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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP42_chr11_100682288_100998941 | 100858086 | G | GGGGTGTG others(3): Show |
intron_variant | MODIFIER | HG03492.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0152 | 1 | 286 | 0.0035 | 10 | c.313 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100858086 | G | GGTGTGTG others(3): Show |
intron_variant | MODIFIER | HG00597.hp1 HG00735.hp1 HG00738.hp1 others(12): Show |
a0001a0002 | a0001c0001a0001c0014a0002c0004 | a0001c0001t0001a0001c0001t0041a0001c0014t0001others(1): Show | a0001c0001t0001g0069a0001c0001t0001g0079a0001c0001t0001g0080others(12): Show | 15 | 286 | 0.0525 | 10 | c.313 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100858086 | G | GTTGTGTG others(3): Show |
intron_variant | MODIFIER | NA19091.hp1 | a0001 | a0001c0012 | a0001c0012t0001 | a0001c0012t0001g0131 | 1 | 286 | 0.0035 | 10 | c.313 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100858117 | G | GTGTGTGT others(3): Show |
intron_variant | MODIFIER | HG00423.hp1 HG02004.hp2 HG02738.hp1 others(3): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0006a0001c0003t0026 | a0001c0001t0001g0062a0001c0001t0001g0066a0001c0003t0006g0159others(3): Show | 6 | 286 | 0.0210 | 10 | c.313 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100875073 | G | GTCTCTCT others(3): Show |
intron_variant | MODIFIER | HG02818.hp2 | a0002 | a0002c0002 | a0002c0002t0008 | a0002c0002t0008g0005 | 1 | 286 | 0.0035 | 10 | c.384 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100893158 | G | GGTGTGTG others(3): Show |
intron_variant | MODIFIER | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(80): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0003a0001c0012others(4): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0013others(14): Show | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0023others(80): Show | 83 | 286 | 0.2902 | 10 | c.385 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903117 | G | GCACACAC others(3): Show |
intron_variant | MODIFIER | HG00639.hp2 HG00735.hp2 HG01069.hp2 others(12): Show |
a0002 | a0002c0002a0002c0004a0002c0006 | a0002c0002t0002a0002c0002t0005a0002c0002t0008others(4): Show | a0002c0002t0002g0050a0002c0002t0002g0102a0002c0002t0002g0139others(12): Show | 15 | 286 | 0.0525 | 10 | c.385 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903117 | G | GCGCACAC others(3): Show |
intron_variant | MODIFIER | NA18943.hp1 NA19087.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0188a0001c0001t0001g0190 | 2 | 286 | 0.0070 | 10 | c.385 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903706 | C | CAAAAAAA others(3): Show |
intron_variant | MODIFIER | HG02970.hp2 NA19240.hp1 |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0015a0002c0002t0001g0017 | 2 | 286 | 0.0070 | 10 | c.385 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903709 | A | AAAAAAAA others(3): Show |
intron_variant | MODIFIER | HG02922.hp2 | a0002 | a0002c0002 | a0002c0002t0011 | a0002c0002t0011g0207 | 1 | 286 | 0.0035 | 10 | c.385 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903709 | A | AAAAAATA others(3): Show |
intron_variant | MODIFIER | HG01109.hp2 HG02572.hp1 |
a0002 | a0002c0006 | a0002c0006t0011 | a0002c0006t0011g0239a0002c0006t0011g0242 | 2 | 286 | 0.0070 | 10 | c.385 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903709 | A | AAAATATA others(3): Show |
intron_variant | MODIFIER | HG01081.hp1 HG02976.hp1 HG03130.hp2 others(1): Show |
a0002 | a0002c0002 | a0002c0002t0008a0002c0002t0009a0002c0002t0035 | a0002c0002t0008g0028a0002c0002t0008g0029a0002c0002t0009g0033others(1): Show | 4 | 286 | 0.0140 | 10 | c.385 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903709 | A | AATATATA others(3): Show |
intron_variant | MODIFIER | HG00544.hp2 HG01257.hp2 HG01361.hp1 others(10): Show |
a0001 | a0001c0001a0001c0008a0001c0014 | a0001c0001t0001a0001c0001t0032a0001c0008t0001others(1): Show | a0001c0001t0001g0023a0001c0001t0001g0086a0001c0001t0001g0117others(10): Show | 13 | 286 | 0.0455 | 10 | c.385 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100917015 | T | TTGTGTGT others(3): Show |
intron_variant | MODIFIER | HG03927.hp2 | a0002 | a0002c0004 | a0002c0004t0007 | a0002c0004t0007g0146 | 1 | 286 | 0.0035 | 10 | c.486 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100935677 | C | CACACACA others(3): Show |
intron_variant | MODIFIER | HG00738.hp1 HG00741.hp1 HG01516.hp1 others(4): Show |
a0002 | a0002c0004 | a0002c0004t0007 | a0002c0004t0007g0016a0002c0004t0007g0060a0002c0004t0007g0074others(4): Show | 7 | 286 | 0.0245 | 10 | c.703 others(25): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100952734 | C | CTTTTTTT others(3): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(215): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0003a0001c0008others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(44): Show | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0011others(215): Show | 218 | 286 | 0.7622 | 10 | c.116 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100972548 | A | ATGGATGG others(3): Show |
intron_variant | MODIFIER | NA18940.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0179 | 1 | 286 | 0.0035 | 10 | c.155 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 17/23 | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTCTTTT others(3): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(5): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0007 | a0001c0001t0001a0002c0002t0002a0002c0002t0005others(1): Show | a0001c0001t0001g0091a0002c0002t0002g0014a0002c0002t0002g0147others(5): Show | 8 | 286 | 0.0280 | 10 | c.245 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTTTTTT others(3): Show |
intron_variant | MODIFIER | HG03688.hp2 HG04199.hp1 HG04204.hp2 others(2): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0009 | a0001c0001t0001a0001c0003t0003a0001c0003t0014others(1): Show | a0001c0001t0001g0177a0001c0003t0003g0219a0001c0003t0014g0234others(2): Show | 5 | 286 | 0.0175 | 10 | c.245 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100985270 | C | CTCTTTAT others(3): Show |
intron_variant | MODIFIER | NA19002.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0224 | 1 | 286 | 0.0035 | 10 | c.245 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | chr11 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12786924 | T | TTTTTATT others(3): Show |
upstream_gene_variant | MODIFIER | NA21309.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0176 | 1 | 230 | 0.0044 | 10 | c.-29 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 2573 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12835606 | C | CACATTGC others(3): Show |
intron_variant | MODIFIER | HG00423.hp1 HG00423.hp2 HG00733.hp1 others(58): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(16): Show | a0001c0001t0001g0009a0001c0001t0001g0013a0001c0001t0001g0016others(58): Show | 61 | 230 | 0.2652 | 10 | c.53+ others(27): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12841577 | G | GTCTGTCT others(3): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00738.hp1 HG01074.hp2 others(12): Show |
a0001 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0035a0001c0001t0001g0041a0001c0001t0001g0189others(12): Show | 15 | 230 | 0.0652 | 10 | c.53+ others(27): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12841637 | C | CAAAAAAA others(3): Show |
intron_variant | MODIFIER | HG02886.hp2 | a0001 | a0001c0001 | a0001c0001t0014 | a0001c0001t0014g0179 | 1 | 230 | 0.0044 | 10 | c.53+ others(27): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12841639 | C | CAAAAAAA others(3): Show |
intron_variant | MODIFIER | HG02922.hp1 HG02965.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0225a0001c0001t0001g0226 | 2 | 230 | 0.0087 | 10 | c.53+ others(27): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12849214 | C | CGTGTGTG others(3): Show |
intron_variant | MODIFIER | HG04204.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0229 | 1 | 230 | 0.0044 | 10 | c.54- others(27): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12868589 | T | TTATATAT others(3): Show |
intron_variant | MODIFIER | HG03491.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0017 | 1 | 230 | 0.0044 | 10 | c.54- others(27): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12868591 | T | TTATATAT others(3): Show |
intron_variant | MODIFIER | HG00733.hp1 HG01517.hp2 HG01934.hp2 others(5): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(1): Show | a0001c0001t0001g0202a0001c0001t0001g0209a0001c0001t0001g0213others(5): Show | 8 | 230 | 0.0348 | 10 | c.54- others(27): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12868591 | T | TTTTATAT others(3): Show |
intron_variant | MODIFIER | HG01952.hp1 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0153 | 1 | 230 | 0.0044 | 10 | c.54- others(27): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12879683 | G | GTGTATAT others(3): Show |
intron_variant | MODIFIER | HG01884.hp1 HG02145.hp1 HG02572.hp1 |
a0001 | a0001c0001a0001c0008 | a0001c0001t0001a0001c0001t0010a0001c0008t0020 | a0001c0001t0001g0183a0001c0001t0010g0182a0001c0008t0020g0181 | 3 | 230 | 0.0130 | 10 | c.54- others(27): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12903126 | G | GAGAGAGA others(3): Show |
intron_variant | MODIFIER | HG01192.hp2 HG03098.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0189a0001c0002t0001g0100 | 2 | 230 | 0.0087 | 10 | c.199 others(27): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12903126 | G | GGAGAGAG others(3): Show |
intron_variant | MODIFIER | HG03516.hp1 NA19083.hp1 |
a0001 | a0001c0001 | a0001c0001t0005a0001c0001t0009 | a0001c0001t0005g0072a0001c0001t0009g0096 | 2 | 230 | 0.0087 | 10 | c.199 others(27): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12903140 | A | AGAGAGAG others(3): Show |
intron_variant | MODIFIER | HG03942.hp2 | a0003 | a0003c0017 | a0003c0017t0003 | a0003c0017t0003g0068 | 1 | 230 | 0.0044 | 10 | c.199 others(27): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12903140 | A | AGTGTGTG others(3): Show |
intron_variant | MODIFIER | HG01070.hp1 HG01074.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0162a0001c0001t0002g0198 | 2 | 230 | 0.0087 | 10 | c.199 others(27): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12931841 | T | TACACACA others(3): Show |
intron_variant | MODIFIER | HG01891.hp1 HG02809.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0033 | a0001c0001t0001g0212a0001c0001t0033g0029 | 2 | 230 | 0.0087 | 10 | c.582 others(27): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12948723 | T | TACACACA others(3): Show |
intron_variant | MODIFIER | HG00738.hp2 HG01070.hp1 HG01074.hp1 others(27): Show |
a0001a0005 | a0001c0001a0001c0003a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0007a0001c0001t0001g0183a0001c0001t0001g0194others(27): Show | 30 | 230 | 0.1304 | 10 | c.862 others(25): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12960565 | C | CAAAAAAA others(3): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(55): Show |
a0001a0004 | a0001c0001a0001c0004a0001c0009others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(13): Show | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0017others(55): Show | 58 | 230 | 0.2522 | 10 | c.152 others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12986673 | C | CAAAAAAA others(3): Show |
intron_variant | MODIFIER | HG01928.hp1 HG02257.hp1 HG02300.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0111a0001c0001t0001g0132a0001c0001t0001g0144 | 3 | 230 | 0.0130 | 10 | c.231 others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12988925 | C | CAAAAAAA others(3): Show |
intron_variant | MODIFIER | HG02027.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0012 | 1 | 230 | 0.0044 | 10 | c.231 others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12994074 | C | CATTGTTT others(3): Show |
downstream_gene_variant | MODIFIER | HG03209.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0035 | 1 | 230 | 0.0044 | 10 | c.*39 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 2432 | chr17 | TogoVar | ||||||
ARHGAP45_chr19_1062167_1091628 | 1064562 | G | GGTTAGTG others(3): Show |
upstream_gene_variant | MODIFIER | HG01978.hp2 | a0001 | a0001c0017 | a0001c0017t0006 | a0001c0017t0006g0219 | 1 | 418 | 0.0024 | 10 | c.-28 others(21): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 2604 | chr19 | TogoVar | ||||||
ARHGAP45_chr19_1062167_1091628 | 1074886 | C | CGGGCGGG others(3): Show |
intron_variant | MODIFIER | HG00140.hp1 HG02071.hp2 |
a0002 | a0002c0001 | a0002c0001t0003a0002c0001t0004 | a0002c0001t0003g0129a0002c0001t0004g0164 | 2 | 418 | 0.0048 | 10 | c.118 others(25): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP4_chrX_153902378_153931264 | 153930653 | A | ATCTTGTG others(3): Show |
upstream_gene_variant | MODIFIER | NA18942.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 308 | 0.0033 | 10 | c.-44 others(21): Show |
ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 4390 | chrX | TogoVar | ||||||
ARHGAP5_chr14_32072304_32164728 | 32153406 | C | CAAAAAAA others(3): Show |
intron_variant | MODIFIER | HG02055.hp1 HG02572.hp1 |
a0001a0006 | a0001c0001a0006c0009 | a0001c0001t0001a0006c0009t0003 | a0001c0001t0001g0166a0006c0009t0003g0172 | 2 | 186 | 0.0108 | 10 | c.418 others(27): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
ARHGAP5_chr14_32072304_32164728 | 32164169 | C | CTTTTTTT others(3): Show |
downstream_gene_variant | MODIFIER | HG02717.hp2 | a0001 | a0001c0018 | a0001c0018t0023 | a0001c0018t0023g0181 | 1 | 186 | 0.0054 | 10 | c.*92 others(21): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4442 | chr14 | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11174562 | C | CTTTCTTT others(3): Show |
intron_variant | MODIFIER | HG01243.hp1 HG03098.hp1 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0005 | a0001c0001t0001g0024a0001c0004t0005g0015 | 2 | 144 | 0.0139 | 10 | c.162 others(29): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11174566 | C | CTTTCTTT others(3): Show |
intron_variant | MODIFIER | HG03486.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0014 | 1 | 144 | 0.0069 | 10 | c.162 others(29): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11174574 | C | CTTTCTTT others(3): Show |
intron_variant | MODIFIER | HG01515.hp1 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0009 | 1 | 144 | 0.0069 | 10 | c.162 others(29): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11176232 | C | CATATATA others(3): Show |
intron_variant | MODIFIER | HG01167.hp1 NA18971.hp1 NA19005.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0037a0001c0001t0001g0089a0001c0001t0002g0132 | 3 | 144 | 0.0208 | 10 | c.162 others(29): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11176300 | C | CATATATA others(3): Show |
intron_variant | MODIFIER | HG01943.hp1 HG02895.hp1 NA18959.hp1 others(1): Show |
a0001a0003 | a0001c0001a0003c0010 | a0001c0001t0001a0001c0001t0004a0003c0010t0017 | a0001c0001t0001g0105a0001c0001t0001g0120a0001c0001t0004g0093others(1): Show | 4 | 144 | 0.0278 | 10 | c.162 others(29): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar |