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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP44_chr17_12784498_12996643 | 12861644 | C | CTTTTTTT others(9): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00639.hp2 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(3): Show | a0001c0001t0001g0146 a0001c0001t0001g0181 a0001c0001t0001g0188 others(7): Show |
10 | 118 | 0.0847 | 16 | c.54- others(33): 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(9): Show |
intron_variant | MODIFIER | HG01884.hp1 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0186 | 1 | 130 | 0.0077 | 16 | c.54- others(33): 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(9): Show |
intron_variant | MODIFIER | NA18994.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0019 | 1 | 143 | 0.0070 | 16 | c.199 others(33): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12931841 | T | TACACACA others(9): Show |
intron_variant | MODIFIER | HG03942.hp1 NA18986.hp1 NA18994.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0004 | a0001c0001t0002g0019 a0001c0001t0003g0083 a0001c0001t0004g0004 others(1): Show |
4 | 43 | 0.0930 | 16 | c.582 others(33): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12978035 | T | TAAAAAAA others(9): Show |
intron_variant | MODIFIER | HG01496.hp2 HG02451.hp1 NA19083.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005 | a0001c0001t0001g0007 a0001c0001t0001g0116 a0001c0001t0001g0174 others(1): Show |
4 | 134 | 0.0299 | 16 | c.176 others(35): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 18/20 | chr17 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12978036 | C | CAAAAAAA others(9): Show |
intron_variant | MODIFIER | HG01884.hp2 HG02280.hp2 HG02922.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0008 | a0001c0001t0001g0224 a0001c0001t0001g0225 a0001c0001t0008g0040 others(2): Show |
5 | 17 | 0.2941 | 16 | c.176 others(35): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12986673 | C | CAAAAAAA others(9): Show |
intron_variant | MODIFIER | HG01070.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0197 | 1 | 136 | 0.0074 | 16 | c.231 others(35): 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(9): Show |
intron_variant | MODIFIER | HG01109.hp2 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0223 | 1 | 67 | 0.0149 | 16 | c.231 others(33): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 20/20 | chr17 | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11174518 | T | TTTCCTTC others(9): Show |
intron_variant | MODIFIER | HG04115.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0048 | 1 | 117 | 0.0085 | 16 | c.162 others(35): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11174573 | C | CCTTCCTT others(9): Show |
intron_variant | MODIFIER | HG01258.hp1 HG02056.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0096 a0001c0001t0001g0118 |
2 | 75 | 0.0267 | 16 | c.162 others(35): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11176232 | C | CATATATA others(9): Show |
intron_variant | MODIFIER | HG02027.hp1 NA18970.hp1 NA18989.hp1 others(1): Show |
a0001 | a0001c0001a0001c0008 | a0001c0001t0001a0001c0001t0004a0001c0008t0001 | a0001c0001t0001g0059 a0001c0001t0001g0068 a0001c0001t0004g0100 others(1): Show |
4 | 36 | 0.1111 | 16 | c.162 others(35): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11185164 | G | GTGTGTGT others(9): Show |
intron_variant | MODIFIER | HG02300.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0086 | 1 | 144 | 0.0069 | 16 | c.127 others(35): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 5/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11201989 | C | CTGTGTGT others(9): Show |
intron_variant | MODIFIER | HG03471.hp1 NA18983.hp1 NA18985.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0010 | a0001c0001t0001g0037 a0001c0001t0001g0066 a0001c0001t0001g0076 others(1): Show |
