regionname | pos | ref | alt | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | ac | an | af | len | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length
|
cds cds pos length
|
aa aa pos length
|
distance | status | chr | external |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARFGEF3_chr6_138156939_138349663 | 138270427 | G | GACACACA others(13): Show |
intron_variant | MODIFIER | HG01361.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0141 | 1 | 190 | 0.0053 | 20 | c.212 others(39): Show |
ARFGEF3 | ENSG00000112379.9 | transcript | ENST00000251691.5 | protein_coding | 12/33 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | |||||
ARFIP1_chr4_152774954_152917357 | 152795820 | A | ATTTTTTT others(13): Show |
intron_variant | MODIFIER | HG02145.hp2 HG02572.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0002t0002 | a0001c0001t0002g0265a0001c0002t0002g0199 | 2 | 342 | 0.0059 | 20 | c.-10 others(39): Show |
ARFIP1 | ENSG00000164144.16 | transcript | ENST00000353617.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARFIP1_chr4_152774954_152917357 | 152808283 | A | ATTTTTTT others(13): Show |
intron_variant | MODIFIER | HG00408.hp2 HG01081.hp1 HG01243.hp1 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003 | a0001c0001t0001g0077a0001c0001t0001g0078a0001c0001t0001g0235others(8): Show | 11 | 342 | 0.0322 | 20 | c.-9- others(37): Show |
ARFIP1 | ENSG00000164144.16 | transcript | ENST00000353617.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARFIP1_chr4_152774954_152917357 | 152847124 | C | CTTTTTTT others(13): Show |
intron_variant | MODIFIER | HG02602.hp1 HG03579.hp1 NA19056.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0264a0001c0001t0001g0293a0001c0001t0001g0303 | 3 | 342 | 0.0088 | 20 | c.94- others(37): Show |
ARFIP1 | ENSG00000164144.16 | transcript | ENST00000353617.7 | protein_coding | 2/8 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARFIP2_chr11_6471519_6486331 | 6472874 | A | ATTCTGCA others(13): Show |
downstream_gene_variant | MODIFIER | HG02922.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009 | 1 | 402 | 0.0025 | 20 | c.*42 others(31): Show |
ARFIP2 | ENSG00000132254.13 | transcript | ENST00000396777.8 | protein_coding | 3644 | chr11 | TogoVar | ||||||
ARG1_chr6_131568226_131589329 | 131584816 | T | TACACACA others(13): Show |
downstream_gene_variant | MODIFIER | HG02647.hp1 HG03195.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0024 | 2 | 420 | 0.0048 | 20 | c.*90 others(29): Show |
ARG1 | ENSG00000118520.16 | transcript | ENST00000368087.8 | protein_coding | 488 | chr6 | TogoVar | ||||||
ARG2_chr14_67614920_67656708 | 67627256 | G | GATATATA others(13): Show |
intron_variant | MODIFIER | HG00639.hp2 HG02109.hp2 NA19030.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0006 | a0001c0001t0001g0172a0001c0001t0003g0061a0001c0001t0006g0218 | 3 | 438 | 0.0069 | 20 | c.184 others(37): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
ARGFX_chr3_121562949_121595622 | 121576707 | T | TTCTCTTT others(13): Show |
intron_variant | MODIFIER | HG02970.hp1 | a0001 | a0001c0001 | a0001c0001t0018 | a0001c0001t0018g0310 | 1 | 410 | 0.0024 | 20 | c.104 others(33): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARGFX_chr3_121562949_121595622 | 121576707 | T | TTTTCTTT others(13): Show |
intron_variant | MODIFIER | HG02109.hp1 NA18942.hp1 NA20129.hp2 |
a0001 | a0001c0001 | a0001c0001t0012a0001c0001t0017 | a0001c0001t0012g0341a0001c0001t0012g0344a0001c0001t0017g0339 | 3 | 410 | 0.0073 | 20 | c.104 others(33): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARGFX_chr3_121562949_121595622 | 121584204 | G | GAGGAAGC others(13): Show |
intron_variant | MODIFIER | HG01255.hp2 HG01358.hp1 HG01952.hp1 others(2): Show |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0176a0002c0002t0001g0195a0002c0002t0001g0203others(2): Show | 5 | 410 | 0.0122 | 20 | c.221 others(35): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARGFX_chr3_121562949_121595622 | 121584204 | G | GAGGAAGG others(13): Show |
intron_variant | MODIFIER | HG02071.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0040 | 1 | 410 | 0.0024 | 20 | c.221 others(35): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARGLU1_chr13_106536673_106573137 | 106540792 | C | CTGGATGG others(13): Show |
downstream_gene_variant | MODIFIER | HG02132.hp2 HG02257.hp1 NA18954.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0007a0001c0001t0016 | a0001c0001t0002g0007a0001c0001t0002g0080a0001c0001t0007g0113others(1): Show | 4 | 376 | 0.0106 | 20 | c.*32 others(31): Show |
ARGLU1 | ENSG00000134884.15 | transcript | ENST00000400198.8 | protein_coding | 880 | chr13 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 147784805 | T | TATTATAA others(13): Show |
intron_variant | MODIFIER | HG01891.hp1 NA19064.hp1 NA19087.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0054a0001c0001t0001g0055a0001c0001t0001g0069 | 3 | 106 | 0.0283 | 20 | c.155 others(39): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147837643 | G | GTTTTTTT others(13): Show |
intron_variant | MODIFIER | HG02109.hp2 HG02451.hp1 HG03130.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0046a0001c0001t0001g0103a0001c0001t0001g0104 | 3 | 106 | 0.0283 | 20 | c.313 others(37): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147873681 | A | AACACACA others(13): Show |
intron_variant | MODIFIER | HG04184.hp2 NA18906.hp1 |
a0001a0004 | a0001c0002a0004c0010 | a0001c0002t0001a0004c0010t0001 | a0001c0002t0001g0033a0004c0010t0001g0048 | 2 | 106 | 0.0189 | 20 | c.703 others(37): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 7/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 147877819 | C | CTTTTTTT others(13): Show |
intron_variant | MODIFIER | HG03471.hp2 | a0001 | a0001c0004 | a0001c0004t0001 | a0001c0004t0001g0045 | 1 | 106 | 0.0094 | 20 | c.833 others(37): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 148017652 | C | CTATATAT others(13): Show |
intron_variant | MODIFIER | HG03098.hp1 | a0001 | a0001c0008 | a0001c0008t0001 | a0001c0008t0001g0060 | 1 | 106 | 0.0094 | 20 | c.171 others(39): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 148017680 | A | ATATATAT others(13): Show |
intron_variant | MODIFIER | HG02895.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006 | 1 | 106 | 0.0094 | 20 | c.171 others(39): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 148017682 | A | ATATATAT others(13): Show |
intron_variant | MODIFIER | NA19043.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0014 | 1 | 106 | 0.0094 | 20 | c.171 others(39): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 148043614 | A | AATATATA others(13): Show |
intron_variant | MODIFIER | HG01243.hp2 HG01261.hp2 HG02055.hp1 others(3): Show |
a0001 | a0001c0001a0001c0009 | a0001c0001t0001a0001c0009t0001 | a0001c0001t0001g0002a0001c0001t0001g0018a0001c0001t0001g0055others(3): Show | 6 | 106 | 0.0566 | 20 | c.186 others(39): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP12_chr10_31800398_31933831 | 31920449 | C | CAAAAAAA others(13): Show |
intron_variant | MODIFIER | HG03209.hp1 | a0001 | a0001c0001 | a0001c0001t0024 | a0001c0001t0024g0042 | 1 | 322 | 0.0031 | 20 | c.-11 others(39): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31933240 | A | ATATATAT others(13): Show |
upstream_gene_variant | MODIFIER | HG01168.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0037 | 1 | 322 | 0.0031 | 20 | c.-46 others(31): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4410 | chr10 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143165960 | G | GAGAAAGA others(13): Show |
intron_variant | MODIFIER | HG06807.hp1 NA18612.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0074a0001c0001t0001g0094 | 2 | 162 | 0.0124 | 20 | c.165 others(39): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143166001 | A | AGAAAGAA others(13): Show |
intron_variant | MODIFIER | HG01069.hp2 HG01243.hp1 HG02145.hp2 others(12): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0001a0001c0002t0002a0002c0004t0001 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0033others(12): Show | 15 | 162 | 0.0926 | 20 | c.165 others(39): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143166001 | A | AGAAAGAA others(13): Show |
intron_variant | MODIFIER | HG02976.hp2 HG03139.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0099a0001c0001t0001g0100 | 2 | 162 | 0.0124 | 20 | c.165 others(39): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143166001 | A | AGAAGGAA others(13): Show |
intron_variant | MODIFIER | HG02572.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0032 | 1 | 162 | 0.0062 | 20 | c.165 others(39): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143320405 | C | CCCCCCCG others(13): Show |
intron_variant | MODIFIER | HG03654.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0070 | 1 | 162 | 0.0062 | 20 | c.474 others(39): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143413966 | T | TGTGTGCG others(13): Show |
intron_variant | MODIFIER | HG00621.hp2 HG00738.hp1 HG00741.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0015a0001c0001t0001g0031a0001c0001t0001g0113others(4): Show | 7 | 162 | 0.0432 | 20 | c.475 others(39): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143413966 | T | TGTGTGTG others(13): Show |
intron_variant | MODIFIER | HG01255.hp2 HG03942.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0109a0001c0001t0001g0154 | 2 | 162 | 0.0124 | 20 | c.475 others(39): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143413966 | T | TGTGTGTG others(13): Show |
intron_variant | MODIFIER | HG02300.hp2 HG02723.hp2 HG03710.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0037a0001c0001t0001g0047a0001c0001t0001g0049others(5): Show | 8 | 162 | 0.0494 | 20 | c.475 others(39): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143413966 | T | TGTGTGTG others(13): Show |
intron_variant | MODIFIER | HG03486.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0106 | 1 | 162 | 0.0062 | 20 | c.475 others(39): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143439422 | C | CAAAAAAA others(13): Show |
intron_variant | MODIFIER | HG01081.hp1 HG04115.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0108a0001c0001t0001g0161 | 2 | 162 | 0.0124 | 20 | c.703 others(37): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143656934 | G | GGTGTGTG others(13): Show |
intron_variant | MODIFIER | HG03486.hp1 NA18947.hp1 NA18991.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0086a0001c0001t0001g0097a0001c0001t0001g0115 | 3 | 162 | 0.0185 | 20 | c.113 others(41): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143673746 | G | GTATATAT others(13): Show |
intron_variant | MODIFIER | HG00738.hp1 HG03491.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0031a0001c0001t0001g0151 | 2 | 162 | 0.0124 | 20 | c.113 others(41): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143673756 | G | GTATATAT others(13): Show |
intron_variant | MODIFIER | NA18962.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0116 | 1 | 162 | 0.0062 | 20 | c.113 others(41): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143673758 | G | GTATATAT others(13): Show |
intron_variant | MODIFIER | HG01081.hp2 HG02071.hp1 HG02698.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0028a0001c0001t0001g0045a0001c0002t0001g0125 | 3 | 162 | 0.0185 | 20 | c.113 others(41): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143673758 | G | GTGTATAT others(13): Show |
intron_variant | MODIFIER | HG01358.hp2 HG01496.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0145a0001c0001t0001g0147 | 2 | 162 | 0.0124 | 20 | c.113 others(41): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143673758 | G | GTGTGTAT others(13): Show |
intron_variant | MODIFIER | HG03490.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0131 | 1 | 162 | 0.0062 | 20 | c.113 others(41): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP17_chr16_24914389_25020369 | 24950836 | C | CAAAAAAA others(13): Show |
intron_variant | MODIFIER | HG02723.hp1 HG02970.hp2 NA19030.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0008a0001c0001t0001g0010a0001c0001t0001g0233 | 3 | 240 | 0.0125 | 20 | c.104 others(39): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 12/19 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 25020176 | A | AAAGGAAG others(13): Show |
upstream_gene_variant | MODIFIER | HG02965.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0229 | 1 | 240 | 0.0042 | 20 | c.-49 others(31): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 4808 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 25020190 | C | CGGAAGGA others(13): Show |
upstream_gene_variant | MODIFIER | HG03139.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004 | 1 | 240 | 0.0042 | 20 | c.-49 others(31): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 4822 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 25020228 | G | GAAGGAAG others(13): Show |
upstream_gene_variant | MODIFIER | HG01243.hp1 HG01496.hp1 HG02809.hp1 others(3): Show |
a0001 | a0001c0001a0001c0003a0001c0005 | a0001c0001t0001a0001c0003t0003a0001c0005t0001 | a0001c0001t0001g0020a0001c0003t0003g0211a0001c0003t0003g0212others(3): Show | 6 | 240 | 0.0250 | 20 | c.-49 others(31): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 4860 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 25020228 | G | GAAGGAAG others(13): Show |
upstream_gene_variant | MODIFIER | HG00642.hp1 HG01099.hp1 HG01243.hp2 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0007 | a0001c0001t0001g0001a0001c0001t0001g0056a0001c0001t0001g0057others(10): Show | 15 | 240 | 0.0625 | 20 | c.-49 others(31): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 4860 | chr16 | TogoVar | ||||||
ARHGAP19_chr10_97217179_97297637 | 97251530 | G | GGGGAGGG others(13): Show |
intron_variant | MODIFIER | HG03492.hp2 | a0002 | a0002c0004 | a0002c0004t0002 | a0002c0004t0002g0176 | 1 | 242 | 0.0041 | 20 | c.927 others(37): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | TogoVar | ||||||
ARHGAP19_chr10_97217179_97297637 | 97251541 | G | GGGGAGGG others(13): Show |
intron_variant | MODIFIER | NA18946.hp2 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0088 | 1 | 242 | 0.0041 | 20 | c.927 others(37): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 6/11 | chr10 | TogoVar | ||||||
ARHGAP20_chr11_110572043_110717437 | 110585408 | C | CCTTGGTT others(13): Show |
intron_variant | MODIFIER | HG03491.hp1 HG03688.hp1 NA19030.hp2 others(1): Show |
a0003a0008 | a0003c0004a0008c0017 | a0003c0004t0002a0003c0004t0017a0008c0017t0002 | a0003c0004t0002g0144a0003c0004t0002g0162a0003c0004t0017g0145others(1): Show | 4 | 226 | 0.0177 | 20 | c.141 others(37): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 12/14 | chr11 | TogoVar | ||||||
ARHGAP20_chr11_110572043_110717437 | 110618161 | G | GAAAAAAA others(13): Show |
intron_variant | MODIFIER | HG04199.hp1 | a0001 | a0001c0002 | a0001c0002t0005 | a0001c0002t0005g0215 | 1 | 226 | 0.0044 | 20 | c.504 others(37): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 4/14 | chr11 | TogoVar | ||||||
ARHGAP20_chr11_110572043_110717437 | 110658780 | A | ATTGTTTT others(13): Show |
intron_variant | MODIFIER | HG02622.hp2 HG03540.hp2 |
a0006 | a0006c0007 | a0006c0007t0010 | a0006c0007t0010g0147a0006c0007t0010g0148 | 2 | 226 | 0.0089 | 20 | c.189 others(39): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | TogoVar | ||||||
ARHGAP20_chr11_110572043_110717437 | 110687035 | C | CATATATA others(13): Show |
intron_variant | MODIFIER | HG00621.hp1 HG00735.hp2 HG01952.hp2 others(5): Show |
a0001a0002a0013 | a0001c0001a0001c0002a0002c0014others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0002t0005others(2): Show | a0001c0001t0001g0139a0001c0001t0001g0171a0001c0001t0001g0183others(5): Show | 8 | 226 | 0.0354 | 20 | c.188 others(37): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24628982 | A | ATATATAT others(13): Show |
intron_variant | MODIFIER | NA20129.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0195 | 1 | 352 | 0.0028 | 20 | c.495 others(37): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar |