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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP27_chr17_45388908_45437870 | 45432378 | TGGGGAAG others(6): Show |
T | intron_variant | MODIFIER | NA18983.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0157 | 1 | 347 | 0.0029 | -13 | c.-28 others(28): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 1/19 | chr17 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6841157 | TTCTCTCT others(6): Show |
T | intron_variant | MODIFIER | HG02922.hp1 HG03579.hp2 |
a0001a0002 | a0001c0003a0002c0017 | a0001c0003t0003a0002c0017t0002 | a0001c0003t0003g0119a0002c0017t0002g0086 | 2 | 248 | 0.0081 | -13 | c.543 others(30): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6841197 | CTCTCTCC others(6): Show |
C | intron_variant | MODIFIER | HG00438.hp1 HG01346.hp2 HG01943.hp2 others(5): Show |
a0001a0002a0003others(1): Show | a0001c0003a0002c0002a0003c0004others(1): Show | a0001c0003t0003a0002c0002t0002a0003c0004t0001others(1): Show | a0001c0003t0003g0013a0001c0003t0003g0201a0002c0002t0002g0083others(5): Show | 8 | 248 | 0.0323 | -13 | c.543 others(30): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161064842 | AAAGAAAG others(6): Show |
A | intron_variant | MODIFIER | HG00323.hp1 HG00423.hp2 HG00738.hp1 others(10): Show |
a0002 | a0002c0002 | a0002c0002t0001a0002c0002t0004 | a0002c0002t0001g0266a0002c0002t0001g0268a0002c0002t0001g0274others(10): Show | 13 | 390 | 0.0333 | -13 | c.97+ others(28): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161066644 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG02273.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0011 | 1 | 390 | 0.0026 | -13 | c.97+ others(28): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161073084 | AGCAGAGA others(6): Show |
A | upstream_gene_variant | MODIFIER | HG00099.hp2 HG00741.hp2 HG01071.hp2 others(26): Show |
a0001a0002a0008 | a0001c0001a0001c0014a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(3): Show | a0001c0001t0001g0002a0001c0001t0001g0074a0001c0001t0001g0076others(25): Show | 29 | 390 | 0.0744 | -13 | c.-34 others(24): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 3194 | chr1 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119303788 | TGTTGTTG others(6): Show |
T | intron_variant | MODIFIER | HG02083.hp1 HG02129.hp1 HG02523.hp1 others(7): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0011a0001c0001t0017a0001c0001t0046others(4): Show | a0001c0001t0011g0300a0001c0001t0011g0301a0001c0001t0017g0175others(7): Show | 10 | 310 | 0.0323 | -13 | c.100 others(30): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119350784 | AGCTGGGG others(6): Show |
A | intron_variant | MODIFIER | NA19060.hp1 | a0001 | a0001c0001 | a0001c0001t0046 | a0001c0001t0046g0307 | 1 | 310 | 0.0032 | -13 | c.101 others(32): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | chr3 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129002957 | CGCCACTA others(6): Show |
C | intron_variant | MODIFIER | HG01123.hp1 HG06807.hp1 |
a0001 | a0001c0003 | a0001c0003t0005 | a0001c0003t0005g0384a0001c0003t0005g0385 | 2 | 398 | 0.0050 | -13 | c.104 others(32): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 11/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129038810 | CCTGGAGT others(6): Show |
C | intron_variant | MODIFIER | NA18955.hp2 NA19002.hp1 |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0183a0001c0001t0004g0184 | 2 | 398 | 0.0050 | -13 | c.104 others(32): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 11/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129051953 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG00558.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0269 | 1 | 398 | 0.0025 | -13 | c.963 others(32): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 10/22 | chr11 | TogoVar | ||||||
ARHGAP33_chr19_35770564_35793822 | 35773965 | CTTTTTTT others(6): Show |
C | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00408.hp1 others(117): Show |
a0001a0002a0004others(4): Show | a0001c0001a0001c0004a0001c0005others(9): Show | a0001c0001t0001a0001c0004t0001a0001c0005t0001others(9): Show | a0001c0001t0001g0002a0001c0001t0001g0004a0001c0001t0001g0007others(31): Show | 120 | 420 | 0.2857 | -13 | c.-16 others(24): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1598 | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46862908 | ATTACGAT others(6): Show |
A | intron_variant | MODIFIER | NA19062.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0264 | 1 | 298 | 0.0034 | -13 | c.-18 others(32): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46983054 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG01891.hp1 HG02622.hp2 HG02647.hp1 others(2): Show |
a0001a0005 | a0001c0001a0005c0012 | a0001c0001t0011a0005c0012t0011 | a0001c0001t0011g0056a0001c0001t0011g0057a0001c0001t0011g0058others(2): Show | 5 | 298 | 0.0168 | -13 | c.382 others(32): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 47006267 | CTTTTTTT others(6): Show |
C | downstream_gene_variant | MODIFIER | HG02071.hp2 NA18943.hp2 |
a0001 | a0001c0001 | a0001c0001t0007a0001c0001t0046 | a0001c0001t0007g0042a0001c0001t0046g0043 | 2 | 298 | 0.0067 | -13 | c.*55 others(24): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1191 | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 47007643 | CTTTTTTT others(6): Show |
C | downstream_gene_variant | MODIFIER | HG01070.hp1 HG01071.hp2 HG02145.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0019a0001c0001t0029a0001c0001t0042 | a0001c0001t0019g0024a0001c0001t0019g0219a0001c0001t0029g0025others(1): Show | 4 | 298 | 0.0134 | -13 | c.*69 others(24): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2567 | chr19 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100699506 | ATTTTTTT others(6): Show |
A | intron_variant | MODIFIER | HG04199.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0177 | 1 | 286 | 0.0035 | -13 | c.154 others(32): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100769712 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | HG03834.hp2 | a0005 | a0005c0016 | a0005c0016t0012 | a0005c0016t0012g0103 | 1 | 286 | 0.0035 | -13 | c.155 others(28): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921237 | ATATATAT others(6): Show |
A | intron_variant | MODIFIER | HG00642.hp1 | a0002 | a0002c0002 | a0002c0002t0005 | a0002c0002t0005g0105 | 1 | 286 | 0.0035 | -13 | c.487 others(28): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921239 | ATATATAT others(6): Show |
A | intron_variant | MODIFIER | HG03669.hp1 NA20752.hp1 |
a0002 | a0002c0002 | a0002c0002t0004a0002c0002t0006 | a0002c0002t0004g0107a0002c0002t0006g0057 | 2 | 286 | 0.0070 | -13 | c.487 others(28): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921241 | ATATATTT others(6): Show |
A | intron_variant | MODIFIER | HG01358.hp2 HG02922.hp1 HG02976.hp2 |
a0002 | a0002c0002 | a0002c0002t0002a0002c0002t0020 | a0002c0002t0002g0245a0002c0002t0002g0246a0002c0002t0020g0104 | 3 | 286 | 0.0105 | -13 | c.487 others(28): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12802946 | TATATATA others(6): Show |
T | intron_variant | MODIFIER | NA18963.hp2 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0083 | 1 | 230 | 0.0044 | -13 | c.53+ others(30): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12802948 | TATATATA others(6): Show |
T | intron_variant | MODIFIER | HG02258.hp2 HG02886.hp2 HG03471.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0014 | a0001c0001t0003g0028a0001c0001t0003g0079a0001c0001t0014g0179 | 3 | 230 | 0.0130 | -13 | c.53+ others(30): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12802950 | TATATATA others(6): Show |
T | intron_variant | MODIFIER | HG01891.hp1 | a0001 | a0001c0001 | a0001c0001t0033 | a0001c0001t0033g0029 | 1 | 230 | 0.0044 | -13 | c.53+ others(30): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12802952 | TATATATA others(6): Show |
T | intron_variant | MODIFIER | NA19007.hp2 NA19054.hp1 |
a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0053a0001c0002t0003g0054 | 2 | 230 | 0.0087 | -13 | c.53+ others(30): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12802954 | TATATATA others(6): Show |
T | intron_variant | MODIFIER | HG02559.hp2 HG02630.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0033a0001c0003t0001g0032 | 2 | 230 | 0.0087 | -13 | c.53+ others(30): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12802956 | TATATATA others(6): Show |
T | intron_variant | MODIFIER | HG00673.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0010 | 1 | 230 | 0.0044 | -13 | c.53+ others(30): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12802957 | ATATATAT others(6): Show |
A | intron_variant | MODIFIER | NA18947.hp2 NA18963.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0013a0001c0001t0004g0014 | 2 | 230 | 0.0087 | -13 | c.53+ others(30): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12860085 | AAAGGCAT others(6): Show |
A | intron_variant | MODIFIER | HG00423.hp2 HG00733.hp1 HG01070.hp1 others(36): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(13): Show | a0001c0001t0001g0001a0001c0001t0001g0033a0001c0001t0001g0124others(36): Show | 39 | 230 | 0.1696 | -13 | c.54- others(30): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12952722 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | NA18906.hp2 | a0001 | a0001c0005 | a0001c0005t0007 | a0001c0005t0007g0039 | 1 | 230 | 0.0044 | -13 | c.113 others(30): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12964466 | TGGAGAAG others(6): Show |
T | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(18): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006a0001c0001t0010others(2): Show | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0020others(18): Show | 21 | 230 | 0.0913 | -13 | c.152 others(32): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12967249 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00642.hp1 others(19): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0006a0001c0001t0010others(3): Show | a0001c0001t0001g0001a0001c0001t0001g0017a0001c0001t0001g0020others(19): Show | 22 | 230 | 0.0957 | -13 | c.152 others(32): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 16/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12975795 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG01981.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0023 | 1 | 230 | 0.0044 | -13 | c.176 others(32): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 18/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12986673 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG02602.hp1 HG02698.hp2 HG03491.hp1 others(1): Show |
a0001a0003 | a0001c0001a0003c0017 | a0001c0001t0001a0001c0001t0003a0003c0017t0003 | a0001c0001t0001g0017a0001c0001t0001g0158a0001c0001t0003g0172others(1): Show | 4 | 230 | 0.0174 | -13 | c.231 others(32): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12991856 | CTTACTTA others(6): Show |
C | downstream_gene_variant | MODIFIER | HG02257.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0132 | 1 | 230 | 0.0044 | -13 | c.*16 others(24): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 214 | chr17 | TogoVar | ||||||
ARHGAP5_chr14_32072304_32164728 | 32153406 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG02809.hp1 | a0013 | a0013c0017 | a0013c0017t0016 | a0013c0017t0016g0005 | 1 | 186 | 0.0054 | -13 | c.418 others(30): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
ARHGAP6_chrX_11132544_11670920 | 11163599 | ACACTAAA others(6): Show |
A | intron_variant | MODIFIER | NA18955.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0122 | 1 | 144 | 0.0069 | -13 | c.180 others(32): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 9/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11174612 | CTTTCTCT others(6): Show |
C | intron_variant | MODIFIER | HG02055.hp1 HG02809.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0015a0001c0003t0001 | a0001c0001t0015g0050a0001c0003t0001g0125 | 2 | 144 | 0.0139 | -13 | c.162 others(32): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44809069 | CCTCAGCC others(6): Show |
C | intron_variant | MODIFIER | HG02165.hp2 HG02965.hp1 HG03098.hp1 |
a0001a0002a0006 | a0001c0008a0002c0046a0006c0030 | a0001c0008t0001a0002c0046t0007a0006c0030t0001 | a0001c0008t0001g0057a0002c0046t0007g0231a0006c0030t0001g0105 | 3 | 390 | 0.0077 | -13 | c.299 others(28): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 4/11 | chr22 | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44854024 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG06807.hp2 NA18906.hp1 |
a0001 | a0001c0001a0001c0024 | a0001c0001t0003a0001c0024t0003 | a0001c0001t0003g0063a0001c0024t0003g0064 | 2 | 390 | 0.0051 | -13 | c.877 others(30): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44856254 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | HG02129.hp1 HG03704.hp1 HG03831.hp1 others(4): Show |
a0002 | a0002c0003a0002c0006a0002c0016others(1): Show | a0002c0003t0004a0002c0006t0004a0002c0016t0004others(1): Show | a0002c0003t0004g0055a0002c0003t0004g0180a0002c0003t0004g0351others(4): Show | 7 | 390 | 0.0180 | -13 | c.878 others(30): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44858692 | AGGCTATG others(6): Show |
A | intron_variant | MODIFIER | NA18961.hp2 | a0003 | a0003c0002 | a0003c0002t0002 | a0003c0002t0002g0026 | 1 | 390 | 0.0026 | -13 | c.878 others(30): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | chr22 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17693079 | CCTTGTTT others(6): Show |
C | intron_variant | MODIFIER | HG03130.hp2 | a0002 | a0002c0018 | a0002c0018t0002 | a0002c0018t0002g0155 | 1 | 168 | 0.0060 | -13 | c.318 others(32): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 27/28 | chr1 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1825177 | CCTGTCCC others(6): Show |
C | intron_variant | MODIFIER | HG01192.hp1 | a0001 | a0001c0009 | a0001c0009t0005 | a0001c0009t0005g0287 | 1 | 363 | 0.0028 | -13 | c.-48 others(30): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF11_chr1_156929840_157050742 | 156962878 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG02132.hp1 HG02135.hp1 |
a0003 | a0003c0003 | a0003c0003t0003 | a0003c0003t0003g0252a0003c0003t0003g0253 | 2 | 362 | 0.0055 | -13 | c.114 others(30): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 13/40 | chr1 | TogoVar | ||||||
ARHGEF11_chr1_156929840_157050742 | 157035818 | AGGAATAT others(6): Show |
A | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(168): Show |
a0001a0002a0003others(4): Show | a0001c0001a0002c0002a0002c0004others(6): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(21): Show | a0001c0001t0001g0332a0001c0001t0001g0333a0001c0001t0001g0334others(167): Show | 171 | 362 | 0.4724 | -13 | c.32+ others(28): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120344265 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG02922.hp2 HG03195.hp1 |
a0001 | a0001c0001 | a0001c0001t0018 | a0001c0001t0018g0280a0001c0001t0018g0281 | 2 | 308 | 0.0065 | -13 | c.32+ others(28): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120351438 | TATATATA others(6): Show |
T | intron_variant | MODIFIER | HG01099.hp1 | a0001 | a0001c0002 | a0001c0002t0034 | a0001c0002t0034g0013 | 1 | 308 | 0.0033 | -13 | c.32+ others(30): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | chr11 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120399321 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG02451.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0133 | 1 | 308 | 0.0033 | -13 | c.33- others(28): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF16_chr1_3449665_3486113 | 3485931 | CAAAAAAA others(6): Show |
C | downstream_gene_variant | MODIFIER | HG03209.hp1 HG03225.hp1 |
a0002 | a0002c0011a0002c0012 | a0002c0011t0002a0002c0012t0010 | a0002c0011t0002g0288a0002c0012t0010g0277 | 2 | 334 | 0.0060 | -13 | c.*53 others(24): Show |
ARHGEF16 | ENSG00000130762.15 | transcript | ENST00000378378.9 | protein_coding | 4819 | chr1 | TogoVar |