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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP10_chr4_147727088_148077776 | 148017652 | C | CTATATA | intron_variant | MODIFIER | HG00558.hp1 HG02976.hp1 NA18612.hp1 |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0002c0003t0001 | a0001c0001t0001g0025a0001c0001t0001g0050a0002c0003t0001g0073 | 3 | 106 | 0.0283 | 6 | c.171 others(25): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 148017680 | A | ATATGAG | intron_variant | MODIFIER | HG02258.hp1 NA18522.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0076a0001c0001t0001g0081 | 2 | 106 | 0.0189 | 6 | c.171 others(25): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 148036066 | C | CTGTGTG | intron_variant | MODIFIER | HG01071.hp2 HG02055.hp2 HG02258.hp2 others(3): Show |
a0001a0002 | a0001c0001a0001c0004a0001c0006others(1): Show | a0001c0001t0001a0001c0004t0001a0001c0006t0001others(1): Show | a0001c0001t0001g0028a0001c0001t0001g0095a0001c0004t0001g0045others(3): Show | 6 | 106 | 0.0566 | 6 | c.186 others(27): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 148043614 | A | AATATAT | intron_variant | MODIFIER | HG01169.hp2 HG02976.hp2 |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0002c0003t0001 | a0001c0001t0001g0035a0002c0003t0001g0009 | 2 | 106 | 0.0189 | 6 | c.186 others(25): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 148065979 | C | CAAAAAA | intron_variant | MODIFIER | HG01167.hp1 HG01169.hp1 HG01884.hp1 others(7): Show |
a0001a0003 | a0001c0001a0001c0011a0003c0007 | a0001c0001t0001a0001c0011t0001a0003c0007t0001 | a0001c0001t0001g0014a0001c0001t0001g0049a0001c0001t0001g0076others(7): Show | 10 | 106 | 0.0943 | 6 | c.227 others(25): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP11A_chr15_32610504_32644941 | 32629941 | A | AGTGTGT | intron_variant | MODIFIER | HG00438.hp2 HG00621.hp1 HG00673.hp2 others(26): Show |
a0001a0007 | a0001c0001a0001c0002a0007c0009 | a0001c0001t0001a0001c0001t0003a0001c0001t0019others(3): Show | a0001c0001t0001g0005a0001c0001t0001g0015a0001c0001t0001g0087others(16): Show | 29 | 335 | 0.0866 | 6 | c.110 others(23): Show |
ARHGAP11A | ENSG00000198826.11 | transcript | ENST00000361627.8 | protein_coding | 8/11 | INFO_REALIGN_3_PRIME | chr15 | TogoVar | |||||
ARHGAP11B_chr15_30621128_30643810 | 30639971 | A | AGTGTGT | downstream_gene_variant | MODIFIER | HG01517.hp2 HG02083.hp2 HG02129.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(5): Show | 9 | 247 | 0.0364 | 6 | c.*12 others(17): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1162 | chr15 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31805648 | T | TCACACA | 3_prime_UTR_variant | MODIFIER | HG00280.hp1 HG00741.hp1 HG01106.hp1 others(23): Show |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0009a0001c0001t0024others(2): Show | a0001c0001t0006g0150a0001c0001t0006g0153a0001c0001t0006g0158others(23): Show | 26 | 322 | 0.0808 | 6 | c.*20 others(17): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 20/20 | 2009 | chr10 | TogoVar | |||||
ARHGAP12_chr10_31800398_31933831 | 31816168 | C | CGTGTGT | intron_variant | MODIFIER | HG00099.hp1 HG00639.hp2 HG00733.hp1 others(28): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0007others(2): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(10): Show | a0001c0001t0001g0119a0001c0001t0001g0135a0001c0001t0001g0142others(28): Show | 31 | 322 | 0.0963 | 6 | c.173 others(25): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 13/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31918315 | T | TCACACA | intron_variant | MODIFIER | HG00544.hp2 HG00621.hp2 HG01358.hp1 others(6): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0008a0001c0001t0012others(2): Show | a0001c0001t0001g0115a0001c0001t0001g0117a0001c0001t0001g0122others(6): Show | 9 | 322 | 0.0280 | 6 | c.-11 others(25): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31923132 | G | GAAAAAA | intron_variant | MODIFIER | HG00735.hp2 HG00738.hp1 HG00741.hp1 others(23): Show |
a0001 | a0001c0001a0001c0003a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(9): Show | a0001c0001t0001g0213a0001c0001t0001g0215a0001c0001t0001g0217others(23): Show | 26 | 322 | 0.0808 | 6 | c.-11 others(25): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31933207 | C | CATATAT | upstream_gene_variant | MODIFIER | HG00544.hp2 HG01358.hp1 HG02273.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0008 | a0001c0001t0001g0101a0001c0001t0001g0109a0001c0001t0001g0111others(4): Show | 7 | 322 | 0.0217 | 6 | c.-46 others(17): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4377 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31933240 | A | ATATATC | upstream_gene_variant | MODIFIER | HG01891.hp2 HG02572.hp2 HG02965.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0005a0001c0001t0011others(1): Show | a0001c0001t0004g0031a0001c0001t0005g0049a0001c0001t0011g0057others(2): Show | 5 | 322 | 0.0155 | 6 | c.-46 others(17): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 4410 | chr10 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143153777 | A | ATCTTCT | intron_variant | MODIFIER | HG01358.hp2 HG03491.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0147a0001c0001t0001g0151 | 2 | 162 | 0.0124 | 6 | c.-14 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143153840 | T | TTCCTCC | intron_variant | MODIFIER | HG00609.hp1 HG00741.hp1 HG02145.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0019a0001c0001t0001g0041a0001c0002t0001g0093 | 3 | 162 | 0.0185 | 6 | c.-14 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143153843 | T | TTCCTCC | intron_variant | MODIFIER | HG01243.hp2 HG01255.hp1 HG02523.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0007a0001c0001t0001g0030a0001c0001t0001g0038others(3): Show | 6 | 162 | 0.0370 | 6 | c.-14 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143153876 | C | CTCCTCT | intron_variant | MODIFIER | HG02280.hp1 HG03654.hp1 NA21309.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0027a0001c0001t0001g0070a0001c0001t0001g0123 | 3 | 162 | 0.0185 | 6 | c.-14 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143188613 | C | CATTATT | intron_variant | MODIFIER | HG00609.hp2 HG02071.hp2 HG02145.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0034others(4): Show | 7 | 162 | 0.0432 | 6 | c.166 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143197967 | T | TACACAC | intron_variant | MODIFIER | HG01255.hp1 HG02965.hp1 NA18955.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0030a0001c0001t0001g0055a0001c0001t0001g0102 | 3 | 162 | 0.0185 | 6 | c.166 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 2/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143207495 | A | AACACAC | intron_variant | MODIFIER | HG01081.hp2 HG03491.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0151a0001c0002t0001g0125 | 2 | 162 | 0.0124 | 6 | c.234 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143209557 | T | TAAAAAA | intron_variant | MODIFIER | HG02886.hp1 HG02965.hp1 HG03490.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0055a0001c0001t0001g0074a0001c0001t0001g0095others(2): Show | 5 | 162 | 0.0309 | 6 | c.235 others(23): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 3/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143239990 | C | CAAAAAA | intron_variant | MODIFIER | HG00609.hp1 HG00621.hp1 HG00621.hp2 others(17): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(1): Show | a0001c0001t0001g0013a0001c0001t0001g0015a0001c0001t0001g0019others(17): Show | 20 | 162 | 0.1235 | 6 | c.385 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143323894 | C | CAAAAAA | intron_variant | MODIFIER | HG02145.hp2 HG02258.hp1 HG02280.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002a0001c0001t0001g0008a0001c0001t0001g0009others(6): Show | 9 | 162 | 0.0556 | 6 | c.474 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143330094 | C | CAAAAAA | intron_variant | MODIFIER | HG00609.hp1 HG01496.hp1 HG01517.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0019a0001c0001t0001g0034a0001c0001t0001g0050others(4): Show | 7 | 162 | 0.0432 | 6 | c.474 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143379487 | A | ATGTGTG | intron_variant | MODIFIER | HG01081.hp1 HG02145.hp2 HG02258.hp1 others(9): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002 | a0001c0001t0001g0009a0001c0001t0001g0069a0001c0001t0001g0099others(9): Show | 12 | 162 | 0.0741 | 6 | c.475 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143397316 | A | ATGTGTG | intron_variant | MODIFIER | HG00733.hp1 HG04199.hp1 NA18955.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0042a0001c0001t0001g0069a0001c0001t0001g0102 | 3 | 162 | 0.0185 | 6 | c.475 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143407987 | G | GTATGTA | intron_variant | MODIFIER | HG00642.hp2 HG01069.hp2 HG02486.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006a0001c0001t0001g0112a0001c0001t0001g0148 | 3 | 162 | 0.0185 | 6 | c.475 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143407987 | G | GTGTATA | intron_variant | MODIFIER | HG02071.hp2 HG02886.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0001a0001c0002t0001g0105 | 2 | 162 | 0.0124 | 6 | c.475 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143413927 | T | TTGTGTG | intron_variant | MODIFIER | HG01081.hp2 HG02071.hp1 HG02109.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0062others(7): Show | 10 | 162 | 0.0617 | 6 | c.475 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143468661 | A | AGTGTGT | intron_variant | MODIFIER | HG02071.hp1 HG02280.hp2 NA18747.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0024a0001c0001t0001g0028a0001c0001t0001g0133 | 3 | 162 | 0.0185 | 6 | c.704 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 8/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143606035 | C | CAAAAAA | intron_variant | MODIFIER | HG00733.hp2 HG01358.hp2 HG03710.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0050a0001c0001t0001g0068a0001c0001t0001g0074others(4): Show | 7 | 162 | 0.0432 | 6 | c.100 others(27): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143656934 | G | GGTGTGT | intron_variant | MODIFIER | HG00733.hp1 HG01358.hp1 HG01515.hp1 others(6): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0042a0001c0001t0001g0064a0001c0001t0001g0080others(6): Show | 9 | 162 | 0.0556 | 6 | c.113 others(27): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143673756 | G | GTATATA | intron_variant | MODIFIER | NA19068.hp2 NA19088.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0160a0001c0003t0001g0054 | 2 | 162 | 0.0124 | 6 | c.113 others(27): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143721061 | C | CAAAAAA | intron_variant | MODIFIER | HG00621.hp1 HG00733.hp2 HG01069.hp1 others(21): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002 | a0001c0001t0001g0007a0001c0001t0001g0013a0001c0001t0001g0014others(21): Show | 24 | 162 | 0.1482 | 6 | c.124 others(27): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143724051 | A | ATGTGTG | intron_variant | MODIFIER | HG00621.hp1 HG00733.hp1 HG00733.hp2 others(31): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0004 | a0001c0001t0001a0001c0002t0001a0002c0004t0001 | a0001c0001t0001g0013a0001c0001t0001g0014a0001c0001t0001g0016others(31): Show | 34 | 162 | 0.2099 | 6 | c.124 others(27): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143730945 | T | TTTTTAA | intron_variant | MODIFIER | HG00609.hp1 HG02071.hp1 HG03490.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002 | a0001c0001t0001g0019a0001c0001t0001g0028a0001c0001t0001g0035others(7): Show | 10 | 162 | 0.0617 | 6 | c.124 others(27): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143765109 | A | ATGTGTG | intron_variant | MODIFIER | HG02486.hp1 HG02486.hp2 HG02523.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006a0001c0001t0001g0010a0001c0001t0001g0052others(4): Show | 7 | 162 | 0.0432 | 6 | c.124 others(25): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 13/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP17_chr16_24914389_25020369 | 24916596 | T | TACACAC | downstream_gene_variant | MODIFIER | HG02257.hp2 HG02970.hp1 HG03209.hp1 |
a0001 | a0001c0004 | a0001c0004t0002 | a0001c0004t0002g0110a0001c0004t0002g0112a0001c0004t0002g0113 | 3 | 240 | 0.0125 | 6 | c.*35 others(17): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 2792 | chr16 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24982985 | T | TATACAC | intron_variant | MODIFIER | HG01243.hp1 HG01496.hp1 HG01884.hp2 others(5): Show |
a0001 | a0001c0003a0001c0005 | a0001c0003t0003a0001c0005t0001 | a0001c0003t0003g0210a0001c0003t0003g0211a0001c0003t0003g0212others(5): Show | 8 | 240 | 0.0333 | 6 | c.54- others(21): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 1/19 | chr16 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129571291 | C | CAAAAAA | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00408.hp2 others(31): Show |
a0001a0002a0006 | a0001c0001a0002c0002a0006c0010 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(6): Show | a0001c0001t0001g0061a0001c0001t0001g0062a0001c0001t0001g0072others(31): Show | 34 | 238 | 0.1429 | 6 | c.*72 others(17): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 4840 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129598941 | G | GGTGTGT | intron_variant | MODIFIER | HG00544.hp2 HG00733.hp1 HG00738.hp1 others(27): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0002c0002t0001 | a0001c0001t0001g0065a0001c0001t0001g0094a0001c0001t0001g0096others(27): Show | 30 | 238 | 0.1261 | 6 | c.171 others(23): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 12/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129625133 | T | TTATATA | intron_variant | MODIFIER | HG02486.hp1 NA20300.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0079a0001c0001t0001g0136 | 2 | 238 | 0.0084 | 6 | c.786 others(23): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129625149 | T | TATGATA | intron_variant | MODIFIER | HG02896.hp1 NA20300.hp1 |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0007a0003c0004t0005 | a0001c0001t0007g0077a0003c0004t0005g0088 | 2 | 238 | 0.0084 | 6 | c.786 others(23): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129626065 | T | TACACAC | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00597.hp1 others(48): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0003a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0074a0001c0001t0001g0086a0001c0001t0001g0089others(48): Show | 51 | 238 | 0.2143 | 6 | c.786 others(23): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129667469 | A | ATGTGTG | intron_variant | MODIFIER | HG01175.hp1 NA18994.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0127a0002c0002t0001g0040 | 2 | 238 | 0.0084 | 6 | c.114 others(25): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129667503 | G | GTGTGTA | intron_variant | MODIFIER | HG00733.hp1 HG01081.hp2 HG01361.hp1 others(8): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(3): Show | a0001c0001t0001g0096a0001c0001t0001g0121a0001c0001t0001g0132others(8): Show | 11 | 238 | 0.0462 | 6 | c.114 others(25): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129668362 | T | TCACACA | intron_variant | MODIFIER | HG00558.hp2 HG00621.hp2 HG01071.hp1 others(29): Show |
a0001a0002a0003 | a0001c0001a0001c0011a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0111a0001c0001t0001g0112a0001c0001t0001g0124others(29): Show | 32 | 238 | 0.1345 | 6 | c.114 others(25): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | TogoVar | ||||||
ARHGAP19_chr10_97217179_97297637 | 97218631 | T | TTTTGTG | downstream_gene_variant | MODIFIER | HG00639.hp1 HG01934.hp1 HG02615.hp1 others(8): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0005a0001c0002t0001 | a0001c0001t0001g0124a0001c0001t0001g0135a0001c0001t0001g0154others(8): Show | 11 | 242 | 0.0455 | 6 | c.*74 others(17): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 3547 | chr10 | TogoVar | ||||||
ARHGAP19_chr10_97217179_97297637 | 97218895 | A | ATGTGTG | downstream_gene_variant | MODIFIER | HG02083.hp1 HG06807.hp2 NA18952.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0204a0001c0001t0001g0208a0001c0001t0001g0217others(1): Show | 4 | 242 | 0.0165 | 6 | c.*72 others(17): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 3283 | chr10 | TogoVar | ||||||
ARHGAP19_chr10_97217179_97297637 | 97219772 | C | CTTTTTT | downstream_gene_variant | MODIFIER | HG00609.hp2 HG00639.hp1 HG00673.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005 | a0001c0001t0001g0125a0001c0001t0001g0141a0001c0001t0005g0235others(6): Show | 9 | 242 | 0.0372 | 6 | c.*63 others(17): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 2406 | chr10 | TogoVar |