4 | 11 | 0.3636 | 16 | c.749 others(33): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 2/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11344700 | A | AGAAAAGA others(9): Show |
intron_variant | MODIFIER | NA19240.hp1 | a0002 | a0002c0005 | a0002c0005t0006 | a0002c0005t0006g0018 | 1 | 141 | 0.0071 | 16 | c.589 others(35): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11346719 | A | AAAAGAAA others(9): Show |
intron_variant | MODIFIER | HG02055.hp1 NA18945.hp1 NA18955.hp1 others(4): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0016others(3): Show | a0001c0001t0001g0065 a0001c0001t0001g0122 a0001c0001t0002g0127 others(4): Show |
7 | 58 | 0.1207 | 16 | c.589 others(35): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11354319 | C | CTATATAT others(9): Show |
intron_variant | MODIFIER | HG02922.hp2 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0011 | 1 | 139 | 0.0072 | 16 | c.589 others(35): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11354327 | C | CTCTCTCT others(9): Show |
intron_variant | MODIFIER | NA19240.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004 | 1 | 75 | 0.0133 | 16 | c.589 others(35): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11411183 | T | TTATATAT others(9): Show |
intron_variant | MODIFIER | HG00621.hp1 HG03486.hp2 HG04115.hp1 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0019 | a0001c0001t0001g0014 a0001c0001t0001g0032 a0001c0001t0001g0048 others(12): Show |
15 | 33 | 0.4545 | 16 | c.589 others(37): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11411183 | T | TTTTATAT others(9): Show |
intron_variant | MODIFIER | HG01106.hp1 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0030 | 1 | 19 | 0.0526 | 16 | c.589 others(37): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11508852 | T | TACACACA others(9): Show |
intron_variant | MODIFIER | HG01243.hp1 HG03486.hp2 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0005 | a0001c0001t0001g0014 a0001c0004t0005g0015 |
2 | 115 | 0.0174 | 16 | c.588 others(37): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11552599 | T | TATATATA others(9): Show |
intron_variant | MODIFIER | HG02698.hp1 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0009 | 1 | 125 | 0.0080 | 16 | c.588 others(37): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11552599 | T | TATATATA others(9): Show |
intron_variant | MODIFIER | HG02965.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0043 | 1 | 125 | 0.0080 | 16 | c.588 others(37): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44754338 | T | TTGTGTGT others(9): Show |
intron_variant | MODIFIER | NA19030.hp2 | a0007 | a0007c0049 | a0007c0049t0006 | a0007c0049t0006g0056 | 1 | 271 | 0.0037 | 16 | 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 | 44754373 | T | TGTGTGTG others(9): Show |
intron_variant | MODIFIER | HG00544.hp2 HG02738.hp2 HG03927.hp1 others(3): Show |
a0002a0003 | a0002c0003a0002c0076a0003c0002others(1): Show | a0002c0003t0004a0002c0076t0004a0003c0002t0002others(1): Show | a0002c0003t0004g0052 a0002c0003t0004g0055 a0002c0076t0004g0144 others(3): Show |
6 | 129 | 0.0465 | 16 | 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 | 44767984 | C | CTTTTTTT others(9): Show |
intron_variant | MODIFIER | NA18992.hp1 NA19240.hp1 |
a0001a0002 | a0001c0018a0002c0003 | a0001c0018t0001a0002c0003t0004 | a0001c0018t0001g0041 a0002c0003t0004g0360 |
2 | 65 | 0.0308 | 16 | c.-72 others(35): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44803727 | T | TCCCAGGA others(9): Show |
intron_variant | MODIFIER | HG01255.hp2 | a0011 | a0011c0032 | a0011c0032t0001 | a0011c0032t0001g0366 | 1 | 388 | 0.0026 | 16 | c.167 others(33): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 3/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44818450 | C | CAAAAAAA others(9): Show |
intron_variant | MODIFIER | HG02280.hp1 HG02647.hp2 HG02896.hp1 others(5): Show |
a0002a0005 | a0002c0003a0002c0023a0002c0047others(1): Show | a0002c0003t0004a0002c0023t0005a0002c0047t0005others(1): Show | a0002c0003t0004g0177 a0002c0003t0004g0351 a0002c0023t0005g0071 others(5): Show |
8 | 267 | 0.0300 | 16 | c.386 others(33): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44827336 | G | GTTTTTTT others(9): Show |
intron_variant | MODIFIER | NA21309.hp2 | a0001 | a0001c0007 | a0001c0007t0001 | a0001c0007t0001g0070 | 1 | 13 | 0.0769 | 16 | c.596 others(33): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44833096 | C | CTTTTCTT others(9): Show |
intron_variant | MODIFIER | HG00323.hp1 HG00544.hp2 HG00741.hp1 others(2): Show |
a0001a0003 | a0001c0008a0003c0002a0003c0005 | a0001c0008t0001a0003c0002t0002a0003c0005t0002 | a0001c0008t0001g0275 a0003c0002t0002g0272 a0003c0002t0002g0273 others(2): Show |
5 | 227 | 0.0220 | 16 | c.596 others(33): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17588849 | A | AGTGTGTG others(9): Show |
intron_variant | MODIFIER | HG02451.hp2 NA18747.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0079 a0001c0001t0003g0143 |
2 | 78 | 0.0256 | 16 | c.257 others(31): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 4/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17621810 | G | GGGCCACA others(9): Show |
intron_variant | MODIFIER | HG00558.hp1 HG00733.hp1 HG01070.hp1 others(56): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0011a0001c0017others(27): Show | a0001c0001t0001a0001c0001t0003a0001c0011t0001others(28): Show | a0001c0001t0001g0009 a0001c0001t0001g0011 a0001c0001t0001g0012 others(56): Show |
59 | 166 | 0.3554 | 16 | c.943 others(29): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 10/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17689574 | C | CCTTCCCT others(9): Show |
intron_variant | MODIFIER | HG01884.hp1 HG02622.hp2 |
a0001a0012 | a0001c0044a0012c0031 | a0001c0044t0004a0012c0031t0006 | a0001c0044t0004g0161 a0012c0031t0006g0165 |
2 | 165 | 0.0121 | 16 | c.318 others(35): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1832648 | A | AGAGACAG others(9): Show |
intron_variant | MODIFIER | NA19080.hp1 | a0002 | a0002c0024 | a0002c0024t0001 | a0002c0024t0001g0148 | 1 | 362 | 0.0028 | 16 | c.-48 others(33): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | chr8 | TogoVar | |||||||
ARHGEF10_chr8_1818926_1963641 | 1839209 | G | GTGGAAGC others(9): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00423.hp2 HG00597.hp1 others(34): Show |
a0001a0002a0004others(4): Show | a0001c0003a0001c0004a0001c0008others(25): Show | a0001c0003t0001a0001c0004t0004a0001c0008t0002others(30): Show | a0001c0003t0001g0030 a0001c0003t0001g0284 a0001c0004t0004g0296 others(34): Show |
37 | 362 | 0.1022 | 16 | c.-47 others(33): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1839727 | C | CGGTGTGG others(9): Show |
intron_variant | MODIFIER | NA19007.hp2 NA19081.hp2 NA19086.hp2 |
a0001a0002 | a0001c0037a0002c0030 | a0001c0037t0004a0001c0037t0009a0002c0030t0003 | a0001c0037t0004g0304 a0001c0037t0009g0305 a0002c0030t0003g0123 |
3 | 362 | 0.0083 | 16 | c.-47 others(33): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1839737 | G | GCTGTCTG others(9): Show |
intron_variant | MODIFIER | HG03209.hp2 | a0001 | a0001c0009 | a0001c0009t0051 | a0001c0009t0051g0274 | 1 | 362 | 0.0028 | 16 | c.-47 others(33): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1840110 | C | CTGTTGTG others(9): Show |
intron_variant | MODIFIER | HG00423.hp2 HG00597.hp1 HG01175.hp1 others(22): Show |
a0001a0002a0004others(1): Show | a0001c0003a0001c0004a0001c0008others(17): Show | a0001c0003t0001a0001c0004t0004a0001c0008t0002others(19): Show | a0001c0003t0001g0030 a0001c0003t0001g0284 a0001c0004t0004g0296 others(22): Show |
25 | 362 | 0.0691 | 16 | c.-47 others(33): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | chr8 | TogoVar | |||||||
ARHGEF10_chr8_1818926_1963641 | 1840174 | C | CTGTTGTG others(9): Show |
intron_variant | MODIFIER | NA18980.hp2 | a0006 | a0006c0113 | a0006c0113t0004 | a0006c0113t0004g0300 | 1 | 362 | 0.0028 | 16 | c.-47 others(33): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | chr8 | TogoVar | |||||||
ARHGEF10_chr8_1818926_1963641 | 1840185 | A | ACTGTCTG others(9): Show |
intron_variant | MODIFIER | HG02258.hp1 | a0018 | a0018c0094 | a0018c0094t0016 | a0018c0094t0016g0146 | 1 | 359 | 0.0028 | 16 | c.-47 others(33): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1840270 | C | CTGTTGTG others(9): Show |
intron_variant | MODIFIER | HG02258.hp1 | a0018 | a0018c0094 | a0018c0094t0016 | a0018c0094t0016g0146 | 1 | 362 | 0.0028 | 16 | c.-47 others(33): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | chr8 | TogoVar | |||||||
ARHGEF10_chr8_1818926_1963641 | 1840351 | T | TGGTGTGG others(9): Show |
intron_variant | MODIFIER | HG03834.hp2 NA21309.hp2 |
a0001 | a0001c0052a0001c0140 | a0001c0052t0045a0001c0140t0004 | a0001c0052t0045g0336 a0001c0140t0004g0294 |
2 | 329 | 0.0061 | 16 | c.-47 others(33): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1840441 | A | ACTGTCTG others(9): Show |
intron_variant | MODIFIER | NA18980.hp2 | a0006 | a0006c0113 | a0006c0113t0004 | a0006c0113t0004g0300 | 1 | 362 | 0.0028 | 16 | c.-47 others(33): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1840505 | A | ACTGTCCG others(9): Show |
intron_variant | MODIFIER | HG01255.hp1 HG02818.hp2 HG03139.hp1 |
a0001 | a0001c0002a0001c0003a0001c0012 | a0001c0002t0026a0001c0003t0026a0001c0012t0063 | a0001c0002t0026g0267 a0001c0003t0026g0268 a0001c0012t0063g0266 |
3 | 362 | 0.0083 | 16 | c.-47 others(33): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1892277 | C | CTGTGTGT others(9): Show |
intron_variant | MODIFIER | HG02559.hp1 | a0001 | a0001c0012 | a0001c0012t0008 | a0001c0012t0008g0348 | 1 | 39 | 0.0256 | 16 | c.118 others(35): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156930060 | T | TTCTTTCT others(9): Show |
downstream_gene_variant | MODIFIER | HG02622.hp1 | a0002 | a0002c0002 | a0002c0002t0024 | a0002c0002t0024g0011 | 1 | 253 | 0.0040 | 16 | c.*59 others(27): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 4779 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 156936495 | A | AATATATA others(9): Show |
intron_variant | MODIFIER | HG02083.hp2 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0094 | 1 | 221 | 0.0045 | 16 | c.463 others(33): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 40/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 157013259 | T | TCACACAC others(9): Show |
intron_variant | MODIFIER | HG02004.hp2 HG02257.hp1 HG02486.hp1 others(8): Show |
a0001a0002a0003 | a0001c0001a0002c0004a0003c0003 | a0001c0001t0004a0001c0001t0007a0001c0001t0015others(4): Show | a0001c0001t0004g0140 a0001c0001t0004g0142 a0001c0001t0007g0165 others(8): Show |
11 | 151 | 0.0728 | 16 | c.33- others(33): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 157013259 | T | TCTCACAC others(9): Show |
intron_variant | MODIFIER | HG00735.hp1 HG01243.hp2 HG01496.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0005 a0001c0001t0004g0167 a0001c0001t0004g0176 |
4 | 144 | 0.0278 | 16 | c.33- others(33): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF11_chr1_156929840_157050742 | 157013299 | A | ACACACAC others(9): Show |
intron_variant | MODIFIER | HG02738.hp1 NA18943.hp1 NA18987.hp1 others(2): Show |
a0002 | a0002c0002a0002c0004 | a0002c0002t0012a0002c0004t0005a0002c0004t0025 | a0002c0002t0012g0191 a0002c0004t0005g0114 a0002c0004t0005g0123 others(2): Show |
5 | 315 | 0.0159 | 16 | c.33- others(33): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | |||||||
ARHGEF12_chr11_120331413_120494937 | 120347151 | C | CCTTTCTT others(9): Show |
intron_variant | MODIFIER | HG01099.hp1 | a0001 | a0001c0002 | a0001c0002t0034 | a0001c0002t0034g0013 | 1 | 257 | 0.0039 | 16 | c.32+ others(31): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |