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 | 12903126 | G | GAGGA | intron_variant | MODIFIER | HG01952.hp2 HG02735.hp2 HG03831.hp2 others(1): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0101a0001c0001t0002g0203a0001c0001t0003g0069others(1): Show | 4 | 230 | 0.0174 | 4 | c.199 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12903140 | A | AGTGT | intron_variant | MODIFIER | HG00642.hp1 HG02572.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006 | a0001c0001t0001g0183a0001c0001t0006g0099 | 2 | 230 | 0.0087 | 4 | c.199 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12910446 | C | CTTTT | intron_variant | MODIFIER | HG00735.hp1 HG01109.hp2 HG01884.hp1 others(16): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(11): Show | a0001c0001t0001g0144a0001c0001t0001g0148a0001c0001t0001g0183others(16): Show | 19 | 230 | 0.0826 | 4 | c.275 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12913968 | C | CAAAA | intron_variant | MODIFIER | HG02027.hp1 HG02129.hp1 HG02602.hp1 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(4): Show | a0001c0001t0001g0158a0001c0001t0001g0163a0001c0001t0001g0180others(6): Show | 9 | 230 | 0.0391 | 4 | c.276 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 4/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12931841 | T | TACAC | intron_variant | MODIFIER | HG02559.hp2 HG02895.hp1 HG02896.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0008a0001c0001t0010 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(4): Show | 7 | 230 | 0.0304 | 4 | c.582 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12938582 | T | TTAAA | intron_variant | MODIFIER | HG00639.hp1 HG00741.hp2 HG01074.hp2 others(44): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0017a0001c0001t0001g0117a0001c0001t0001g0136others(44): Show | 47 | 230 | 0.2044 | 4 | c.583 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 7/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12946799 | T | TAAAA | intron_variant | MODIFIER | HG01934.hp1 HG02145.hp2 HG02559.hp1 others(5): Show |
a0001 | a0001c0001a0001c0005a0001c0006 | a0001c0001t0001a0001c0001t0008a0001c0001t0014others(4): Show | a0001c0001t0001g0027a0001c0001t0008g0037a0001c0001t0008g0223others(5): Show | 8 | 230 | 0.0348 | 4 | c.862 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12948723 | T | TACAC | intron_variant | MODIFIER | HG00140.hp1 HG01074.hp2 HG01169.hp1 others(21): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0006a0001c0001t0010a0001c0001t0025others(8): Show | a0001c0001t0006g0168a0001c0001t0010g0034a0001c0001t0025g0036others(21): Show | 24 | 230 | 0.1044 | 4 | c.862 others(19): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12956866 | A | AACAC | intron_variant | MODIFIER | HG01109.hp2 HG01243.hp2 HG01891.hp1 others(14): Show |
a0001 | a0001c0001a0001c0005a0001c0006others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(6): Show | a0001c0001t0001g0030a0001c0001t0001g0147a0001c0001t0001g0189others(14): Show | 17 | 230 | 0.0739 | 4 | c.134 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12962080 | A | AATAT | intron_variant | MODIFIER | HG00673.hp2 HG03942.hp1 NA18942.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0011 | a0001c0001t0004g0002a0001c0001t0004g0004a0001c0001t0004g0010others(5): Show | 8 | 230 | 0.0348 | 4 | c.152 others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12963046 | C | CAAAA | intron_variant | MODIFIER | HG01074.hp2 HG01169.hp1 HG01192.hp2 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0001a0001c0001t0010a0001c0002t0001others(5): Show | a0001c0001t0001g0194a0001c0001t0010g0182a0001c0002t0001g0089others(10): Show | 13 | 230 | 0.0565 | 4 | c.152 others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12966155 | C | CAAAA | intron_variant | MODIFIER | HG01934.hp1 HG02109.hp1 HG02451.hp2 others(13): Show |
a0001 | a0001c0001a0001c0003a0001c0005others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(7): Show | a0001c0001t0001g0189a0001c0001t0003g0028a0001c0001t0003g0075others(13): Show | 16 | 230 | 0.0696 | 4 | c.152 others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12970378 | A | AAAAG | intron_variant | MODIFIER | HG00639.hp2 HG00735.hp1 HG01074.hp2 others(40): Show |
a0001a0003a0005 | a0001c0001a0001c0002a0001c0004others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(14): Show | a0001c0001t0001g0005a0001c0001t0001g0007a0001c0001t0001g0017others(40): Show | 43 | 230 | 0.1870 | 4 | c.152 others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12975119 | G | GGATT | intron_variant | MODIFIER | HG02698.hp2 HG03704.hp2 HG03942.hp2 |
a0001a0003 | a0001c0001a0003c0017 | a0001c0001t0003a0001c0001t0011a0003c0017t0003 | a0001c0001t0003g0172a0001c0001t0011g0073a0003c0017t0003g0068 | 3 | 230 | 0.0130 | 4 | c.176 others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12986673 | C | CAAAA | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00733.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006a0001c0001t0013 | a0001c0001t0001g0183a0001c0001t0006g0024a0001c0001t0006g0097others(4): Show | 7 | 230 | 0.0304 | 4 | c.231 others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12991576 | T | TTATC | 3_prime_UTR_variant | MODIFIER | HG01884.hp2 HG01934.hp1 HG02280.hp2 others(3): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0008a0001c0005t0032 | a0001c0001t0008g0037a0001c0001t0008g0042a0001c0001t0008g0043others(3): Show | 6 | 230 | 0.0261 | 4 | c.*14 others(15): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 21/21 | 1411 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||
ARHGAP44_chr17_12784498_12996643 | 12991773 | G | GTCTT | downstream_gene_variant | MODIFIER | HG02922.hp1 HG02965.hp1 HG03041.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0185a0001c0001t0001g0225a0001c0001t0001g0226 | 3 | 230 | 0.0130 | 4 | c.*16 others(15): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 131 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12991846 | A | AACTT | downstream_gene_variant | MODIFIER | HG00639.hp2 HG00738.hp1 HG00738.hp2 others(13): Show |
a0001a0005 | a0001c0001a0001c0003a0005c0013 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0030a0001c0001t0001g0041a0001c0001t0001g0094others(13): Show | 16 | 230 | 0.0696 | 4 | c.*16 others(15): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 204 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12991869 | T | TTTAC | downstream_gene_variant | MODIFIER | HG01243.hp2 HG01891.hp2 HG02109.hp2 others(2): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0003a0001c0003t0001 | a0001c0001t0001g0009a0001c0001t0001g0147a0001c0001t0001g0189others(2): Show | 5 | 230 | 0.0217 | 4 | c.*16 others(15): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 227 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12992119 | C | CTGAT | downstream_gene_variant | MODIFIER | HG00673.hp2 HG02027.hp2 HG02074.hp1 others(12): Show |
a0001a0006 | a0001c0001a0006c0015 | a0001c0001t0004a0001c0001t0011a0001c0001t0024others(2): Show | a0001c0001t0004g0002a0001c0001t0004g0004a0001c0001t0004g0010others(12): Show | 15 | 230 | 0.0652 | 4 | c.*19 others(15): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 477 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12992127 | T | TTTGA | downstream_gene_variant | MODIFIER | HG00735.hp1 HG01192.hp1 HG02602.hp1 others(9): Show |
a0001a0003 | a0001c0001a0001c0003a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0025others(4): Show | a0001c0001t0001g0017a0001c0001t0001g0138a0001c0001t0001g0158others(9): Show | 12 | 230 | 0.0522 | 4 | c.*19 others(15): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 485 | chr17 | TogoVar | ||||||
ARHGAP45_chr19_1062167_1091628 | 1075236 | C | CTTTT | intron_variant | MODIFIER | HG00323.hp2 HG00621.hp1 HG01978.hp2 others(5): Show |
a0001 | a0001c0002a0001c0004a0001c0017 | a0001c0002t0001a0001c0004t0006a0001c0017t0006 | a0001c0002t0001g0277a0001c0004t0006g0039a0001c0004t0006g0211others(4): Show | 8 | 418 | 0.0191 | 4 | c.118 others(21): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP45_chr19_1062167_1091628 | 1090460 | A | ATTTT | downstream_gene_variant | MODIFIER | HG00140.hp1 HG00735.hp1 HG00735.hp2 others(29): Show |
a0001a0002a0003others(4): Show | a0001c0004a0002c0001a0002c0019others(6): Show | a0001c0004t0024a0002c0001t0003a0002c0001t0005others(9): Show | a0001c0004t0024g0232a0002c0001t0003g0003a0002c0001t0003g0013others(26): Show | 32 | 418 | 0.0766 | 4 | c.*44 others(15): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 3833 | chr19 | TogoVar | ||||||
ARHGAP4_chrX_153902378_153931264 | 153930679 | A | AGAGG | upstream_gene_variant | MODIFIER | NA18942.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 308 | 0.0033 | 4 | c.-44 others(15): Show |
ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 4416 | chrX | TogoVar | ||||||
ARHGAP5_chr14_32072304_32164728 | 32130525 | C | CATTG | intron_variant | MODIFIER | HG00609.hp2 HG01243.hp1 HG02258.hp2 others(8): Show |
a0001a0002a0009others(1): Show | a0001c0002a0001c0018a0002c0003others(2): Show | a0001c0002t0005a0001c0018t0023a0002c0003t0001others(3): Show | a0001c0002t0005g0004a0001c0002t0005g0167a0001c0002t0005g0168others(7): Show | 11 | 186 | 0.0591 | 4 | c.386 others(25): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
ARHGAP5_chr14_32072304_32164728 | 32148163 | A | AATCT | intron_variant | MODIFIER | HG00609.hp1 HG00639.hp1 HG00639.hp2 others(48): Show |
a0001a0007a0010others(1): Show | a0001c0001a0001c0012a0007c0013others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0014others(47): Show | 51 | 186 | 0.2742 | 4 | c.394 others(23): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
ARHGAP5_chr14_32072304_32164728 | 32153406 | C | CAAAA | intron_variant | MODIFIER | HG01884.hp2 HG02132.hp2 HG02165.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0014 | a0001c0001t0001g0060a0001c0001t0001g0066a0001c0001t0003g0144others(2): Show | 5 | 186 | 0.0269 | 4 | c.418 others(21): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
ARHGAP6_chrX_11132544_11670920 | 11136871 | G | GAACT | downstream_gene_variant | MODIFIER | HG01256.hp1 HG01515.hp1 HG02145.hp1 others(10): Show |
a0002a0004 | a0002c0002a0004c0008 | a0002c0002t0003a0002c0002t0009a0002c0002t0016others(1): Show | a0002c0002t0003g0005a0002c0002t0003g0006a0002c0002t0003g0009others(10): Show | 13 | 144 | 0.0903 | 4 | c.*19 others(15): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 672 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11140434 | A | AAAAT | intron_variant | MODIFIER | HG02145.hp1 HG03516.hp1 NA20129.hp1 |
a0002a0004 | a0002c0002a0004c0008 | a0002c0002t0003a0002c0002t0009a0004c0008t0012 | a0002c0002t0003g0012a0002c0002t0009g0127a0004c0008t0012g0002 | 3 | 144 | 0.0208 | 4 | c.225 others(21): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 12/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11173475 | T | TGAAA | intron_variant | MODIFIER | NA18953.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0062 | 1 | 144 | 0.0069 | 4 | c.163 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11174518 | T | TTTCC | intron_variant | MODIFIER | HG01074.hp1 HG02040.hp1 HG03490.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0038a0001c0001t0001g0042a0001c0001t0001g0071others(2): Show | 5 | 144 | 0.0347 | 4 | c.162 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11174573 | C | CCTTT | intron_variant | MODIFIER | HG00642.hp1 HG01928.hp1 HG02083.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0067a0001c0001t0001g0086a0001c0001t0004g0069others(1): Show | 4 | 144 | 0.0278 | 4 | c.162 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11174623 | T | TTTTC | intron_variant | MODIFIER | HG00140.hp1 HG01109.hp1 HG01243.hp1 others(11): Show |
a0001a0004 | a0001c0001a0001c0004a0004c0008 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(2): Show | a0001c0001t0001g0028a0001c0001t0001g0052a0001c0001t0001g0072others(11): Show | 14 | 144 | 0.0972 | 4 | c.162 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11176232 | C | CATAT | intron_variant | MODIFIER | HG02074.hp1 HG02132.hp1 HG02451.hp1 others(15): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0011others(4): Show | a0001c0001t0001g0017a0001c0001t0001g0025a0001c0001t0001g0059others(15): Show | 18 | 144 | 0.1250 | 4 | c.162 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11176255 | A | ATATT | intron_variant | MODIFIER | HG01515.hp1 HG02698.hp1 HG02735.hp1 others(5): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0005 | a0001c0001t0001a0002c0002t0003a0002c0005t0006 | a0001c0001t0001g0004a0002c0002t0003g0005a0002c0002t0003g0006others(5): Show | 8 | 144 | 0.0556 | 4 | c.162 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11176257 | A | ATTTT | intron_variant | MODIFIER | HG02258.hp1 HG02451.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0018 | a0001c0001t0001g0020a0002c0002t0018g0029 | 2 | 144 | 0.0139 | 4 | c.162 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11176300 | C | CATAT | intron_variant | MODIFIER | HG01069.hp1 HG02055.hp1 HG02135.hp1 others(14): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0009others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0010others(5): Show | a0001c0001t0001g0004a0001c0001t0001g0020a0001c0001t0001g0052others(14): Show | 17 | 144 | 0.1181 | 4 | c.162 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11176355 | C | CCTAG | intron_variant | MODIFIER | HG02300.hp2 NA18965.hp1 NA19083.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0072a0001c0001t0001g0073a0001c0001t0001g0084 | 3 | 144 | 0.0208 | 4 | c.162 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11190460 | G | GATAT | intron_variant | MODIFIER | HG00738.hp1 HG01255.hp1 HG01258.hp1 others(3): Show |
a0001a0005 | a0001c0001a0005c0006 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(2): Show | a0001c0001t0001g0091a0001c0001t0002g0137a0001c0001t0004g0095others(3): Show | 6 | 144 | 0.0417 | 4 | c.821 others(21): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 3/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11201989 | C | CTGTG | intron_variant | MODIFIER | HG00609.hp1 HG00673.hp1 HG01109.hp1 others(12): Show |
a0001a0005 | a0001c0001a0005c0006 | a0001c0001t0001a0001c0001t0002a0005c0006t0001 | a0001c0001t0001g0028a0001c0001t0001g0033a0001c0001t0001g0060others(12): Show | 15 | 144 | 0.1042 | 4 | c.749 others(21): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 2/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11202799 | C | CAAAA | intron_variant | MODIFIER | HG06807.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0013 | 1 | 144 | 0.0069 | 4 | c.749 others(21): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 2/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11214257 | G | GCACA | intron_variant | MODIFIER | HG00642.hp1 HG00738.hp1 HG01243.hp1 others(8): Show |
a0001a0002 | a0001c0001a0001c0004a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(3): Show | a0001c0001t0001g0003a0001c0001t0001g0098a0001c0001t0002g0128others(8): Show | 11 | 144 | 0.0764 | 4 | c.749 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 2/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11230610 | A | AGTGT | intron_variant | MODIFIER | HG01258.hp1 HG01934.hp1 HG02071.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0023a0001c0001t0001g0035a0001c0001t0001g0091others(2): Show | 5 | 144 | 0.0347 | 4 | c.748 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 2/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11241531 | C | CGTGT | intron_variant | MODIFIER | HG03130.hp1 NA18948.hp1 NA18966.hp1 others(5): Show |
a0001 | a0001c0001a0001c0007 | a0001c0001t0001a0001c0001t0004a0001c0001t0014others(1): Show | a0001c0001t0001g0022a0001c0001t0001g0053a0001c0001t0001g0061others(5): Show | 8 | 144 | 0.0556 | 4 | c.748 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 2/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11241571 | T | TGCGC | intron_variant | MODIFIER | NA20905.hp1 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0006 | 1 | 144 | 0.0069 | 4 | c.748 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 2/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11241573 | T | TGTGC | intron_variant | MODIFIER | HG02735.hp1 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0016 | 1 | 144 | 0.0069 | 4 | c.748 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 2/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11266033 | C | CTGTG | intron_variant | MODIFIER | HG01074.hp1 HG01243.hp1 HG01934.hp1 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0001t0002a0001c0004t0005 | a0001c0001t0001g0023a0001c0001t0002g0136a0001c0004t0005g0015 | 3 | 144 | 0.0208 | 4 | c.589 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11266072 | T | TGTGA | intron_variant | MODIFIER | HG02258.hp1 HG02451.hp2 NA19012.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0018 | a0001c0001t0001g0003a0001c0001t0001g0020a0002c0002t0018g0029 | 3 | 144 | 0.0208 | 4 | c.589 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11280745 | C | CAAAA | intron_variant | MODIFIER | HG01106.hp1 HG02451.hp1 HG02698.hp1 others(17): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0007others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(6): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0014others(17): Show | 20 | 144 | 0.1389 | 4 | c.589 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11294242 | G | GTAGA | intron_variant | MODIFIER | HG02735.hp1 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0016 | 1 | 144 | 0.0069 | 4 | c.589 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar |