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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP20_chr11_110572043_110717437 | 110648210 | AATATATA others(9): Show |
A | intron_variant | MODIFIER | HG02273.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0109 | 1 | 226 | 0.0044 | -16 | c.189 others(35): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24622433 | CATATATA others(9): Show |
C | intron_variant | MODIFIER | HG00423.hp1 HG00438.hp2 HG00609.hp1 others(40): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0174a0001c0001t0001g0181a0001c0001t0001g0183others(40): Show | 43 | 352 | 0.1222 | -16 | c.525 others(31): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24628952 | CTATATAT others(9): Show |
C | intron_variant | MODIFIER | HG02257.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0192 | 1 | 352 | 0.0028 | -16 | c.495 others(33): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24695050 | CAAAAAAA others(9): Show |
C | intron_variant | MODIFIER | HG01891.hp2 HG02523.hp2 HG03209.hp1 others(1): Show |
a0001a0005a0007 | a0001c0001a0001c0014a0005c0005others(1): Show | a0001c0001t0001a0001c0014t0004a0005c0005t0004others(1): Show | a0001c0001t0001g0171a0001c0014t0004g0286a0005c0005t0004g0287others(1): Show | 4 | 352 | 0.0114 | -16 | c.64- others(33): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | TogoVar | ||||||
ARHGAP22_chr10_48441036_48610073 | 48450049 | GCTGACTG others(9): Show |
G | intron_variant | MODIFIER | HG00735.hp1 HG02258.hp2 HG02280.hp2 others(5): Show |
a0001a0007a0008 | a0001c0004a0007c0011a0008c0014 | a0001c0004t0004a0001c0004t0006a0007c0011t0004others(1): Show | a0001c0004t0004g0034a0001c0004t0004g0108a0001c0004t0004g0158others(5): Show | 8 | 270 | 0.0296 | -16 | c.186 others(33): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 9/9 | chr10 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38504978 | CTTTTTTT others(9): Show |
C | intron_variant | MODIFIER | HG01243.hp2 HG02486.hp1 HG02622.hp2 others(3): Show |
a0001a0004 | a0001c0009a0004c0017a0004c0019others(1): Show | a0001c0009t0003a0004c0017t0004a0004c0019t0004others(1): Show | a0001c0009t0003g0173a0004c0017t0004g0138a0004c0017t0004g0139others(3): Show | 6 | 309 | 0.0194 | -16 | c.344 others(35): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85590184 | GCCTGCCT others(9): Show |
G | intron_variant | MODIFIER | HG01884.hp2 NA18906.hp1 |
a0001 | a0001c0004a0001c0008 | a0001c0004t0003a0001c0008t0017 | a0001c0004t0003g0089a0001c0008t0017g0057 | 2 | 108 | 0.0185 | -16 | c.180 others(35): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85590188 | GCCTGCCT others(9): Show |
G | intron_variant | MODIFIER | HG02622.hp2 | a0001 | a0001c0001 | a0001c0001t0015 | a0001c0001t0015g0049 | 1 | 108 | 0.0093 | -16 | c.180 others(35): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85590192 | GCCTTCCT others(9): Show |
G | intron_variant | MODIFIER | HG00323.hp1 HG00423.hp2 HG00735.hp2 others(23): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0002t0002a0001c0003t0001others(4): Show | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0018others(23): Show | 26 | 108 | 0.2407 | -16 | c.180 others(35): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85607754 | TCAAAAAT others(9): Show |
T | intron_variant | MODIFIER | HG00323.hp1 HG00423.hp2 HG00735.hp2 others(21): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0002a0001c0003t0001others(2): Show | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0018others(21): Show | 24 | 108 | 0.2222 | -16 | c.180 others(35): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85643234 | GTTTTTTT others(9): Show |
G | intron_variant | MODIFIER | HG02451.hp1 HG02486.hp1 HG02486.hp2 others(2): Show |
a0001 | a0001c0001a0001c0003a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0005a0001c0003t0001others(2): Show | a0001c0001t0001g0090a0001c0001t0005g0036a0001c0003t0001g0086others(2): Show | 5 | 108 | 0.0463 | -16 | c.180 others(35): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85669644 | AATATATA others(9): Show |
A | intron_variant | MODIFIER | HG06807.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0068 | 1 | 108 | 0.0093 | -16 | c.181 others(35): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85743392 | CAAAAAAA others(9): Show |
C | intron_variant | MODIFIER | HG00323.hp2 HG00423.hp1 HG00639.hp1 others(23): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(10): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0019others(23): Show | 26 | 108 | 0.2407 | -16 | c.268 others(35): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85784905 | CTCTATCT others(9): Show |
C | intron_variant | MODIFIER | HG00423.hp2 HG01346.hp1 HG01433.hp1 others(12): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0020a0001c0002t0002others(6): Show | a0001c0001t0001g0008a0001c0001t0001g0016a0001c0001t0001g0018others(12): Show | 15 | 108 | 0.1389 | -16 | c.268 others(35): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85827461 | CGTGTGTG others(9): Show |
C | intron_variant | MODIFIER | HG02723.hp2 | a0001 | a0001c0003 | a0001c0003t0005 | a0001c0003t0005g0059 | 1 | 108 | 0.0093 | -16 | c.269 others(35): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85997265 | GATAGGTA others(9): Show |
G | intron_variant | MODIFIER | HG03130.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0065 | 1 | 108 | 0.0093 | -16 | c.200 others(35): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85997371 | TATAGATA others(9): Show |
T | intron_variant | MODIFIER | HG00323.hp2 HG00423.hp2 HG01074.hp1 others(13): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0002a0001c0003t0001others(3): Show | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(13): Show | 16 | 108 | 0.1482 | -16 | c.200 others(35): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP25_chr2_68729811_68831833 | 68784178 | TCTCTCTC others(9): Show |
T | intron_variant | MODIFIER | NA19030.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0143 | 1 | 368 | 0.0027 | -16 | c.349 others(33): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3/10 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142890147 | AAAAAATA others(9): Show |
A | intron_variant | MODIFIER | HG03490.hp2 HG03492.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0034a0001c0001t0003g0033 | 2 | 198 | 0.0101 | -16 | c.487 others(33): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142963163 | GGTATATA others(9): Show |
G | intron_variant | MODIFIER | HG00323.hp1 | a0001 | a0001c0001 | a0001c0001t0036 | a0001c0001t0036g0160 | 1 | 198 | 0.0051 | -16 | c.110 others(37): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143185553 | CTTTTCCA others(9): Show |
C | intron_variant | MODIFIER | HG02615.hp1 | a0002 | a0002c0007 | a0002c0007t0004 | a0002c0007t0004g0110 | 1 | 198 | 0.0051 | -16 | c.198 others(37): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP27_chr17_45388908_45437870 | 45412962 | CTTTTTTT others(9): Show |
C | intron_variant | MODIFIER | HG01243.hp1 HG01952.hp1 HG02976.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0010 | a0001c0001t0003g0216a0001c0001t0010g0008a0001c0001t0010g0019 | 4 | 347 | 0.0115 | -16 | c.658 others(33): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | TogoVar | ||||||
ARHGAP27_chr17_45388908_45437870 | 45419512 | GTATATAT others(9): Show |
G | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp1 HG01074.hp2 others(25): Show |
a0001a0004a0007 | a0001c0001a0004c0004a0007c0008 | a0001c0001t0002a0001c0001t0003a0001c0001t0008others(3): Show | a0001c0001t0002g0157a0001c0001t0002g0271a0001c0001t0002g0272others(17): Show | 28 | 347 | 0.0807 | -16 | c.657 others(35): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6729546 | ACTCACAC others(9): Show |
A | upstream_gene_variant | MODIFIER | HG03471.hp1 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0002 | 1 | 248 | 0.0040 | -16 | c.-27 others(25): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 169 | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6909285 | CTTTTCTT others(9): Show |
C | intron_variant | MODIFIER | HG02896.hp1 HG02897.hp2 HG03540.hp2 others(1): Show |
a0001a0003 | a0001c0001a0003c0022 | a0001c0001t0007a0003c0022t0003 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0007g0212others(1): Show | 4 | 248 | 0.0161 | -16 | c.209 others(33): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP29_chr1_94163905_94242584 | 94177142 | GTGTTTAA others(9): Show |
G | intron_variant | MODIFIER | HG03130.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0044 | 1 | 356 | 0.0028 | -16 | c.290 others(33): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 22/22 | chr1 | TogoVar | ||||||
ARHGAP29_chr1_94163905_94242584 | 94201506 | TTCTCTCT others(9): Show |
T | intron_variant | MODIFIER | HG02683.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0215 | 1 | 356 | 0.0028 | -16 | c.128 others(33): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161053462 | TTCTCTCT others(9): Show |
T | intron_variant | MODIFIER | HG00544.hp2 HG00597.hp2 HG00609.hp2 others(126): Show |
a0001a0003a0009 | a0001c0001a0003c0004a0009c0013 | a0001c0001t0001a0001c0001t0002a0003c0004t0001others(1): Show | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0011others(125): Show | 129 | 390 | 0.3308 | -16 | c.537 others(29): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 5/11 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161055940 | ATAAAATA others(9): Show |
A | intron_variant | MODIFIER | HG02922.hp1 HG02922.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0157a0001c0001t0001g0164 | 2 | 390 | 0.0051 | -16 | c.345 others(31): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 3/11 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161064775 | AAGAAAAA others(9): Show |
A | intron_variant | MODIFIER | NA18747.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0224 | 1 | 390 | 0.0026 | -16 | c.97+ others(31): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161064819 | GAAAGAAA others(9): Show |
G | intron_variant | MODIFIER | HG00408.hp2 NA18973.hp1 NA19012.hp1 others(2): Show |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0021a0002c0002t0001g0022a0002c0002t0001g0023others(2): Show | 5 | 390 | 0.0128 | -16 | c.97+ others(31): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119332629 | TCTCTCTC others(9): Show |
T | intron_variant | MODIFIER | HG02280.hp2 | a0001 | a0001c0010 | a0001c0010t0014 | a0001c0010t0014g0004 | 1 | 310 | 0.0032 | -16 | c.101 others(35): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP31_chr3_119289383_119425714 | 119332631 | TCTCTCAC others(9): Show |
T | intron_variant | MODIFIER | HG01099.hp2 HG01243.hp2 HG01884.hp1 others(24): Show |
a0001a0002a0004others(4): Show | a0001c0001a0001c0002a0001c0004others(7): Show | a0001c0001t0008a0001c0001t0020a0001c0001t0029others(14): Show | a0001c0001t0008g0224a0001c0001t0020g0064a0001c0001t0029g0054others(24): Show | 27 | 310 | 0.0871 | -16 | c.101 others(35): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP31_chr3_119289383_119425714 | 119332633 | TCTCACAC others(9): Show |
T | intron_variant | MODIFIER | HG03491.hp2 HG03492.hp1 NA21309.hp2 |
a0001a0013 | a0001c0001a0013c0020 | a0001c0001t0006a0013c0020t0013 | a0001c0001t0006g0065a0001c0001t0006g0066a0013c0020t0013g0051 | 3 | 310 | 0.0097 | -16 | c.101 others(35): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP32_chr11_128960060_129197325 | 129060336 | CATAGATA others(9): Show |
C | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp2 HG01258.hp2 others(25): Show |
a0001a0002a0007 | a0001c0001a0001c0014a0002c0007others(3): Show | a0001c0001t0002a0001c0001t0004a0001c0014t0004others(4): Show | a0001c0001t0002g0156a0001c0001t0002g0158a0001c0001t0004g0154others(25): Show | 28 | 398 | 0.0704 | -16 | c.963 others(33): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 10/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129189807 | AACTTGTC others(9): Show |
A | intron_variant | MODIFIER | HG02257.hp1 | a0002 | a0002c0007 | a0002c0007t0001 | a0002c0007t0001g0391 | 1 | 398 | 0.0025 | -16 | c.116 others(33): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 1/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129193316 | GGGGGGGG others(9): Show |
G | upstream_gene_variant | MODIFIER | HG02080.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0009 | 1 | 398 | 0.0025 | -16 | c.-11 others(27): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 992 | chr11 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46888261 | AATATATA others(9): Show |
A | intron_variant | MODIFIER | HG01433.hp2 HG02155.hp1 HG02698.hp1 others(2): Show |
a0001a0003 | a0001c0001a0003c0013 | a0001c0001t0004a0001c0001t0041a0003c0013t0004 | a0001c0001t0004g0080a0001c0001t0004g0082a0001c0001t0004g0233others(2): Show | 5 | 298 | 0.0168 | -16 | c.-18 others(37): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46936901 | GCAATCTC others(9): Show |
G | intron_variant | MODIFIER | NA18612.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0265 | 1 | 298 | 0.0034 | -16 | c.368 others(33): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 2/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46939372 | CATTTATT others(9): Show |
C | intron_variant | MODIFIER | HG02451.hp2 HG02572.hp2 NA18906.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0018a0001c0001t0045 | a0001c0001t0003g0054a0001c0001t0018g0040a0001c0001t0018g0227others(1): Show | 4 | 298 | 0.0134 | -16 | c.382 others(35): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 47006267 | CTTTTTTT others(9): Show |
C | downstream_gene_variant | MODIFIER | HG02896.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0030 | 1 | 298 | 0.0034 | -16 | c.*55 others(27): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1191 | chr19 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144559354 | CAAAAAAA others(9): Show |
C | intron_variant | MODIFIER | HG02257.hp1 | a0001 | a0001c0007 | a0001c0007t0003 | a0001c0007t0003g0078 | 1 | 246 | 0.0041 | -16 | c.513 others(33): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38603407 | GTCTATCT others(9): Show |
G | intron_variant | MODIFIER | HG02559.hp1 | a0004 | a0004c0011 | a0004c0011t0004 | a0004c0011t0004g0114 | 1 | 350 | 0.0029 | -16 | c.137 others(33): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ARHGAP40_chr20_38596809_38655653 | 38627375 | GGTGTGTG others(9): Show |
G | intron_variant | MODIFIER | HG00642.hp2 | a0002 | a0002c0003 | a0002c0003t0004 | a0002c0003t0004g0304 | 1 | 350 | 0.0029 | -16 | c.558 others(31): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ARHGAP40_chr20_38596809_38655653 | 38642714 | ATCCATCC others(9): Show |
A | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00323.hp2 others(170): Show |
a0001a0002a0005others(8): Show | a0001c0001a0001c0002a0001c0004others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(18): Show | a0001c0001t0001g0004a0001c0001t0001g0005a0001c0001t0001g0016others(154): Show | 173 | 350 | 0.4943 | -16 | c.136 others(33): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 10/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100699496 | ATATATAT others(9): Show |
A | intron_variant | MODIFIER | NA19043.hp1 | a0002 | a0002c0002 | a0002c0002t0028 | a0002c0002t0028g0001 | 1 | 286 | 0.0035 | -16 | c.154 others(35): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100699498 | ATATATAT others(9): Show |
A | intron_variant | MODIFIER | HG01081.hp1 HG02055.hp2 HG02698.hp1 others(7): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0005 | a0001c0001t0001a0001c0001t0002a0002c0002t0004others(4): Show | a0001c0001t0001g0026a0001c0001t0001g0027a0001c0001t0002g0265others(7): Show | 10 | 286 | 0.0350 | -16 | c.154 others(35): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100699500 | ATATATAT others(9): Show |
A | intron_variant | MODIFIER | HG00544.hp2 HG00733.hp2 HG00735.hp2 others(2): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0002c0002t0002others(2): Show | a0001c0001t0001g0023a0001c0001t0002g0003a0002c0002t0002g0244others(2): Show | 5 | 286 | 0.0175 | -16 | c.154 others(35): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100714389 | TTGTGTGT others(9): Show |
T | intron_variant | MODIFIER | HG01891.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0067 | 1 | 286 | 0.0035 | -16 | c.154 others(35): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100728713 | CGTATATA others(9): Show |
C | intron_variant | MODIFIER | NA19057.hp1 NA19077.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0198a0001c0001t0001g0199 | 2 | 286 | 0.0070 | -16 | c.154 others(35): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | chr11 | TogoVar |