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 | 100715048 | CAAA | C | intron_variant | MODIFIER | HG00323.hp2 HG00597.hp2 HG00673.hp2 others(42): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0008others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0003t0003others(12): Show | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0088others(42): Show | 45 | 286 | 0.1573 | -3 | c.154 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100735002 | AAAC | A | intron_variant | MODIFIER | HG01081.hp1 HG02055.hp2 HG02630.hp1 others(1): Show |
a0002 | a0002c0002a0002c0005 | a0002c0002t0002a0002c0002t0008a0002c0005t0010 | a0002c0002t0002g0139a0002c0002t0008g0028a0002c0002t0008g0029others(1): Show | 4 | 286 | 0.0140 | -3 | c.155 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100751773 | CTTT | C | intron_variant | MODIFIER | HG00673.hp2 HG01109.hp2 HG01515.hp2 others(9): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0010others(2): Show | a0001c0001t0001a0001c0003t0003a0001c0010t0001others(4): Show | a0001c0001t0001g0279a0001c0003t0003g0269a0001c0003t0003g0273others(9): Show | 12 | 286 | 0.0420 | -3 | c.155 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100764005 | CTCT | C | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(54): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0002c0002others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(19): Show | a0001c0001t0001g0007a0001c0001t0001g0062a0001c0001t0001g0066others(54): Show | 57 | 286 | 0.1993 | -3 | c.155 others(20): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100765367 | TGTG | T | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(56): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0002c0002others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(19): Show | a0001c0001t0001g0007a0001c0001t0001g0011a0001c0001t0001g0062others(56): Show | 59 | 286 | 0.2063 | -3 | c.155 others(20): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100767670 | AAAG | A | intron_variant | MODIFIER | HG01081.hp1 HG01891.hp1 HG02055.hp2 others(2): Show |
a0002 | a0002c0002a0002c0005 | a0002c0002t0008a0002c0002t0009a0002c0005t0010 | a0002c0002t0008g0028a0002c0002t0008g0029a0002c0002t0009g0043others(2): Show | 5 | 286 | 0.0175 | -3 | c.155 others(20): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100769712 | CTTT | C | intron_variant | MODIFIER | HG01109.hp2 HG01243.hp2 HG01346.hp1 others(9): Show |
a0001a0002 | a0001c0001a0001c0010a0002c0002others(1): Show | a0001c0001t0001a0001c0010t0001a0002c0002t0002others(5): Show | a0001c0001t0001g0178a0001c0001t0001g0188a0001c0010t0001g0238others(9): Show | 12 | 286 | 0.0420 | -3 | c.155 others(18): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100794075 | CAAA | C | intron_variant | MODIFIER | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(43): Show |
a0001a0002a0004 | a0001c0001a0001c0003a0002c0002others(3): Show | a0001c0001t0001a0001c0001t0013a0001c0001t0032others(16): Show | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0066others(43): Show | 46 | 286 | 0.1608 | -3 | c.251 others(18): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100828164 | TGCC | T | intron_variant | MODIFIER | HG00423.hp2 HG00544.hp1 HG00597.hp1 others(60): Show |
a0001a0002 | a0001c0001a0001c0012a0001c0014others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(12): Show | a0001c0001t0001g0011a0001c0001t0001g0069a0001c0001t0001g0070others(60): Show | 63 | 286 | 0.2203 | -3 | c.313 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100850873 | CTTT | C | intron_variant | MODIFIER | HG00323.hp1 HG00323.hp2 HG00639.hp2 others(74): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0003a0001c0008others(7): Show | a0001c0001t0001a0001c0001t0037a0001c0003t0001others(22): Show | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0091others(74): Show | 77 | 286 | 0.2692 | -3 | c.313 others(20): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100862423 | TTTC | T | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(29): Show |
a0001a0002 | a0001c0001a0001c0008a0002c0002others(2): Show | a0001c0001t0001a0001c0008t0001a0001c0008t0010others(11): Show | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0144others(29): Show | 32 | 286 | 0.1119 | -3 | c.384 others(20): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100868627 | CTCT | C | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp1 HG00408.hp2 others(34): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(6): Show | a0001c0001t0001g0135a0001c0001t0001g0266a0001c0001t0001g0279others(34): Show | 37 | 286 | 0.1294 | -3 | c.384 others(20): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100899731 | TTTG | T | intron_variant | MODIFIER | HG00733.hp2 HG01074.hp2 HG01081.hp1 others(43): Show |
a0001a0002 | a0001c0003a0001c0008a0002c0002others(2): Show | a0001c0003t0003a0001c0003t0022a0001c0008t0001others(12): Show | a0001c0003t0003g0155a0001c0003t0003g0272a0001c0003t0022g0209others(43): Show | 46 | 286 | 0.1608 | -3 | c.385 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100914509 | GAAC | G | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(216): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0008a0001c0010others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(46): Show | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0011others(216): Show | 219 | 286 | 0.7657 | -3 | c.486 others(18): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100928772 | ACCC | A | intron_variant | MODIFIER | HG00738.hp1 HG00741.hp1 HG01516.hp1 others(5): Show |
a0002 | a0002c0004 | a0002c0004t0007 | a0002c0004t0007g0016a0002c0004t0007g0060a0002c0004t0007g0074others(5): Show | 8 | 286 | 0.0280 | -3 | c.598 others(20): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 6/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100956181 | ACAT | A | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(261): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0003a0001c0008others(13): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(50): Show | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0011others(261): Show | 264 | 286 | 0.9231 | -3 | c.116 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100958128 | TTTG | T | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(261): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0003a0001c0008others(13): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(50): Show | a0001c0001t0001g0002a0001c0001t0001g0007a0001c0001t0001g0011others(261): Show | 264 | 286 | 0.9231 | -3 | c.116 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | CTTT | C | intron_variant | MODIFIER | HG00323.hp2 HG01884.hp1 HG01934.hp1 others(9): Show |
a0001a0004 | a0001c0001a0004c0013 | a0001c0001t0001a0001c0001t0013a0001c0001t0036others(1): Show | a0001c0001t0001g0007a0001c0001t0001g0117a0001c0001t0001g0130others(9): Show | 12 | 286 | 0.0420 | -3 | c.245 others(22): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12816560 | AATT | A | intron_variant | MODIFIER | HG03471.hp2 HG03579.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | 230 | 0.0087 | -3 | c.53+ others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12828028 | CAAA | C | intron_variant | MODIFIER | HG01192.hp1 HG01884.hp1 HG02145.hp1 others(9): Show |
a0001 | a0001c0001a0001c0006a0001c0008 | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(4): Show | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(9): Show | 12 | 230 | 0.0522 | -3 | c.53+ others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12834841 | CTTA | C | intron_variant | MODIFIER | HG02630.hp2 HG02809.hp2 HG02895.hp1 others(2): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(2): Show | 5 | 230 | 0.0217 | -3 | c.53+ others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12842414 | CAAA | C | intron_variant | MODIFIER | HG01891.hp2 HG02922.hp2 HG03471.hp2 others(4): Show |
a0001 | a0001c0001a0001c0003a0001c0005 | a0001c0001t0001a0001c0001t0003a0001c0003t0001others(1): Show | a0001c0001t0001g0009a0001c0001t0001g0017a0001c0001t0001g0227others(4): Show | 7 | 230 | 0.0304 | -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 | 12842431 | AAAG | A | intron_variant | MODIFIER | HG00423.hp1 HG00733.hp1 HG01243.hp1 others(8): Show |
a0001 | a0001c0001a0001c0003a0001c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0019others(3): Show | a0001c0001t0001g0194a0001c0001t0001g0209a0001c0001t0001g0213others(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 | 12849048 | CAAA | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00423.hp1 others(94): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(32): Show | a0001c0001t0001g0020a0001c0001t0001g0021a0001c0001t0001g0022others(94): Show | 97 | 230 | 0.4217 | -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 | 12857765 | GTTA | G | intron_variant | MODIFIER | HG01934.hp1 HG02258.hp1 HG03098.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0007a0001c0001t0008others(1): Show | a0001c0001t0001g0035a0001c0001t0001g0214a0001c0001t0007g0038others(2): Show | 5 | 230 | 0.0217 | -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 | 12885520 | TTGA | T | intron_variant | MODIFIER | HG00639.hp2 HG01928.hp1 HG02027.hp2 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0094a0001c0001t0001g0111a0001c0001t0001g0117others(9): Show | 12 | 230 | 0.0522 | -3 | c.54- others(18): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12894695 | TGTC | T | intron_variant | MODIFIER | HG00639.hp2 HG01928.hp1 HG02027.hp2 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0094a0001c0001t0001g0111a0001c0001t0001g0117others(9): Show | 12 | 230 | 0.0522 | -3 | c.54- others(16): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12900913 | CTTT | C | intron_variant | MODIFIER | HG01070.hp2 HG01109.hp2 HG01192.hp1 others(33): Show |
a0001 | a0001c0001a0001c0002a0001c0005others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(11): Show | a0001c0001t0001g0007a0001c0001t0001g0009a0001c0001t0001g0020others(33): Show | 36 | 230 | 0.1565 | -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 | 12903114 | GAGA | G | intron_variant | MODIFIER | HG01081.hp2 HG03239.hp1 HG03453.hp1 others(2): Show |
a0001 | a0001c0001a0001c0008 | a0001c0001t0002a0001c0001t0011a0001c0001t0013others(1): Show | a0001c0001t0002g0121a0001c0001t0002g0229a0001c0001t0011g0083others(2): Show | 5 | 230 | 0.0217 | -3 | c.199 others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12903116 | GAGA | G | intron_variant | MODIFIER | HG02257.hp2 NA18989.hp1 |
a0001 | a0001c0001a0001c0009 | a0001c0001t0003a0001c0009t0002 | a0001c0001t0003g0047a0001c0009t0002g0110 | 2 | 230 | 0.0087 | -3 | c.199 others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12903118 | GAGA | G | intron_variant | MODIFIER | HG00423.hp1 HG02451.hp1 NA18942.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0019 | a0001c0001t0001g0174a0001c0001t0004g0170a0001c0001t0019g0210 | 3 | 230 | 0.0130 | -3 | c.199 others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12912837 | AGAG | A | intron_variant | MODIFIER | HG03831.hp2 HG03942.hp1 NA18947.hp2 others(2): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(2): Show | a0001c0001t0001g0013a0001c0001t0002g0019a0001c0001t0003g0088others(2): Show | 5 | 230 | 0.0217 | -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 | 12918059 | TCTC | T | intron_variant | MODIFIER | HG01884.hp1 HG02145.hp1 HG02572.hp1 |
a0001 | a0001c0001a0001c0008 | a0001c0001t0001a0001c0001t0010a0001c0008t0020 | a0001c0001t0001g0183a0001c0001t0010g0182a0001c0008t0020g0181 | 3 | 230 | 0.0130 | -3 | c.388 others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 5/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12967249 | CTTT | C | intron_variant | MODIFIER | HG01106.hp2 HG01192.hp1 HG01891.hp1 others(20): Show |
a0001 | a0001c0001a0001c0003a0001c0005others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(9): Show | a0001c0001t0001g0005a0001c0001t0001g0009a0001c0001t0001g0027others(20): Show | 23 | 230 | 0.1000 | -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 | 12970365 | CAAA | C | intron_variant | MODIFIER | HG02258.hp1 HG02647.hp2 HG03209.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(1): Show | a0001c0001t0001g0030a0001c0001t0003g0076a0001c0001t0009g0096others(2): Show | 5 | 230 | 0.0217 | -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 | 12978694 | TTTC | T | intron_variant | MODIFIER | HG00639.hp2 HG00642.hp2 HG00738.hp1 others(63): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(20): Show | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0020others(63): Show | 66 | 230 | 0.2870 | -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 | 12981400 | CTTT | C | intron_variant | MODIFIER | HG00673.hp2 HG03942.hp1 NA18942.hp2 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0004a0001c0001t0011others(1): Show | a0001c0001t0003g0088a0001c0001t0004g0002a0001c0001t0004g0004others(8): Show | 11 | 230 | 0.0478 | -3 | c.193 others(22): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 19/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12989100 | CCAA | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0013 | a0001c0001t0006g0024a0001c0001t0006g0097a0001c0001t0006g0099others(7): Show | 10 | 230 | 0.0435 | -3 | c.231 others(20): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 20/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12991792 | CTCT | C | downstream_gene_variant | MODIFIER | HG00639.hp2 HG00738.hp1 HG01070.hp2 others(11): Show |
a0001a0005 | a0001c0001a0001c0003a0005c0013 | a0001c0001t0001a0001c0001t0003a0001c0001t0027others(2): Show | a0001c0001t0001g0041a0001c0001t0001g0094a0001c0001t0001g0111others(11): Show | 14 | 230 | 0.0609 | -3 | c.*16 others(14): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 150 | chr17 | TogoVar | ||||||
ARHGAP45_chr19_1062167_1091628 | 1075034 | CCAA | C | intron_variant | MODIFIER | HG00438.hp1 HG00609.hp2 HG01891.hp1 others(35): Show |
a0002a0011a0012 | a0002c0001a0002c0015a0002c0019others(5): Show | a0002c0001t0004a0002c0015t0001a0002c0019t0009others(5): Show | a0002c0001t0004g0006a0002c0001t0004g0010a0002c0001t0004g0033others(26): Show | 38 | 418 | 0.0909 | -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 | 1076483 | CTTT | C | intron_variant | MODIFIER | HG00438.hp1 HG00609.hp2 HG01934.hp1 others(21): Show |
a0002a0009a0022 | a0002c0001a0002c0015a0002c0031others(4): Show | a0002c0001t0004a0002c0015t0001a0002c0031t0004others(4): Show | a0002c0001t0004g0006a0002c0001t0004g0010a0002c0001t0004g0032others(14): Show | 24 | 418 | 0.0574 | -3 | c.118 others(22): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP45_chr19_1062167_1091628 | 1086993 | ATTT | A | downstream_gene_variant | MODIFIER | HG02257.hp2 HG02615.hp1 HG02622.hp1 others(4): Show |
a0001a0003a0004others(2): Show | a0001c0002a0001c0036a0003c0040others(3): Show | a0001c0002t0001a0001c0036t0026a0003c0040t0028others(3): Show | a0001c0002t0001g0018a0001c0036t0026g0304a0003c0040t0028g0144others(3): Show | 7 | 418 | 0.0168 | -3 | c.*98 others(12): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 366 | chr19 | TogoVar | ||||||
ARHGAP45_chr19_1062167_1091628 | 1088889 | CAGT | C | downstream_gene_variant | MODIFIER | HG01106.hp2 HG01109.hp1 HG01192.hp2 others(15): Show |
a0001a0004 | a0001c0004a0001c0017a0004c0005 | a0001c0004t0006a0001c0017t0006a0004c0005t0008 | a0001c0004t0006g0015a0001c0004t0006g0016a0001c0004t0006g0017others(9): Show | 18 | 418 | 0.0431 | -3 | c.*28 others(14): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 2262 | chr19 | TogoVar | ||||||
ARHGAP5_chr14_32072304_32164728 | 32123582 | GCTT | G | intron_variant | MODIFIER | HG00609.hp2 HG02809.hp1 |
a0009a0013 | a0009c0014a0013c0017 | a0009c0014t0015a0013c0017t0016 | a0009c0014t0015g0159a0013c0017t0016g0005 | 2 | 186 | 0.0108 | -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 | 32143202 | AGTT | A | intron_variant | MODIFIER | HG02132.hp1 HG03130.hp2 HG03516.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0048a0001c0001t0001g0049a0001c0001t0001g0050others(2): Show | 5 | 186 | 0.0269 | -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 | 32143239 | GTTA | G | intron_variant | MODIFIER | HG01255.hp2 HG02698.hp1 HG02965.hp2 others(3): Show |
a0001a0007 | a0001c0001a0007c0013 | a0001c0001t0001a0007c0013t0018 | a0001c0001t0001g0002a0001c0001t0001g0028a0001c0001t0001g0068others(2): Show | 6 | 186 | 0.0323 | -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 | 32153406 | CAAA | C | intron_variant | MODIFIER | HG00609.hp1 HG01169.hp2 HG01192.hp2 others(17): Show |
a0001a0003 | a0001c0001a0001c0019a0003c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(3): Show | a0001c0001t0001g0008a0001c0001t0001g0012a0001c0001t0001g0013others(17): Show | 20 | 186 | 0.1075 | -3 | c.418 others(20): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
ARHGAP5_chr14_32072304_32164728 | 32161233 | TCAA | T | downstream_gene_variant | MODIFIER | HG00609.hp1 HG02129.hp1 NA19000.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0037a0001c0001t0001g0041a0001c0001t0001g0086 | 3 | 186 | 0.0161 | -3 | c.*62 others(14): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 1506 | chr14 | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11166798 | TAGA | T | intron_variant | MODIFIER | HG02258.hp1 HG02451.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0018 | a0001c0001t0001g0020a0002c0002t0018g0029 | 2 | 144 | 0.0139 | -3 | c.180 others(22): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 9/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11167655 | CGAT | C | 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 |