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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP42_chr11_100682288_100998941 | 100875073 | GTCTCTC | G | intron_variant | MODIFIER | HG01257.hp2 HG01516.hp2 HG02523.hp1 others(1): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0005 | a0001c0001t0001g0086a0001c0001t0001g0124a0001c0001t0001g0281others(1): Show | 4 | 286 | 0.0140 | -6 | c.384 others(25): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100875103 | CTCTCTG | C | intron_variant | MODIFIER | HG01070.hp2 HG02630.hp2 NA19240.hp2 |
a0002 | a0002c0002a0002c0009 | a0002c0002t0002a0002c0002t0017a0002c0009t0027 | a0002c0002t0002g0045a0002c0002t0017g0046a0002c0009t0027g0094 | 3 | 286 | 0.0105 | -6 | c.384 others(25): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100875107 | CTGTGTG | C | intron_variant | MODIFIER | HG02132.hp2 HG02257.hp1 HG03579.hp2 others(2): Show |
a0001a0003a0006 | a0001c0001a0003c0007a0006c0017 | a0001c0001t0001a0003c0007t0005a0006c0017t0001 | a0001c0001t0001g0002a0001c0001t0001g0072a0001c0001t0001g0203others(2): Show | 5 | 286 | 0.0175 | -6 | c.384 others(25): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903709 | AATATAT | A | intron_variant | MODIFIER | HG00642.hp1 HG00642.hp2 HG01978.hp1 others(4): Show |
a0002 | a0002c0002a0002c0006 | a0002c0002t0004a0002c0002t0005a0002c0002t0009others(1): Show | a0002c0002t0004g0064a0002c0002t0004g0083a0002c0002t0005g0105others(4): Show | 7 | 286 | 0.0245 | -6 | c.385 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100914509 | GAACAAC | G | intron_variant | MODIFIER | HG01081.hp1 HG02257.hp2 HG02976.hp1 others(1): Show |
a0002 | a0002c0002 | a0002c0002t0008a0002c0002t0009 | a0002c0002t0008g0028a0002c0002t0008g0029a0002c0002t0008g0230others(1): Show | 4 | 286 | 0.0140 | -6 | c.486 others(21): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100917015 | TTGTGTG | T | intron_variant | MODIFIER | HG00408.hp1 HG00597.hp2 HG00639.hp2 others(20): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0037a0001c0003t0003a0001c0003t0014others(4): Show | a0001c0001t0037g0041a0001c0003t0003g0118a0001c0003t0003g0119others(20): Show | 23 | 286 | 0.0804 | -6 | c.486 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100938953 | CACTTAT | C | intron_variant | MODIFIER | HG01891.hp1 HG02055.hp2 HG03098.hp2 others(4): Show |
a0002 | a0002c0005 | a0002c0005t0010a0002c0005t0016 | a0002c0005t0010g0030a0002c0005t0010g0044a0002c0005t0010g0056others(4): Show | 7 | 286 | 0.0245 | -6 | c.832 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 8/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100978565 | TATTATA | T | intron_variant | MODIFIER | HG01123.hp2 HG01261.hp1 HG02074.hp1 others(37): Show |
a0001a0006 | a0001c0001a0006c0017 | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(3): Show | a0001c0001t0001g0002a0001c0001t0001g0027a0001c0001t0001g0047others(37): Show | 40 | 286 | 0.1399 | -6 | c.239 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 21/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | CTTTTTT | C | intron_variant | MODIFIER | HG02055.hp1 HG02970.hp1 NA18953.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0039a0002c0002t0040 | a0001c0001t0001g0027a0001c0001t0001g0070a0001c0001t0001g0192others(3): Show | 6 | 286 | 0.0210 | -6 | c.245 others(25): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100996990 | TTTTTTC | T | downstream_gene_variant | MODIFIER | HG00423.hp1 HG00733.hp1 HG01070.hp1 others(11): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0006a0001c0003t0006a0001c0003t0014others(2): Show | a0001c0001t0006g0081a0001c0003t0006g0112a0001c0003t0006g0159others(11): Show | 14 | 286 | 0.0490 | -6 | c.*81 others(17): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3050 | chr11 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12802927 | TTATATA | T | intron_variant | MODIFIER | HG01934.hp2 HG02145.hp2 HG02735.hp1 others(2): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0027others(1): Show | a0001c0001t0001g0127a0001c0001t0001g0163a0001c0001t0002g0219others(2): Show | 5 | 230 | 0.0217 | -6 | c.53+ others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12802965 | ATATATT | A | intron_variant | MODIFIER | HG01243.hp2 HG02280.hp1 HG03098.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0013a0001c0002t0001others(1): Show | a0001c0001t0001g0147a0001c0001t0001g0189a0001c0001t0013g0161others(2): Show | 5 | 230 | 0.0217 | -6 | c.53+ others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12822353 | AGATGAT | A | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00639.hp1 others(72): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(29): Show | a0001c0001t0001g0027a0001c0001t0001g0035a0001c0001t0001g0041others(72): Show | 75 | 230 | 0.3261 | -6 | c.53+ others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12868589 | TTTTATA | T | intron_variant | MODIFIER | HG00140.hp2 HG00423.hp1 HG00639.hp2 others(11): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0027a0001c0001t0001g0132a0001c0001t0001g0144others(11): Show | 14 | 230 | 0.0609 | -6 | c.54- others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12868591 | TTATATA | T | intron_variant | MODIFIER | HG01192.hp1 HG01928.hp2 HG02809.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005a0001c0001t0009others(1): Show | a0001c0001t0001g0152a0001c0001t0005g0050a0001c0001t0009g0191others(1): Show | 4 | 230 | 0.0174 | -6 | c.54- others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12885324 | GGTGTGT | G | intron_variant | MODIFIER | HG01192.hp1 HG01891.hp2 HG02109.hp1 others(17): Show |
a0001 | a0001c0001a0001c0006 | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(5): Show | a0001c0001t0001g0009a0001c0001t0001g0033a0001c0001t0001g0035others(17): Show | 20 | 230 | 0.0870 | -6 | c.54- others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12886969 | TTTTTTG | T | intron_variant | MODIFIER | HG01884.hp1 HG02572.hp1 HG02622.hp2 others(4): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0013a0001c0001t0001g0027a0001c0001t0001g0183others(4): Show | 7 | 230 | 0.0304 | -6 | c.54- others(21): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12903140 | AGTGTGT | A | intron_variant | MODIFIER | HG02109.hp1 HG02809.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0009 | a0001c0001t0003g0075a0001c0001t0009g0191 | 2 | 230 | 0.0087 | -6 | c.199 others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12931841 | TACACAC | T | intron_variant | MODIFIER | HG00642.hp1 HG00642.hp2 HG00733.hp1 others(53): Show |
a0001a0003a0005 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(13): Show | a0001c0001t0001g0009a0001c0001t0001g0035a0001c0001t0001g0041others(53): Show | 56 | 230 | 0.2435 | -6 | c.582 others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12956866 | AACACAC | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00639.hp1 others(101): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(32): Show | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0007others(101): Show | 104 | 230 | 0.4522 | -6 | c.134 others(23): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 15/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12976243 | ACACACC | A | intron_variant | MODIFIER | NA18951.hp1 NA18951.hp2 NA18984.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003a0001c0001t0005 | a0001c0001t0002g0108a0001c0001t0003g0049a0001c0001t0005g0057others(1): Show | 4 | 230 | 0.0174 | -6 | c.176 others(25): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12978553 | CTCCCAG | C | intron_variant | MODIFIER | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(64): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(21): Show | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0020others(64): Show | 67 | 230 | 0.2913 | -6 | c.176 others(25): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP45_chr19_1062167_1091628 | 1070504 | TTCTTTC | T | intron_variant | MODIFIER | HG01243.hp1 HG02630.hp2 HG02647.hp2 others(5): Show |
a0002a0004 | a0002c0001a0004c0005a0004c0048 | a0002c0001t0004a0004c0005t0003a0004c0005t0008others(1): Show | a0002c0001t0004g0148a0004c0005t0003g0181a0004c0005t0003g0187others(5): Show | 8 | 418 | 0.0191 | -6 | c.421 others(23): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP45_chr19_1062167_1091628 | 1082278 | GCGGGGC | G | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(138): Show |
a0001a0002a0003others(6): Show | a0001c0002a0001c0004a0001c0017others(13): Show | a0001c0002t0001a0001c0002t0002a0001c0002t0013others(20): Show | a0001c0002t0001g0002a0001c0002t0001g0007a0001c0002t0001g0018others(103): Show | 141 | 418 | 0.3373 | -6 | c.251 others(23): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP5_chr14_32072304_32164728 | 32143202 | AGTTGTT | A | intron_variant | MODIFIER | HG00609.hp2 HG03130.hp1 HG03704.hp2 |
a0001a0009 | a0001c0001a0009c0014 | a0001c0001t0001a0009c0014t0015 | a0001c0001t0001g0093a0001c0001t0001g0157a0009c0014t0015g0159 | 3 | 186 | 0.0161 | -6 | c.386 others(25): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
ARHGAP6_chrX_11132544_11670920 | 11176232 | CATATAT | C | intron_variant | MODIFIER | HG03471.hp1 | a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0141 | 1 | 144 | 0.0069 | -6 | c.162 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11176300 | CATATAT | C | intron_variant | MODIFIER | HG01433.hp1 HG01515.hp1 HG02572.hp1 others(5): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0010others(1): Show | a0001c0001t0001g0003a0001c0001t0001g0054a0001c0001t0001g0061others(5): Show | 8 | 144 | 0.0556 | -6 | c.162 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11179765 | CATATAT | C | intron_variant | MODIFIER | HG02258.hp1 HG02451.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0018 | a0001c0001t0001g0020a0002c0002t0018g0029 | 2 | 144 | 0.0139 | -6 | c.133 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 6/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11185142 | CTGTGTG | C | intron_variant | MODIFIER | HG01074.hp1 HG01243.hp1 HG01515.hp1 others(13): Show |
a0001a0002 | a0001c0001a0001c0004a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(3): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0024others(13): Show | 16 | 144 | 0.1111 | -6 | c.127 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 5/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11201989 | CTGTGTG | C | intron_variant | MODIFIER | HG02145.hp1 HG03139.hp1 |
a0001a0004 | a0001c0001a0004c0008 | a0001c0001t0020a0004c0008t0012 | a0001c0001t0020g0131a0004c0008t0012g0002 | 2 | 144 | 0.0139 | -6 | c.749 others(23): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 2/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11241531 | CGTGTGT | C | intron_variant | MODIFIER | HG01167.hp1 HG02895.hp1 HG03098.hp1 others(2): Show |
a0001a0003 | a0001c0001a0003c0010 | a0001c0001t0001a0001c0001t0002a0001c0001t0019others(1): Show | a0001c0001t0001g0024a0001c0001t0001g0045a0001c0001t0002g0132others(2): Show | 5 | 144 | 0.0347 | -6 | c.748 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 2/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11266033 | CTGTGTG | C | intron_variant | MODIFIER | NA18983.hp1 NA18985.hp1 NA20805.hp1 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0013a0002c0002t0009 | a0001c0001t0001g0074a0001c0001t0013g0066a0002c0002t0009g0140 | 3 | 144 | 0.0208 | -6 | c.589 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11320766 | TACACAC | T | intron_variant | MODIFIER | HG02572.hp1 HG03471.hp1 NA19082.hp1 others(1): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0010a0002c0002t0003a0002c0002t0016 | a0001c0001t0010g0141a0001c0001t0010g0142a0002c0002t0003g0012others(1): Show | 4 | 144 | 0.0278 | -6 | c.589 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11335238 | ATATTTT | A | intron_variant | MODIFIER | HG01256.hp1 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0019 | 1 | 144 | 0.0069 | -6 | c.589 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11351047 | TACACAC | T | intron_variant | MODIFIER | HG02451.hp2 HG02647.hp1 HG03130.hp1 |
a0001 | a0001c0001a0001c0007 | a0001c0001t0001a0001c0001t0002a0001c0007t0001 | a0001c0001t0001g0020a0001c0001t0002g0129a0001c0007t0001g0021 | 3 | 144 | 0.0208 | -6 | c.589 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11353549 | AGTGTGT | A | intron_variant | MODIFIER | HG01106.hp1 HG02451.hp1 HG02809.hp1 others(10): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(3): Show | a0001c0001t0001g0003a0001c0001t0001g0043a0001c0001t0001g0046others(10): Show | 13 | 144 | 0.0903 | -6 | c.589 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11354295 | TTCTCTC | T | intron_variant | MODIFIER | HG00609.hp1 HG00738.hp1 HG01358.hp1 others(21): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0014 | a0001c0001t0001g0022a0001c0001t0001g0025a0001c0001t0001g0026others(21): Show | 24 | 144 | 0.1667 | -6 | c.589 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11354323 | CTCTCTA | C | intron_variant | MODIFIER | HG00621.hp1 HG01069.hp1 HG01192.hp1 others(14): Show |
a0001a0002 | a0001c0001a0001c0009a0002c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(4): Show | a0001c0001t0001g0042a0001c0001t0001g0055a0001c0001t0001g0064others(14): Show | 17 | 144 | 0.1181 | -6 | c.589 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11354325 | CTCTATA | C | intron_variant | MODIFIER | HG01258.hp1 HG02015.hp1 HG02074.hp1 others(5): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0005 | a0001c0001t0001g0041a0001c0001t0001g0057a0001c0001t0001g0063others(5): Show | 8 | 144 | 0.0556 | -6 | c.589 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11354327 | CTATATA | C | intron_variant | MODIFIER | HG00642.hp1 HG03098.hp1 HG04204.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0105others(2): Show | 5 | 144 | 0.0347 | -6 | c.589 others(25): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11358433 | CTTTCTT | C | intron_variant | MODIFIER | HG02922.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0138 | 1 | 144 | 0.0069 | -6 | c.589 others(27): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11358481 | CTTTCTT | C | intron_variant | MODIFIER | HG02074.hp1 NA18940.hp1 NA19056.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0081a0001c0001t0001g0098a0001c0001t0001g0123 | 3 | 144 | 0.0208 | -6 | c.589 others(27): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11362650 | TATAATA | T | intron_variant | MODIFIER | HG02015.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0041 | 1 | 144 | 0.0069 | -6 | c.589 others(27): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11372771 | CAAAAAA | C | intron_variant | MODIFIER | HG02647.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0129 | 1 | 144 | 0.0069 | -6 | c.589 others(27): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11373094 | AACACAC | A | intron_variant | MODIFIER | HG01934.hp1 HG02451.hp1 HG03516.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0023a0001c0001t0001g0036a0001c0001t0001g0116others(1): Show | 4 | 144 | 0.0278 | -6 | c.589 others(27): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11417059 | CATATAT | C | intron_variant | MODIFIER | HG01934.hp1 HG02622.hp2 NA19066.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0023a0001c0001t0001g0044a0001c0001t0001g0067 | 3 | 144 | 0.0208 | -6 | c.589 others(27): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11427815 | AGAGGAG | A | intron_variant | MODIFIER | HG01106.hp1 HG01109.hp1 HG01167.hp1 others(23): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0001c0007others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(9): Show | a0001c0001t0001g0017a0001c0001t0001g0020a0001c0001t0001g0028others(23): Show | 26 | 144 | 0.1806 | -6 | c.589 others(27): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11450203 | AGTGTGT | A | intron_variant | MODIFIER | HG01258.hp1 HG01934.hp1 HG01943.hp1 others(11): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0004a0002c0002t0003 | a0001c0001t0001g0020a0001c0001t0001g0023a0001c0001t0001g0027others(11): Show | 14 | 144 | 0.0972 | -6 | c.589 others(27): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11475560 | TACACAC | T | intron_variant | MODIFIER | HG01074.hp1 HG01167.hp1 HG01256.hp1 others(14): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0008 | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(3): Show | a0001c0001t0001g0017a0001c0001t0001g0024a0001c0001t0001g0054others(14): Show | 17 | 144 | 0.1181 | -6 | c.588 others(27): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11489632 | GCCAACC | G | intron_variant | MODIFIER | HG01258.hp1 HG01934.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0023a0001c0001t0001g0091 | 2 | 144 | 0.0139 | -6 | c.588 others(27): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar |