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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP5_chr14_32072304_32164728 | 32145456 | C | CTGT | intron_variant | MODIFIER | HG00609.hp2 HG01109.hp2 HG01243.hp1 others(20): Show |
a0001a0003a0004others(2): Show | a0001c0001a0001c0002a0001c0018others(4): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(9): Show | a0001c0001t0001g0150 a0001c0001t0003g0144 a0001c0001t0003g0148 others(19): Show |
23 | 184 | 0.1250 | 3 | c.386 others(20): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | ||||||
ARHGAP5_chr14_32072304_32164728 | 32159829 | T | TAAA | downstream_gene_variant | MODIFIER | HG01243.hp1 HG01884.hp2 HG02258.hp2 others(18): Show |
a0001a0003a0009 | a0001c0001a0001c0002a0001c0018others(2): Show | a0001c0001t0003a0001c0001t0007a0001c0001t0014others(6): Show | a0001c0001t0003g0144 a0001c0001t0003g0148 a0001c0001t0003g0160 others(17): Show |
21 | 182 | 0.1154 | 3 | c.*48 others(14): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 102 | chr14 | TogoVar | |||||||
ARHGAP5_chr14_32072304_32164728 | 32163485 | C | CAAA | downstream_gene_variant | MODIFIER | HG01109.hp1 HG01515.hp2 HG02280.hp2 others(3): Show |
a0001a0002a0007 | a0001c0001a0001c0012a0002c0004others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0012t0027others(2): Show | a0001c0001t0001g0152 a0001c0001t0003g0148 a0001c0001t0003g0163 others(3): Show |
6 | 56 | 0.1071 | 3 | c.*85 others(14): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3758 | chr14 | TogoVar | |||||||
ARHGAP5_chr14_32072304_32164728 | 32164169 | C | CTTT | downstream_gene_variant | MODIFIER | HG00140.hp1 HG00639.hp1 HG01106.hp2 others(6): Show |
a0001a0002a0010 | a0001c0001a0002c0004a0010c0017 | a0001c0001t0001a0001c0001t0003a0001c0001t0028others(2): Show | a0001c0001t0001g0032 a0001c0001t0001g0067 a0001c0001t0001g0069 others(6): Show |
9 | 78 | 0.1154 | 3 | c.*92 others(14): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4442 | chr14 | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11140434 | A | AAAT | intron_variant | MODIFIER | HG01256.hp1 HG01515.hp1 HG02698.hp1 others(6): Show |
a0002 | a0002c0002 | a0002c0002t0003a0002c0002t0009a0002c0002t0014 | a0002c0002t0003g0005 a0002c0002t0003g0008 a0002c0002t0003g0009 others(6): Show |
9 | 137 | 0.0657 | 3 | c.225 others(20): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 12/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11166829 | T | TAAC | intron_variant | MODIFIER | HG02145.hp1 HG02622.hp1 HG03516.hp1 others(1): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0007 | a0001c0001t0002a0002c0002t0003a0002c0002t0009others(1): Show | a0001c0001t0002g0133 a0002c0002t0003g0012 a0002c0002t0009g0128 others(1): Show |
4 | 144 | 0.0278 | 3 | c.180 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 9/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11174623 | T | TTTC | intron_variant | MODIFIER | HG00673.hp1 NA18966.hp1 NA18984.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0057 a0001c0001t0001g0090 a0001c0001t0001g0101 |
3 | 77 | 0.0390 | 3 | c.162 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11195959 | C | CAAA | intron_variant | MODIFIER | HG02145.hp1 HG03516.hp1 NA18906.hp1 others(2): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0002c0005others(1): Show | a0001c0001t0008a0002c0002t0003a0002c0002t0009others(2): Show | a0001c0001t0008g0049 a0002c0002t0003g0010 a0002c0002t0009g0128 others(2): Show |
5 | 93 | 0.0538 | 3 | c.820 others(18): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 3/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11216717 | T | TTTC | intron_variant | MODIFIER | HG01106.hp1 HG01243.hp1 HG01515.hp1 others(27): Show |
a0001a0002a0003 | a0001c0001a0001c0004a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(7): Show | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0014 others(27): Show |
30 | 144 | 0.2083 | 3 | c.749 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 2/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11266913 | T | TCTG | intron_variant | MODIFIER | HG01515.hp1 HG02145.hp1 HG02451.hp1 others(10): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0007 | a0001c0001t0001a0002c0002t0003a0002c0002t0006others(2): Show | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0116 others(10): Show |
13 | 144 | 0.0903 | 3 | c.589 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11370893 | A | AAAC | intron_variant | MODIFIER | HG01258.hp1 HG01934.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0023 a0001c0001t0001g0096 |
2 | 143 | 0.0140 | 3 | c.589 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11427815 | A | AGAG | intron_variant | MODIFIER | HG01256.hp1 HG02622.hp2 HG02922.hp2 others(5): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0003a0002c0002t0009 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0066 others(5): Show |
8 | 38 | 0.2105 | 3 | c.589 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11558836 | C | CAAA | intron_variant | MODIFIER | HG02145.hp1 HG02451.hp2 HG02622.hp1 others(9): Show |
a0001a0002a0003 | a0001c0001a0001c0006a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0006t0001others(2): Show | a0001c0001t0001g0020 a0001c0001t0001g0039 a0001c0001t0001g0040 others(9): Show |
12 | 46 | 0.2609 | 3 | c.588 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11559929 | A | AAAT | intron_variant | MODIFIER | HG01106.hp1 HG01109.hp1 HG01934.hp1 others(14): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(3): Show | a0001c0001t0001g0020 a0001c0001t0001g0023 a0001c0001t0001g0027 others(14): Show |
17 | 107 | 0.1589 | 3 | c.588 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11571709 | A | AAAT | intron_variant | MODIFIER | HG01167.hp1 HG01243.hp1 HG01358.hp1 others(7): Show |
a0001a0003 | a0001c0001a0001c0003a0001c0004others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0003t0001others(2): Show | a0001c0001t0001g0014 a0001c0001t0001g0022 a0001c0001t0001g0033 others(7): Show |
10 | 100 | 0.1000 | 3 | c.588 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11590847 | A | AAGG | intron_variant | MODIFIER | HG03654.hp1 NA19056.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0055 a0001c0001t0001g0079 |
2 | 143 | 0.0140 | 3 | c.588 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11590852 | A | AAGG | intron_variant | MODIFIER | HG02135.hp1 NA18961.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0093 a0001c0001t0001g0104 |
2 | 119 | 0.0168 | 3 | c.588 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11590857 | A | AAGG | intron_variant | MODIFIER | HG01515.hp1 HG02027.hp1 HG03130.hp1 others(1): Show |
a0001a0002 | a0001c0001a0001c0006a0002c0002 | a0001c0001t0001a0001c0006t0001a0002c0002t0003 | a0001c0001t0001g0059 a0001c0001t0001g0063 a0001c0006t0001g0021 others(1): Show |
4 | 122 | 0.0328 | 3 | c.588 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11590862 | A | AAAG | intron_variant | MODIFIER | HG00673.hp1 HG01515.hp1 HG02027.hp1 others(4): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0003 | a0001c0001t0001g0059 a0001c0001t0001g0063 a0001c0001t0001g0084 others(4): Show |
7 | 74 | 0.0946 | 3 | c.588 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11590862 | A | AAGG | intron_variant | MODIFIER | HG01109.hp1 HG02040.hp1 NA18970.hp1 others(2): Show |
a0001 | a0001c0001a0001c0003a0001c0008 | a0001c0001t0001a0001c0003t0001a0001c0008t0001 | a0001c0001t0001g0028 a0001c0001t0001g0068 a0001c0001t0001g0092 others(2): Show |
5 | 72 | 0.0694 | 3 | c.588 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP6_chrX_11132544_11670920 | 11660530 | C | CAAA | intron_variant | MODIFIER | HG01258.hp1 HG01928.hp1 HG01943.hp1 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0018 | a0001c0001t0001g0091 a0001c0001t0001g0092 a0001c0001t0001g0093 others(11): Show |
14 | 18 | 0.7778 | 3 | c.588 others(20): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44767984 | C | CTTT | intron_variant | MODIFIER | HG02280.hp1 HG02895.hp2 HG02897.hp2 others(6): Show |
a0001a0002a0005others(2): Show | a0001c0007a0001c0008a0002c0023others(3): Show | a0001c0007t0001a0001c0008t0001a0002c0023t0005others(3): Show | a0001c0007t0001g0069 a0001c0008t0001g0038 a0002c0023t0005g0071 others(6): Show |
9 | 72 | 0.1250 | 3 | c.-72 others(22): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44771242 | A | ATTT | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(61): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0004a0001c0007others(25): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(31): Show | a0001c0001t0001g0042 a0001c0001t0001g0161 a0001c0001t0003g0023 others(61): Show |
64 | 182 | 0.3516 | 3 | c.-71 others(22): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44778953 | T | TGCC | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(305): Show |
a0001a0002a0003others(25): Show | a0001c0001a0001c0004a0001c0007others(71): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(84): Show | a0001c0001t0001g0017 a0001c0001t0001g0024 a0001c0001t0001g0042 others(305): Show |
308 | 388 | 0.7938 | 3 | c.-71 others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | chr22 | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44779564 | A | ATTT | intron_variant | MODIFIER | HG00621.hp1 HG00639.hp1 HG00642.hp2 others(76): Show |
a0001a0002a0003others(11): Show | a0001c0001a0001c0004a0001c0007others(34): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(40): Show | a0001c0001t0001g0017 a0001c0001t0003g0063 a0001c0001t0010g0198 others(76): Show |
79 | 154 | 0.5130 | 3 | c.-71 others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44787919 | C | CTTT | intron_variant | MODIFIER | HG01934.hp1 HG02109.hp2 HG02615.hp2 others(5): Show |
a0001a0002a0008others(1): Show | a0001c0007a0002c0011a0002c0016others(3): Show | a0001c0007t0001a0002c0011t0005a0002c0016t0004others(3): Show | a0001c0007t0001g0058 a0001c0007t0001g0202 a0002c0011t0005g0061 others(5): Show |
8 | 284 | 0.0282 | 3 | c.79+ others(18): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44790676 | C | CAAA | intron_variant | MODIFIER | HG00423.hp1 HG00673.hp2 HG00735.hp2 others(20): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0004a0001c0007others(12): Show | a0001c0001t0003a0001c0004t0001a0001c0004t0003others(13): Show | a0001c0001t0003g0063 a0001c0001t0003g0080 a0001c0004t0001g0335 others(20): Show |
23 | 190 | 0.1211 | 3 | c.79+ others(18): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44795040 | C | CAAA | intron_variant | MODIFIER | HG02074.hp1 HG02809.hp1 HG03130.hp2 others(3): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0007a0002c0011others(3): Show | a0001c0001t0003a0001c0007t0001a0002c0011t0005others(3): Show | a0001c0001t0003g0305 a0001c0007t0001g0069 a0002c0011t0005g0016 others(3): Show |
6 | 244 | 0.0246 | 3 | c.80- others(18): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44797217 | C | CTTT | intron_variant | MODIFIER | HG00140.hp2 HG00323.hp2 HG00408.hp1 others(96): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0004a0001c0007others(22): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(28): Show | a0001c0001t0001g0101 a0001c0001t0001g0200 a0001c0001t0001g0371 others(96): Show |
99 | 286 | 0.3462 | 3 | c.80- others(18): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44797979 | A | ATTT | intron_variant | MODIFIER | HG02602.hp1 HG03017.hp1 HG03704.hp1 others(7): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0003a0002c0016others(3): Show | a0001c0001t0003a0001c0001t0010a0002c0003t0004others(4): Show | a0001c0001t0003g0293 a0001c0001t0010g0198 a0002c0003t0004g0021 others(7): Show |
10 | 238 | 0.0420 | 3 | c.80- others(18): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44816803 | C | CAAA | intron_variant | MODIFIER | HG01496.hp2 HG01516.hp2 HG01891.hp2 others(17): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0004a0001c0007others(8): Show | a0001c0001t0003a0001c0004t0010a0001c0007t0001others(8): Show | a0001c0001t0003g0074 a0001c0001t0003g0201 a0001c0004t0010g0302 others(17): Show |
20 | 284 | 0.0704 | 3 | c.386 others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 5/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44827336 | G | GTTT | intron_variant | MODIFIER | HG00280.hp2 HG00558.hp1 HG00558.hp2 others(78): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0004a0001c0007others(16): Show | a0001c0001t0001a0001c0001t0003a0001c0004t0001others(20): Show | a0001c0001t0001g0024 a0001c0001t0001g0371 a0001c0001t0003g0080 others(78): Show |
81 | 93 | 0.8710 | 3 | c.596 others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44829118 | C | CAAA | intron_variant | MODIFIER | HG00738.hp2 HG01496.hp2 HG02559.hp1 others(26): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0007a0001c0010others(18): Show | a0001c0001t0003a0001c0007t0001a0001c0010t0001others(18): Show | a0001c0001t0003g0109 a0001c0001t0003g0110 a0001c0007t0001g0058 others(26): Show |
29 | 84 | 0.3452 | 3 | c.596 others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44830024 | C | CTTT | intron_variant | MODIFIER | HG02257.hp2 HG02559.hp2 HG02647.hp1 others(6): Show |
a0001a0002a0013 | a0001c0007a0002c0003a0002c0006others(4): Show | a0001c0007t0001a0002c0003t0004a0002c0006t0004others(4): Show | a0001c0007t0001g0202 a0001c0007t0001g0324 a0002c0003t0004g0011 others(6): Show |
9 | 144 | 0.0625 | 3 | c.596 others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44856254 | C | CTTT | intron_variant | MODIFIER | HG00741.hp1 HG01891.hp1 HG02074.hp2 others(12): Show |
a0001a0008a0012others(2): Show | a0001c0001a0001c0004a0001c0007others(6): Show | a0001c0001t0001a0001c0004t0001a0001c0007t0001others(6): Show | a0001c0001t0001g0017 a0001c0001t0001g0101 a0001c0004t0001g0136 others(12): Show |
15 | 39 | 0.3846 | 3 | c.878 others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44858533 | C | CTTT | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(75): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0004a0001c0008others(12): Show | a0001c0001t0003a0001c0001t0011a0001c0004t0003others(14): Show | a0001c0001t0003g0023 a0001c0001t0003g0028 a0001c0001t0003g0063 others(75): Show |
78 | 114 | 0.6842 | 3 | c.878 others(20): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44863816 | G | GCCT | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(178): Show |
a0001a0002a0003others(11): Show | a0001c0001a0001c0004a0001c0008others(39): Show | a0001c0001t0003a0001c0001t0011a0001c0004t0003others(42): Show | a0001c0001t0003g0006 a0001c0001t0003g0023 a0001c0001t0003g0028 others(178): Show |
181 | 388 | 0.4665 | 3 | c.*12 others(14): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1033 | chr22 | TogoVar | |||||||
ARHGAP8_chr22_44747575_44867784 | 44867113 | C | CAAA | downstream_gene_variant | MODIFIER | HG00099.hp2 HG01109.hp2 HG01192.hp2 others(18): Show |
a0002a0006a0015others(1): Show | a0002c0011a0002c0013a0002c0020others(9): Show | a0002c0011t0005a0002c0011t0007a0002c0013t0007others(10): Show | a0002c0011t0005g0333 a0002c0011t0007g0031 a0002c0011t0007g0182 others(18): Show |
21 | 201 | 0.1045 | 3 | c.*45 others(14): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 4330 | chr22 | TogoVar | |||||||
ARHGDIB_chr12_14937031_14966601 | 14939333 | C | CAAA | downstream_gene_variant | MODIFIER | HG00099.hp1 HG01175.hp1 HG01934.hp2 others(10): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0003a0001c0002t0001 | a0001c0001t0001g0050 a0001c0001t0001g0051 a0001c0001t0001g0065 others(8): Show |
13 | 321 | 0.0405 | 3 | c.*31 others(14): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 2697 | chr12 | TogoVar | |||||||
ARHGDIB_chr12_14937031_14966601 | 14952277 | C | CAAA | intron_variant | MODIFIER | HG01891.hp2 HG02109.hp2 HG02280.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0085 a0001c0002t0001g0010 a0001c0002t0001g0086 others(4): Show |
10 | 199 | 0.0503 | 3 | c.-12 others(20): Show |
ARHGDIB | ENSG00000111348.9 | transcript | ENST00000228945.9 | protein_coding | 1/5 | chr12 | TogoVar | |||||||
ARHGEF10L_chr1_17534698_17702869 | 17611987 | C | CCAT | intron_variant | MODIFIER | HG00642.hp1 HG03225.hp1 HG03471.hp1 |
a0002 | a0002c0007 | a0002c0007t0002 | a0002c0007t0002g0013 a0002c0007t0002g0105 a0002c0007t0002g0111 |
3 | 166 | 0.0181 | 3 | c.610 others(20): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17666990 | G | GGAA | intron_variant | MODIFIER | HG00642.hp1 HG00741.hp1 HG01109.hp1 others(24): Show |
a0001a0002a0004others(4): Show | a0001c0011a0001c0017a0001c0020others(11): Show | a0001c0011t0001a0001c0017t0002a0001c0020t0001others(11): Show | a0001c0011t0001g0004 a0001c0011t0001g0138 a0001c0011t0001g0152 others(24): Show |
27 | 166 | 0.1627 | 3 | c.300 others(22): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17695790 | T | TCTG | intron_variant | MODIFIER | HG00323.hp1 HG00323.hp2 HG00544.hp1 others(121): Show |
a0001a0002a0003others(14): Show | a0001c0001a0001c0006a0001c0011others(30): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(35): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0009 others(121): Show |
124 | 166 | 0.7470 | 3 | c.330 others(20): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17696212 | C | CAAA | intron_variant | MODIFIER | HG00738.hp1 HG01884.hp1 HG02622.hp2 others(2): Show |
a0001a0012a0020 | a0001c0001a0001c0013a0001c0044others(2): Show | a0001c0001t0001a0001c0013t0001a0001c0044t0004others(2): Show | a0001c0001t0001g0125 a0001c0013t0001g0008 a0001c0044t0004g0161 others(2): Show |
5 | 19 | 0.2632 | 3 | c.330 others(20): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 28/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1841892 | G | GACC | intron_variant | MODIFIER | HG03942.hp1 NA18960.hp1 NA19000.hp2 |
a0001a0002 | a0001c0003a0001c0115a0002c0061 | a0001c0003t0001a0001c0115t0004a0002c0061t0025 | a0001c0003t0001g0284 a0001c0115t0004g0281 a0002c0061t0025g0286 |
3 | 312 | 0.0096 | 3 | c.-47 others(20): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | chr8 | TogoVar | |||||||
ARHGEF10_chr8_1818926_1963641 | 1841910 | G | GACC | intron_variant | MODIFIER | HG00738.hp2 HG02074.hp2 NA19012.hp1 |
a0001a0002 | a0001c0003a0002c0034a0002c0152 | a0001c0003t0001a0002c0034t0010a0002c0152t0002 | a0001c0003t0001g0177 a0002c0034t0010g0135 a0002c0152t0002g0024 |
3 | 299 | 0.0100 | 3 | c.-47 others(20): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | chr8 | TogoVar | |||||||
ARHGEF10_chr8_1818926_1963641 | 1871112 | C | CAAA | intron_variant | MODIFIER | HG01515.hp1 HG01517.hp2 HG02083.hp2 others(10): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0003a0001c0005others(6): Show | a0001c0001t0014a0001c0001t0019a0001c0003t0001others(8): Show | a0001c0001t0014g0185 a0001c0001t0019g0317 a0001c0003t0001g0159 others(10): Show |
13 | 170 | 0.0765 | 3 | c.679 others(20): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 7/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1889168 | G | GGAT | intron_variant | MODIFIER | HG00642.hp1 HG00738.hp2 HG01346.hp1 others(4): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0019a0001c0002t0001a0001c0002t0012others(4): Show | a0001c0001t0019g0245 a0001c0002t0001g0068 a0001c0002t0012g0190 others(4): Show |
7 | 362 | 0.0193 | 3 | c.118 others(22): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1889281 | G | GTGA | intron_variant | MODIFIER | NA18941.hp2 NA18943.hp2 NA18966.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0010 | a0001c0001t0002a0001c0002t0001a0001c0002t0002others(1): Show | a0001c0001t0002g0249 a0001c0002t0001g0248 a0001c0002t0002g0002 others(2): Show |
5 | 361 | 0.0139 | 3 | c.118 others(22): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | chr8 | TogoVar | |||||||
ARHGEF10_chr8_1818926_1963641 | 1893092 | C | CAAA | intron_variant | MODIFIER | HG00597.hp1 HG00597.hp2 HG00673.hp2 others(43): Show |
a0001a0004a0006others(3): Show | a0001c0002a0001c0003a0001c0004others(30): Show | a0001c0002t0001a0001c0003t0001a0001c0003t0009others(39): Show | a0001c0002t0001g0053 a0001c0002t0001g0071 a0001c0002t0001g0341 others(43): Show |
46 | 240 | 0.1917 | 3 | c.118 others(20): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar |