Run ID: SRR11462861
Sample name:
Date: 02-04-2023 21:20:19
Number of reads: 730252
Percentage reads mapped: 48.68
Strain: La1.8.1
Drug-resistance: Other
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
La1 | M.bovis | None | None | 1.0 |
La1.8 | M.bovis | None | None | 1.0 |
La1.8.1 | M.bovis | None | None | 1.0 |
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 | 7283 | c.-19G>T | upstream_gene_variant | 0.14 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7584 | p.Ser95Ala | missense_variant | 0.17 |
gyrA | 7607 | c.306C>G | synonymous_variant | 0.14 |
gyrA | 7619 | c.318C>G | synonymous_variant | 0.19 |
gyrA | 7629 | p.Val110Ile | missense_variant | 0.19 |
gyrA | 7658 | c.357A>G | synonymous_variant | 0.19 |
gyrA | 7661 | c.360C>T | synonymous_variant | 0.16 |
gyrA | 8285 | c.984C>T | synonymous_variant | 0.98 |
gyrA | 8501 | c.1200G>C | synonymous_variant | 0.13 |
gyrA | 8714 | p.Lys471Asn | missense_variant | 0.13 |
gyrA | 8897 | c.1596T>C | synonymous_variant | 0.16 |
gyrA | 8903 | c.1602T>C | synonymous_variant | 0.16 |
gyrA | 8915 | c.1614A>G | synonymous_variant | 0.17 |
gyrA | 8933 | c.1632G>C | synonymous_variant | 0.17 |
gyrA | 8934 | p.Gln545Lys | missense_variant | 0.17 |
gyrA | 8939 | c.1638T>C | synonymous_variant | 0.16 |
gyrA | 8942 | c.1641G>C | synonymous_variant | 0.16 |
gyrA | 8944 | p.Gly548Asp | missense_variant | 0.16 |
gyrA | 8946 | c.1645_1647delTTGinsCTC | synonymous_variant | 0.15 |
gyrA | 8990 | c.1689C>G | synonymous_variant | 0.2 |
gyrA | 8996 | c.1695T>C | synonymous_variant | 0.18 |
gyrA | 8998 | p.Leu566Trp | missense_variant | 0.18 |
gyrA | 9018 | p.Gln573Lys | missense_variant | 0.19 |
gyrA | 9023 | c.1722A>C | synonymous_variant | 0.17 |
gyrA | 9026 | c.1725G>C | synonymous_variant | 0.14 |
gyrA | 9029 | c.1728T>C | synonymous_variant | 0.14 |
gyrA | 9032 | c.1731T>C | synonymous_variant | 0.14 |
gyrA | 9143 | c.1842T>C | synonymous_variant | 1.0 |
gyrA | 9217 | p.Asp639Ala | missense_variant | 1.0 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 576751 | p.Lys468Asn | missense_variant | 0.25 |
rpoB | 760140 | p.Pro112Ser | missense_variant | 0.12 |
rpoB | 760148 | p.Asp114Glu | missense_variant | 0.15 |
rpoB | 760157 | c.351A>G | synonymous_variant | 0.19 |
rpoB | 760181 | c.375T>C | synonymous_variant | 0.19 |
rpoB | 760184 | c.378A>G | synonymous_variant | 0.21 |
rpoB | 760196 | c.390C>G | synonymous_variant | 0.21 |
rpoB | 760223 | c.417T>C | synonymous_variant | 0.2 |
rpoB | 760233 | c.427_429delAGTinsTCG | synonymous_variant | 0.21 |
rpoB | 760241 | c.435G>C | synonymous_variant | 0.21 |
rpoB | 760244 | c.438G>C | synonymous_variant | 0.19 |
rpoB | 760256 | c.450C>T | synonymous_variant | 0.21 |
rpoB | 760357 | p.Thr184Asn | missense_variant | 0.15 |
rpoB | 760361 | c.555T>C | synonymous_variant | 0.15 |
rpoB | 760370 | c.564C>G | synonymous_variant | 0.14 |
rpoB | 760376 | p.Asp190Glu | missense_variant | 0.18 |
rpoB | 760380 | p.Thr192Pro | missense_variant | 0.18 |
rpoB | 760400 | c.594G>C | synonymous_variant | 0.16 |
rpoB | 760407 | p.Ser201Ala | missense_variant | 0.15 |
rpoB | 760430 | c.624T>C | synonymous_variant | 0.14 |
rpoB | 760436 | c.630C>G | synonymous_variant | 0.14 |
rpoB | 760460 | c.654G>C | synonymous_variant | 0.21 |
rpoB | 760475 | c.669A>G | synonymous_variant | 0.22 |
rpoB | 760481 | c.675G>C | synonymous_variant | 0.22 |
rpoB | 760484 | c.678A>G | synonymous_variant | 0.21 |
rpoB | 760487 | c.681G>C | synonymous_variant | 0.23 |
rpoB | 760508 | c.702G>C | synonymous_variant | 0.3 |
rpoB | 760511 | c.705G>C | synonymous_variant | 0.3 |
rpoB | 760514 | c.708C>G | synonymous_variant | 0.3 |
rpoB | 760532 | c.726T>C | synonymous_variant | 0.33 |
rpoB | 760533 | p.Val243Leu | missense_variant | 0.33 |
rpoB | 760541 | c.735G>C | synonymous_variant | 0.31 |
rpoB | 760547 | c.741G>C | synonymous_variant | 0.33 |
rpoB | 760553 | c.747C>G | synonymous_variant | 0.35 |
rpoB | 760565 | c.759A>C | synonymous_variant | 0.31 |
rpoB | 760568 | c.762G>C | synonymous_variant | 0.31 |
rpoB | 760571 | c.765G>C | synonymous_variant | 0.31 |
rpoB | 760589 | c.783C>G | synonymous_variant | 0.26 |
rpoB | 760591 | p.Val262Ala | missense_variant | 0.26 |
rpoB | 760611 | c.805_807delTTGinsCTC | synonymous_variant | 0.25 |
rpoB | 760634 | c.828T>C | synonymous_variant | 0.18 |
rpoB | 760646 | c.840C>G | synonymous_variant | 0.15 |
rpoB | 760649 | c.843G>C | synonymous_variant | 0.15 |
rpoB | 760652 | c.846C>G | synonymous_variant | 0.15 |
rpoB | 760655 | c.849A>G | synonymous_variant | 0.16 |
rpoB | 760661 | c.855A>G | synonymous_variant | 0.19 |
rpoB | 760670 | c.864G>C | synonymous_variant | 0.19 |
rpoB | 760674 | c.868T>C | synonymous_variant | 0.22 |
rpoB | 760679 | c.873A>G | synonymous_variant | 0.18 |
rpoB | 760683 | c.877T>C | synonymous_variant | 0.19 |
rpoB | 760946 | c.1140A>G | synonymous_variant | 0.13 |
rpoB | 760953 | p.Ile383Leu | missense_variant | 0.14 |
rpoB | 760958 | c.1152G>C | synonymous_variant | 0.14 |
rpoB | 760961 | c.1155C>G | synonymous_variant | 0.14 |
rpoB | 760965 | p.Met387Leu | missense_variant | 0.14 |
rpoB | 760970 | c.1164G>C | synonymous_variant | 0.15 |
rpoB | 760973 | c.1167G>C | synonymous_variant | 0.15 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.17 |
rpoB | 760985 | c.1179G>C | synonymous_variant | 0.18 |
rpoB | 760988 | c.1182C>G | synonymous_variant | 0.17 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.17 |
rpoB | 760997 | c.1191G>C | synonymous_variant | 0.17 |
rpoB | 761006 | c.1200C>G | synonymous_variant | 0.21 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.21 |
rpoB | 761027 | c.1221A>C | synonymous_variant | 0.25 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.24 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.23 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.22 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.23 |
rpoB | 761058 | p.Val418Ser | missense_variant | 0.23 |
rpoB | 761063 | c.1257C>G | synonymous_variant | 0.24 |
rpoB | 761088 | c.1282_1284delAGCinsTCG | synonymous_variant | 0.23 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 0.22 |
rpoB | 761097 | c.1291_1293delAGCinsTCA | synonymous_variant | 0.23 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.24 |
rpoB | 761126 | c.1320G>C | synonymous_variant | 0.25 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.24 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.24 |
rpoB | 761147 | c.1341C>T | synonymous_variant | 0.21 |
rpoB | 761150 | c.1344A>T | synonymous_variant | 0.21 |
rpoB | 762053 | c.2247T>C | synonymous_variant | 0.14 |
rpoB | 762065 | c.2259T>C | synonymous_variant | 0.19 |
rpoB | 762074 | c.2268C>G | synonymous_variant | 0.19 |
rpoB | 762083 | c.2277T>C | synonymous_variant | 0.19 |
rpoB | 762086 | c.2280G>C | synonymous_variant | 0.21 |
rpoB | 762101 | c.2295C>G | synonymous_variant | 0.26 |
rpoB | 762114 | p.Ile770Val | missense_variant | 0.24 |
rpoB | 762131 | c.2325C>G | synonymous_variant | 0.24 |
rpoB | 762137 | c.2331C>T | synonymous_variant | 0.23 |
rpoB | 762140 | c.2334G>C | synonymous_variant | 0.23 |
rpoB | 762143 | c.2337T>C | synonymous_variant | 0.23 |
rpoB | 762149 | c.2343G>C | synonymous_variant | 0.23 |
rpoB | 762156 | p.Val784Ile | missense_variant | 0.23 |
rpoB | 762170 | c.2364C>T | synonymous_variant | 0.27 |
rpoB | 762185 | c.2379G>C | synonymous_variant | 0.31 |
rpoB | 762218 | c.2412T>C | synonymous_variant | 0.3 |
rpoB | 762233 | c.2427G>C | synonymous_variant | 0.24 |
rpoB | 762251 | c.2445G>C | synonymous_variant | 0.22 |
rpoB | 762254 | c.2448T>C | synonymous_variant | 0.22 |
rpoB | 762257 | c.2451C>G | synonymous_variant | 0.22 |
rpoB | 762275 | c.2469C>G | synonymous_variant | 0.17 |
rpoB | 762284 | c.2478G>C | synonymous_variant | 0.17 |
rpoB | 762905 | p.Asp1033Glu | missense_variant | 0.17 |
rpoC | 762929 | c.-441G>T | upstream_gene_variant | 0.26 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 0.23 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.31 |
rpoC | 762989 | c.-381G>T | upstream_gene_variant | 0.32 |
rpoC | 762995 | c.-375G>C | upstream_gene_variant | 0.33 |
rpoC | 763013 | c.-357C>G | upstream_gene_variant | 0.31 |
rpoC | 763022 | c.-348C>G | upstream_gene_variant | 0.29 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.29 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763053 | c.-317_-315delTTGinsCTC | upstream_gene_variant | 0.27 |
rpoC | 763067 | c.-303C>G | upstream_gene_variant | 0.21 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.22 |
rpoB | 763074 | p.Thr1090Val | missense_variant | 0.22 |
rpoC | 763088 | c.-282C>G | upstream_gene_variant | 0.23 |
rpoC | 763115 | c.-255T>C | upstream_gene_variant | 0.22 |
rpoC | 763127 | c.-243G>C | upstream_gene_variant | 0.19 |
rpoC | 763133 | c.-237G>C | upstream_gene_variant | 0.21 |
rpoC | 763573 | c.204G>C | synonymous_variant | 0.16 |
rpoC | 763615 | c.246G>C | synonymous_variant | 0.17 |
rpoC | 763618 | c.249C>T | synonymous_variant | 0.16 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.19 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.16 |
rpoC | 763666 | c.297G>T | synonymous_variant | 0.16 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.13 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.12 |
rpoC | 764278 | c.909A>G | synonymous_variant | 0.16 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.13 |
rpoC | 764560 | c.1191T>C | synonymous_variant | 0.15 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.2 |
rpoC | 764611 | c.1242G>C | synonymous_variant | 0.29 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.3 |
rpoC | 764635 | c.1266C>G | synonymous_variant | 0.3 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.26 |
rpoC | 764656 | c.1287C>G | synonymous_variant | 0.27 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.27 |
rpoC | 764665 | c.1296C>G | synonymous_variant | 0.28 |
rpoC | 764668 | c.1299C>T | synonymous_variant | 0.27 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.22 |
rpoC | 764701 | c.1332C>G | synonymous_variant | 0.26 |
rpoC | 764716 | c.1347G>C | synonymous_variant | 0.24 |
rpoC | 764746 | c.1377G>C | synonymous_variant | 0.23 |
rpoC | 764755 | c.1386C>T | synonymous_variant | 0.22 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.23 |
rpoC | 764780 | c.1411_1413delAGCinsTCG | synonymous_variant | 0.21 |
rpoC | 764797 | c.1428G>C | synonymous_variant | 0.24 |
rpoC | 764803 | c.1434C>G | synonymous_variant | 0.23 |
rpoC | 764812 | c.1443C>G | synonymous_variant | 0.23 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.22 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.18 |
rpoC | 764827 | c.1458G>C | synonymous_variant | 0.2 |
rpoC | 764854 | c.1485G>C | synonymous_variant | 0.21 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.17 |
rpoC | 764863 | c.1494G>C | synonymous_variant | 0.17 |
rpoC | 764869 | c.1500C>T | synonymous_variant | 0.17 |
rpoC | 764872 | c.1503A>T | synonymous_variant | 0.18 |
rpoC | 764878 | c.1509C>G | synonymous_variant | 0.17 |
rpoC | 764887 | c.1518G>T | synonymous_variant | 0.19 |
rpoC | 764888 | c.1519T>C | synonymous_variant | 0.21 |
rpoC | 764893 | c.1524T>C | synonymous_variant | 0.19 |
rpoC | 764902 | c.1533C>G | synonymous_variant | 0.19 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.2 |
rpoC | 764912 | p.Met515Gln | missense_variant | 0.2 |
rpoC | 764917 | c.1548G>C | synonymous_variant | 0.2 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 0.2 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 0.25 |
rpoC | 764948 | c.1579_1581delTTGinsCTC | synonymous_variant | 0.24 |
rpoC | 764953 | c.1584G>C | synonymous_variant | 0.23 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.23 |
rpoC | 765034 | c.1665T>C | synonymous_variant | 0.17 |
rpoC | 765040 | c.1671T>C | synonymous_variant | 0.17 |
rpoC | 765041 | c.1672T>C | synonymous_variant | 0.17 |
rpoC | 765047 | c.1678T>C | synonymous_variant | 0.19 |
rpoC | 765055 | c.1686C>G | synonymous_variant | 0.18 |
rpoC | 765076 | c.1707A>G | synonymous_variant | 0.2 |
rpoC | 765079 | c.1710T>G | synonymous_variant | 0.2 |
rpoC | 765082 | c.1713G>T | synonymous_variant | 0.2 |
rpoC | 765085 | c.1716T>C | synonymous_variant | 0.21 |
rpoC | 765089 | c.1720_1722delTTGinsCTC | synonymous_variant | 0.21 |
rpoC | 765100 | c.1731G>C | synonymous_variant | 0.21 |
rpoC | 765103 | c.1734G>T | synonymous_variant | 0.21 |
rpoC | 765121 | c.1752G>T | synonymous_variant | 0.14 |
rpoC | 766846 | c.3477C>T | synonymous_variant | 0.14 |
rpoC | 766858 | c.3489C>T | synonymous_variant | 0.14 |
rpoC | 766861 | c.3492G>C | synonymous_variant | 0.16 |
rpoC | 766867 | c.3498C>G | synonymous_variant | 0.16 |
rpoC | 766882 | c.3513C>T | synonymous_variant | 0.18 |
rpoC | 766885 | c.3516G>C | synonymous_variant | 0.17 |
rpoC | 766894 | c.3525T>C | synonymous_variant | 0.17 |
rpoC | 766895 | c.3526T>C | synonymous_variant | 0.17 |
rpoC | 766900 | c.3531T>C | synonymous_variant | 0.17 |
rpoC | 766909 | c.3540G>C | synonymous_variant | 0.17 |
rpoC | 766911 | p.Ile1181Thr | missense_variant | 0.17 |
rpoC | 766915 | p.Asp1182Glu | missense_variant | 0.18 |
rpoC | 766918 | c.3549C>T | synonymous_variant | 0.18 |
rpoC | 766919 | p.Ala1184Ser | missense_variant | 0.17 |
rpoC | 766931 | p.Ala1188Ser | missense_variant | 0.15 |
rpoC | 766942 | c.3573C>T | synonymous_variant | 0.15 |
rpoC | 766945 | c.3576A>C | synonymous_variant | 0.16 |
rpoC | 766948 | c.3579G>C | synonymous_variant | 0.16 |
rpoC | 766963 | c.3594T>C | synonymous_variant | 0.19 |
rpoC | 766981 | c.3612T>G | synonymous_variant | 0.2 |
rpoC | 766990 | c.3621G>C | synonymous_variant | 0.2 |
rpoC | 767002 | c.3633G>C | synonymous_variant | 0.21 |
rpoC | 767008 | c.3639G>C | synonymous_variant | 0.22 |
rpoC | 767014 | c.3645G>C | synonymous_variant | 0.22 |
rpoC | 767017 | c.3648C>G | synonymous_variant | 0.22 |
rpoC | 767041 | c.3672G>C | synonymous_variant | 0.16 |
rpoC | 767044 | c.3675G>C | synonymous_variant | 0.16 |
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 | 781751 | c.192G>C | synonymous_variant | 0.16 |
rpsL | 781760 | c.201T>C | synonymous_variant | 0.18 |
rpsL | 781769 | c.210G>A | synonymous_variant | 0.21 |
rpsL | 781772 | c.213C>T | synonymous_variant | 0.21 |
rpsL | 781781 | c.222G>T | synonymous_variant | 0.23 |
rpsL | 781802 | c.243G>C | synonymous_variant | 0.2 |
rpsL | 781805 | c.246G>C | synonymous_variant | 0.2 |
rpsL | 781808 | c.249C>T | synonymous_variant | 0.22 |
rpsL | 781814 | c.255C>T | synonymous_variant | 0.22 |
rpsL | 781817 | c.258G>T | synonymous_variant | 0.22 |
rpsL | 781829 | c.270G>C | synonymous_variant | 0.26 |
rpsL | 781832 | c.273T>G | synonymous_variant | 0.26 |
rpsL | 781838 | c.279G>T | synonymous_variant | 0.24 |
rpsL | 781841 | c.282C>T | synonymous_variant | 0.22 |
rpsL | 781865 | c.306G>C | synonymous_variant | 0.25 |
rpsL | 781871 | c.312G>C | synonymous_variant | 0.26 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.2 |
rpsL | 781898 | c.339A>G | synonymous_variant | 0.2 |
rpsL | 781901 | c.342C>G | synonymous_variant | 0.21 |
rpsL | 781907 | c.348T>C | synonymous_variant | 0.21 |
rpsL | 781916 | c.357T>G | synonymous_variant | 0.22 |
rplC | 800612 | c.-197A>G | upstream_gene_variant | 0.27 |
rplC | 800618 | c.-191T>G | upstream_gene_variant | 0.26 |
rplC | 800633 | c.-176T>C | upstream_gene_variant | 0.28 |
rplC | 800645 | c.-164C>T | upstream_gene_variant | 0.27 |
rplC | 800648 | c.-161A>G | upstream_gene_variant | 0.27 |
rplC | 800654 | c.-155T>C | upstream_gene_variant | 0.26 |
rplC | 800672 | c.-137G>C | upstream_gene_variant | 0.22 |
rplC | 800690 | c.-119C>T | upstream_gene_variant | 0.22 |
rplC | 800693 | c.-116A>G | upstream_gene_variant | 0.22 |
rplC | 800703 | c.-106T>C | upstream_gene_variant | 0.22 |
rplC | 800715 | c.-94_-92delATCinsCTG | upstream_gene_variant | 0.21 |
rplC | 800720 | c.-89T>C | upstream_gene_variant | 0.21 |
rplC | 800723 | c.-86C>G | upstream_gene_variant | 0.22 |
rplC | 800735 | c.-74C>G | upstream_gene_variant | 0.22 |
rplC | 800738 | c.-71T>C | upstream_gene_variant | 0.24 |
rplC | 800762 | c.-47T>G | upstream_gene_variant | 0.21 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
fbiC | 1305494 | c.2565_*55delGGCCTAGCCCCGGCGACGATGCCGGGTCGCGGGATGCGGCCCGTTGAGGAGCGGGGCAATCT | frameshift_variant&stop_lost&splice_region_variant | 0.15 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471918 | n.73A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1471923 | n.78T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1471925 | n.80T>C | non_coding_transcript_exon_variant | 0.57 |
rrs | 1471932 | n.87A>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1471934 | n.89A>G | non_coding_transcript_exon_variant | 0.57 |
rrs | 1471938 | n.93T>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1471972 | n.127T>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1471981 | n.136C>T | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472023 | n.178G>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472061 | n.216A>T | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472067 | n.222G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472068 | n.223T>C | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472069 | n.224G>A | non_coding_transcript_exon_variant | 0.88 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472148 | n.303T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472225 | n.380C>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.9 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472287 | n.442C>T | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472327 | n.482G>A | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.86 |
rrs | 1472396 | n.551A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472431 | n.586G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472438 | n.593T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472450 | n.605A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472451 | n.606C>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472460 | n.615T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472461 | n.616G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472462 | n.617T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472467 | n.622G>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472612 | n.767G>T | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472682 | n.837T>A | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472683 | n.838T>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1472836 | n.991G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472837 | n.992C>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472839 | n.994C>G | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472843 | n.998_999insT | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472857 | n.1012A>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472858 | n.1013G>C | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472860 | n.1015C>G | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472861 | n.1016G>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472864 | n.1019C>G | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472872 | n.1027G>C | non_coding_transcript_exon_variant | 0.68 |
rrs | 1472874 | n.1029C>T | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472876 | n.1031G>C | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472878 | n.1033G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1473081 | n.1236C>G | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473082 | n.1237G>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473088 | n.1243A>G | non_coding_transcript_exon_variant | 0.84 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.77 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.77 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473129 | n.1284C>G | non_coding_transcript_exon_variant | 0.77 |
rrs | 1473130 | n.1285G>C | non_coding_transcript_exon_variant | 0.77 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.59 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.45 |
rrl | 1473679 | n.22T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1473695 | n.38A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473696 | n.39T>C | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473697 | n.40C>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473698 | n.41G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473699 | n.42A>G | non_coding_transcript_exon_variant | 0.22 |
rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1473757 | n.100T>G | non_coding_transcript_exon_variant | 0.62 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1473793 | n.136G>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1473797 | n.140G>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1473802 | n.145C>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1473814 | n.157A>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1473815 | n.158T>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1473816 | n.159C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1473844 | n.187C>A | non_coding_transcript_exon_variant | 0.7 |
rrl | 1473870 | n.213G>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1473871 | n.214T>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.7 |
rrl | 1473888 | n.231T>A | non_coding_transcript_exon_variant | 0.7 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1473922 | n.265A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473933 | n.276_277insAT | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473936 | n.281_282delGC | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473943 | n.286G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473945 | n.288T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473946 | n.289A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473968 | n.311C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473971 | n.314G>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474007 | n.350A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1474127 | n.470G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474139 | n.482C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474140 | n.483C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474151 | n.494C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474174 | n.517A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474180 | n.523_524insA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474202 | n.545T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474218 | n.561T>A | 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 | 1.0 |
rrl | 1474308 | n.651G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474353 | n.696A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474355 | n.698A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474356 | n.699T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474359 | n.702C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474373 | n.717dupT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474402 | n.745T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474409 | n.756_776delACCCACACGCGCATACGCGCG | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474435 | n.778G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474437 | n.782_784delATA | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474444 | n.787G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474447 | n.790G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474448 | n.791T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474450 | n.793T>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474495 | n.838G>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474496 | n.839C>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474498 | n.841G>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474505 | n.848C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474508 | n.851C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1474626 | n.969T>C | non_coding_transcript_exon_variant | 0.79 |
rrl | 1474627 | n.970G>A | non_coding_transcript_exon_variant | 0.79 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.79 |
rrl | 1474638 | n.981C>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1474639 | n.982G>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474674 | n.1017A>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474675 | n.1018C>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474676 | n.1019T>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1474709 | n.1053_1056delTGGT | non_coding_transcript_exon_variant | 0.88 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474803 | n.1146G>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474812 | n.1155G>A | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474822 | n.1165G>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474824 | n.1167A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475433 | n.1776A>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475443 | n.1786G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475444 | n.1787G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1475479 | n.1822C>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475482 | n.1825A>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475483 | n.1826C>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475485 | n.1828C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475486 | n.1829A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475487 | n.1830C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475505 | n.1848G>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475536 | n.1879C>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475538 | n.1881T>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475550 | n.1893A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475601 | n.1945_1950delGGAATA | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475609 | n.1954_1955insCTGGT | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475614 | n.1957A>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475615 | n.1958C>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475617 | n.1960C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475619 | n.1962C>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475622 | n.1965G>A | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475627 | n.1970G>C | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475633 | n.1976G>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475636 | n.1979A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475638 | n.1981C>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475639 | n.1982C>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 0.85 |
rrl | 1475655 | n.1998T>A | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.9 |
rrl | 1475688 | n.2031G>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475699 | n.2042C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1475713 | n.2056C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1475763 | n.2106C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1475883 | n.2226A>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475897 | n.2240T>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.81 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.8 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.81 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476032 | n.2375C>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476033 | n.2376T>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476035 | n.2378G>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476044 | n.2387T>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476045 | n.2388G>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476046 | n.2389G>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476047 | n.2390G>C | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476087 | n.2430C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476089 | n.2432T>C | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476091 | n.2434_2435insC | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476103 | n.2446C>A | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476110 | n.2453G>T | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476215 | n.2558C>T | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476256 | n.2599A>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476297 | n.2640C>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476298 | n.2641C>G | non_coding_transcript_exon_variant | 0.84 |
rrl | 1476300 | n.2643G>A | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476524 | n.2867C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476529 | n.2872A>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476597 | n.2940G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476603 | n.2946G>A | 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 | 0.64 |
rrl | 1476616 | n.2959A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.61 |
rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 0.47 |
rrl | 1476665 | n.3008T>G | non_coding_transcript_exon_variant | 0.4 |
rrl | 1476666 | n.3009C>T | non_coding_transcript_exon_variant | 0.38 |
rpsA | 1833676 | c.135A>G | synonymous_variant | 0.17 |
rpsA | 1833694 | c.153G>T | synonymous_variant | 0.16 |
rpsA | 1833697 | c.156C>G | synonymous_variant | 0.15 |
rpsA | 1833709 | c.168C>T | synonymous_variant | 0.18 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.23 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.23 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.24 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.25 |
rpsA | 1833746 | c.205_206delTCinsAG | synonymous_variant | 0.21 |
rpsA | 1833769 | c.228C>G | synonymous_variant | 0.18 |
rpsA | 1833770 | p.Asn77Ser | missense_variant | 0.18 |
rpsA | 1833781 | c.240T>C | synonymous_variant | 0.19 |
rpsA | 1833782 | p.Ser81Asn | missense_variant | 0.19 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.19 |
rpsA | 1833793 | c.252C>T | synonymous_variant | 0.19 |
rpsA | 1833795 | p.Glu85Ala | missense_variant | 0.19 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.19 |
rpsA | 1833805 | c.264C>T | synonymous_variant | 0.18 |
rpsA | 1833808 | c.267G>C | synonymous_variant | 0.18 |
rpsA | 1833811 | c.270G>C | synonymous_variant | 0.18 |
rpsA | 1833829 | c.288A>G | synonymous_variant | 0.33 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 0.32 |
rpsA | 1833838 | c.297G>C | synonymous_variant | 0.34 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.33 |
rpsA | 1833847 | c.306C>G | synonymous_variant | 0.36 |
rpsA | 1833856 | c.315A>G | synonymous_variant | 0.37 |
rpsA | 1833859 | c.318C>T | synonymous_variant | 0.37 |
rpsA | 1833874 | c.333T>C | synonymous_variant | 0.38 |
rpsA | 1833886 | c.345C>G | synonymous_variant | 0.37 |
rpsA | 1833894 | p.Ala118Glu | missense_variant | 0.41 |
rpsA | 1833928 | c.387G>C | synonymous_variant | 0.44 |
rpsA | 1833940 | c.399C>G | synonymous_variant | 0.41 |
rpsA | 1833952 | c.411C>T | synonymous_variant | 0.38 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 0.38 |
rpsA | 1833961 | c.420C>G | synonymous_variant | 0.37 |
rpsA | 1833970 | c.429G>C | synonymous_variant | 0.38 |
rpsA | 1833973 | c.432G>C | synonymous_variant | 0.37 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.33 |
rpsA | 1833985 | c.444G>C | synonymous_variant | 0.34 |
rpsA | 1833988 | c.447C>G | synonymous_variant | 0.36 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.37 |
rpsA | 1834009 | c.468C>T | synonymous_variant | 0.33 |
rpsA | 1834012 | c.471G>T | synonymous_variant | 0.34 |
rpsA | 1834024 | c.483G>C | synonymous_variant | 0.33 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.33 |
rpsA | 1834054 | c.513C>G | synonymous_variant | 0.36 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.28 |
rpsA | 1834093 | c.552G>C | synonymous_variant | 0.27 |
rpsA | 1834099 | c.558C>G | synonymous_variant | 0.26 |
rpsA | 1834102 | c.561T>C | synonymous_variant | 0.26 |
rpsA | 1834105 | c.564C>T | synonymous_variant | 0.24 |
rpsA | 1834108 | c.567C>A | synonymous_variant | 0.25 |
rpsA | 1834114 | c.573G>C | synonymous_variant | 0.31 |
rpsA | 1834135 | c.594G>C | synonymous_variant | 0.3 |
rpsA | 1834151 | p.Asn204His | missense_variant | 0.27 |
rpsA | 1834154 | p.Asn205Gln | missense_variant | 0.27 |
rpsA | 1834157 | c.616T>C | synonymous_variant | 0.27 |
rpsA | 1834162 | c.621A>G | synonymous_variant | 0.26 |
rpsA | 1834165 | c.624A>G | synonymous_variant | 0.26 |
rpsA | 1834167 | c.628_629delAC | frameshift_variant | 0.25 |
rpsA | 1834172 | c.631_632insGG | frameshift_variant | 0.28 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 0.39 |
rpsA | 1834183 | c.642T>C | synonymous_variant | 0.48 |
rpsA | 1834210 | c.669C>T | synonymous_variant | 0.5 |
rpsA | 1834213 | c.672G>C | synonymous_variant | 0.5 |
rpsA | 1834219 | c.678C>G | synonymous_variant | 0.48 |
rpsA | 1834222 | c.681T>C | synonymous_variant | 0.47 |
rpsA | 1834225 | c.684C>G | synonymous_variant | 0.47 |
rpsA | 1834231 | c.690T>C | synonymous_variant | 0.5 |
rpsA | 1834234 | c.693G>C | synonymous_variant | 0.51 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.55 |
rpsA | 1834243 | c.702G>C | synonymous_variant | 0.53 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.61 |
rpsA | 1834255 | c.714C>G | synonymous_variant | 0.61 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.57 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.59 |
rpsA | 1834279 | c.738C>T | synonymous_variant | 0.57 |
rpsA | 1834298 | p.Gln253Thr | missense_variant | 0.53 |
rpsA | 1834303 | c.762T>G | synonymous_variant | 0.5 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.5 |
rpsA | 1834327 | c.786G>C | synonymous_variant | 0.46 |
rpsA | 1834340 | p.Met267Leu | missense_variant | 0.44 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.44 |
rpsA | 1834354 | c.813G>C | synonymous_variant | 0.43 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.42 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.4 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.41 |
rpsA | 1834378 | c.837T>C | synonymous_variant | 0.42 |
rpsA | 1834384 | c.843A>G | synonymous_variant | 0.42 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.39 |
rpsA | 1834396 | c.855G>T | synonymous_variant | 0.33 |
rpsA | 1834399 | p.His286Gln | missense_variant | 0.33 |
rpsA | 1834408 | c.867C>G | synonymous_variant | 0.34 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.33 |
rpsA | 1834417 | c.876G>C | synonymous_variant | 0.34 |
rpsA | 1834423 | c.882G>C | synonymous_variant | 0.35 |
rpsA | 1834435 | c.894G>C | synonymous_variant | 0.36 |
rpsA | 1834451 | c.910_912delTTGinsCTC | synonymous_variant | 0.36 |
rpsA | 1834456 | c.915T>C | synonymous_variant | 0.35 |
rpsA | 1834465 | c.924T>C | synonymous_variant | 0.35 |
rpsA | 1834468 | c.927A>G | synonymous_variant | 0.35 |
rpsA | 1834489 | c.948T>C | synonymous_variant | 0.4 |
rpsA | 1834501 | c.960G>C | synonymous_variant | 0.39 |
rpsA | 1834504 | c.963G>C | synonymous_variant | 0.37 |
rpsA | 1834513 | c.972C>G | synonymous_variant | 0.36 |
rpsA | 1834528 | c.987T>C | synonymous_variant | 0.38 |
rpsA | 1834540 | c.999G>C | synonymous_variant | 0.38 |
rpsA | 1834543 | c.1002C>G | synonymous_variant | 0.38 |
rpsA | 1834546 | c.1005T>C | synonymous_variant | 0.38 |
rpsA | 1834552 | c.1011G>C | synonymous_variant | 0.38 |
rpsA | 1834555 | c.1014T>C | synonymous_variant | 0.39 |
rpsA | 1834556 | p.Ala339Ser | missense_variant | 0.39 |
rpsA | 1834570 | c.1029C>T | synonymous_variant | 0.39 |
rpsA | 1834600 | c.1059G>C | synonymous_variant | 0.42 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 0.5 |
rpsA | 1834612 | c.1071G>T | synonymous_variant | 0.48 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 0.5 |
rpsA | 1834622 | c.1081_1083delTCGinsAGC | synonymous_variant | 0.5 |
rpsA | 1834633 | c.1092A>G | synonymous_variant | 0.55 |
rpsA | 1834639 | c.1098T>C | synonymous_variant | 0.55 |
rpsA | 1834667 | p.Ala376Ser | missense_variant | 0.38 |
rpsA | 1834690 | c.1149T>C | synonymous_variant | 0.35 |
rpsA | 1834700 | p.Gln387Asn | missense_variant | 0.35 |
rpsA | 1834706 | p.Asn389Glu | missense_variant | 0.32 |
rpsA | 1834733 | p.Ala398Pro | missense_variant | 0.2 |
rpsA | 1834859 | p.Ala440Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
ndh | 2102193 | p.Arg284Trp | missense_variant | 1.0 |
ndh | 2103173 | c.-132delG | upstream_gene_variant | 1.0 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155503 | c.609C>T | synonymous_variant | 1.0 |
katG | 2155743 | c.369G>C | synonymous_variant | 0.16 |
katG | 2155755 | c.357C>T | synonymous_variant | 0.15 |
katG | 2155787 | p.Ala109Ser | missense_variant | 0.13 |
katG | 2155796 | p.Ala106Ser | missense_variant | 0.13 |
katG | 2156025 | c.87C>A | synonymous_variant | 1.0 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2168011 | p.Ser868Arg | missense_variant | 1.0 |
PPE35 | 2168319 | p.Thr765Ile | missense_variant | 1.0 |
PPE35 | 2168814 | c.1798dupA | frameshift_variant | 1.0 |
PPE35 | 2169156 | p.Thr486Met | missense_variant | 0.12 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2517945 | c.-170_-168delATCinsGTG | upstream_gene_variant | 0.14 |
kasA | 2517950 | c.-165C>G | upstream_gene_variant | 0.14 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
eis | 2715125 | p.Thr70Ala | missense_variant | 1.0 |
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 | 3877613 | p.Ile299Val | missense_variant | 0.13 |
rpoA | 3877656 | c.852T>C | synonymous_variant | 0.2 |
rpoA | 3877659 | c.849G>T | synonymous_variant | 0.2 |
rpoA | 3877668 | c.840A>G | synonymous_variant | 0.21 |
rpoA | 3877677 | c.831G>C | synonymous_variant | 0.24 |
rpoA | 3877683 | c.825G>C | synonymous_variant | 0.23 |
rpoA | 3877686 | c.822A>G | synonymous_variant | 0.24 |
rpoA | 3877704 | c.804G>T | synonymous_variant | 0.3 |
rpoA | 3877728 | c.780C>G | synonymous_variant | 0.31 |
rpoA | 3877731 | c.777G>T | synonymous_variant | 0.32 |
rpoA | 3877743 | c.765T>C | synonymous_variant | 0.33 |
rpoA | 3877746 | c.762G>C | synonymous_variant | 0.3 |
rpoA | 3877752 | p.Asp252Glu | missense_variant | 0.29 |
rpoA | 3877764 | p.Ala248Ser | missense_variant | 0.3 |
rpoA | 3877770 | p.Ser246Ala | missense_variant | 0.31 |
rpoA | 3877776 | c.732T>C | synonymous_variant | 0.37 |
rpoA | 3877782 | c.726T>C | synonymous_variant | 0.39 |
rpoA | 3877818 | c.690A>G | synonymous_variant | 0.5 |
rpoA | 3877836 | c.672A>G | synonymous_variant | 0.55 |
rpoA | 3877839 | c.669G>C | synonymous_variant | 0.54 |
rpoA | 3877842 | c.666A>G | synonymous_variant | 0.53 |
rpoA | 3877856 | c.652T>C | synonymous_variant | 0.54 |
rpoA | 3877866 | c.642G>C | synonymous_variant | 0.5 |
rpoA | 3877875 | c.633T>C | synonymous_variant | 0.47 |
rpoA | 3877881 | c.627G>T | synonymous_variant | 0.5 |
rpoA | 3877893 | c.615C>G | synonymous_variant | 0.46 |
rpoA | 3877898 | p.Pro204Ala | missense_variant | 0.49 |
rpoA | 3877900 | p.Ser203Thr | missense_variant | 0.5 |
rpoA | 3877902 | p.Ile202Met | missense_variant | 0.5 |
rpoA | 3877905 | c.603A>G | synonymous_variant | 0.5 |
rpoA | 3877908 | c.600T>C | synonymous_variant | 0.49 |
rpoA | 3877920 | c.588G>C | synonymous_variant | 0.5 |
rpoA | 3877935 | p.Lys191Arg | missense_variant | 0.5 |
rpoA | 3877938 | c.570C>T | synonymous_variant | 0.5 |
rpoA | 3877962 | c.546G>T | synonymous_variant | 0.48 |
rpoA | 3877971 | p.Asp179Glu | missense_variant | 0.53 |
rpoA | 3877989 | c.519A>G | synonymous_variant | 0.57 |
rpoA | 3877998 | c.510G>C | synonymous_variant | 0.54 |
rpoA | 3878001 | c.507A>G | synonymous_variant | 0.5 |
rpoA | 3878010 | c.498C>G | synonymous_variant | 0.5 |
rpoA | 3878013 | c.495T>C | synonymous_variant | 0.5 |
rpoA | 3878019 | c.489A>G | synonymous_variant | 0.5 |
rpoA | 3878025 | c.483C>T | synonymous_variant | 0.46 |
rpoA | 3878028 | c.480G>C | synonymous_variant | 0.45 |
rpoA | 3878031 | c.477T>C | synonymous_variant | 0.45 |
rpoA | 3878034 | c.474A>G | synonymous_variant | 0.45 |
rpoA | 3878040 | c.468T>C | synonymous_variant | 0.43 |
rpoA | 3878046 | c.462T>G | synonymous_variant | 0.42 |
rpoA | 3878050 | p.Arg153Lys | missense_variant | 0.42 |
rpoA | 3878055 | c.453A>G | synonymous_variant | 0.44 |
rpoA | 3878061 | c.447G>C | synonymous_variant | 0.46 |
rpoA | 3878067 | c.441C>G | synonymous_variant | 0.46 |
rpoA | 3878070 | c.438T>C | synonymous_variant | 0.48 |
rpoA | 3878082 | c.426T>G | synonymous_variant | 0.52 |
rpoA | 3878102 | p.Val136Ile | missense_variant | 0.5 |
rpoA | 3878103 | c.405A>G | synonymous_variant | 0.5 |
rpoA | 3878106 | c.402G>C | synonymous_variant | 0.52 |
rpoA | 3878118 | c.390T>C | synonymous_variant | 0.51 |
rpoA | 3878127 | c.381G>C | synonymous_variant | 0.48 |
rpoA | 3878136 | c.372C>T | synonymous_variant | 0.5 |
rpoA | 3878161 | c.345_346delCG | frameshift_variant | 0.48 |
rpoA | 3878166 | c.341_342insGT | frameshift_variant | 0.47 |
rpoA | 3878172 | c.336G>C | synonymous_variant | 0.45 |
rpoA | 3878175 | c.333G>T | synonymous_variant | 0.45 |
rpoA | 3878187 | c.321C>G | synonymous_variant | 0.41 |
rpoA | 3878193 | c.315T>C | synonymous_variant | 0.41 |
rpoA | 3878196 | p.Glu104Ala | missense_variant | 0.38 |
rpoA | 3878199 | c.309T>C | synonymous_variant | 0.38 |
rpoA | 3878205 | c.303T>C | synonymous_variant | 0.4 |
rpoA | 3878217 | p.Leu97Val | missense_variant | 0.44 |
rpoA | 3878241 | p.Glu89Asp | missense_variant | 0.35 |
rpoA | 3878250 | c.258C>G | synonymous_variant | 0.33 |
rpoA | 3878253 | c.255G>C | synonymous_variant | 0.31 |
rpoA | 3878256 | c.252G>C | synonymous_variant | 0.33 |
rpoA | 3878264 | p.Ser82Gly | missense_variant | 0.33 |
rpoA | 3878271 | c.237T>C | synonymous_variant | 0.36 |
rpoA | 3878283 | p.Glu75Asp | missense_variant | 0.38 |
rpoA | 3878295 | c.213A>G | synonymous_variant | 0.36 |
rpoA | 3878298 | c.210A>G | synonymous_variant | 0.38 |
rpoA | 3878301 | c.207C>G | synonymous_variant | 0.36 |
rpoA | 3878304 | c.204G>C | synonymous_variant | 0.36 |
rpoA | 3878310 | c.198G>C | synonymous_variant | 0.38 |
rpoA | 3878322 | c.186A>G | synonymous_variant | 0.32 |
rpoA | 3878331 | c.177A>G | synonymous_variant | 0.32 |
rpoA | 3878334 | c.174T>C | synonymous_variant | 0.24 |
rpoA | 3878337 | c.171T>C | synonymous_variant | 0.24 |
rpoA | 3878346 | c.162T>C | synonymous_variant | 0.29 |
rpoA | 3878355 | c.153C>G | synonymous_variant | 0.29 |
rpoA | 3878364 | c.144A>C | synonymous_variant | 0.31 |
rpoA | 3878367 | c.141C>G | synonymous_variant | 0.25 |
rpoA | 3878370 | c.138T>C | synonymous_variant | 0.25 |
rpoA | 3878373 | c.135G>C | synonymous_variant | 0.25 |
rpoA | 3878385 | c.123C>G | synonymous_variant | 0.25 |
rpoA | 3878391 | c.117T>C | synonymous_variant | 0.18 |
rpoA | 3878394 | c.114G>C | synonymous_variant | 0.18 |
rpoA | 3878400 | c.108T>C | synonymous_variant | 0.18 |
rpoA | 3878409 | c.99C>G | synonymous_variant | 0.15 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
clpC1 | 4038725 | c.1980C>G | synonymous_variant | 0.2 |
clpC1 | 4038740 | c.1965G>C | synonymous_variant | 0.3 |
clpC1 | 4038743 | c.1962G>C | synonymous_variant | 0.32 |
clpC1 | 4038755 | c.1950G>C | synonymous_variant | 0.34 |
clpC1 | 4038764 | c.1941C>G | synonymous_variant | 0.34 |
clpC1 | 4038767 | c.1938G>C | synonymous_variant | 0.36 |
clpC1 | 4038770 | c.1935C>T | synonymous_variant | 0.36 |
clpC1 | 4038773 | c.1932T>C | synonymous_variant | 0.37 |
clpC1 | 4038794 | p.Ser637Thr | missense_variant | 0.39 |
clpC1 | 4038808 | c.1896_1897insC | frameshift_variant | 0.42 |
clpC1 | 4038811 | c.1893delT | frameshift_variant | 0.38 |
clpC1 | 4038860 | c.1845G>C | synonymous_variant | 0.52 |
clpC1 | 4038878 | c.1827A>G | synonymous_variant | 0.53 |
clpC1 | 4038896 | c.1809C>G | synonymous_variant | 0.61 |
clpC1 | 4038905 | c.1800A>G | synonymous_variant | 0.64 |
clpC1 | 4038911 | c.1794G>T | synonymous_variant | 0.58 |
clpC1 | 4038914 | c.1791G>C | synonymous_variant | 0.56 |
clpC1 | 4038923 | c.1782A>G | synonymous_variant | 0.56 |
clpC1 | 4038926 | c.1779G>C | synonymous_variant | 0.55 |
clpC1 | 4038932 | c.1773G>C | synonymous_variant | 0.55 |
clpC1 | 4038941 | c.1764G>C | synonymous_variant | 0.53 |
clpC1 | 4038953 | c.1752A>G | synonymous_variant | 0.58 |
clpC1 | 4038956 | c.1749T>C | synonymous_variant | 0.59 |
clpC1 | 4038965 | c.1740T>C | synonymous_variant | 0.57 |
clpC1 | 4038971 | c.1734T>C | synonymous_variant | 0.56 |
clpC1 | 4038974 | c.1731T>C | synonymous_variant | 0.56 |
clpC1 | 4038986 | p.Asp573Glu | missense_variant | 0.56 |
clpC1 | 4038989 | c.1716T>C | synonymous_variant | 0.56 |
clpC1 | 4038997 | c.1708T>C | synonymous_variant | 0.56 |
clpC1 | 4039004 | c.1701C>G | synonymous_variant | 0.51 |
clpC1 | 4039016 | c.1689C>G | synonymous_variant | 0.51 |
clpC1 | 4039022 | c.1683A>G | synonymous_variant | 0.53 |
clpC1 | 4039085 | c.1620A>G | synonymous_variant | 0.46 |
clpC1 | 4039091 | c.1614G>C | synonymous_variant | 0.44 |
clpC1 | 4039097 | c.1608G>T | synonymous_variant | 0.4 |
clpC1 | 4039100 | c.1605C>G | synonymous_variant | 0.4 |
clpC1 | 4039106 | c.1599G>C | synonymous_variant | 0.4 |
clpC1 | 4039112 | c.1593C>G | synonymous_variant | 0.4 |
clpC1 | 4039118 | c.1587C>G | synonymous_variant | 0.38 |
clpC1 | 4039121 | c.1584T>C | synonymous_variant | 0.37 |
clpC1 | 4039124 | c.1581C>G | synonymous_variant | 0.38 |
clpC1 | 4039142 | c.1563A>G | synonymous_variant | 0.31 |
clpC1 | 4039145 | c.1560G>C | synonymous_variant | 0.31 |
clpC1 | 4039169 | p.Glu512Asp | missense_variant | 0.23 |
clpC1 | 4039172 | c.1533A>G | synonymous_variant | 0.23 |
clpC1 | 4039178 | c.1527G>C | synonymous_variant | 0.21 |
clpC1 | 4039181 | c.1522_1524delTTGinsCTC | synonymous_variant | 0.21 |
clpC1 | 4039187 | c.1518G>T | synonymous_variant | 0.19 |
clpC1 | 4039199 | p.Ala502Glu | missense_variant | 0.21 |
clpC1 | 4039499 | c.1206G>C | synonymous_variant | 0.19 |
clpC1 | 4039517 | c.1188C>G | synonymous_variant | 0.31 |
clpC1 | 4039526 | c.1179G>C | synonymous_variant | 0.31 |
clpC1 | 4039541 | c.1164C>G | synonymous_variant | 0.28 |
clpC1 | 4039547 | c.1158C>G | synonymous_variant | 0.25 |
clpC1 | 4039556 | c.1149G>C | synonymous_variant | 0.25 |
clpC1 | 4039565 | c.1140G>C | synonymous_variant | 0.24 |
clpC1 | 4039570 | p.Met379Leu | missense_variant | 0.25 |
clpC1 | 4039574 | p.Ala377Ser | missense_variant | 0.26 |
clpC1 | 4039577 | c.1128T>C | synonymous_variant | 0.26 |
clpC1 | 4039580 | c.1125C>G | synonymous_variant | 0.26 |
clpC1 | 4039586 | c.1119G>C | synonymous_variant | 0.27 |
clpC1 | 4039589 | p.Val372Ile | missense_variant | 0.27 |
clpC1 | 4039592 | c.1113G>C | synonymous_variant | 0.24 |
clpC1 | 4039616 | c.1089G>C | synonymous_variant | 0.3 |
clpC1 | 4039642 | p.Thr355Ala | missense_variant | 0.37 |
clpC1 | 4039649 | c.1056G>C | synonymous_variant | 0.36 |
clpC1 | 4039652 | p.Thr351Ser | missense_variant | 0.35 |
clpC1 | 4039661 | c.1044T>C | synonymous_variant | 0.37 |
clpC1 | 4039670 | c.1035G>C | synonymous_variant | 0.36 |
clpC1 | 4039673 | c.1032G>C | synonymous_variant | 0.37 |
clpC1 | 4039694 | c.1011G>C | synonymous_variant | 0.36 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.35 |
clpC1 | 4039748 | c.957G>C | synonymous_variant | 0.3 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.33 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.33 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.29 |
clpC1 | 4039769 | c.936C>G | synonymous_variant | 0.28 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.27 |
clpC1 | 4039781 | c.924G>C | synonymous_variant | 0.26 |
clpC1 | 4039817 | c.888A>T | synonymous_variant | 0.27 |
clpC1 | 4039820 | c.885T>G | synonymous_variant | 0.28 |
clpC1 | 4039823 | c.882T>C | synonymous_variant | 0.29 |
clpC1 | 4039829 | c.874_876delTTGinsCTC | synonymous_variant | 0.29 |
clpC1 | 4039832 | c.873C>G | synonymous_variant | 0.29 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.33 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.35 |
clpC1 | 4039876 | p.Asn277Asp | missense_variant | 0.33 |
clpC1 | 4039895 | p.Lys270Arg | missense_variant | 0.31 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.31 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.31 |
clpC1 | 4039925 | c.780C>T | synonymous_variant | 0.26 |
clpC1 | 4039928 | c.775_777delAGCinsTCG | synonymous_variant | 0.26 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.25 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.27 |
clpC1 | 4039943 | c.762G>C | synonymous_variant | 0.3 |
clpC1 | 4039946 | c.759A>C | synonymous_variant | 0.31 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.31 |
clpC1 | 4039964 | c.741C>G | synonymous_variant | 0.32 |
clpC1 | 4039982 | c.723G>C | synonymous_variant | 0.35 |
clpC1 | 4039988 | c.717C>G | synonymous_variant | 0.29 |
clpC1 | 4039994 | p.Glu237Asn | missense_variant | 0.24 |
clpC1 | 4040002 | p.His235Asn | missense_variant | 0.23 |
clpC1 | 4040003 | c.702G>C | synonymous_variant | 0.23 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.2 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.19 |
clpC1 | 4040030 | c.675C>G | synonymous_variant | 0.19 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.2 |
clpC1 | 4040045 | c.660C>G | synonymous_variant | 0.2 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
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 |
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 |
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 |
fbiC | 1305494 | c.2565_*56delCNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNNN | frameshift_variant&stop_lost&splice_region_variant | 1.0 |