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 | 100980559 | C | CTTCTTTT others(7): Show |
intron_variant | MODIFIER | HG00423.hp2 HG03017.hp1 NA19002.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0019 | a0001c0001t0001g0140 a0001c0001t0001g0225 a0001c0001t0019g0078 |
3 | 26 | 0.1154 | 14 | c.245 others(33): 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(7): Show |
intron_variant | MODIFIER | HG00738.hp2 HG03579.hp2 |
a0001a0002 | a0001c0001a0002c0009 | a0001c0001t0001a0002c0009t0004 | a0001c0001t0001g0002 a0002c0009t0004g0237 |
2 | 25 | 0.0800 | 14 | c.245 others(33): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12825416 | T | TTGTGTGT others(7): Show |
intron_variant | MODIFIER | HG02071.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0015 | 1 | 120 | 0.0083 | 14 | c.53+ others(31): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12841594 | T | TCTCTCTC others(7): Show |
intron_variant | MODIFIER | HG01192.hp1 HG02074.hp2 HG02258.hp2 others(8): Show |
a0001a0003 | a0001c0001a0001c0004a0003c0013 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0026 a0001c0001t0001g0174 a0001c0001t0002g0142 others(8): Show |
11 | 134 | 0.0821 | 14 | c.53+ others(31): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12841594 | T | TCTCTCTC others(7): Show |
intron_variant | MODIFIER | HG03942.hp2 | a0004 | a0004c0017 | a0004c0017t0003 | a0004c0017t0003g0050 | 1 | 124 | 0.0081 | 14 | c.53+ others(31): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12841594 | T | TGTCTCTC others(7): Show |
intron_variant | MODIFIER | HG02647.hp1 HG02922.hp1 HG02965.hp1 others(1): Show |
a0001 | a0001c0001a0001c0011 | a0001c0001t0001a0001c0001t0008a0001c0011t0001 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0008g0228 others(1): Show |
4 | 127 | 0.0315 | 14 | c.53+ others(31): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12841594 | T | TGTCTCTC others(7): Show |
intron_variant | MODIFIER | HG02145.hp2 HG02559.hp1 NA21309.hp1 |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0001t0027a0001c0006t0001 | a0001c0001t0001g0176 a0001c0001t0027g0222 a0001c0006t0001g0221 |
3 | 126 | 0.0238 | 14 | c.53+ others(31): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12841633 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | NA21309.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0176 | 1 | 222 | 0.0045 | 14 | c.53+ others(31): 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(7): Show |
intron_variant | MODIFIER | HG02559.hp2 HG03453.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0010 | a0001c0001t0001g0033 a0001c0001t0010g0032 |
2 | 99 | 0.0202 | 14 | c.53+ others(31): 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(7): Show |
intron_variant | MODIFIER | HG02559.hp1 | a0001 | a0001c0006 | a0001c0006t0001 | a0001c0006t0001g0221 | 1 | 98 | 0.0102 | 14 | c.53+ others(31): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12861644 | C | CTTTTTTT others(7): Show |
intron_variant | MODIFIER | HG01891.hp2 HG01934.hp1 HG02258.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(1): Show | a0001c0001t0001g0009 a0001c0001t0003g0060 a0001c0001t0003g0072 others(3): Show |
6 | 114 | 0.0526 | 14 | c.54- others(31): 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(7): Show |
intron_variant | MODIFIER | NA18947.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0012 | 1 | 143 | 0.0070 | 14 | c.199 others(31): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12903126 | G | GAGAGAGA others(7): Show |
intron_variant | MODIFIER | HG01891.hp1 | a0001 | a0001c0001 | a0001c0001t0033 | a0001c0001t0033g0029 | 1 | 143 | 0.0070 | 14 | c.199 others(31): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12931841 | T | TACACACA others(7): Show |
intron_variant | MODIFIER | HG02698.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0172 | 1 | 40 | 0.0250 | 14 | c.582 others(31): 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(7): Show |
intron_variant | MODIFIER | HG01255.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0143 | 1 | 43 | 0.0233 | 14 | c.862 others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12986673 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG02273.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0093 | 1 | 136 | 0.0074 | 14 | c.231 others(33): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12989101 | C | CCGAAAAA others(7): Show |
intron_variant | MODIFIER | HG00642.hp2 HG03017.hp2 HG06807.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0030 | a0001c0001t0001g0101 a0001c0001t0001g0132 a0001c0001t0001g0152 others(1): Show |
4 | 70 | 0.0571 | 14 | c.231 others(31): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 20/20 | chr17 | TogoVar | |||||||
ARHGAP4_chrX_153902378_153931264 | 153930667 | A | ACCTCAGT others(7): Show |
upstream_gene_variant | MODIFIER | NA18942.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 306 | 0.0033 | 14 | c.-44 others(25): Show |
ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 4404 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11174570 | C | CTTTCTTT others(7): Show |
intron_variant | MODIFIER | NA18906.hp2 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0010 | 1 | 143 | 0.0070 | 14 | c.162 others(33): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11176232 | C | CATATATA others(7): Show |
intron_variant | MODIFIER | HG02083.hp1 HG02738.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0080 a0001c0001t0001g0091 |
2 | 34 | 0.0588 | 14 | c.162 others(33): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11176300 | C | CATATATA others(7): Show |
intron_variant | MODIFIER | HG00738.hp1 HG04228.hp1 NA18966.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0017 a0001c0001t0001g0026 a0001c0001t0001g0101 others(2): Show |
5 | 17 | 0.2941 | 14 | c.162 others(33): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11201989 | C | CTGTGTGT others(7): Show |
intron_variant | MODIFIER | HG00642.hp1 HG02572.hp1 HG02622.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(1): Show | a0001c0001t0001g0014 a0001c0001t0001g0025 a0001c0001t0001g0046 others(5): Show |
8 | 15 | 0.5333 | 14 | c.749 others(31): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 2/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11354327 | C | CTATATAT others(7): Show |
intron_variant | MODIFIER | HG06807.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0013 | 1 | 75 | 0.0133 | 14 | c.589 others(33): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11354327 | C | CTCTCTCT others(7): Show |
intron_variant | MODIFIER | HG02451.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0116 | 1 | 75 | 0.0133 | 14 | c.589 others(33): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11411183 | T | TTATATAT others(7): Show |
intron_variant | MODIFIER | HG00738.hp1 HG01515.hp1 HG02015.hp1 others(15): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0009 | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(3): Show | a0001c0001t0001g0027 a0001c0001t0001g0041 a0001c0001t0001g0054 others(15): Show |
18 | 36 | 0.5000 | 14 | c.589 others(35): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11411183 | T | TTTTATAT others(7): Show |
intron_variant | MODIFIER | NA18906.hp1 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0049 | 1 | 19 | 0.0526 | 14 | c.589 others(35): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11417059 | C | CATATATA others(7): Show |
intron_variant | MODIFIER | HG01433.hp1 HG03130.hp1 |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0006t0001 | a0001c0001t0001g0056 a0001c0006t0001g0021 |
2 | 12 | 0.1667 | 14 | c.589 others(35): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11497559 | T | TTCTCTCT others(7): Show |
intron_variant | MODIFIER | HG03688.hp1 HG04204.hp1 NA18612.hp1 others(1): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0003 | a0001c0001t0001g0054 a0001c0001t0001g0075 a0001c0001t0001g0089 others(1): Show |
4 | 18 | 0.2222 | 14 | c.588 others(35): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11520131 | T | TTATATAT others(7): Show |
intron_variant | MODIFIER | HG02135.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0104 | 1 | 29 | 0.0345 | 14 | c.588 others(35): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11552599 | T | TATATATA others(7): Show |
intron_variant | MODIFIER | NA19082.hp1 NA20905.hp1 |
a0002 | a0002c0002 | a0002c0002t0003a0002c0002t0014 | a0002c0002t0003g0005 a0002c0002t0014g0006 |
2 | 126 | 0.0159 | 14 | c.588 others(35): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11590865 | A | AGAAAAGA others(7): Show |
intron_variant | MODIFIER | HG00140.hp1 HG02486.hp1 |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0130 a0001c0001t0002g0132 |
2 | 129 | 0.0155 | 14 | c.588 others(33): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44754338 | T | TTGTGTGT others(7): Show |
intron_variant | MODIFIER | HG01934.hp1 | a0012 | a0012c0035 | a0012c0035t0001 | a0012c0035t0001g0001 | 1 | 271 | 0.0037 | 14 | c.-72 others(31): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44754373 | T | TGTGTGTG others(7): Show |
intron_variant | MODIFIER | HG03492.hp1 HG04184.hp1 NA19057.hp2 |
a0001a0003 | a0001c0004a0001c0007a0003c0036 | a0001c0004t0003a0001c0007t0001a0003c0036t0002 | a0001c0004t0003g0050 a0001c0007t0001g0051 a0003c0036t0002g0143 |
3 | 126 | 0.0238 | 14 | c.-72 others(31): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44767984 | C | CTTTTTTT others(7): Show |
intron_variant | MODIFIER | NA18941.hp2 | a0002 | a0002c0006 | a0002c0006t0004 | a0002c0006t0004g0300 | 1 | 64 | 0.0156 | 14 | c.-72 others(33): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44818450 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG02055.hp2 HG02615.hp1 NA18975.hp1 others(1): Show |
a0001a0002a0003 | a0001c0018a0002c0013a0003c0062 | a0001c0018t0001a0002c0013t0005a0003c0062t0002 | a0001c0018t0001g0041 a0001c0018t0001g0108 a0002c0013t0005g0043 others(1): Show |
4 | 263 | 0.0152 | 14 | c.386 others(31): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44867283 | C | CAAAAAAA others(7): Show |
downstream_gene_variant | MODIFIER | HG01358.hp1 HG03669.hp1 NA19012.hp1 others(1): Show |
a0001 | a0001c0001a0001c0004a0001c0024 | a0001c0001t0001a0001c0004t0001a0001c0024t0001 | a0001c0001t0001g0024 a0001c0001t0001g0161 a0001c0004t0001g0335 others(1): Show |
4 | 134 | 0.0299 | 14 | c.*46 others(25): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 4500 | chr22 | TogoVar | |||||||
ARHGDIA_chr17_81862721_81876337 | 81866967 | G | GCAGCTGG others(7): Show |
downstream_gene_variant | MODIFIER | HG02818.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 382 | 0.0026 | 14 | c.*19 others(25): Show |
ARHGDIA | ENSG00000141522.12 | transcript | ENST00000269321.12 | protein_coding | 753 | chr17 | TogoVar | |||||||
ARHGDIB_chr12_14937031_14966601 | 14948100 | G | GCGCGCAC others(7): Show |
intron_variant | MODIFIER | HG00738.hp2 HG01257.hp2 NA20805.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0002t0001 | a0001c0001t0002g0273 a0001c0002t0001g0054 |
3 | 111 | 0.0270 | 14 | c.266 others(29): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 3/5 | chr12 | TogoVar | |||||||
ARHGEF10L_chr1_17534698_17702869 | 17588849 | A | AGTGTGTG others(7): Show |
intron_variant | MODIFIER | HG01496.hp2 HG02148.hp1 NA18906.hp2 others(1): Show |
a0001a0020 | a0001c0001a0020c0049 | a0001c0001t0001a0020c0049t0004 | a0001c0001t0001g0022 a0001c0001t0001g0034 a0001c0001t0001g0158 others(1): Show |
4 | 80 | 0.0500 | 14 | c.257 others(29): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17588880 | G | GTGTGTGT others(7): Show |
intron_variant | MODIFIER | HG02630.hp2 HG03098.hp2 |
a0002a0004 | a0002c0018a0004c0005 | a0002c0018t0002a0004c0005t0002 | a0002c0018t0002g0015 a0004c0005t0002g0117 |
2 | 107 | 0.0187 | 14 | c.257 others(29): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1892277 | C | CTGTGTGT others(7): Show |
intron_variant | MODIFIER | HG02886.hp2 NA18964.hp2 NA18967.hp1 others(3): Show |
a0001a0006 | a0001c0043a0001c0085a0001c0144others(3): Show | a0001c0043t0014a0001c0085t0001a0001c0144t0052others(3): Show | a0001c0043t0014g0262 a0001c0085t0001g0207 a0001c0144t0052g0339 others(3): Show |
6 | 44 | 0.1364 | 14 | c.118 others(33): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156930032 | T | TTTTCTTT others(7): Show |
downstream_gene_variant | MODIFIER | HG00741.hp1 HG02280.hp2 HG02630.hp2 others(9): Show |
a0002a0007 | a0002c0004a0007c0014 | a0002c0004t0005a0002c0004t0014a0002c0004t0026others(1): Show | a0002c0004t0005g0014 a0002c0004t0005g0015 a0002c0004t0005g0022 others(9): Show |
12 | 276 | 0.0435 | 14 | c.*59 others(25): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4807 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 156930044 | C | CTCTTTCT others(7): Show |
downstream_gene_variant | MODIFIER | HG02055.hp1 HG02257.hp2 HG02602.hp2 others(6): Show |
a0001a0002a0004 | a0001c0001a0002c0004a0004c0006 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(2): Show | a0001c0001t0001g0337 a0001c0001t0004g0138 a0001c0001t0004g0139 others(6): Show |
9 | 212 | 0.0425 | 14 | c.*59 others(25): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4795 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 156936495 | A | AATATATA others(7): Show |
intron_variant | MODIFIER | HG03927.hp2 NA19074.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0007 | a0001c0001t0001g0326 a0001c0001t0007g0150 |
2 | 222 | 0.0090 | 14 | c.463 others(31): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 156936497 | A | AATATATA others(7): Show |
intron_variant | MODIFIER | HG00621.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0047 | 1 | 78 | 0.0128 | 14 | c.463 others(31): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 157008406 | G | GCACACAC others(7): Show |
intron_variant | MODIFIER | HG02486.hp2 | a0002 | a0002c0002 | a0002c0002t0029 | a0002c0002t0029g0187 | 1 | 9 | 0.1111 | 14 | c.33- others(31): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 157013259 | T | TCACACAC others(7): Show |
intron_variant | MODIFIER | HG02451.hp2 HG02630.hp1 HG02647.hp2 others(2): Show |
a0002a0003 | a0002c0004a0003c0003 | a0002c0004t0008a0002c0004t0014a0003c0003t0003 | a0002c0004t0008g0198 a0002c0004t0008g0199 a0002c0004t0014g0205 others(2): Show |
5 | 145 | 0.0345 | 14 | c.33- others(31): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 157013259 | T | TCTCACAC others(7): Show |
intron_variant | MODIFIER | HG01169.hp1 HG01192.hp1 HG01346.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0151 a0001c0001t0004g0153 a0001c0001t0004g0154 others(3): Show |
6 | 146 | 0.0411 | 14 | c.33- others(31): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 157013299 | A | ACACACAC others(7): Show |
intron_variant | MODIFIER | HG04184.hp1 | a0002 | a0002c0004 | a0002c0004t0009 | a0002c0004t0009g0118 | 1 | 311 | 0.0032 | 14 | c.33- others(31): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF12_chr11_120331413_120494937 | 120347204 | C | CTTTCTTT others(7): Show |
intron_variant | MODIFIER | NA18967.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0288 | 1 | 304 | 0.0033 | 14 | c.32+ others(29): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |