Run ID: ERR3468488
Sample name:
Date: 01-04-2023 02:15:32
Number of reads: 389699
Percentage reads mapped: 35.69
Strain: La1.8.1
Drug-resistance: RR-TB
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 |
---|---|---|---|---|---|
rpoB | 761196 | p.Leu464Met | missense_variant | 0.29 | rifampicin |
rrs | 1472644 | n.799C>T | non_coding_transcript_exon_variant | 0.8 | streptomycin |
rrs | 1473247 | n.1402C>A | non_coding_transcript_exon_variant | 0.83 | kanamycin, capreomycin, aminoglycosides, amikacin |
rrs | 1473329 | n.1484G>T | non_coding_transcript_exon_variant | 0.82 | kanamycin, capreomycin, aminoglycosides, amikacin |
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 |
gyrB | 6998 | p.Arg587Ser | missense_variant | 0.15 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 8048 | c.747C>A | synonymous_variant | 1.0 |
gyrA | 8285 | c.984C>T | synonymous_variant | 1.0 |
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 | 491382 | p.Glu200Asp | missense_variant | 0.4 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
rpoB | 759994 | p.Arg63His | missense_variant | 0.33 |
rpoB | 760007 | c.201C>A | synonymous_variant | 0.33 |
rpoB | 760631 | c.825G>A | synonymous_variant | 0.2 |
rpoB | 760920 | p.Leu372Ile | missense_variant | 0.23 |
rpoB | 760925 | c.1119T>C | synonymous_variant | 0.23 |
rpoB | 760926 | p.Thr374Ala | missense_variant | 0.23 |
rpoB | 760940 | c.1134G>C | synonymous_variant | 0.25 |
rpoB | 760944 | p.Gln380Glu | missense_variant | 0.25 |
rpoB | 760953 | p.Ile383Val | missense_variant | 0.25 |
rpoB | 760958 | c.1152G>C | synonymous_variant | 0.25 |
rpoB | 760959 | p.Val385Thr | missense_variant | 0.25 |
rpoB | 760965 | p.Met387Leu | missense_variant | 0.25 |
rpoB | 760970 | c.1164G>C | synonymous_variant | 0.27 |
rpoB | 760973 | c.1167G>C | synonymous_variant | 0.25 |
rpoB | 760982 | c.1176G>C | synonymous_variant | 0.31 |
rpoB | 760985 | c.1179G>T | synonymous_variant | 0.21 |
rpoB | 760991 | c.1185G>C | synonymous_variant | 0.29 |
rpoB | 760997 | c.1191G>C | synonymous_variant | 0.13 |
rpoB | 761015 | c.1209G>C | synonymous_variant | 0.5 |
rpoB | 761018 | c.1212G>A | synonymous_variant | 0.48 |
rpoB | 761027 | c.1221A>G | synonymous_variant | 0.54 |
rpoB | 761036 | c.1230G>C | synonymous_variant | 0.45 |
rpoB | 761037 | c.1231T>C | synonymous_variant | 0.5 |
rpoB | 761051 | c.1245G>C | synonymous_variant | 0.48 |
rpoB | 761057 | c.1251G>C | synonymous_variant | 0.54 |
rpoB | 761084 | c.1278C>A | synonymous_variant | 0.55 |
rpoB | 761088 | c.1282_1283delAGinsTC | synonymous_variant | 0.55 |
rpoB | 761096 | c.1290G>C | synonymous_variant | 0.45 |
rpoB | 761097 | c.1291_1293delAGCinsTCG | synonymous_variant | 0.55 |
rpoB | 761102 | c.1296A>G | synonymous_variant | 0.57 |
rpoB | 761126 | c.1320G>C | synonymous_variant | 0.55 |
rpoB | 761132 | c.1326G>C | synonymous_variant | 0.55 |
rpoB | 761133 | c.1327T>C | synonymous_variant | 0.57 |
rpoB | 761150 | c.1344A>C | synonymous_variant | 0.62 |
rpoB | 761156 | c.1350G>C | synonymous_variant | 0.6 |
rpoB | 761165 | c.1359G>C | synonymous_variant | 0.5 |
rpoB | 761180 | c.1374A>C | synonymous_variant | 0.43 |
rpoB | 761186 | p.Glu460Asp | missense_variant | 0.36 |
rpoB | 761195 | c.1389G>C | synonymous_variant | 0.29 |
rpoB | 761201 | c.1395G>A | synonymous_variant | 0.15 |
rpoB | 761207 | c.1401C>T | synonymous_variant | 0.25 |
rpoB | 761222 | c.1416G>C | synonymous_variant | 0.17 |
rpoB | 761231 | c.1425C>A | synonymous_variant | 0.25 |
rpoB | 761234 | c.1428G>T | synonymous_variant | 0.17 |
rpoB | 761243 | c.1437G>C | synonymous_variant | 0.21 |
rpoC | 762827 | c.-543G>C | upstream_gene_variant | 0.25 |
rpoC | 762831 | c.-539_-538delAGinsTC | upstream_gene_variant | 0.29 |
rpoB | 762849 | p.Tyr1015Asp | missense_variant | 0.33 |
rpoB | 762855 | p.Val1017Ile | missense_variant | 0.33 |
rpoB | 762858 | p.Thr1018Ser | missense_variant | 0.44 |
rpoC | 762863 | c.-507T>C | upstream_gene_variant | 0.44 |
rpoB | 762879 | p.Met1025Leu | missense_variant | 0.3 |
rpoC | 762887 | c.-483G>C | upstream_gene_variant | 0.3 |
rpoC | 762917 | c.-453C>G | upstream_gene_variant | 0.17 |
rpoC | 762923 | c.-447C>G | upstream_gene_variant | 0.23 |
rpoC | 762926 | c.-444C>G | upstream_gene_variant | 0.15 |
rpoC | 762929 | c.-441G>C | upstream_gene_variant | 0.22 |
rpoC | 762938 | c.-432G>C | upstream_gene_variant | 0.15 |
rpoC | 762947 | c.-423C>G | upstream_gene_variant | 0.45 |
rpoC | 762962 | c.-408C>T | upstream_gene_variant | 0.46 |
rpoC | 762971 | c.-399G>A | upstream_gene_variant | 0.15 |
rpoC | 762989 | c.-381G>C | upstream_gene_variant | 0.33 |
rpoC | 762995 | c.-375G>T | upstream_gene_variant | 0.27 |
rpoC | 763004 | c.-366G>A | upstream_gene_variant | 0.25 |
rpoB | 763005 | p.Cys1067Val | missense_variant | 0.25 |
rpoB | 763014 | p.Met1070Leu | missense_variant | 0.25 |
rpoB | 763017 | p.Gln1071Glu | missense_variant | 0.25 |
rpoC | 763028 | c.-342T>C | upstream_gene_variant | 0.23 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763040 | c.-330C>G | upstream_gene_variant | 0.23 |
rpoC | 763049 | c.-321G>A | upstream_gene_variant | 0.27 |
rpoC | 763052 | c.-318G>C | upstream_gene_variant | 0.27 |
rpoC | 763053 | c.-317T>C | upstream_gene_variant | 0.27 |
rpoC | 763067 | c.-303C>G | upstream_gene_variant | 0.33 |
rpoC | 763070 | c.-300T>C | upstream_gene_variant | 0.25 |
rpoB | 763075 | p.Thr1090Ile | missense_variant | 0.25 |
rpoB | 763077 | p.Val1091His | missense_variant | 0.25 |
rpoC | 763082 | c.-288C>A | upstream_gene_variant | 0.25 |
rpoC | 763103 | c.-267G>C | upstream_gene_variant | 0.2 |
rpoC | 763465 | c.96G>A | synonymous_variant | 0.29 |
rpoC | 763468 | c.99G>C | synonymous_variant | 0.38 |
rpoC | 763486 | c.117T>C | synonymous_variant | 0.42 |
rpoC | 763492 | c.123G>C | synonymous_variant | 0.46 |
rpoC | 763507 | c.138G>C | synonymous_variant | 0.5 |
rpoC | 763528 | c.159G>C | synonymous_variant | 0.42 |
rpoC | 763531 | c.162G>T | synonymous_variant | 0.15 |
rpoC | 763532 | p.Thr55Ser | missense_variant | 0.4 |
rpoC | 763537 | c.168C>T | synonymous_variant | 0.2 |
rpoC | 763546 | c.177A>G | synonymous_variant | 0.42 |
rpoC | 763558 | c.189C>T | synonymous_variant | 0.28 |
rpoC | 763570 | c.201G>C | synonymous_variant | 0.38 |
rpoC | 763594 | c.225C>T | synonymous_variant | 0.27 |
rpoC | 763600 | c.231C>G | synonymous_variant | 0.23 |
rpoC | 763603 | c.234C>T | synonymous_variant | 0.19 |
rpoC | 763609 | c.240C>T | synonymous_variant | 0.19 |
rpoC | 763615 | c.246G>C | synonymous_variant | 0.41 |
rpoC | 763630 | c.261G>C | synonymous_variant | 0.37 |
rpoC | 763633 | c.264T>C | synonymous_variant | 0.16 |
rpoC | 763636 | c.267T>C | synonymous_variant | 0.2 |
rpoC | 763642 | c.273G>C | synonymous_variant | 0.32 |
rpoC | 763660 | c.291T>G | synonymous_variant | 0.13 |
rpoC | 763666 | c.297G>C | synonymous_variant | 0.13 |
rpoC | 763675 | c.306C>G | synonymous_variant | 0.12 |
rpoC | 763696 | c.327T>C | synonymous_variant | 0.12 |
rpoC | 763699 | c.330G>T | synonymous_variant | 0.25 |
rpoC | 763708 | c.339G>C | synonymous_variant | 0.2 |
rpoC | 763714 | c.345G>C | synonymous_variant | 0.23 |
rpoC | 763717 | c.348T>C | synonymous_variant | 0.23 |
rpoC | 763720 | c.351G>C | synonymous_variant | 0.13 |
rpoC | 763732 | c.363C>T | synonymous_variant | 0.21 |
rpoC | 763744 | c.375G>C | synonymous_variant | 0.17 |
rpoC | 763751 | p.Ile128Val | missense_variant | 0.17 |
rpoC | 764503 | c.1134G>C | synonymous_variant | 0.25 |
rpoC | 764509 | c.1140G>C | synonymous_variant | 0.22 |
rpoC | 764521 | c.1152T>C | synonymous_variant | 0.2 |
rpoC | 764536 | c.1167G>T | synonymous_variant | 0.2 |
rpoC | 764539 | c.1170C>G | synonymous_variant | 0.2 |
rpoC | 764548 | c.1179G>A | synonymous_variant | 0.27 |
rpoC | 764566 | c.1197C>G | synonymous_variant | 0.31 |
rpoC | 764572 | c.1203G>C | synonymous_variant | 0.31 |
rpoC | 764575 | c.1206T>G | synonymous_variant | 0.25 |
rpoC | 764576 | c.1207_1208delTCinsAG | synonymous_variant | 0.23 |
rpoC | 764581 | c.1212T>C | synonymous_variant | 0.23 |
rpoC | 764582 | p.Leu405Met | missense_variant | 0.23 |
rpoC | 764602 | c.1233C>T | synonymous_variant | 0.43 |
rpoC | 764605 | c.1236G>T | synonymous_variant | 0.43 |
rpoC | 764611 | c.1242G>T | synonymous_variant | 0.4 |
rpoC | 764620 | c.1251G>C | synonymous_variant | 0.5 |
rpoC | 764632 | c.1263T>C | synonymous_variant | 0.56 |
rpoC | 764650 | c.1281G>T | synonymous_variant | 0.55 |
rpoC | 764662 | c.1293G>C | synonymous_variant | 0.67 |
rpoC | 764677 | c.1308C>G | synonymous_variant | 0.62 |
rpoC | 764695 | c.1326T>C | synonymous_variant | 0.47 |
rpoC | 764706 | p.Leu446Gln | missense_variant | 0.58 |
rpoC | 764722 | c.1353G>C | synonymous_variant | 0.65 |
rpoC | 764746 | c.1377G>C | synonymous_variant | 0.68 |
rpoC | 764752 | c.1383G>T | synonymous_variant | 0.48 |
rpoC | 764764 | c.1395T>C | synonymous_variant | 0.64 |
rpoC | 764767 | c.1398G>C | synonymous_variant | 0.44 |
rpoC | 764780 | c.1411_1413delAGCinsTCG | synonymous_variant | 0.43 |
rpoC | 764791 | c.1422C>T | synonymous_variant | 0.33 |
rpoC | 764797 | c.1428G>C | synonymous_variant | 0.65 |
rpoC | 764803 | c.1434C>T | synonymous_variant | 0.25 |
rpoC | 764804 | p.Gln479Tyr | missense_variant | 0.53 |
rpoC | 764809 | c.1440C>T | synonymous_variant | 0.29 |
rpoC | 764810 | p.Pro481Ala | missense_variant | 0.12 |
rpoC | 764815 | c.1446A>G | synonymous_variant | 0.59 |
rpoC | 764818 | c.1449G>C | synonymous_variant | 0.25 |
rpoC | 764824 | c.1455T>C | synonymous_variant | 0.53 |
rpoC | 764827 | c.1458G>T | synonymous_variant | 0.4 |
rpoC | 764837 | p.Val490Ile | missense_variant | 0.5 |
rpoC | 764843 | p.Ala492Thr | missense_variant | 0.47 |
rpoC | 764854 | c.1485G>C | synonymous_variant | 0.26 |
rpoC | 764858 | c.1489T>C | synonymous_variant | 0.28 |
rpoC | 764863 | c.1494G>C | synonymous_variant | 0.18 |
rpoC | 764869 | c.1500C>T | synonymous_variant | 0.59 |
rpoC | 764875 | c.1506C>T | synonymous_variant | 0.47 |
rpoC | 764878 | c.1509C>G | synonymous_variant | 0.2 |
rpoC | 764887 | c.1518G>C | synonymous_variant | 0.3 |
rpoC | 764888 | c.1519_1521delTTGinsCTC | synonymous_variant | 0.42 |
rpoC | 764893 | c.1524T>C | synonymous_variant | 0.25 |
rpoC | 764902 | c.1533C>G | synonymous_variant | 0.23 |
rpoC | 764908 | c.1539G>A | synonymous_variant | 0.2 |
rpoC | 764911 | c.1542A>G | synonymous_variant | 0.33 |
rpoC | 764912 | p.Met515Gln | missense_variant | 0.33 |
rpoC | 764917 | c.1548G>C | synonymous_variant | 0.33 |
rpoC | 764920 | c.1551G>C | synonymous_variant | 0.36 |
rpoC | 764923 | c.1554A>G | synonymous_variant | 0.14 |
rpoC | 764935 | c.1566T>C | synonymous_variant | 0.2 |
rpoC | 764941 | c.1572G>T | synonymous_variant | 0.21 |
rpoC | 764948 | c.1579T>C | synonymous_variant | 0.31 |
rpoC | 764958 | p.Glu530Gly | missense_variant | 0.17 |
rpoC | 764962 | c.1593G>C | synonymous_variant | 0.28 |
rpoC | 764968 | c.1599T>C | synonymous_variant | 0.28 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 779004 | c.-524G>A | upstream_gene_variant | 0.13 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
rpsL | 781559 | c.-1G>A | upstream_gene_variant | 0.22 |
rpsL | 781572 | p.Gln5Asn | missense_variant | 0.2 |
rpsL | 781595 | c.36T>C | synonymous_variant | 0.2 |
rpsL | 781598 | c.39G>C | synonymous_variant | 0.18 |
rpsL | 781606 | p.Ile16Thr | missense_variant | 0.18 |
rpsL | 781608 | p.Ser17Ala | missense_variant | 0.18 |
rpsL | 781622 | c.63C>G | synonymous_variant | 0.18 |
rpsL | 781625 | c.66G>A | synonymous_variant | 0.18 |
rpsL | 781628 | c.69T>C | synonymous_variant | 0.18 |
rpsL | 781631 | c.72G>C | synonymous_variant | 0.18 |
rpsL | 781655 | c.96T>C | synonymous_variant | 0.22 |
rpsL | 781658 | c.99A>G | synonymous_variant | 0.22 |
rpsL | 781664 | c.105C>T | synonymous_variant | 0.29 |
rpsL | 781682 | c.123T>C | synonymous_variant | 0.22 |
rpsL | 781685 | c.126G>C | synonymous_variant | 0.22 |
rpsL | 781880 | c.321C>G | synonymous_variant | 0.17 |
rpsL | 781889 | c.330C>T | synonymous_variant | 0.15 |
rpsL | 781892 | c.333A>G | synonymous_variant | 0.15 |
rpsL | 781898 | c.339A>C | synonymous_variant | 0.15 |
rplC | 801454 | p.Glu216Gln | missense_variant | 0.83 |
fbiC | 1302899 | c.-32A>G | upstream_gene_variant | 1.0 |
fbiC | 1304566 | p.Phe546Leu | missense_variant | 0.25 |
fbiC | 1304610 | c.1680C>G | synonymous_variant | 0.38 |
fbiC | 1304613 | c.1683T>C | synonymous_variant | 0.38 |
fbiC | 1304619 | c.1689G>A | synonymous_variant | 0.33 |
fbiC | 1304625 | c.1695C>T | synonymous_variant | 0.33 |
fbiC | 1304634 | c.1704C>G | synonymous_variant | 0.33 |
fbiC | 1304640 | c.1710A>C | synonymous_variant | 0.38 |
fbiC | 1304658 | c.1728C>G | synonymous_variant | 0.33 |
fbiC | 1304660 | p.Tyr577Phe | missense_variant | 0.33 |
fbiC | 1304662 | p.Ser578Thr | missense_variant | 0.33 |
fbiC | 1304671 | c.1742delT | frameshift_variant | 0.33 |
fbiC | 1304674 | p.Gly582Arg | missense_variant | 0.33 |
fbiC | 1304677 | c.1747_1748insC | frameshift_variant | 0.33 |
fbiC | 1304691 | c.1761G>T | synonymous_variant | 0.33 |
fbiC | 1304694 | c.1764A>G | synonymous_variant | 0.33 |
fbiC | 1304700 | c.1770G>A | synonymous_variant | 0.33 |
fbiC | 1304703 | c.1773C>G | synonymous_variant | 0.33 |
fbiC | 1304715 | c.1785G>C | synonymous_variant | 0.33 |
fbiC | 1304718 | c.1788C>A | synonymous_variant | 0.33 |
fbiC | 1304724 | c.1794A>G | synonymous_variant | 0.25 |
fbiC | 1304727 | c.1797A>G | synonymous_variant | 0.25 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1471878 | n.33C>T | non_coding_transcript_exon_variant | 0.25 |
rrs | 1471935 | n.90T>C | non_coding_transcript_exon_variant | 1.0 |
rrs | 1472023 | n.178G>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472028 | n.183A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472030 | n.185G>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472033 | n.188A>T | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472040 | n.195T>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472045 | n.200T>G | non_coding_transcript_exon_variant | 0.33 |
rrs | 1472053 | n.211_212delGC | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472057 | n.212C>A | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472062 | n.217G>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472068 | n.223T>C | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472069 | n.224G>A | non_coding_transcript_exon_variant | 0.43 |
rrs | 1472075 | n.230A>G | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472102 | n.257G>A | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472106 | n.261G>A | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472108 | n.263C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472112 | n.267C>T | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472113 | n.268T>C | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472150 | n.305T>A | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472172 | n.327T>C | non_coding_transcript_exon_variant | 0.94 |
rrs | 1472225 | n.380C>G | non_coding_transcript_exon_variant | 0.81 |
rrs | 1472251 | n.406G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472286 | n.441C>G | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472289 | n.444T>G | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472290 | n.445C>G | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472297 | n.453_465delGTCCGGGTTCTCT | non_coding_transcript_exon_variant | 0.7 |
rrs | 1472315 | n.470T>G | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472324 | n.479G>C | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472325 | n.480G>C | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472328 | n.483G>C | non_coding_transcript_exon_variant | 0.58 |
rrs | 1472344 | n.499C>T | non_coding_transcript_exon_variant | 0.64 |
rrs | 1472382 | n.537G>A | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472389 | n.544G>A | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472400 | n.555C>T | non_coding_transcript_exon_variant | 0.27 |
rrs | 1472414 | n.569C>T | non_coding_transcript_exon_variant | 0.38 |
rrs | 1472422 | n.577T>C | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472435 | n.590T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472439 | n.594C>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472446 | n.601T>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472448 | n.603T>C | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472449 | n.604C>A | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472450 | n.605A>G | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472452 | n.607G>A | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472456 | n.611T>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472462 | n.617T>C | non_coding_transcript_exon_variant | 0.36 |
rrs | 1472463 | n.618G>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472464 | n.619A>G | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472467 | n.622G>T | non_coding_transcript_exon_variant | 0.4 |
rrs | 1472471 | n.626G>A | non_coding_transcript_exon_variant | 0.44 |
rrs | 1472489 | n.644A>T | non_coding_transcript_exon_variant | 0.21 |
rrs | 1472494 | n.649A>G | non_coding_transcript_exon_variant | 0.5 |
rrs | 1472495 | n.650C>A | non_coding_transcript_exon_variant | 0.45 |
rrs | 1472498 | n.653C>T | non_coding_transcript_exon_variant | 0.57 |
rrs | 1472530 | n.685G>A | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472558 | n.713G>A | non_coding_transcript_exon_variant | 0.72 |
rrs | 1472569 | n.724G>A | non_coding_transcript_exon_variant | 0.73 |
rrs | 1472582 | n.737G>T | non_coding_transcript_exon_variant | 0.67 |
rrs | 1472607 | n.762G>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472655 | n.810G>T | non_coding_transcript_exon_variant | 0.76 |
rrs | 1472660 | n.815T>C | non_coding_transcript_exon_variant | 0.95 |
rrs | 1472661 | n.816A>G | non_coding_transcript_exon_variant | 0.17 |
rrs | 1472673 | n.830delT | non_coding_transcript_exon_variant | 0.8 |
rrs | 1472692 | n.847T>C | non_coding_transcript_exon_variant | 0.71 |
rrs | 1472713 | n.868T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1472714 | n.869A>G | non_coding_transcript_exon_variant | 0.91 |
rrs | 1472790 | n.945T>C | non_coding_transcript_exon_variant | 0.32 |
rrs | 1472824 | n.979T>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472825 | n.980G>A | non_coding_transcript_exon_variant | 0.22 |
rrs | 1472828 | n.983T>C | non_coding_transcript_exon_variant | 0.25 |
rrs | 1472837 | n.992C>A | non_coding_transcript_exon_variant | 0.29 |
rrs | 1472875 | n.1030T>G | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472878 | n.1033G>T | non_coding_transcript_exon_variant | 0.75 |
rrs | 1472880 | n.1035G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472895 | n.1050C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472952 | n.1107T>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472955 | n.1110C>T | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472956 | n.1111T>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472969 | n.1124A>G | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472973 | n.1128A>T | non_coding_transcript_exon_variant | 0.92 |
rrs | 1472978 | n.1133T>C | non_coding_transcript_exon_variant | 0.83 |
rrs | 1472987 | n.1142G>A | non_coding_transcript_exon_variant | 0.84 |
rrs | 1472990 | n.1145A>G | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473026 | n.1181T>C | non_coding_transcript_exon_variant | 0.93 |
rrs | 1473035 | n.1190G>A | non_coding_transcript_exon_variant | 0.83 |
rrs | 1473055 | n.1210C>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1473056 | n.1211A>T | non_coding_transcript_exon_variant | 0.84 |
rrs | 1473066 | n.1221A>G | non_coding_transcript_exon_variant | 0.85 |
rrs | 1473082 | n.1237G>A | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473093 | n.1248C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473099 | n.1254T>G | non_coding_transcript_exon_variant | 0.14 |
rrs | 1473100 | n.1255G>A | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473102 | n.1257C>T | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473104 | n.1259C>T | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473110 | n.1265T>G | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473111 | n.1266A>G | non_coding_transcript_exon_variant | 0.96 |
rrs | 1473115 | n.1270G>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473121 | n.1276T>C | non_coding_transcript_exon_variant | 0.95 |
rrs | 1473122 | n.1277T>A | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473123 | n.1278A>T | non_coding_transcript_exon_variant | 0.15 |
rrs | 1473129 | n.1284C>T | non_coding_transcript_exon_variant | 0.17 |
rrs | 1473145 | n.1300C>T | non_coding_transcript_exon_variant | 0.8 |
rrs | 1473166 | n.1321G>A | non_coding_transcript_exon_variant | 0.78 |
rrs | 1473252 | n.1407T>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473259 | n.1414C>T | non_coding_transcript_exon_variant | 0.81 |
rrs | 1473276 | n.1431A>G | non_coding_transcript_exon_variant | 0.94 |
rrs | 1473301 | n.1456T>C | non_coding_transcript_exon_variant | 0.2 |
rrs | 1473315 | n.1470T>C | non_coding_transcript_exon_variant | 0.82 |
rrs | 1473316 | n.1471C>T | non_coding_transcript_exon_variant | 0.72 |
rrl | 1473717 | n.60G>A | non_coding_transcript_exon_variant | 0.27 |
rrl | 1473731 | n.74T>A | non_coding_transcript_exon_variant | 0.3 |
rrl | 1473756 | n.99G>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473757 | n.100T>G | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473758 | n.101G>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1473770 | n.113T>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473806 | n.149C>T | non_coding_transcript_exon_variant | 0.67 |
rrl | 1473814 | n.157A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1473815 | n.158T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1473830 | n.173T>C | non_coding_transcript_exon_variant | 0.62 |
rrl | 1473832 | n.175C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1473833 | n.176_177insT | non_coding_transcript_exon_variant | 0.75 |
rrl | 1473844 | n.187C>T | non_coding_transcript_exon_variant | 0.56 |
rrl | 1473870 | n.213G>A | non_coding_transcript_exon_variant | 0.29 |
rrl | 1473871 | n.214T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1473876 | n.219G>A | non_coding_transcript_exon_variant | 0.67 |
rrl | 1473887 | n.230T>C | non_coding_transcript_exon_variant | 0.33 |
rrl | 1473888 | n.231T>C | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473898 | n.241C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1473899 | n.242A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1473916 | n.259C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1473923 | n.266C>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1474164 | n.507C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474183 | n.526T>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474184 | n.527C>T | non_coding_transcript_exon_variant | 0.44 |
rrl | 1474185 | n.528G>A | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474201 | n.544T>C | non_coding_transcript_exon_variant | 0.58 |
rrl | 1474202 | n.545T>C | non_coding_transcript_exon_variant | 0.54 |
rrl | 1474218 | n.561T>A | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474249 | n.592G>C | non_coding_transcript_exon_variant | 0.84 |
rrl | 1474269 | n.612C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1474281 | n.624A>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1474286 | n.629C>A | non_coding_transcript_exon_variant | 0.76 |
rrl | 1474310 | n.653T>G | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474311 | n.654G>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1474316 | n.659T>C | non_coding_transcript_exon_variant | 0.77 |
rrl | 1474348 | n.691C>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474351 | n.694G>T | non_coding_transcript_exon_variant | 0.93 |
rrl | 1474353 | n.696A>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474354 | n.697C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1474356 | n.699T>C | non_coding_transcript_exon_variant | 0.81 |
rrl | 1474362 | n.705A>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474381 | n.724T>A | non_coding_transcript_exon_variant | 0.87 |
rrl | 1474387 | n.730C>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1474402 | n.745T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1474413 | n.756A>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1474414 | n.757C>T | non_coding_transcript_exon_variant | 0.53 |
rrl | 1474447 | n.790G>A | non_coding_transcript_exon_variant | 0.17 |
rrl | 1474450 | n.793T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474454 | n.797G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474466 | n.809G>A | non_coding_transcript_exon_variant | 0.91 |
rrl | 1474488 | n.831G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474496 | n.839C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474497 | n.840G>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474506 | n.849C>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474507 | n.850G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474516 | n.859C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474529 | n.872A>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474530 | n.873G>A | non_coding_transcript_exon_variant | 0.94 |
rrl | 1474537 | n.880G>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474539 | n.882C>T | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474540 | n.883T>G | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474583 | n.926C>T | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474632 | n.975G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474636 | n.979A>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474637 | n.980C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474638 | n.981C>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474639 | n.982G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474663 | n.1006C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474664 | n.1007G>A | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474676 | n.1019T>A | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474709 | n.1053_1056delTGGT | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474717 | n.1060_1061insGTGAG | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474722 | n.1065T>C | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474723 | n.1066G>A | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474734 | n.1077G>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474736 | n.1079C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474749 | n.1092C>T | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474751 | n.1094G>A | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474753 | n.1097delC | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474760 | n.1103A>G | non_coding_transcript_exon_variant | 1.0 |
rrl | 1474777 | n.1120T>C | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474779 | n.1122G>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474782 | n.1125G>A | non_coding_transcript_exon_variant | 0.99 |
rrl | 1474783 | n.1126G>A | non_coding_transcript_exon_variant | 0.95 |
rrl | 1474794 | n.1137C>T | non_coding_transcript_exon_variant | 0.98 |
rrl | 1474823 | n.1166C>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474827 | n.1170C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1474830 | n.1173A>G | non_coding_transcript_exon_variant | 0.97 |
rrl | 1474831 | n.1174A>C | non_coding_transcript_exon_variant | 0.14 |
rrl | 1474864 | n.1207C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1474869 | n.1212G>A | non_coding_transcript_exon_variant | 0.74 |
rrl | 1474904 | n.1247G>C | non_coding_transcript_exon_variant | 0.84 |
rrl | 1474905 | n.1248T>C | non_coding_transcript_exon_variant | 0.7 |
rrl | 1474913 | n.1256T>C | non_coding_transcript_exon_variant | 0.8 |
rrl | 1474932 | n.1275C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1474938 | n.1281G>A | non_coding_transcript_exon_variant | 0.23 |
rrl | 1474946 | n.1289C>T | non_coding_transcript_exon_variant | 0.38 |
rrl | 1475060 | n.1404delC | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475065 | n.1408G>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475067 | n.1410A>G | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475068 | n.1411A>G | non_coding_transcript_exon_variant | 0.65 |
rrl | 1475076 | n.1419C>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475078 | n.1421T>C | non_coding_transcript_exon_variant | 0.65 |
rrl | 1475079 | n.1422T>C | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475081 | n.1424C>T | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475090 | n.1433A>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475093 | n.1436C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475104 | n.1447T>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475108 | n.1451C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475111 | n.1454G>A | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475114 | n.1457C>T | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475116 | n.1459G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475119 | n.1462C>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1475124 | n.1467A>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1475129 | n.1472G>A | non_coding_transcript_exon_variant | 0.65 |
rrl | 1475163 | n.1506T>C | non_coding_transcript_exon_variant | 0.13 |
rrl | 1475406 | n.1749T>G | non_coding_transcript_exon_variant | 0.33 |
rrl | 1475414 | n.1757G>C | non_coding_transcript_exon_variant | 0.4 |
rrl | 1475419 | n.1762C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475422 | n.1765A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475429 | n.1772G>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475443 | n.1786G>A | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475452 | n.1795C>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1475460 | n.1803A>G | non_coding_transcript_exon_variant | 0.56 |
rrl | 1475480 | n.1823A>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475481 | n.1824C>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475482 | n.1825A>T | non_coding_transcript_exon_variant | 0.62 |
rrl | 1475526 | n.1869C>A | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475531 | n.1874C>T | non_coding_transcript_exon_variant | 0.7 |
rrl | 1475538 | n.1881T>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1475539 | n.1882A>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1475545 | n.1888T>G | non_coding_transcript_exon_variant | 0.17 |
rrl | 1475548 | n.1891C>T | non_coding_transcript_exon_variant | 0.25 |
rrl | 1475649 | n.1992A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475655 | n.1998T>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475657 | n.2000A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1475659 | n.2002G>A | non_coding_transcript_exon_variant | 0.75 |
rrl | 1475722 | n.2065G>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1475753 | n.2096C>G | non_coding_transcript_exon_variant | 0.98 |
rrl | 1475775 | n.2118G>T | non_coding_transcript_exon_variant | 0.96 |
rrl | 1475869 | n.2212C>A | non_coding_transcript_exon_variant | 0.88 |
rrl | 1475881 | n.2224T>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475883 | n.2226A>C | non_coding_transcript_exon_variant | 0.86 |
rrl | 1475884 | n.2227A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475899 | n.2242G>A | non_coding_transcript_exon_variant | 0.84 |
rrl | 1475916 | n.2259C>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475943 | n.2286G>A | non_coding_transcript_exon_variant | 0.82 |
rrl | 1475952 | n.2295A>G | non_coding_transcript_exon_variant | 0.79 |
rrl | 1475963 | n.2306G>A | non_coding_transcript_exon_variant | 0.78 |
rrl | 1475970 | n.2313C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1475975 | n.2318C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1475977 | n.2320A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475978 | n.2321C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1475988 | n.2331A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1475996 | n.2339T>A | non_coding_transcript_exon_variant | 0.68 |
rrl | 1475997 | n.2340A>G | non_coding_transcript_exon_variant | 0.9 |
rrl | 1475997 | n.2340A>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1475998 | n.2341C>T | non_coding_transcript_exon_variant | 0.71 |
rrl | 1476001 | n.2344T>C | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476024 | n.2367T>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476025 | n.2368G>T | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476030 | n.2373A>G | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476032 | n.2375C>G | non_coding_transcript_exon_variant | 0.23 |
rrl | 1476033 | n.2376T>C | non_coding_transcript_exon_variant | 0.88 |
rrl | 1476033 | n.2376T>G | non_coding_transcript_exon_variant | 0.69 |
rrl | 1476034 | n.2377C>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476045 | n.2388G>C | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476046 | n.2389G>T | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476047 | n.2390G>C | non_coding_transcript_exon_variant | 0.21 |
rrl | 1476049 | n.2392C>T | non_coding_transcript_exon_variant | 0.9 |
rrl | 1476056 | n.2399G>A | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476058 | n.2401T>C | non_coding_transcript_exon_variant | 0.67 |
rrl | 1476076 | n.2419A>G | non_coding_transcript_exon_variant | 0.48 |
rrl | 1476079 | n.2422G>A | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476080 | n.2423T>A | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476080 | n.2423T>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476081 | n.2424A>T | non_coding_transcript_exon_variant | 0.32 |
rrl | 1476086 | n.2429G>A | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476088 | n.2431A>C | non_coding_transcript_exon_variant | 0.44 |
rrl | 1476095 | n.2438C>T | non_coding_transcript_exon_variant | 0.33 |
rrl | 1476099 | n.2442A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476103 | n.2446C>A | non_coding_transcript_exon_variant | 0.39 |
rrl | 1476104 | n.2447T>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476105 | n.2450delA | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476110 | n.2453G>C | non_coding_transcript_exon_variant | 0.57 |
rrl | 1476110 | n.2453G>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476113 | n.2456T>G | non_coding_transcript_exon_variant | 0.35 |
rrl | 1476115 | n.2458T>C | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476130 | n.2473G>A | non_coding_transcript_exon_variant | 0.45 |
rrl | 1476131 | n.2474C>T | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476160 | n.2503T>C | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476165 | n.2508T>A | non_coding_transcript_exon_variant | 0.68 |
rrl | 1476194 | n.2537A>G | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476200 | n.2543A>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476201 | n.2544C>T | non_coding_transcript_exon_variant | 0.86 |
rrl | 1476214 | n.2557G>T | non_coding_transcript_exon_variant | 0.83 |
rrl | 1476221 | n.2564T>C | non_coding_transcript_exon_variant | 0.17 |
rrl | 1476224 | n.2567A>G | non_coding_transcript_exon_variant | 0.93 |
rrl | 1476245 | n.2588C>T | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476250 | n.2593C>G | non_coding_transcript_exon_variant | 0.75 |
rrl | 1476251 | n.2594T>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476252 | n.2595T>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476256 | n.2599A>T | non_coding_transcript_exon_variant | 0.89 |
rrl | 1476257 | n.2600G>C | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476260 | n.2603A>G | non_coding_transcript_exon_variant | 0.91 |
rrl | 1476281 | n.2624T>C | non_coding_transcript_exon_variant | 0.92 |
rrl | 1476308 | n.2651G>T | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476309 | n.2652G>C | non_coding_transcript_exon_variant | 0.26 |
rrl | 1476311 | n.2654G>C | non_coding_transcript_exon_variant | 0.63 |
rrl | 1476312 | n.2655T>C | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476337 | n.2680C>T | non_coding_transcript_exon_variant | 0.74 |
rrl | 1476359 | n.2702C>G | non_coding_transcript_exon_variant | 0.76 |
rrl | 1476381 | n.2724G>C | non_coding_transcript_exon_variant | 0.78 |
rrl | 1476428 | n.2771C>T | non_coding_transcript_exon_variant | 0.94 |
rrl | 1476466 | n.2809C>T | non_coding_transcript_exon_variant | 0.82 |
rrl | 1476506 | n.2849T>C | non_coding_transcript_exon_variant | 0.77 |
rrl | 1476515 | n.2858C>T | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476523 | n.2866T>C | non_coding_transcript_exon_variant | 0.65 |
rrl | 1476524 | n.2867C>A | non_coding_transcript_exon_variant | 0.73 |
rrl | 1476525 | n.2868A>G | non_coding_transcript_exon_variant | 0.59 |
rrl | 1476530 | n.2873C>T | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476536 | n.2879G>A | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476538 | n.2881A>G | non_coding_transcript_exon_variant | 0.64 |
rrl | 1476539 | n.2882A>G | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476540 | n.2883C>G | non_coding_transcript_exon_variant | 0.81 |
rrl | 1476547 | n.2890C>T | non_coding_transcript_exon_variant | 0.66 |
rrl | 1476584 | n.2927C>T | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476585 | n.2928A>G | non_coding_transcript_exon_variant | 0.6 |
rrl | 1476586 | n.2929C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476594 | n.2937C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476596 | n.2939C>T | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476601 | n.2944G>A | non_coding_transcript_exon_variant | 0.22 |
rrl | 1476603 | n.2946G>A | non_coding_transcript_exon_variant | 0.43 |
rrl | 1476613 | n.2956G>A | non_coding_transcript_exon_variant | 0.2 |
rrl | 1476614 | n.2957A>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476619 | n.2962C>T | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476628 | n.2971T>A | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476629 | n.2972C>A | non_coding_transcript_exon_variant | 0.38 |
rrl | 1476630 | n.2973A>G | non_coding_transcript_exon_variant | 0.5 |
rrl | 1476661 | n.3004A>G | non_coding_transcript_exon_variant | 0.25 |
fabG1 | 1673312 | c.-128C>T | upstream_gene_variant | 0.22 |
inhA | 1673715 | c.-487C>G | upstream_gene_variant | 0.88 |
rpsA | 1833709 | c.168C>T | synonymous_variant | 0.42 |
rpsA | 1833721 | c.180A>G | synonymous_variant | 0.17 |
rpsA | 1833724 | c.183C>T | synonymous_variant | 0.42 |
rpsA | 1833727 | c.186G>C | synonymous_variant | 0.45 |
rpsA | 1833730 | c.189C>T | synonymous_variant | 0.45 |
rpsA | 1833733 | c.192C>T | synonymous_variant | 0.18 |
rpsA | 1833734 | p.Ala65Ser | missense_variant | 0.45 |
rpsA | 1833742 | c.201A>G | synonymous_variant | 0.42 |
rpsA | 1833763 | c.222C>T | synonymous_variant | 0.21 |
rpsA | 1833769 | c.228C>G | synonymous_variant | 0.21 |
rpsA | 1833770 | p.Asn77Gly | missense_variant | 0.36 |
rpsA | 1833775 | p.Glu78Asp | missense_variant | 0.36 |
rpsA | 1833778 | c.237C>T | synonymous_variant | 0.21 |
rpsA | 1833781 | c.240T>C | synonymous_variant | 0.36 |
rpsA | 1833787 | c.246C>T | synonymous_variant | 0.25 |
rpsA | 1833790 | c.249T>C | synonymous_variant | 0.36 |
rpsA | 1833793 | c.252C>T | synonymous_variant | 0.43 |
rpsA | 1833794 | p.Glu85Gln | missense_variant | 0.36 |
rpsA | 1833802 | c.261A>G | synonymous_variant | 0.25 |
rpsA | 1833823 | c.282G>A | synonymous_variant | 0.45 |
rpsA | 1833832 | c.291G>A | synonymous_variant | 0.36 |
rpsA | 1833838 | c.297G>T | synonymous_variant | 0.22 |
rpsA | 1833841 | c.300C>G | synonymous_variant | 0.38 |
rpsA | 1833937 | c.396G>A | synonymous_variant | 0.14 |
rpsA | 1833952 | c.411C>T | synonymous_variant | 0.19 |
rpsA | 1833955 | c.414G>C | synonymous_variant | 0.23 |
rpsA | 1833970 | c.429G>T | synonymous_variant | 0.29 |
rpsA | 1833979 | c.438T>C | synonymous_variant | 0.38 |
rpsA | 1833991 | c.450C>A | synonymous_variant | 0.33 |
rpsA | 1833994 | c.453G>C | synonymous_variant | 0.2 |
rpsA | 1833997 | c.456G>C | synonymous_variant | 0.43 |
rpsA | 1834000 | c.459G>C | synonymous_variant | 0.43 |
rpsA | 1834009 | c.468C>T | synonymous_variant | 0.23 |
rpsA | 1834012 | c.471G>C | synonymous_variant | 0.5 |
rpsA | 1834015 | c.474G>C | synonymous_variant | 0.27 |
rpsA | 1834024 | c.483G>C | synonymous_variant | 0.38 |
rpsA | 1834025 | p.Gln162Ala | missense_variant | 0.5 |
rpsA | 1834030 | c.489C>G | synonymous_variant | 0.62 |
rpsA | 1834039 | c.498C>T | synonymous_variant | 0.38 |
rpsA | 1834040 | p.Lys167Gln | missense_variant | 0.62 |
rpsA | 1834043 | p.Glu168Gln | missense_variant | 0.62 |
rpsA | 1834051 | c.510G>A | synonymous_variant | 0.62 |
rpsA | 1834054 | c.513C>G | synonymous_variant | 0.25 |
rpsA | 1834069 | c.528G>C | synonymous_variant | 0.29 |
rpsA | 1834240 | c.699T>C | synonymous_variant | 0.25 |
rpsA | 1834246 | c.705G>T | synonymous_variant | 0.29 |
rpsA | 1834249 | c.708T>C | synonymous_variant | 0.29 |
rpsA | 1834261 | c.720A>G | synonymous_variant | 0.25 |
rpsA | 1834264 | c.723G>C | synonymous_variant | 0.25 |
rpsA | 1834294 | c.753G>T | synonymous_variant | 0.27 |
rpsA | 1834298 | p.Gln253Glu | missense_variant | 0.3 |
rpsA | 1834306 | c.765T>C | synonymous_variant | 0.3 |
rpsA | 1834307 | p.Asp256Gln | missense_variant | 0.3 |
rpsA | 1834312 | c.771G>A | synonymous_variant | 0.3 |
rpsA | 1834327 | c.786G>T | synonymous_variant | 0.33 |
rpsA | 1834333 | p.Asp264Glu | missense_variant | 0.36 |
rpsA | 1834336 | c.795C>T | synonymous_variant | 0.36 |
rpsA | 1834340 | p.Met267Leu | missense_variant | 0.36 |
rpsA | 1834348 | c.807T>C | synonymous_variant | 0.4 |
rpsA | 1834354 | c.813G>C | synonymous_variant | 0.33 |
rpsA | 1834357 | c.816T>C | synonymous_variant | 0.44 |
rpsA | 1834360 | c.819G>C | synonymous_variant | 0.33 |
rpsA | 1834361 | c.820T>C | synonymous_variant | 0.33 |
rpsA | 1834366 | c.825A>G | synonymous_variant | 0.38 |
rpsA | 1834375 | c.834G>T | synonymous_variant | 0.38 |
rpsA | 1834378 | c.837T>G | synonymous_variant | 0.38 |
rpsA | 1834387 | c.846C>T | synonymous_variant | 0.38 |
rpsA | 1834395 | p.Arg285Gln | missense_variant | 0.25 |
rpsA | 1834397 | p.His286Thr | missense_variant | 0.25 |
rpsA | 1834411 | c.870T>C | synonymous_variant | 0.2 |
rpsA | 1834489 | c.948T>A | synonymous_variant | 0.2 |
rpsA | 1834606 | c.1065C>T | synonymous_variant | 0.29 |
rpsA | 1834612 | c.1071G>T | synonymous_variant | 0.29 |
rpsA | 1834619 | c.1078T>C | synonymous_variant | 0.29 |
rpsA | 1834627 | c.1086C>G | synonymous_variant | 0.29 |
rpsA | 1834774 | c.1233C>T | synonymous_variant | 0.29 |
rpsA | 1834859 | p.Ala440Thr | missense_variant | 1.0 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1918395 | c.456G>T | synonymous_variant | 0.14 |
ndh | 2102193 | p.Arg284Trp | missense_variant | 0.29 |
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 | 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 | 2169769 | p.Ala282Thr | missense_variant | 0.2 |
Rv1979c | 2222308 | p.Asp286Gly | missense_variant | 1.0 |
Rv1979c | 2222467 | p.Thr233Asn | missense_variant | 0.25 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
kasA | 2518132 | c.18C>T | synonymous_variant | 1.0 |
eis | 2715125 | p.Thr70Ala | missense_variant | 1.0 |
ahpC | 2726579 | c.387T>C | synonymous_variant | 0.29 |
folC | 2747020 | c.579C>G | synonymous_variant | 0.25 |
folC | 2747023 | c.576C>G | synonymous_variant | 0.29 |
folC | 2747030 | p.Pro190Gln | missense_variant | 0.29 |
folC | 2747033 | p.Ala189Gly | missense_variant | 0.29 |
folC | 2747037 | p.Asn188Asp | missense_variant | 0.29 |
folC | 2747047 | c.552C>G | synonymous_variant | 0.29 |
folC | 2747059 | c.540T>C | synonymous_variant | 0.22 |
folC | 2747068 | p.Met177Leu | missense_variant | 0.22 |
folC | 2747101 | c.498G>T | synonymous_variant | 0.22 |
folC | 2747104 | p.Asp165Glu | missense_variant | 0.22 |
folC | 2747110 | c.489T>C | synonymous_variant | 0.22 |
folC | 2747113 | c.486C>A | synonymous_variant | 0.22 |
folC | 2747119 | c.480C>T | synonymous_variant | 0.22 |
folC | 2747122 | c.477G>C | synonymous_variant | 0.22 |
folC | 2747131 | c.468C>T | synonymous_variant | 0.22 |
pepQ | 2859782 | p.Gln213* | stop_gained | 0.25 |
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 | 3878591 | c.-84C>A | upstream_gene_variant | 0.5 |
rpoA | 3878630 | c.-124delC | upstream_gene_variant | 1.0 |
clpC1 | 4038403 | c.2302T>C | synonymous_variant | 1.0 |
clpC1 | 4039610 | c.1095G>C | synonymous_variant | 0.33 |
clpC1 | 4039640 | p.Thr355Ala | missense_variant | 0.25 |
clpC1 | 4039646 | p.Glu353Ala | missense_variant | 0.25 |
clpC1 | 4039649 | c.1056G>C | synonymous_variant | 0.22 |
clpC1 | 4039652 | p.Thr351Ser | missense_variant | 0.44 |
clpC1 | 4039655 | c.1050G>C | synonymous_variant | 0.22 |
clpC1 | 4039661 | p.Gly348Ala | missense_variant | 0.44 |
clpC1 | 4039664 | c.1041G>C | synonymous_variant | 0.22 |
clpC1 | 4039670 | p.Val345Ile | missense_variant | 0.29 |
clpC1 | 4039673 | c.1032G>C | synonymous_variant | 0.22 |
clpC1 | 4039682 | c.1023C>T | synonymous_variant | 0.3 |
clpC1 | 4039685 | c.1020C>T | synonymous_variant | 0.33 |
clpC1 | 4039691 | c.1014G>C | synonymous_variant | 0.3 |
clpC1 | 4039694 | c.1011G>T | synonymous_variant | 0.38 |
clpC1 | 4039697 | c.1008C>A | synonymous_variant | 0.2 |
clpC1 | 4039700 | c.1005C>T | synonymous_variant | 0.5 |
clpC1 | 4039706 | c.999G>A | synonymous_variant | 0.2 |
clpC1 | 4039714 | p.Tyr331His | missense_variant | 0.5 |
clpC1 | 4039721 | c.984C>T | synonymous_variant | 0.2 |
clpC1 | 4039724 | c.981A>G | synonymous_variant | 0.8 |
clpC1 | 4039727 | c.978C>T | synonymous_variant | 0.27 |
clpC1 | 4039730 | c.975C>G | synonymous_variant | 0.18 |
clpC1 | 4039733 | c.972G>T | synonymous_variant | 0.36 |
clpC1 | 4039739 | c.966C>T | synonymous_variant | 0.4 |
clpC1 | 4039742 | c.963C>T | synonymous_variant | 0.55 |
clpC1 | 4039748 | c.957G>C | synonymous_variant | 0.6 |
clpC1 | 4039751 | c.954A>G | synonymous_variant | 0.67 |
clpC1 | 4039757 | c.948A>G | synonymous_variant | 0.67 |
clpC1 | 4039760 | c.945T>C | synonymous_variant | 0.22 |
clpC1 | 4039766 | c.939T>C | synonymous_variant | 0.86 |
clpC1 | 4039769 | c.936C>T | synonymous_variant | 0.75 |
clpC1 | 4039773 | p.Lys311Met | missense_variant | 0.33 |
clpC1 | 4039775 | c.930G>C | synonymous_variant | 0.8 |
clpC1 | 4039778 | c.927A>G | synonymous_variant | 0.8 |
clpC1 | 4039781 | c.924G>C | synonymous_variant | 0.4 |
clpC1 | 4039787 | c.918G>C | synonymous_variant | 0.4 |
clpC1 | 4039793 | c.912C>G | synonymous_variant | 0.8 |
clpC1 | 4039796 | c.909C>T | synonymous_variant | 0.4 |
clpC1 | 4039814 | c.891C>G | synonymous_variant | 0.5 |
clpC1 | 4039817 | c.888A>C | synonymous_variant | 0.5 |
clpC1 | 4039820 | c.885T>C | synonymous_variant | 0.5 |
clpC1 | 4039826 | c.879C>G | synonymous_variant | 0.4 |
clpC1 | 4039831 | c.874T>C | synonymous_variant | 0.5 |
clpC1 | 4039838 | p.Leu289Ile | missense_variant | 0.33 |
clpC1 | 4039850 | c.855T>C | synonymous_variant | 0.57 |
clpC1 | 4039865 | c.840T>C | synonymous_variant | 0.5 |
clpC1 | 4039875 | p.Asn277Arg | missense_variant | 0.5 |
clpC1 | 4039889 | c.816G>C | synonymous_variant | 0.5 |
clpC1 | 4039898 | c.807C>G | synonymous_variant | 0.62 |
clpC1 | 4039904 | c.801A>G | synonymous_variant | 0.62 |
clpC1 | 4039907 | c.798G>A | synonymous_variant | 0.71 |
clpC1 | 4039929 | c.775_776delAGinsTC | synonymous_variant | 0.62 |
clpC1 | 4039931 | c.774T>C | synonymous_variant | 0.62 |
clpC1 | 4039934 | c.771G>C | synonymous_variant | 0.67 |
clpC1 | 4039943 | c.762G>C | synonymous_variant | 0.7 |
clpC1 | 4039946 | c.759A>T | synonymous_variant | 0.7 |
clpC1 | 4039949 | c.756G>C | synonymous_variant | 0.7 |
clpC1 | 4039952 | c.753T>C | synonymous_variant | 0.73 |
clpC1 | 4039958 | c.747G>C | synonymous_variant | 0.73 |
clpC1 | 4039964 | c.741C>G | synonymous_variant | 0.17 |
clpC1 | 4039981 | p.Leu242Ile | missense_variant | 0.7 |
clpC1 | 4039982 | c.723G>C | synonymous_variant | 0.7 |
clpC1 | 4039988 | c.717C>G | synonymous_variant | 0.56 |
clpC1 | 4039991 | c.714G>C | synonymous_variant | 0.67 |
clpC1 | 4039994 | p.Glu237Asp | missense_variant | 0.5 |
clpC1 | 4040001 | p.His235Arg | missense_variant | 0.5 |
clpC1 | 4040003 | c.702G>C | synonymous_variant | 0.5 |
clpC1 | 4040009 | c.696C>G | synonymous_variant | 0.56 |
clpC1 | 4040015 | c.690G>C | synonymous_variant | 0.5 |
clpC1 | 4040021 | c.684A>C | synonymous_variant | 0.56 |
clpC1 | 4040024 | c.681A>G | synonymous_variant | 0.6 |
clpC1 | 4040033 | c.672G>C | synonymous_variant | 0.44 |
clpC1 | 4040042 | c.663C>T | synonymous_variant | 0.33 |
clpC1 | 4040048 | c.657C>T | synonymous_variant | 0.3 |
clpC1 | 4040054 | c.651G>A | synonymous_variant | 0.3 |
clpC1 | 4040057 | c.648C>T | synonymous_variant | 0.3 |
clpC1 | 4040063 | c.642G>C | synonymous_variant | 0.2 |
clpC1 | 4040066 | c.639G>C | synonymous_variant | 0.22 |
clpC1 | 4040069 | c.636G>C | synonymous_variant | 0.2 |
clpC1 | 4040090 | c.615T>C | synonymous_variant | 0.22 |
clpC1 | 4040096 | c.609G>C | synonymous_variant | 0.22 |
clpC1 | 4040267 | c.438A>G | synonymous_variant | 0.14 |
clpC1 | 4040273 | c.432T>C | synonymous_variant | 0.14 |
clpC1 | 4040276 | c.429C>G | synonymous_variant | 0.15 |
clpC1 | 4040279 | c.426C>G | synonymous_variant | 0.15 |
clpC1 | 4040291 | c.414G>C | synonymous_variant | 0.15 |
clpC1 | 4040303 | c.402G>C | synonymous_variant | 0.17 |
clpC1 | 4040306 | c.399G>T | synonymous_variant | 0.17 |
clpC1 | 4040310 | p.Thr132Asn | missense_variant | 0.17 |
clpC1 | 4040312 | c.393G>C | synonymous_variant | 0.17 |
clpC1 | 4040315 | p.Glu130Asp | missense_variant | 0.17 |
clpC1 | 4040321 | c.384C>T | synonymous_variant | 0.18 |
clpC1 | 4040324 | c.381G>C | synonymous_variant | 0.18 |
clpC1 | 4040336 | c.369G>T | synonymous_variant | 0.25 |
clpC1 | 4040345 | c.360C>A | synonymous_variant | 0.25 |
clpC1 | 4040348 | c.357G>A | synonymous_variant | 0.25 |
clpC1 | 4040354 | c.351A>G | synonymous_variant | 0.29 |
clpC1 | 4040363 | c.342A>T | synonymous_variant | 0.25 |
clpC1 | 4040372 | c.333C>T | synonymous_variant | 0.22 |
clpC1 | 4040375 | c.330G>C | synonymous_variant | 0.22 |
clpC1 | 4040380 | c.325T>C | synonymous_variant | 0.22 |
clpC1 | 4040387 | c.318A>G | synonymous_variant | 0.22 |
clpC1 | 4040390 | c.315C>G | synonymous_variant | 0.22 |
clpC1 | 4040393 | c.312G>T | synonymous_variant | 0.2 |
clpC1 | 4040486 | c.219G>T | synonymous_variant | 0.18 |
clpC1 | 4040522 | c.183T>C | synonymous_variant | 0.17 |
clpC1 | 4040528 | c.177G>C | synonymous_variant | 0.17 |
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 | 0.18 |
clpC1 | 4040540 | c.165G>C | synonymous_variant | 0.18 |
clpC1 | 4040546 | c.159G>T | synonymous_variant | 0.2 |
clpC1 | 4040560 | c.145C>T | synonymous_variant | 0.18 |
clpC1 | 4040561 | c.144A>G | synonymous_variant | 0.18 |
clpC1 | 4040570 | c.135C>A | synonymous_variant | 0.2 |
clpC1 | 4040576 | c.129C>T | synonymous_variant | 0.2 |
embC | 4240664 | p.Trp268Arg | missense_variant | 0.2 |
embC | 4240671 | p.Thr270Ile | missense_variant | 1.0 |
embC | 4242642 | p.Arg927His | missense_variant | 1.0 |
embA | 4242970 | c.-263C>T | upstream_gene_variant | 1.0 |
embA | 4243269 | p.Ala13Thr | missense_variant | 0.2 |
embA | 4244220 | c.988C>T | synonymous_variant | 1.0 |
embB | 4246551 | p.Asn13Ser | missense_variant | 1.0 |
embB | 4246567 | c.54_55insT | frameshift_variant | 0.29 |
embB | 4246864 | c.351C>T | synonymous_variant | 1.0 |
embB | 4247646 | p.Glu378Ala | missense_variant | 1.0 |
embB | 4248734 | p.Arg741Trp | missense_variant | 1.0 |
embB | 4249747 | c.3234C>T | synonymous_variant | 0.25 |
aftB | 4267167 | p.Gln557Pro | missense_variant | 1.0 |
aftB | 4267277 | c.1560G>A | synonymous_variant | 0.25 |
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 |
ethA | 4326024 | p.Pro484Ser | missense_variant | 1.0 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |