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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP44_chr17_12784498_12996643 | 12863148 | T | TAAG | intron_variant | MODIFIER | HG01884.hp1 HG01891.hp1 HG02145.hp1 others(8): Show |
a0001 | a0001c0001a0001c0004a0001c0005others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(7): Show | a0001c0001t0001g0174a0001c0001t0001g0183a0001c0001t0003g0028others(8): Show | 11 | 230 | 0.0478 | 3 | c.54- others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12868572 | A | ATGC | intron_variant | MODIFIER | HG02622.hp1 HG02895.hp1 HG02896.hp2 others(5): Show |
a0001 | a0001c0001a0001c0005a0001c0006 | a0001c0001t0001a0001c0001t0008a0001c0005t0001others(1): Show | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(5): Show | 8 | 230 | 0.0348 | 3 | c.54- others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12870048 | C | CTTT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(112): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(35): Show | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(112): Show | 115 | 230 | 0.5000 | 3 | c.54- others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12897710 | C | CTTT | intron_variant | MODIFIER | HG01517.hp2 HG01891.hp2 HG01981.hp2 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0009a0001c0001t0001g0174a0001c0001t0002g0008others(10): Show | 13 | 230 | 0.0565 | 3 | c.198 others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12903121 | A | AGAG | intron_variant | MODIFIER | HG00733.hp1 HG01928.hp2 HG02071.hp1 others(16): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0002g0122others(16): Show | 19 | 230 | 0.0826 | 3 | c.199 others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12910446 | C | CTTT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(136): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(36): Show | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(136): Show | 139 | 230 | 0.6044 | 3 | c.275 others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12912318 | C | CAGT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(189): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(13): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(50): Show | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0009others(189): Show | 192 | 230 | 0.8348 | 3 | c.275 others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12913968 | C | CAAA | intron_variant | MODIFIER | HG02074.hp1 HG02559.hp1 HG02647.hp1 others(6): Show |
a0001 | a0001c0001a0001c0005a0001c0006others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0005t0001others(4): Show | a0001c0001t0001g0148a0001c0001t0004g0109a0001c0005t0001g0173others(6): Show | 9 | 230 | 0.0391 | 3 | c.276 others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12919387 | C | CTTT | intron_variant | MODIFIER | HG01934.hp1 HG02258.hp2 HG02922.hp2 others(5): Show |
a0001 | a0001c0001a0001c0003a0001c0005 | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(3): Show | a0001c0001t0001g0030a0001c0001t0003g0078a0001c0001t0003g0079others(5): Show | 8 | 230 | 0.0348 | 3 | c.388 others(18): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12920375 | C | CAAA | intron_variant | MODIFIER | HG00423.hp2 HG00673.hp2 HG00733.hp1 others(99): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(31): Show | a0001c0001t0001g0001a0001c0001t0001g0009a0001c0001t0001g0013others(99): Show | 102 | 230 | 0.4435 | 3 | c.464 others(18): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 6/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12938582 | T | TTAA | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(15): Show |
a0001 | a0001c0001a0001c0005a0001c0012 | a0001c0001t0002a0001c0001t0003a0001c0001t0006others(7): Show | a0001c0001t0002g0008a0001c0001t0003g0047a0001c0001t0003g0048others(15): Show | 18 | 230 | 0.0783 | 3 | c.583 others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 7/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12946478 | T | TAAA | intron_variant | MODIFIER | HG03942.hp1 NA18942.hp2 NA18963.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(2): Show | a0001c0001t0002g0019a0001c0001t0003g0088a0001c0001t0004g0002others(6): Show | 9 | 230 | 0.0391 | 3 | c.861 others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12946799 | T | TAAA | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(145): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(35): Show | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(145): Show | 148 | 230 | 0.6435 | 3 | c.862 others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12963046 | C | CAAA | intron_variant | MODIFIER | HG01192.hp1 HG01517.hp1 HG01891.hp2 others(5): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0008others(2): Show | a0001c0001t0003a0001c0001t0025a0001c0001t0027others(5): Show | a0001c0001t0003g0074a0001c0001t0025g0036a0001c0001t0027g0222others(5): Show | 8 | 230 | 0.0348 | 3 | c.152 others(22): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12966155 | C | CAAA | intron_variant | MODIFIER | HG00733.hp1 HG01081.hp1 HG01243.hp2 others(26): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0114a0001c0001t0001g0140a0001c0001t0001g0147others(26): Show | 29 | 230 | 0.1261 | 3 | c.152 others(22): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12970378 | A | AAAG | intron_variant | MODIFIER | HG00673.hp2 HG01109.hp2 HG01192.hp1 others(30): Show |
a0001 | a0001c0001a0001c0005a0001c0006others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(15): Show | a0001c0001t0001g0009a0001c0001t0001g0027a0001c0001t0001g0147others(30): Show | 33 | 230 | 0.1435 | 3 | c.152 others(22): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12976612 | C | CAAA | intron_variant | MODIFIER | HG00673.hp2 HG01074.hp2 HG01106.hp2 others(42): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(4): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(16): Show | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0009others(42): Show | 45 | 230 | 0.1957 | 3 | c.176 others(22): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12989101 | C | CAAA | intron_variant | MODIFIER | HG00423.hp2 HG00741.hp2 HG01884.hp1 others(8): Show |
a0001 | a0001c0001a0001c0003a0001c0004others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0005others(6): Show | a0001c0001t0002g0015a0001c0001t0002g0023a0001c0001t0002g0156others(8): Show | 11 | 230 | 0.0478 | 3 | c.231 others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12992148 | T | TTGA | downstream_gene_variant | MODIFIER | HG02572.hp1 NA18906.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0183a0001c0001t0003g0090 | 2 | 230 | 0.0087 | 3 | c.*19 others(14): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 506 | chr17 | TogoVar | ||||||
ARHGAP45_chr19_1062167_1091628 | 1075236 | C | CTTT | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(204): Show |
a0001a0002a0004others(7): Show | a0001c0002a0001c0004a0001c0017others(22): Show | a0001c0002t0001a0001c0002t0002a0001c0002t0013others(41): Show | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0018others(148): Show | 207 | 418 | 0.4952 | 3 | c.118 others(20): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP45_chr19_1062167_1091628 | 1090460 | A | ATTT | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00323.hp1 others(68): Show |
a0001a0002a0003others(6): Show | a0001c0002a0001c0004a0002c0001others(16): Show | a0001c0002t0001a0001c0004t0001a0001c0004t0005others(25): Show | a0001c0002t0001g0021a0001c0002t0001g0043a0001c0004t0001g0230others(54): Show | 71 | 418 | 0.1699 | 3 | c.*44 others(14): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 3833 | chr19 | TogoVar | ||||||
ARHGAP4_chrX_153902378_153931264 | 153906428 | C | CGTG | downstream_gene_variant | MODIFIER | NA19063.hp1 | a0008 | a0008c0014 | a0008c0014t0001 | a0008c0014t0001g0089 | 1 | 308 | 0.0033 | 3 | c.*12 others(14): Show |
ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 949 | chrX | TogoVar | ||||||
ARHGAP4_chrX_153902378_153931264 | 153916741 | C | CAAA | intron_variant | MODIFIER | NA19076.hp1 | a0014 | a0014c0022 | a0014c0022t0001 | a0014c0022t0001g0108 | 1 | 308 | 0.0033 | 3 | c.103 others(22): Show |
ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 7/21 | chrX | TogoVar | ||||||
ARHGAP5_chr14_32072304_32164728 | 32086574 | T | TATA | intron_variant | MODIFIER | HG01243.hp1 HG02258.hp2 HG02572.hp2 others(3): Show |
a0001 | a0001c0002a0001c0018 | a0001c0002t0005a0001c0018t0023 | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(2): Show | 6 | 186 | 0.0323 | 3 | c.-16 others(22): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
ARHGAP5_chr14_32072304_32164728 | 32143202 | A | AGTT | intron_variant | MODIFIER | HG00140.hp2 HG00609.hp1 HG00621.hp2 others(78): Show |
a0001a0003a0004others(3): Show | a0001c0001a0003c0004a0004c0005others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(10): Show | a0001c0001t0001g0001a0001c0001t0001g0006a0001c0001t0001g0009others(77): Show | 81 | 186 | 0.4355 | 3 | c.386 others(22): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
ARHGAP5_chr14_32072304_32164728 | 32145456 | C | CTGT | intron_variant | MODIFIER | HG00609.hp2 HG01109.hp2 HG01243.hp1 others(20): Show |
a0001a0002a0006others(2): Show | a0001c0001a0001c0002a0001c0018others(4): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(9): Show | a0001c0001t0001g0150a0001c0001t0003g0144a0001c0001t0003g0148others(19): Show | 23 | 186 | 0.1237 | 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 |
a0001a0002a0006 | a0001c0001a0001c0002a0001c0018others(2): Show | a0001c0001t0003a0001c0001t0007a0001c0001t0014others(6): Show | a0001c0001t0003g0144a0001c0001t0003g0148a0001c0001t0003g0160others(17): Show | 21 | 186 | 0.1129 | 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 |
a0001a0003a0008 | a0001c0001a0001c0012a0003c0004others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0012t0027others(2): Show | a0001c0001t0001g0152a0001c0001t0003g0148a0001c0001t0003g0163others(3): Show | 6 | 186 | 0.0323 | 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 |
a0001a0003a0013 | a0001c0001a0003c0004a0013c0017 | a0001c0001t0001a0001c0001t0003a0001c0001t0028others(2): Show | a0001c0001t0001g0032a0001c0001t0001g0067a0001c0001t0001g0069others(6): Show | 9 | 186 | 0.0484 | 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 | a0002c0002t0003a0002c0002t0009a0002c0002t0016 | a0002c0002t0003g0005a0002c0002t0003g0006a0002c0002t0003g0009others(6): Show | 9 | 144 | 0.0625 | 3 | c.225 others(20): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 12/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11160456 | C | CAAA | intron_variant | MODIFIER | HG02735.hp1 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0016 | 1 | 144 | 0.0069 | 3 | c.181 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 9/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11166829 | T | TAAC | intron_variant | MODIFIER | HG02145.hp1 HG02622.hp1 HG03516.hp1 others(1): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0008 | a0001c0001t0002a0002c0002t0003a0002c0002t0009others(1): Show | a0001c0001t0002g0134a0002c0002t0003g0012a0002c0002t0009g0127others(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 | 11174609 | T | TTTC | intron_variant | MODIFIER | NA19066.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0067 | 1 | 144 | 0.0069 | 3 | c.162 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11174623 | T | TTTC | intron_variant | MODIFIER | HG00673.hp1 NA18966.hp1 NA18984.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0057a0001c0001t0001g0085a0001c0001t0001g0096 | 3 | 144 | 0.0208 | 3 | c.162 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11174635 | C | CTCT | intron_variant | MODIFIER | HG02027.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0058 | 1 | 144 | 0.0069 | 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 |
a0001a0002a0004 | a0001c0001a0002c0002a0002c0005others(1): Show | a0001c0001t0008a0002c0002t0003a0002c0002t0009others(2): Show | a0001c0001t0008g0049a0002c0002t0003g0010a0002c0002t0009g0127others(2): Show | 5 | 144 | 0.0347 | 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 |
a0001a0002a0004 | a0001c0001a0001c0004a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(7): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0014others(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 | 11254716 | C | CAAA | intron_variant | MODIFIER | HG02717.hp1 HG03209.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0046a0001c0001t0001g0114 | 2 | 144 | 0.0139 | 3 | c.589 others(16): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11266913 | T | TCTG | intron_variant | MODIFIER | HG01515.hp1 HG02145.hp1 HG02451.hp1 others(10): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0008 | a0001c0001t0001a0002c0002t0003a0002c0002t0006others(2): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0116others(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 | 11280745 | C | CAAA | intron_variant | MODIFIER | HG01243.hp1 HG03486.hp1 |
a0001 | a0001c0004 | a0001c0004t0005 | a0001c0004t0005g0015a0001c0004t0005g0047 | 2 | 144 | 0.0139 | 3 | c.589 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11304777 | C | CTTT | intron_variant | MODIFIER | HG02735.hp1 HG03209.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0003 | a0001c0001t0001g0046a0002c0002t0003g0016 | 2 | 144 | 0.0139 | 3 | c.589 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11310160 | C | CAAA | intron_variant | MODIFIER | HG02698.hp1 NA19082.hp1 |
a0002 | a0002c0002 | a0002c0002t0003a0002c0002t0016 | a0002c0002t0003g0005a0002c0002t0016g0007 | 2 | 144 | 0.0139 | 3 | c.589 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11354295 | T | TTTC | intron_variant | MODIFIER | NA18985.hp1 | a0001 | a0001c0001 | a0001c0001t0013 | a0001c0001t0013g0066 | 1 | 144 | 0.0069 | 3 | c.589 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11358386 | A | AGAT | intron_variant | MODIFIER | NA18985.hp1 | a0001 | a0001c0001 | a0001c0001t0013 | a0001c0001t0013g0066 | 1 | 144 | 0.0069 | 3 | c.589 others(24): 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 | a0001c0001t0001g0023a0001c0001t0001g0091 | 2 | 144 | 0.0139 | 3 | c.589 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11399354 | C | CAAA | intron_variant | MODIFIER | HG03579.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0052 | 1 | 144 | 0.0069 | 3 | c.589 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11422399 | G | GAGT | intron_variant | MODIFIER | NA19055.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0082 | 1 | 144 | 0.0069 | 3 | c.589 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11424133 | A | AGAG | intron_variant | MODIFIER | NA19055.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0082 | 1 | 144 | 0.0069 | 3 | c.589 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11426359 | A | ATTT | intron_variant | MODIFIER | HG01109.hp1 NA20129.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0006 | a0001c0001t0001g0028a0002c0002t0006g0031 | 2 | 144 | 0.0139 | 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 | a0001c0001t0001a0001c0001t0013a0002c0002t0003others(1): Show | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0094others(5): Show | 8 | 144 | 0.0556 | 3 | c.589 others(24): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar |