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 | 100699504 | ATATTTTT others(7): Show |
A | intron_variant | MODIFIER | HG01433.hp1 NA18991.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0213a0002c0002t0001g0012 | 2 | 286 | 0.0070 | -14 | c.154 others(33): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100714389 | TTGTGTGT others(7): Show |
T | intron_variant | MODIFIER | HG02970.hp1 | a0002 | a0002c0002 | a0002c0002t0040 | a0002c0002t0040g0101 | 1 | 286 | 0.0035 | -14 | c.154 others(33): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100728713 | CGTATATA others(7): Show |
C | intron_variant | MODIFIER | HG03579.hp2 NA19043.hp1 NA19054.hp2 others(2): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0002c0002t0028 | a0001c0001t0001g0002a0001c0001t0001g0026a0001c0001t0001g0200others(2): Show | 5 | 286 | 0.0175 | -14 | c.154 others(33): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100728714 | GTATATAT others(7): Show |
G | intron_variant | MODIFIER | HG01243.hp2 | a0002 | a0002c0002 | a0002c0002t0029 | a0002c0002t0029g0227 | 1 | 286 | 0.0035 | -14 | c.154 others(33): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100751773 | CTTTTTTT others(7): Show |
C | intron_variant | MODIFIER | HG01346.hp1 HG02257.hp2 HG02896.hp1 |
a0002 | a0002c0002 | a0002c0002t0002a0002c0002t0008 | a0002c0002t0002g0010a0002c0002t0008g0009a0002c0002t0008g0230 | 3 | 286 | 0.0105 | -14 | c.155 others(33): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100794075 | CAAAAAAA others(7): Show |
C | intron_variant | MODIFIER | HG01433.hp1 HG02056.hp2 HG02083.hp2 others(6): Show |
a0001a0002 | a0001c0001a0001c0008a0002c0002 | a0001c0001t0001a0001c0008t0001a0002c0002t0001others(2): Show | a0001c0001t0001g0197a0001c0008t0001g0187a0002c0002t0001g0012others(6): Show | 9 | 286 | 0.0315 | -14 | c.251 others(30): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100875099 | CTCTCTCT others(7): Show |
C | intron_variant | MODIFIER | HG01433.hp1 HG02280.hp1 HG02615.hp2 others(3): Show |
a0001a0002 | a0001c0003a0002c0002 | a0001c0003t0003a0002c0002t0001a0002c0002t0002 | a0001c0003t0003g0219a0002c0002t0001g0012a0002c0002t0001g0013others(3): Show | 6 | 286 | 0.0210 | -14 | c.384 others(33): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100875101 | CTCTCTCT others(7): Show |
C | intron_variant | MODIFIER | HG02071.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0185 | 1 | 286 | 0.0035 | -14 | c.384 others(33): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100875107 | CTGTGTGT others(7): Show |
C | intron_variant | MODIFIER | HG04199.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0177 | 1 | 286 | 0.0035 | -14 | c.384 others(33): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100903709 | AATATATA others(7): Show |
A | intron_variant | MODIFIER | HG00639.hp1 HG02083.hp1 HG02486.hp1 others(7): Show |
a0001a0006 | a0001c0001a0001c0010a0001c0012others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0031others(4): Show | a0001c0001t0001g0062a0001c0001t0001g0126a0001c0001t0001g0184others(7): Show | 10 | 286 | 0.0350 | -14 | 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 | 100921235 | ATATATAT others(7): Show |
A | intron_variant | MODIFIER | HG01361.hp2 HG02965.hp2 |
a0002 | a0002c0002 | a0002c0002t0005a0002c0002t0009 | a0002c0002t0005g0111a0002c0002t0009g0037 | 2 | 286 | 0.0070 | -14 | c.487 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921237 | ATATATAT others(7): Show |
A | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00639.hp2 others(4): Show |
a0002 | a0002c0002 | a0002c0002t0002a0002c0002t0005a0002c0002t0009 | a0002c0002t0002g0252a0002c0002t0005g0048a0002c0002t0005g0049others(4): Show | 7 | 286 | 0.0245 | -14 | c.487 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921239 | ATATATAT others(7): Show |
A | intron_variant | MODIFIER | HG01109.hp1 NA20129.hp2 |
a0002 | a0002c0002 | a0002c0002t0005a0002c0002t0020 | a0002c0002t0005g0110a0002c0002t0020g0106 | 2 | 286 | 0.0070 | -14 | c.487 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12788456 | TTTTTCTT others(7): Show |
T | upstream_gene_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG01884.hp2 others(6): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(3): Show | a0001c0001t0001g0030a0001c0001t0002g0167a0001c0001t0006g0168others(6): Show | 9 | 230 | 0.0391 | -14 | c.-13 others(25): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1041 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12802927 | TTATATAT others(7): Show |
T | intron_variant | MODIFIER | HG00735.hp1 HG01074.hp2 HG01891.hp2 others(15): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(6): Show | a0001c0001t0001g0030a0001c0001t0001g0227a0001c0001t0001g0228others(15): Show | 18 | 230 | 0.0783 | -14 | c.53+ others(31): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12849568 | CTTTTTTT others(7): Show |
C | intron_variant | MODIFIER | NA18968.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0128 | 1 | 230 | 0.0044 | -14 | c.54- others(31): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12868589 | TTTTATAT others(7): Show |
T | intron_variant | MODIFIER | HG01934.hp1 HG02132.hp1 HG02970.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(5): Show | a0001c0001t0001g0124a0001c0001t0003g0078a0001c0001t0003g0164others(7): Show | 10 | 230 | 0.0435 | -14 | c.54- others(31): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12903083 | TGAGAGAG others(7): Show |
T | intron_variant | MODIFIER | HG00639.hp1 HG01258.hp2 HG02109.hp2 others(5): Show |
a0001 | a0001c0001a0001c0003a0001c0004others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0013others(4): Show | a0001c0001t0001g0193a0001c0001t0003g0065a0001c0001t0013g0161others(5): Show | 8 | 230 | 0.0348 | -14 | c.199 others(31): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12903140 | AGTGTGTG others(7): Show |
A | intron_variant | MODIFIER | HG03225.hp1 | a0001 | a0001c0001 | a0001c0001t0012 | a0001c0001t0012g0095 | 1 | 230 | 0.0044 | -14 | c.199 others(31): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12931841 | TACACACA others(7): Show |
T | intron_variant | MODIFIER | HG01884.hp1 HG02145.hp1 HG02572.hp1 others(4): Show |
a0001 | a0001c0001a0001c0008 | a0001c0001t0001a0001c0001t0010a0001c0008t0020 | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0138others(4): Show | 7 | 230 | 0.0304 | -14 | c.582 others(31): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP45_chr19_1062167_1091628 | 1066626 | AGACGGAC others(7): Show |
A | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00438.hp1 HG00609.hp2 others(94): Show |
a0002a0003a0004others(11): Show | a0002c0001a0002c0015a0002c0019others(27): Show | a0002c0001t0004a0002c0001t0005a0002c0001t0016others(33): Show | a0002c0001t0004g0006a0002c0001t0004g0010a0002c0001t0004g0032others(79): Show | 97 | 418 | 0.2321 | -14 | c.-77 others(23): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 540 | chr19 | TogoVar | ||||||
ARHGAP45_chr19_1062167_1091628 | 1076483 | CTTTTTTT others(7): Show |
C | intron_variant | MODIFIER | HG03130.hp1 | a0001 | a0001c0036 | a0001c0036t0026 | a0001c0036t0026g0304 | 1 | 418 | 0.0024 | -14 | c.118 others(33): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP4_chrX_153902378_153931264 | 153930827 | TTGGGCTC others(7): Show |
T | upstream_gene_variant | MODIFIER | NA18942.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 1 | 308 | 0.0033 | -14 | c.-46 others(25): Show |
ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 4564 | chrX | TogoVar | ||||||
ARHGAP5_chr14_32072304_32164728 | 32153406 | CAAAAAAA others(7): Show |
C | intron_variant | MODIFIER | NA21309.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0089 | 1 | 186 | 0.0054 | -14 | c.418 others(31): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
ARHGAP6_chrX_11132544_11670920 | 11201989 | CTGTGTGT others(7): Show |
C | intron_variant | MODIFIER | HG01074.hp1 HG01243.hp1 HG02717.hp1 others(2): Show |
a0001a0002 | a0001c0001a0001c0004a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0004t0005others(1): Show | a0001c0001t0001g0114a0001c0001t0002g0136a0001c0004t0005g0015others(2): Show | 5 | 144 | 0.0347 | -14 | c.749 others(31): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 2/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11241531 | CGTGTGTG others(7): Show |
C | intron_variant | MODIFIER | HG02258.hp1 HG02451.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0018 | a0001c0001t0001g0020a0002c0002t0018g0029 | 2 | 144 | 0.0139 | -14 | c.748 others(33): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 2/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11320766 | TACACACA others(7): Show |
T | intron_variant | MODIFIER | HG03516.hp1 | a0002 | a0002c0002 | a0002c0002t0009 | a0002c0002t0009g0127 | 1 | 144 | 0.0069 | -14 | c.589 others(33): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11353549 | AGTGTGTG others(7): Show |
A | intron_variant | MODIFIER | NA20129.hp1 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0012 | 1 | 144 | 0.0069 | -14 | c.589 others(33): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11354323 | CTCTCTAT others(7): Show |
C | intron_variant | MODIFIER | NA19070.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0097 | 1 | 144 | 0.0069 | -14 | c.589 others(33): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11411183 | TTATATAT others(7): Show |
T | intron_variant | MODIFIER | HG01433.hp1 HG02647.hp1 HG02735.hp1 others(1): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0002c0002t0003 | a0001c0001t0001g0054a0001c0001t0002g0129a0002c0002t0003g0012others(1): Show | 4 | 144 | 0.0278 | -14 | c.589 others(35): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11417059 | CATATATA others(7): Show |
C | intron_variant | MODIFIER | HG01358.hp1 HG02015.hp1 HG02027.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0015 | a0001c0001t0001g0033a0001c0001t0001g0041a0001c0001t0001g0058others(5): Show | 8 | 144 | 0.0556 | -14 | c.589 others(35): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11502710 | GATTTTCT others(7): Show |
G | intron_variant | MODIFIER | HG01106.hp1 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0030 | 1 | 144 | 0.0069 | -14 | c.588 others(35): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11520131 | TTATATAT others(7): Show |
T | intron_variant | MODIFIER | HG00140.hp1 HG00673.hp1 HG03710.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0036a0001c0001t0001g0038a0001c0001t0001g0039others(3): Show | 6 | 144 | 0.0417 | -14 | c.588 others(35): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11527011 | AGTGTGTG others(7): Show |
A | intron_variant | MODIFIER | HG01167.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0132 | 1 | 144 | 0.0069 | -14 | c.588 others(35): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11605541 | TGAGTACA others(7): Show |
T | intron_variant | MODIFIER | HG06807.hp2 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0013 | 1 | 144 | 0.0069 | -14 | c.588 others(33): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11660530 | CAAAAAAA others(7): Show |
C | intron_variant | MODIFIER | HG00140.hp1 NA18953.hp1 NA18960.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0062a0001c0001t0001g0063a0001c0001t0001g0064others(1): Show | 4 | 144 | 0.0278 | -14 | c.588 others(31): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44772223 | CTTTTTTT others(7): Show |
C | intron_variant | MODIFIER | HG01891.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0017 | 1 | 390 | 0.0026 | -14 | c.-71 others(33): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44829118 | CAAAAAAA others(7): Show |
C | intron_variant | MODIFIER | NA18993.hp1 NA18993.hp2 NA19011.hp2 |
a0001a0003a0019 | a0001c0008a0003c0002a0019c0045 | a0001c0008t0003a0003c0002t0002a0019c0045t0004 | a0001c0008t0003g0299a0003c0002t0002g0345a0019c0045t0004g0295 | 3 | 390 | 0.0077 | -14 | c.596 others(31): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44851606 | CTTGAGTC others(7): Show |
C | intron_variant | MODIFIER | HG00280.hp1 HG00323.hp1 HG01257.hp1 others(1): Show |
a0001a0003 | a0001c0007a0003c0002 | a0001c0007t0001a0003c0002t0002 | a0001c0007t0001g0140a0003c0002t0002g0272a0003c0002t0002g0273others(1): Show | 4 | 390 | 0.0103 | -14 | c.877 others(31): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44856254 | CTTTTTTT others(7): Show |
C | intron_variant | MODIFIER | HG00544.hp1 HG00609.hp1 HG00609.hp2 others(60): Show |
a0002a0005a0010others(2): Show | a0002c0003a0002c0006a0002c0011others(9): Show | a0002c0003t0003a0002c0003t0004a0002c0006t0004others(10): Show | a0002c0003t0003g0276a0002c0003t0004g0002a0002c0003t0004g0011others(60): Show | 63 | 390 | 0.1615 | -14 | c.878 others(31): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGDIG_chr16_275591_288010 | 286215 | CCACCGCC others(7): Show |
C | downstream_gene_variant | MODIFIER | NA18940.hp1 NA18956.hp2 NA18971.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0001 | 4 | 442 | 0.0091 | -14 | c.*34 others(25): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 3206 | chr16 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1888397 | CAGTGGGG others(7): Show |
C | intron_variant | MODIFIER | HG01975.hp2 | a0002 | a0002c0025 | a0002c0025t0024 | a0002c0025t0024g0106 | 1 | 363 | 0.0028 | -14 | c.118 others(33): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | chr8 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 156954380 | CAAAAAAA others(7): Show |
C | intron_variant | MODIFIER | HG02280.hp2 HG03041.hp1 HG03209.hp2 others(3): Show |
a0002a0003 | a0002c0004a0003c0003 | a0002c0004t0005a0002c0004t0026a0003c0003t0006 | a0002c0004t0005g0015a0002c0004t0005g0105a0002c0004t0005g0107others(3): Show | 6 | 362 | 0.0166 | -14 | c.179 others(31): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 21/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 157040310 | CAGCTAAA others(7): Show |
C | intron_variant | MODIFIER | NA18951.hp2 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0110 | 1 | 362 | 0.0028 | -14 | c.32+ others(29): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120334863 | GTATATAT others(7): Show |
G | upstream_gene_variant | MODIFIER | HG00597.hp2 HG00738.hp1 HG02145.hp2 others(11): Show |
a0001 | a0001c0002a0001c0004a0001c0006 | a0001c0002t0003a0001c0002t0019a0001c0004t0005others(1): Show | a0001c0002t0003g0028a0001c0002t0003g0029a0001c0002t0003g0062others(11): Show | 14 | 308 | 0.0455 | -14 | c.-23 others(25): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1549 | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120347266 | CTGTCTGT others(7): Show |
C | intron_variant | MODIFIER | HG00735.hp2 HG00738.hp1 HG01123.hp1 others(50): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0001c0006others(2): Show | a0001c0001t0002a0001c0001t0006a0001c0001t0007others(11): Show | a0001c0001t0002g0019a0001c0001t0002g0102a0001c0001t0002g0124others(50): Show | 53 | 308 | 0.1721 | -14 | c.32+ others(30): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF15_chr17_8305241_8327511 | 8326050 | GGCATTAC others(7): Show |
G | downstream_gene_variant | MODIFIER | HG02970.hp1 | a0004 | a0004c0005 | a0004c0005t0003 | a0004c0005t0003g0009 | 1 | 428 | 0.0023 | -14 | c.*50 others(25): Show |
ARHGEF15 | ENSG00000198844.12 | transcript | ENST00000361926.8 | protein_coding | 3540 | chr17 | TogoVar | ||||||
ARHGEF16_chr1_3449665_3486113 | 3470301 | GGTGTCTG others(7): Show |
G | intron_variant | MODIFIER | HG01123.hp2 HG01243.hp1 HG01261.hp1 others(19): Show |
a0002a0012a0013 | a0002c0003a0002c0022a0012c0031others(1): Show | a0002c0003t0002a0002c0022t0002a0012c0031t0002others(1): Show | a0002c0003t0002g0002a0002c0003t0002g0004a0002c0003t0002g0005others(10): Show | 22 | 334 | 0.0659 | -14 | c.102 others(31): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARHGEF16_chr1_3449665_3486113 | 3471083 | GGGGTGTG others(7): Show |
G | intron_variant | MODIFIER | HG02809.hp2 HG02965.hp2 HG03098.hp2 |
a0002 | a0002c0014 | a0002c0014t0006 | a0002c0014t0006g0009a0002c0014t0006g0088 | 3 | 334 | 0.0090 | -14 | c.102 others(33): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARHGEF16_chr1_3449665_3486113 | 3471109 | CCTGGGCA others(7): Show |
C | intron_variant | MODIFIER | HG02074.hp1 | a0002 | a0002c0002 | a0002c0002t0003 | a0002c0002t0003g0037 | 1 | 334 | 0.0030 | -14 | c.102 others(33): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 6/14 | chr1 | TogoVar |