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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP15_chr2_143124419_143773352 | 143258252 | C | CATAT | intron_variant | MODIFIER | HG00733.hp2 HG01361.hp1 HG01517.hp1 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009a0001c0001t0001g0074a0001c0001t0001g0092others(8): Show | 11 | 162 | 0.0679 | 4 | c.474 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143263907 | C | CTTTT | intron_variant | MODIFIER | HG01243.hp1 HG02071.hp1 HG02976.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0001a0002c0004t0001 | a0001c0001t0001g0028a0001c0001t0001g0088a0001c0001t0001g0091others(3): Show | 6 | 162 | 0.0370 | 4 | c.474 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143309866 | T | TTGTG | intron_variant | MODIFIER | HG02523.hp1 HG02602.hp1 HG03490.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0037a0001c0001t0001g0052a0001c0001t0001g0053others(7): Show | 10 | 162 | 0.0617 | 4 | c.474 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143346220 | T | TCTCA | intron_variant | MODIFIER | HG00642.hp2 HG01243.hp1 HG02145.hp1 others(7): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0001a0002c0004t0001 | a0001c0001t0001g0011a0001c0001t0001g0041a0001c0001t0001g0074others(7): Show | 10 | 162 | 0.0617 | 4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143346236 | T | TCACA | intron_variant | MODIFIER | HG02145.hp1 HG02559.hp1 HG02976.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0041a0001c0001t0001g0099a0001c0001t0001g0120 | 3 | 162 | 0.0185 | 4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143365012 | A | AAAAT | intron_variant | MODIFIER | HG00609.hp2 HG00733.hp1 HG01081.hp2 others(28): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0001a0001c0001t0001g0024a0001c0001t0001g0026others(28): Show | 31 | 162 | 0.1914 | 4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143372011 | G | GAAAT | intron_variant | MODIFIER | HG00609.hp1 HG01261.hp2 HG02886.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0022others(3): Show | 6 | 162 | 0.0370 | 4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143373063 | G | GAGAA | intron_variant | MODIFIER | HG00609.hp2 HG00642.hp1 HG00733.hp1 others(98): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0004others(98): Show | 101 | 162 | 0.6235 | 4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143379480 | C | CATAT | intron_variant | MODIFIER | HG01261.hp1 HG02109.hp2 HG02723.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0039a0001c0001t0001g0062a0001c0001t0001g0118others(1): Show | 4 | 162 | 0.0247 | 4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143379487 | A | ATGTG | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp2 HG01069.hp1 others(23): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0006a0001c0001t0001g0015a0001c0001t0001g0019others(23): Show | 26 | 162 | 0.1605 | 4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143397316 | A | ATGTG | intron_variant | MODIFIER | HG00609.hp1 HG00642.hp1 HG01071.hp2 others(19): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0019others(19): Show | 22 | 162 | 0.1358 | 4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143407985 | G | GTGTA | intron_variant | MODIFIER | HG00738.hp2 HG01256.hp2 HG01261.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0017a0001c0001t0001g0018a0001c0001t0001g0080others(3): Show | 6 | 162 | 0.0370 | 4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143407987 | G | GTGTA | intron_variant | MODIFIER | HG00642.hp1 HG01071.hp2 HG02129.hp1 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0021a0001c0001t0001g0046a0001c0001t0001g0048others(12): Show | 15 | 162 | 0.0926 | 4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143411244 | C | CATTA | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(140): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(3): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(140): Show | 143 | 162 | 0.8827 | 4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143412372 | G | GATAA | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(146): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(3): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(146): Show | 149 | 162 | 0.9198 | 4 | c.475 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143461281 | C | CAAAA | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp2 HG00733.hp1 others(21): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0015a0001c0001t0001g0019others(21): Show | 24 | 162 | 0.1482 | 4 | c.703 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143462773 | A | AGATG | intron_variant | MODIFIER | HG00733.hp2 NA19240.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0058a0001c0001t0001g0141 | 2 | 162 | 0.0124 | 4 | c.704 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143468659 | A | AGTGT | intron_variant | MODIFIER | HG03491.hp1 HG04199.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0069a0001c0001t0001g0151 | 2 | 162 | 0.0124 | 4 | c.704 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143468661 | A | AGTGT | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp2 HG00642.hp1 others(37): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0001a0001c0003t0001 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0005others(37): Show | 40 | 162 | 0.2469 | 4 | c.704 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143468663 | A | AGTGT | intron_variant | MODIFIER | HG03710.hp2 HG04228.hp1 NA19000.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0068a0001c0001t0001g0079a0001c0001t0001g0153 | 3 | 162 | 0.0185 | 4 | c.704 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143511568 | T | TTTTG | intron_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(83): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0004others(1): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(2): Show | a0001c0001t0001g0003a0001c0001t0001g0007a0001c0001t0001g0008others(83): Show | 86 | 162 | 0.5309 | 4 | c.827 others(21): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 9/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143590942 | G | GCTCT | intron_variant | MODIFIER | HG00741.hp1 HG01081.hp2 HG02109.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0004a0001c0001t0001g0096a0001c0002t0001g0065others(2): Show | 5 | 162 | 0.0309 | 4 | c.100 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143606035 | C | CAAAA | intron_variant | MODIFIER | HG01071.hp2 HG02071.hp1 HG02615.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0008a0001c0001t0001g0020a0001c0001t0001g0021others(6): Show | 9 | 162 | 0.0556 | 4 | c.100 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143610719 | G | GTATT | intron_variant | MODIFIER | HG01361.hp2 HG01515.hp1 HG01517.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0098a0001c0001t0001g0120a0001c0001t0001g0123others(7): Show | 10 | 162 | 0.0617 | 4 | c.100 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143684073 | T | TTATC | intron_variant | MODIFIER | HG00642.hp2 HG00733.hp1 HG00738.hp2 others(47): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0001a0001c0002t0001a0002c0004t0001 | a0001c0001t0001g0011a0001c0001t0001g0020a0001c0001t0001g0029others(47): Show | 50 | 162 | 0.3086 | 4 | c.113 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143700685 | T | TATGA | intron_variant | MODIFIER | NA18991.hp1 NA19088.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0033a0001c0001t0001g0083 | 2 | 162 | 0.0124 | 4 | c.113 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143724051 | A | ATGTG | intron_variant | MODIFIER | HG00642.hp2 HG00738.hp2 HG00741.hp1 others(34): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0020others(34): Show | 37 | 162 | 0.2284 | 4 | c.124 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143730945 | T | TTTAA | intron_variant | MODIFIER | HG02145.hp1 HG02145.hp2 HG02258.hp1 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004a0001c0001t0001g0008a0001c0001t0001g0009others(11): Show | 14 | 162 | 0.0864 | 4 | c.124 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143737726 | T | TTTTA | intron_variant | MODIFIER | HG03209.hp1 HG03710.hp2 NA18966.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003a0001c0001t0001g0056a0001c0001t0001g0068 | 3 | 162 | 0.0185 | 4 | c.124 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143765080 | T | TTATC | intron_variant | MODIFIER | NA19043.hp1 NA19240.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0005a0001c0001t0001g0122 | 2 | 162 | 0.0124 | 4 | c.124 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143765109 | A | ATGTG | intron_variant | MODIFIER | HG01515.hp1 HG01517.hp2 HG02109.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002 | a0001c0001t0001g0004a0001c0001t0001g0063a0001c0001t0001g0096others(4): Show | 7 | 162 | 0.0432 | 4 | c.124 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP17_chr16_24914389_25020369 | 24916423 | C | CTTTT | downstream_gene_variant | MODIFIER | HG01358.hp2 HG02040.hp1 HG02055.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0062a0001c0001t0001g0088a0001c0001t0001g0116others(6): Show | 9 | 240 | 0.0375 | 4 | c.*37 others(15): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2965 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24916596 | T | TACAC | downstream_gene_variant | MODIFIER | HG02486.hp2 HG02572.hp2 HG02922.hp2 others(3): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0002a0001c0004t0008 | a0001c0001t0001g0121a0001c0001t0001g0198a0001c0004t0002g0103others(3): Show | 6 | 240 | 0.0250 | 4 | c.*35 others(15): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2792 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24958237 | A | AAAAC | intron_variant | MODIFIER | HG00323.hp2 HG00438.hp1 HG00609.hp2 others(139): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(9): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0006others(134): Show | 142 | 240 | 0.5917 | 4 | c.724 others(21): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 9/19 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24961972 | G | GTTTT | intron_variant | MODIFIER | HG01243.hp1 HG01496.hp1 HG01884.hp1 others(22): Show |
a0001 | a0001c0001a0001c0003a0001c0004others(1): Show | a0001c0001t0001a0001c0001t0005a0001c0003t0003others(3): Show | a0001c0001t0001g0029a0001c0001t0001g0107a0001c0001t0001g0229others(21): Show | 25 | 240 | 0.1042 | 4 | c.574 others(21): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24999399 | T | TTTTA | intron_variant | MODIFIER | HG00642.hp2 HG01123.hp1 HG01168.hp2 others(52): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(2): Show | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0005others(51): Show | 55 | 240 | 0.2292 | 4 | c.53+ others(21): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 25003038 | C | CAAAA | intron_variant | MODIFIER | HG01243.hp2 HG01256.hp1 HG01516.hp1 others(17): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0051a0001c0001t0001g0052a0001c0001t0001g0084others(17): Show | 20 | 240 | 0.0833 | 4 | c.53+ others(21): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 25020117 | A | AAAAG | upstream_gene_variant | MODIFIER | HG00323.hp1 HG01884.hp1 HG01934.hp2 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005a0001c0001t0007 | a0001c0001t0001g0017a0001c0001t0001g0021a0001c0001t0001g0025others(11): Show | 15 | 240 | 0.0625 | 4 | c.-48 others(15): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 4749 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 25020176 | A | AACGG | upstream_gene_variant | MODIFIER | HG01167.hp2 HG01168.hp2 HG01169.hp1 others(10): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0016a0001c0001t0001g0028a0001c0001t0001g0116others(10): Show | 13 | 240 | 0.0542 | 4 | c.-49 others(15): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 4808 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 25020190 | C | CGGAA | upstream_gene_variant | MODIFIER | HG02895.hp1 HG02970.hp2 HG03139.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004 | a0001c0001t0001g0146a0001c0001t0001g0233a0001c0001t0002g0031others(1): Show | 4 | 240 | 0.0167 | 4 | c.-49 others(15): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 4822 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 25020228 | G | GAAGA | upstream_gene_variant | MODIFIER | HG06807.hp1 NA18747.hp1 NA19240.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0027a0001c0001t0001g0064a0001c0001t0001g0099 | 3 | 240 | 0.0125 | 4 | c.-49 others(15): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 4860 | chr16 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129602987 | T | TTATA | intron_variant | MODIFIER | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(19): Show |
a0001a0002 | a0001c0001a0001c0011a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0109others(19): Show | 22 | 238 | 0.0924 | 4 | c.136 others(23): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 10/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129608064 | G | GAAAA | intron_variant | MODIFIER | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(7): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0002c0002t0001others(1): Show | a0001c0001t0001g0080a0001c0001t0001g0108a0001c0001t0001g0153others(7): Show | 10 | 238 | 0.0420 | 4 | c.112 others(19): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 8/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129619979 | A | AGAAG | intron_variant | MODIFIER | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(12): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0007a0002c0002t0001others(1): Show | a0001c0001t0001g0079a0001c0001t0001g0080a0001c0001t0001g0108others(12): Show | 15 | 238 | 0.0630 | 4 | c.787 others(21): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129625357 | T | TGATA | intron_variant | MODIFIER | NA19004.hp1 NA19011.hp1 NA19090.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0005a0001c0001t0009a0002c0002t0005 | a0001c0001t0005g0212a0001c0001t0009g0069a0002c0002t0005g0024 | 3 | 238 | 0.0126 | 4 | c.786 others(21): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129625551 | T | TTATA | intron_variant | MODIFIER | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(49): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0017others(1): Show | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(48): Show | 52 | 238 | 0.2185 | 4 | c.786 others(21): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129625732 | T | TAATA | intron_variant | MODIFIER | HG02451.hp1 HG03195.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0010 | a0001c0001t0002g0145a0001c0001t0010g0137 | 2 | 238 | 0.0084 | 4 | c.786 others(21): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129625732 | T | TTATA | intron_variant | MODIFIER | HG00597.hp2 HG03209.hp2 NA18612.hp1 others(3): Show |
a0001a0002 | a0001c0001a0001c0011a0002c0002 | a0001c0001t0005a0001c0001t0009a0001c0011t0001others(1): Show | a0001c0001t0005g0207a0001c0001t0005g0212a0001c0001t0009g0069others(3): Show | 6 | 238 | 0.0252 | 4 | c.786 others(21): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129626065 | T | TACAC | intron_variant | MODIFIER | HG00140.hp1 HG00408.hp1 HG00544.hp1 others(26): Show |
a0001a0002a0009 | a0001c0001a0002c0002a0002c0006others(1): Show | a0001c0001t0001a0001c0001t0002a0002c0002t0001others(3): Show | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0072others(26): Show | 29 | 238 | 0.1219 | 4 | c.786 others(21): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129631941 | G | GAATT | intron_variant | MODIFIER | HG00140.hp1 HG00544.hp2 HG00609.hp2 others(65): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0011a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0001a0001c0001t0001g0061a0001c0001t0001g0062others(64): Show | 68 | 238 | 0.2857 | 4 | c.616 others(21): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4/14 | chr6 | TogoVar |