view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | 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 | 100903117 | G | GCACACAC others(3): Show |
intron_variant | MODIFIER | HG00639.hp2 HG00735.hp2 HG01069.hp2 others(11): Show |
a0002 | a0002c0002a0002c0004 | a0002c0002t0002a0002c0002t0005a0002c0002t0008others(3): Show | a0002c0002t0002g0053 a0002c0002t0002g0119 a0002c0002t0002g0141 others(11): Show |
14 | 53 | 0.2642 | 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 | a0001c0001t0001g0189 a0001c0001t0001g0191 |
2 | 41 | 0.0488 | 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 | a0002c0002t0001g0013 a0002c0002t0001g0016 |
2 | 263 | 0.0076 | 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 | a0002c0002t0011g0224 | 1 | 68 | 0.0147 | 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 | a0002c0006t0011g0239 a0002c0006t0011g0242 |
2 | 69 | 0.0290 | 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 | a0002c0002t0008g0028 a0002c0002t0008g0029 a0002c0002t0009g0033 others(1): Show |
4 | 71 | 0.0563 | 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 | a0001c0001t0001g0022 a0001c0001t0001g0073 a0001c0001t0001g0109 others(10): Show |
13 | 80 | 0.1625 | 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 | a0002c0004t0007g0145 | 1 | 4 | 0.2500 | 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 | a0002c0004t0007g0014 a0002c0004t0007g0061 a0002c0004t0007g0076 others(4): Show |
7 | 153 | 0.0458 | 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(214): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0003a0001c0008others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(43): Show | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0011 others(214): Show |
217 | 236 | 0.9195 | 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 | a0001c0001t0001g0180 | 1 | 284 | 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 | a0001c0001t0001g0091 a0002c0002t0002g0012 a0002c0002t0002g0150 others(5): Show |
8 | 31 | 0.2581 | 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 | a0001c0001t0001g0178 a0001c0003t0003g0214 a0001c0003t0014g0234 others(2): Show |
5 | 28 | 0.1786 | 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 | a0001c0001t0001g0225 | 1 | 284 | 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 | 87 | 0.0115 | 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 |
a0001a0002a0006 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(16): Show | a0001c0001t0001g0009 a0001c0001t0001g0012 a0001c0001t0001g0015 others(58): Show |
61 | 228 | 0.2675 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0044 a0001c0001t0001g0181 others(12): Show |
15 | 223 | 0.0673 | 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 | a0001c0001t0014g0178 | 1 | 98 | 0.0102 | 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 | a0001c0001t0001g0224 a0001c0001t0001g0225 |
2 | 227 | 0.0088 | 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 | a0001c0001t0002g0230 | 1 | 104 | 0.0096 | 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 | 100 | 0.0100 | 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 | a0001c0001t0001g0192 a0001c0001t0001g0204 a0001c0001t0001g0213 others(5): Show |
8 | 137 | 0.0584 | 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 | 130 | 0.0077 | 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 | a0001c0001t0001g0187 a0001c0001t0010g0186 a0001c0008t0020g0185 |
3 | 226 | 0.0133 | 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 | a0001c0001t0001g0181 a0001c0002t0001g0097 |
2 | 144 | 0.0139 | 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 | a0001c0001t0005g0058 a0001c0001t0009g0095 |
2 | 144 | 0.0139 | 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 | a0004 | a0004c0017 | a0004c0017t0003 | a0004c0017t0003g0050 | 1 | 107 | 0.0093 | 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 | a0001c0001t0002g0155 a0001c0001t0002g0198 |
2 | 108 | 0.0185 | 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 | a0001c0001t0001g0212 a0001c0001t0033g0029 |
2 | 41 | 0.0488 | 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 |
a0001a0003 | a0001c0001a0001c0003a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0007 a0001c0001t0001g0187 a0001c0001t0001g0200 others(27): Show |
30 | 72 | 0.4167 | 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 |
a0001a0006 | a0001c0001a0001c0004a0001c0009others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(13): Show | a0001c0001t0001g0001 a0001c0001t0001g0015 a0001c0001t0001g0017 others(55): Show |
58 | 228 | 0.2544 | 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 | a0001c0001t0001g0111 a0001c0001t0001g0118 a0001c0001t0001g0119 |
3 | 138 | 0.0217 | 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 | a0001c0001t0004g0013 | 1 | 160 | 0.0063 | 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 | a0001c0001t0001g0037 | 1 | 228 | 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 | a0001c0017t0006g0195 | 1 | 416 | 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 | a0002c0001t0003g0110 a0002c0001t0004g0139 |
2 | 415 | 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 | 306 | 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 |
a0001a0009 | a0001c0001a0009c0009 | a0001c0001t0001a0009c0009t0003 | a0001c0001t0001g0166 a0009c0009t0003g0172 |
2 | 24 | 0.0833 | 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 | 70 | 0.0143 | 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 | a0001c0001t0001g0024 a0001c0004t0005g0015 |
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 | 143 | 0.0070 | 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 | a0002c0002t0003g0008 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0095 a0001c0001t0002g0134 |
3 | 35 | 0.0857 | 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 |
a0001a0004 | a0001c0001a0004c0009 | a0001c0001t0001a0001c0001t0004a0004c0009t0001 | a0001c0001t0001g0110 a0001c0001t0001g0120 a0001c0001t0004g0098 others(1): Show |
4 | 16 | 0.2500 | 10 | c.162 others(29): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11185142 | C | CTGTGTGT others(3): Show |
intron_variant | MODIFIER | HG02258.hp1 HG02451.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0015 | a0001c0001t0001g0020 a0002c0002t0015g0029 |
2 | 96 | 0.0208 | 10 | c.127 others(29): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 5/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11196135 | A | AAAAACAA others(3): Show |
intron_variant | MODIFIER | HG01243.hp1 HG02922.hp2 HG03098.hp1 others(5): Show |
a0001a0002 | a0001c0001a0001c0004a0002c0002 | a0001c0001t0001a0001c0001t0008a0001c0004t0005others(2): Show | a0001c0001t0001g0024 a0001c0001t0008g0049 a0001c0004t0005g0015 others(5): Show |
8 | 108 | 0.0741 | 10 | c.820 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 3/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11201989 | C | CTGTGTGT others(3): Show |
intron_variant | MODIFIER | HG01167.hp1 HG01928.hp1 HG02129.hp1 others(16): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0006others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(4): Show | a0001c0001t0001g0017 a0001c0001t0001g0026 a0001c0001t0001g0068 others(16): Show |
19 | 26 | 0.7308 | 10 | c.749 others(27): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 2/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11241531 | C | CGTGTGTG others(3): Show |
intron_variant | MODIFIER | NA19088.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0112 | 1 | 67 | 0.0149 | 10 | c.748 others(29): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 2/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11266072 | T | TGTGTGTG others(3): Show |
intron_variant | MODIFIER | HG01106.hp1 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0030 | 1 | 117 | 0.0085 | 10 | c.589 others(29): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11320766 | T | TACACACA others(3): Show |
intron_variant | MODIFIER | NA18612.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0054 | 1 | 28 | 0.0357 | 10 | c.589 others(29): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar |