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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP40_chr20_38596809_38655653 | 38616935 | C | CTTTATTT others(5): Show |
intron_variant | MODIFIER | HG00140.hp2 HG00438.hp2 HG01256.hp2 others(46): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0002a0001c0007others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(17): Show | a0001c0001t0001g0023a0001c0001t0001g0140a0001c0001t0001g0241others(42): Show | 49 | 350 | 0.1400 | 12 | c.138 others(29): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ARHGAP40_chr20_38596809_38655653 | 38627352 | A | ATGTGTGT others(5): Show |
intron_variant | MODIFIER | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(74): Show |
a0001a0004a0005others(7): Show | a0001c0002a0001c0008a0004c0011others(9): Show | a0001c0002t0001a0001c0002t0002a0001c0002t0003others(18): Show | a0001c0002t0001g0025a0001c0002t0001g0125a0001c0002t0001g0126others(69): Show | 77 | 350 | 0.2200 | 12 | c.558 others(27): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100779485 | T | TATACACA others(5): Show |
intron_variant | MODIFIER | HG00423.hp1 NA19091.hp1 |
a0001 | a0001c0003a0001c0012 | a0001c0003t0026a0001c0012t0001 | a0001c0003t0026g0181a0001c0012t0001g0131 | 2 | 286 | 0.0070 | 12 | c.250 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100779485 | T | TATATACA others(5): Show |
intron_variant | MODIFIER | HG01123.hp2 HG01261.hp1 HG01346.hp2 others(9): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0003t0003others(1): Show | a0001c0001t0001g0113a0001c0001t0001g0117a0001c0001t0001g0149others(9): Show | 12 | 286 | 0.0420 | 12 | c.250 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100806837 | G | GTTTATTT others(5): Show |
intron_variant | MODIFIER | HG02280.hp2 HG02809.hp1 HG03453.hp1 others(1): Show |
a0002 | a0002c0002 | a0002c0002t0002a0002c0002t0004a0002c0002t0008 | a0002c0002t0002g0173a0002c0002t0002g0174a0002c0002t0004g0172others(1): Show | 4 | 286 | 0.0140 | 12 | c.312 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100806837 | G | GTTTGTTT others(5): Show |
intron_variant | MODIFIER | HG01346.hp1 HG02257.hp2 HG02818.hp2 |
a0002 | a0002c0002 | a0002c0002t0002a0002c0002t0008 | a0002c0002t0002g0010a0002c0002t0008g0005a0002c0002t0008g0230 | 3 | 286 | 0.0105 | 12 | c.312 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100837666 | C | CTTTTTTT others(5): Show |
intron_variant | MODIFIER | HG00597.hp1 HG00735.hp1 HG00738.hp2 others(11): Show |
a0001a0002 | a0001c0001a0002c0009 | a0001c0001t0001a0001c0001t0006a0001c0001t0041others(1): Show | a0001c0001t0001g0087a0001c0001t0001g0092a0001c0001t0001g0100others(11): Show | 14 | 286 | 0.0490 | 12 | c.313 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100858086 | G | GGTGTGTG others(5): Show |
intron_variant | MODIFIER | HG01346.hp2 HG03239.hp2 HG04199.hp2 others(6): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0001a0001c0001t0024a0002c0004t0007 | a0001c0001t0001g0076a0001c0001t0001g0124a0001c0001t0001g0130others(6): Show | 9 | 286 | 0.0315 | 12 | c.313 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100858117 | G | GTGTGTGT others(5): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(57): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0001c0008others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0003t0006others(13): Show | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0072others(57): Show | 60 | 286 | 0.2098 | 12 | c.313 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100893158 | G | GGTGTGTG others(5): Show |
intron_variant | MODIFIER | HG00408.hp2 HG01123.hp2 HG01257.hp2 others(39): Show |
a0001 | a0001c0001a0001c0003a0001c0008 | a0001c0001t0001a0001c0001t0002a0001c0001t0030others(5): Show | a0001c0001t0001g0047a0001c0001t0001g0062a0001c0001t0001g0066others(39): Show | 42 | 286 | 0.1469 | 12 | c.385 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903117 | G | GCACACAC others(5): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG01123.hp1 others(12): Show |
a0001a0002a0003 | a0001c0008a0002c0002a0002c0004others(2): Show | a0001c0008t0001a0002c0002t0004a0002c0002t0005others(6): Show | a0001c0008t0001g0004a0002c0002t0004g0107a0002c0002t0004g0172others(12): Show | 15 | 286 | 0.0525 | 12 | c.385 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903117 | G | GCGCACAC others(5): Show |
intron_variant | MODIFIER | HG01928.hp1 HG01934.hp2 HG02165.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0013 | a0001c0001t0001g0011a0001c0001t0001g0092a0001c0001t0001g0098others(4): Show | 7 | 286 | 0.0245 | 12 | c.385 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903117 | G | GCGCGCAC others(5): Show |
intron_variant | MODIFIER | HG02486.hp1 | a0001 | a0001c0010 | a0001c0010t0001 | a0001c0010t0001g0238 | 1 | 286 | 0.0035 | 12 | c.385 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903706 | C | CAAAAAAA others(5): Show |
intron_variant | MODIFIER | HG01496.hp1 HG01981.hp1 |
a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0147a0002c0002t0002g0208 | 2 | 286 | 0.0070 | 12 | c.385 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903709 | A | AAAAAAAA others(5): Show |
intron_variant | MODIFIER | HG01891.hp2 HG02280.hp1 |
a0002 | a0002c0002 | a0002c0002t0001a0002c0002t0002 | a0002c0002t0001g0013a0002c0002t0002g0067 | 2 | 286 | 0.0070 | 12 | c.385 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903709 | A | AAAAAAAA others(5): Show |
intron_variant | MODIFIER | HG01106.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0097 | 1 | 286 | 0.0035 | 12 | c.385 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903709 | A | AAAAAAAA others(5): Show |
intron_variant | MODIFIER | HG02622.hp1 | a0002 | a0002c0006 | a0002c0006t0011 | a0002c0006t0011g0241 | 1 | 286 | 0.0035 | 12 | c.385 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903709 | A | AATATATA others(5): Show |
intron_variant | MODIFIER | HG00597.hp1 HG01192.hp2 HG03239.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0024 | a0001c0001t0001g0091a0001c0001t0001g0100a0001c0001t0001g0120others(7): Show | 10 | 286 | 0.0350 | 12 | c.385 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100908087 | G | GTAGTAAA others(5): Show |
intron_variant | MODIFIER | NA18953.hp2 | a0001 | a0001c0001 | a0001c0001t0013 | a0001c0001t0013g0122 | 1 | 286 | 0.0035 | 12 | c.385 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100917015 | T | TTGTGTGT others(5): Show |
intron_variant | MODIFIER | HG03239.hp2 | a0002 | a0002c0004 | a0002c0004t0007 | a0002c0004t0007g0075 | 1 | 286 | 0.0035 | 12 | c.486 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100935677 | C | CACACACA others(5): Show |
intron_variant | MODIFIER | HG01070.hp2 HG02559.hp2 HG03139.hp1 others(1): Show |
a0002 | a0002c0002a0002c0011 | a0002c0002t0017a0002c0002t0018a0002c0011t0017 | a0002c0002t0017g0046a0002c0002t0018g0193a0002c0002t0018g0194others(1): Show | 4 | 286 | 0.0140 | 12 | c.703 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 7/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100952734 | C | CTTTTTTT others(5): Show |
intron_variant | MODIFIER | HG02976.hp1 HG03688.hp1 |
a0002 | a0002c0002a0002c0004 | a0002c0002t0009a0002c0004t0007 | a0002c0002t0009g0033a0002c0004t0007g0125 | 2 | 286 | 0.0070 | 12 | c.116 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100972516 | T | TTGGATGG others(5): Show |
intron_variant | MODIFIER | HG00738.hp1 HG00741.hp1 HG01516.hp1 others(6): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0001a0002c0004t0007 | a0001c0001t0001g0093a0001c0001t0001g0095a0002c0004t0007g0016others(6): Show | 9 | 286 | 0.0315 | 12 | c.155 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTCTTTT others(5): Show |
intron_variant | MODIFIER | HG01109.hp1 HG03017.hp2 NA18522.hp1 |
a0002 | a0002c0002 | a0002c0002t0002a0002c0002t0005a0002c0002t0008 | a0002c0002t0002g0102a0002c0002t0005g0110a0002c0002t0008g0175 | 3 | 286 | 0.0105 | 12 | c.245 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100987806 | A | AAAATAAA others(5): Show |
intron_variant | MODIFIER | HG01256.hp2 HG02129.hp2 HG03834.hp1 others(13): Show |
a0001a0006 | a0001c0001a0006c0017 | a0001c0001t0001a0006c0017t0001 | a0001c0001t0001g0011a0001c0001t0001g0026a0001c0001t0001g0027others(13): Show | 16 | 286 | 0.0559 | 12 | c.253 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100987843 | A | AAATAAAT others(5): Show |
intron_variant | MODIFIER | HG01074.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0244 | 1 | 286 | 0.0035 | 12 | c.253 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100995655 | G | GAATAAAT others(5): Show |
downstream_gene_variant | MODIFIER | HG00323.hp1 HG00639.hp2 HG00642.hp1 others(54): Show |
a0001a0002a0003 | a0001c0001a0001c0008a0002c0002others(4): Show | a0001c0001t0001a0001c0008t0010a0002c0002t0002others(13): Show | a0001c0001t0001g0027a0001c0001t0001g0113a0001c0001t0001g0186others(54): Show | 57 | 286 | 0.1993 | 12 | c.*68 others(23): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1715 | chr11 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12796136 | A | ATATCTAT others(5): Show |
intron_variant | MODIFIER | HG03139.hp1 HG03486.hp1 NA18906.hp1 |
a0001 | a0001c0001a0001c0005a0001c0006 | a0001c0001t0003a0001c0005t0001a0001c0006t0003 | a0001c0001t0003g0090a0001c0005t0001g0173a0001c0006t0003g0091 | 3 | 230 | 0.0130 | 12 | c.53+ others(27): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12825416 | T | TTGTGTGT others(5): Show |
intron_variant | MODIFIER | HG00423.hp2 HG02027.hp2 HG03491.hp1 others(6): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(1): Show | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0002g0015others(6): Show | 9 | 230 | 0.0391 | 12 | c.53+ others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12841577 | G | GTCTGTCT others(5): Show |
intron_variant | MODIFIER | HG00639.hp1 HG00741.hp2 HG01081.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0003a0001c0001t0005a0001c0002t0003 | a0001c0001t0003g0064a0001c0001t0003g0065a0001c0001t0003g0066others(2): Show | 5 | 230 | 0.0217 | 12 | c.53+ others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12841585 | G | GTCTCTCT others(5): Show |
intron_variant | MODIFIER | NA18906.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0090 | 1 | 230 | 0.0044 | 12 | c.53+ others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12841594 | T | TCTCTCTC others(5): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00673.hp2 HG01928.hp2 others(16): Show |
a0001 | a0001c0001a0001c0002a0001c0006others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(5): Show | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(16): Show | 19 | 230 | 0.0826 | 12 | c.53+ others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12841594 | T | TGTCTCTC others(5): Show |
intron_variant | MODIFIER | HG02559.hp2 HG02886.hp2 HG03453.hp2 others(1): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0001t0010a0001c0001t0014others(1): Show | a0001c0001t0001g0033a0001c0001t0010g0034a0001c0001t0014g0179others(1): Show | 4 | 230 | 0.0174 | 12 | c.53+ others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12841639 | C | CAAAAAAA others(5): Show |
intron_variant | MODIFIER | HG03041.hp2 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0223 | 1 | 230 | 0.0044 | 12 | c.53+ others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12849214 | C | CGTGTGTG others(5): Show |
intron_variant | MODIFIER | HG00423.hp2 HG02027.hp2 HG02071.hp2 others(6): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(1): Show | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0017others(6): Show | 9 | 230 | 0.0391 | 12 | c.54- others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12861653 | T | TTTTTTTT others(5): Show |
intron_variant | MODIFIER | HG00423.hp2 HG00642.hp1 HG00733.hp1 others(31): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(8): Show | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0016others(31): Show | 34 | 230 | 0.1478 | 12 | c.54- others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12861653 | T | TTTTTTTT others(5): Show |
intron_variant | MODIFIER | HG03491.hp1 HG03831.hp2 HG03942.hp1 others(4): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0013a0001c0001t0001g0017a0001c0001t0002g0019others(4): Show | 7 | 230 | 0.0304 | 12 | c.54- others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12868591 | T | TTATATAT others(5): Show |
intron_variant | MODIFIER | HG02145.hp1 HG02572.hp1 HG03239.hp2 |
a0001 | a0001c0001a0001c0003a0001c0008 | a0001c0001t0001a0001c0003t0001a0001c0008t0020 | a0001c0001t0001g0183a0001c0003t0001g0211a0001c0008t0020g0181 | 3 | 230 | 0.0130 | 12 | c.54- others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12903126 | G | GGAGAGAG others(5): Show |
intron_variant | MODIFIER | HG02647.hp2 | a0001 | a0001c0001 | a0001c0001t0029 | a0001c0001t0029g0177 | 1 | 230 | 0.0044 | 12 | c.199 others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12903140 | A | AGTGTGTG others(5): Show |
intron_variant | MODIFIER | HG01167.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0206 | 1 | 230 | 0.0044 | 12 | c.199 others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12931841 | T | TACACACA others(5): Show |
intron_variant | MODIFIER | HG03704.hp2 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0073 | 1 | 230 | 0.0044 | 12 | c.582 others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12931841 | T | TACACACA others(5): Show |
intron_variant | MODIFIER | HG01192.hp1 HG02451.hp1 HG03486.hp2 others(2): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0001t0003a0001c0001t0025others(1): Show | a0001c0001t0001g0174a0001c0001t0001g0176a0001c0001t0003g0090others(2): Show | 5 | 230 | 0.0217 | 12 | c.582 others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12948723 | T | TACACACA others(5): Show |
intron_variant | MODIFIER | HG03942.hp2 NA18989.hp1 |
a0001a0003 | a0001c0009a0003c0017 | a0001c0009t0002a0003c0017t0003 | a0001c0009t0002g0110a0003c0017t0003g0068 | 2 | 230 | 0.0087 | 12 | c.862 others(27): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12978035 | T | TAAAAAAA others(5): Show |
intron_variant | MODIFIER | HG03492.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0120 | 1 | 230 | 0.0044 | 12 | c.176 others(31): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 18/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12978036 | C | CAAAAAAA others(5): Show |
intron_variant | MODIFIER | HG02145.hp2 HG03486.hp1 |
a0001 | a0001c0001a0001c0006 | a0001c0001t0027a0001c0006t0003 | a0001c0001t0027g0222a0001c0006t0003g0091 | 2 | 230 | 0.0087 | 12 | c.176 others(31): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12986673 | C | CAAAAAAA others(5): Show |
intron_variant | MODIFIER | HG01243.hp1 | a0001 | a0001c0001 | a0001c0001t0021 | a0001c0001t0021g0195 | 1 | 230 | 0.0044 | 12 | c.231 others(31): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12989101 | C | CCCAAAAA others(5): Show |
intron_variant | MODIFIER | HG02145.hp2 | a0001 | a0001c0001 | a0001c0001t0027 | a0001c0001t0027g0222 | 1 | 230 | 0.0044 | 12 | c.231 others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 20/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12989101 | C | CCCCAAAA others(5): Show |
intron_variant | MODIFIER | HG01928.hp1 HG02300.hp1 HG04228.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0111a0001c0001t0001g0144a0001c0001t0001g0148others(1): Show | 4 | 230 | 0.0174 | 12 | c.231 others(29): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 20/20 | chr17 | TogoVar | ||||||
ARHGAP5_chr14_32072304_32164728 | 32148163 | A | AATCTATC others(5): Show |
intron_variant | MODIFIER | HG02738.hp2 HG03516.hp1 HG03654.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0012 | a0001c0001t0001g0050a0001c0001t0001g0128a0001c0001t0001g0175others(1): Show | 4 | 186 | 0.0215 | 12 | c.394 others(31): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
ARHGAP6_chrX_11132544_11670920 | 11174573 | C | CCTTCCTT others(5): Show |
intron_variant | MODIFIER | HG01261.hp1 HG02145.hp1 HG02300.hp2 others(1): Show |
a0001a0004 | a0001c0001a0004c0008 | a0001c0001t0001a0004c0008t0012 | a0001c0001t0001g0080a0001c0001t0001g0084a0001c0001t0001g0120others(1): Show | 4 | 144 | 0.0278 | 12 | c.162 others(31): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar |