synonymous_variant | 0.21 |
clpC1 | 4039661 | c.1044T>C | synonymous_variant | 0.24 |
clpC1 | 4039670 | c.1035G>T | synonymous_variant | 0.18 |
clpC1 | 4039673 | c.1032G>C | synonymous_variant | 0.17 |
clpC1 | 4039682 | c.1023C>T | synonymous_variant | 0.16 |
clpC1 | 4039685 | c.1020C>T | synonymous_variant | 0.15 |
clpC1 | 4039691 | c.1014G>C | synonymous_variant | 0.15 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.16 |
clpC1 | 4039697 | c.1008C>T | synonymous_variant | 0.16 |
clpC1 | 4039700 | c.1005C>T | synonymous_variant | 0.15 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.24 |
clpC1 | 4039742 | c.963C>T | synonymous_variant | 0.33 |
clpC1 | 4039748 | c.957G>C | synonymous_variant | 0.32 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.35 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.33 |
clpC1 | 4039769 | c.936C>T | synonymous_variant | 0.31 |
clpC1 | 4039775 | c.930G>C | synonymous_variant | 0.28 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.27 |
clpC1 | 4039781 | c.924G>C | synonymous_variant | 0.27 |
clpC1 | 4039787 | c.918G>C | synonymous_variant | 0.27 |
clpC1 | 4039793 | c.912C>G | synonymous_variant | 0.28 |
clpC1 | 4039802 | c.903G>T | synonymous_variant | 0.27 |
clpC1 | 4039814 | c.891C>G | synonymous_variant | 0.27 |
clpC1 | 4039817 | c.888A>C | synonymous_variant | 0.26 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.26 |
clpC1 | 4039826 | c.879C>G | synonymous_variant | 0.29 |
clpC1 | 4039829 | c.874_876delTTGinsCTC | synonymous_variant | 0.29 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.26 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.25 |
clpC1 | 4040426 | c.279T>C | synonymous_variant | 0.12 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.16 |
clpC1 | 4040528 | c.177G>C | synonymous_variant | 0.16 |
clpC1 | 4040531 | c.174T>A | synonymous_variant | 0.17 |
clpC1 | 4040534 | c.171A>G | synonymous_variant | 0.17 |
clpC1 | 4040537 | c.168G>C | synonymous_variant | 0.17 |
clpC1 | 4040540 | c.165G>C | synonymous_variant | 0.17 |
clpC1 | 4040546 | c.159G>T | synonymous_variant | 0.19 |
clpC1 | 4040560 | c.145C>T | synonymous_variant | 0.15 |
clpC1 | 4040561 | c.144A>G | synonymous_variant | 0.15 |
clpC1 | 4040570 | c.135C>A | synonymous_variant | 0.15 |
clpC1 | 4040573 | c.132T>C | synonymous_variant | 0.15 |
clpC1 | 4040576 | c.129C>T | synonymous_variant | 0.15 |
clpC1 | 4040582 | c.123G>C | synonymous_variant | 0.16 |
clpC1 | 4040585 | c.120A>G | synonymous_variant | 0.16 |
clpC1 | 4040588 | c.117T>C | synonymous_variant | 0.16 |
clpC1 | 4040591 | c.114C>T | synonymous_variant | 0.17 |
clpC1 | 4040594 | c.111G>C | synonymous_variant | 0.17 |
clpC1 | 4040600 | c.103_105delTTAinsCTC | synonymous_variant | 0.18 |
clpC1 | 4040606 | c.99T>C | synonymous_variant | 0.18 |
clpC1 | 4040615 | c.90C>G | synonymous_variant | 0.2 |
clpC1 | 4040648 | c.57G>A | synonymous_variant | 0.18 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4241384 | p.Pro508Thr | missense_variant | 0.82 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4242970 | c.-263C>T | upstream_gene_variant | 1.0 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embB | 4246551 | p.Asn13Ser | missense_variant | 1.0 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4249640 | c.3127T>C | synonymous_variant | 0.96 |
aftB | 4267858 | p.Ile327Val | missense_variant | 1.0 |
aftB | 4269351 | c.-515C>T | upstream_gene_variant | 1.0 |
ubiA | 4269387 | p.Glu149Asp | missense_variant | 1.0 |
ubiA | 4269599 | p.Glu79* | stop_gained | 0.12 |
aftB | 4269606 | c.-770T>C | upstream_gene_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |