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 | 110648226 | TATATATA others(7): Show |
T | intron_variant | MODIFIER | HG01891.hp1 HG02109.hp1 HG02486.hp2 others(5): Show |
a0001a0002 | a0001c0001a0001c0005a0002c0006 | a0001c0001t0004a0001c0001t0006a0001c0005t0005others(1): Show | a0001c0001t0004g0004a0001c0001t0004g0143a0001c0001t0006g0199others(4): Show | 8 | 226 | 0.0354 | -14 | c.189 others(33): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24622433 | CATATATA others(7): Show |
C | intron_variant | MODIFIER | HG00099.hp2 HG01192.hp1 HG01433.hp2 others(18): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0003others(2): Show | a0001c0001t0001a0001c0001t0016a0002c0002t0001others(3): Show | a0001c0001t0001g0191a0001c0001t0001g0196a0001c0001t0001g0199others(18): Show | 21 | 352 | 0.0597 | -14 | c.525 others(29): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 8/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24628833 | GTACATAT others(7): Show |
G | intron_variant | MODIFIER | HG01516.hp1 HG01517.hp1 |
a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0158a0001c0001t0009g0159 | 2 | 352 | 0.0057 | -14 | c.495 others(31): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24628952 | CTATATAT others(7): Show |
C | intron_variant | MODIFIER | HG01516.hp2 NA18522.hp1 |
a0002a0005 | a0002c0002a0005c0005 | a0002c0002t0014a0005c0005t0001 | a0002c0002t0014g0105a0005c0005t0001g0284 | 2 | 352 | 0.0057 | -14 | c.495 others(31): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24649751 | TAGAAAAC others(7): Show |
T | intron_variant | MODIFIER | HG02922.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0138 | 1 | 352 | 0.0028 | -14 | c.269 others(33): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 4/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24695050 | CAAAAAAA others(7): Show |
C | intron_variant | MODIFIER | HG00597.hp2 | a0003 | a0003c0003 | a0003c0003t0001 | a0003c0003t0001g0230 | 1 | 352 | 0.0028 | -14 | c.64- others(31): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38447437 | GAAAAAAA others(7): Show |
G | intron_variant | MODIFIER | HG00544.hp1 HG02040.hp1 |
a0001 | a0001c0003a0001c0007 | a0001c0003t0001a0001c0007t0003 | a0001c0003t0001g0109a0001c0007t0003g0110 | 2 | 309 | 0.0065 | -14 | c.64- others(31): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP23_chr17_38423464_38517385 | 38453418 | CGTGCGTG others(7): Show |
C | intron_variant | MODIFIER | HG01358.hp1 HG01884.hp2 HG02145.hp1 others(3): Show |
a0001a0003a0005others(1): Show | a0001c0011a0001c0032a0003c0014others(2): Show | a0001c0011t0006a0001c0032t0001a0003c0014t0001others(2): Show | a0001c0011t0006g0071a0001c0011t0006g0074a0001c0032t0001g0201others(3): Show | 6 | 309 | 0.0194 | -14 | c.64- others(29): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP23_chr17_38423464_38517385 | 38504978 | CTTTTTTT others(7): Show |
C | intron_variant | MODIFIER | HG02145.hp1 HG02280.hp2 HG02723.hp2 others(3): Show |
a0001a0006 | a0001c0001a0001c0002a0001c0031others(2): Show | a0001c0001t0001a0001c0002t0002a0001c0031t0003others(2): Show | a0001c0001t0001g0152a0001c0002t0002g0306a0001c0031t0003g0065others(3): Show | 6 | 309 | 0.0194 | -14 | c.344 others(33): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85485372 | AAAAAATA others(7): Show |
A | intron_variant | MODIFIER | HG01243.hp1 HG02145.hp2 |
a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0074a0001c0001t0005g0101 | 2 | 108 | 0.0185 | -14 | c.-21 others(31): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85485374 | AAAATATA others(7): Show |
A | intron_variant | MODIFIER | HG03130.hp2 | a0002 | a0002c0006 | a0002c0006t0018 | a0002c0006t0018g0040 | 1 | 108 | 0.0093 | -14 | c.-21 others(31): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85643234 | GTTTTTTT others(7): Show |
G | intron_variant | MODIFIER | HG02622.hp2 | a0001 | a0001c0001 | a0001c0001t0015 | a0001c0001t0015g0049 | 1 | 108 | 0.0093 | -14 | c.180 others(33): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85655788 | TATATAGA others(7): Show |
T | intron_variant | MODIFIER | NA21309.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0060 | 1 | 108 | 0.0093 | -14 | c.181 others(33): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85669644 | AATATATA others(7): Show |
A | intron_variant | MODIFIER | HG02109.hp1 HG02622.hp2 |
a0001 | a0001c0001a0001c0007 | a0001c0001t0015a0001c0007t0003 | a0001c0001t0015g0049a0001c0007t0003g0072 | 2 | 108 | 0.0185 | -14 | c.181 others(33): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85724489 | GTGTATAT others(7): Show |
G | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp2 HG01884.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0002a0001c0002t0007others(3): Show | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0039others(7): Show | 10 | 108 | 0.0926 | -14 | c.268 others(31): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85827461 | CGTGTGTG others(7): Show |
C | intron_variant | MODIFIER | HG01243.hp2 HG02145.hp1 |
a0001a0002 | a0001c0004a0002c0006 | a0001c0004t0003a0002c0006t0006 | a0001c0004t0003g0071a0002c0006t0006g0031 | 2 | 108 | 0.0185 | -14 | c.269 others(33): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142890151 | AATATATA others(7): Show |
A | intron_variant | MODIFIER | HG02965.hp1 NA18944.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0004a0001c0002t0001 | a0001c0001t0004g0105a0001c0002t0001g0156 | 2 | 198 | 0.0101 | -14 | c.487 others(31): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143029392 | GTTTTTTT others(7): Show |
G | intron_variant | MODIFIER | HG02886.hp2 | a0001 | a0001c0001 | a0001c0001t0024 | a0001c0001t0024g0112 | 1 | 198 | 0.0051 | -14 | c.114 others(33): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143162284 | TACACACA others(7): Show |
T | intron_variant | MODIFIER | HG00323.hp2 HG00408.hp1 HG00438.hp1 others(35): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(20): Show | a0001c0001t0001g0018a0001c0001t0001g0116a0001c0001t0001g0131others(35): Show | 38 | 198 | 0.1919 | -14 | c.198 others(35): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143168445 | CTTTTTTT others(7): Show |
C | intron_variant | MODIFIER | NA18612.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0184 | 1 | 198 | 0.0051 | -14 | c.198 others(35): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP27_chr17_45388908_45437870 | 45412962 | CTTTTTTT others(7): Show |
C | intron_variant | MODIFIER | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(22): Show |
a0001a0002a0004others(1): Show | a0001c0001a0002c0002a0002c0010others(3): Show | a0001c0001t0002a0002c0002t0001a0002c0010t0001others(4): Show | a0001c0001t0002g0262a0002c0002t0001g0097a0002c0010t0001g0035others(14): Show | 25 | 347 | 0.0721 | -14 | c.658 others(31): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | TogoVar | ||||||
ARHGAP27_chr17_45388908_45437870 | 45419508 | GTATGTAT others(7): Show |
G | intron_variant | MODIFIER | HG00735.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0156 | 1 | 347 | 0.0029 | -14 | c.657 others(33): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | TogoVar | ||||||
ARHGAP27_chr17_45388908_45437870 | 45419512 | GTATATAT others(7): Show |
G | intron_variant | MODIFIER | HG04184.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0219 | 1 | 347 | 0.0029 | -14 | c.657 others(33): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6729326 | GCACACAC others(7): Show |
G | upstream_gene_variant | MODIFIER | NA18988.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0213 | 1 | 248 | 0.0040 | -14 | c.-49 others(23): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 389 | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6828384 | GGAGGAGA others(7): Show |
G | intron_variant | MODIFIER | HG02055.hp1 HG02145.hp1 HG02615.hp1 others(3): Show |
a0001a0002a0006 | a0001c0001a0001c0012a0002c0005others(1): Show | a0001c0001t0001a0001c0012t0001a0002c0005t0002others(1): Show | a0001c0001t0001g0124a0001c0001t0001g0149a0001c0001t0001g0150others(3): Show | 6 | 248 | 0.0242 | -14 | c.325 others(31): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6854742 | GCTGCAGC others(7): Show |
G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(64): Show |
a0001a0002a0005others(2): Show | a0001c0001a0001c0003a0001c0012others(6): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(13): Show | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(64): Show | 67 | 248 | 0.2702 | -14 | c.636 others(31): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP29_chr1_94163905_94242584 | 94201506 | TTCTCTCT others(7): Show |
T | intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp1 others(326): Show |
a0001a0003a0004others(5): Show | a0001c0001a0001c0002a0001c0005others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(46): Show | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0008others(285): Show | 329 | 356 | 0.9242 | -14 | c.128 others(31): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | TogoVar | ||||||
ARHGAP29_chr1_94163905_94242584 | 94240282 | TCAATCTC others(7): Show |
T | upstream_gene_variant | MODIFIER | HG03486.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0294 | 1 | 356 | 0.0028 | -14 | c.-29 others(25): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2699 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161053462 | TTCTCTCT others(7): Show |
T | intron_variant | MODIFIER | HG01934.hp2 HG01978.hp2 HG03490.hp2 others(2): Show |
a0001a0007 | a0001c0001a0007c0011 | a0001c0001t0001a0007c0011t0001 | a0001c0001t0001g0161a0001c0001t0001g0171a0001c0001t0001g0212others(2): Show | 5 | 390 | 0.0128 | -14 | c.537 others(27): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 5/11 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161064765 | GAAAGAAA others(7): Show |
G | intron_variant | MODIFIER | HG01071.hp2 NA19030.hp1 NA20805.hp2 |
a0001a0008 | a0001c0001a0008c0012 | a0001c0001t0001a0008c0012t0001 | a0001c0001t0001g0074a0001c0001t0001g0116a0008c0012t0001g0075 | 3 | 390 | 0.0077 | -14 | c.97+ others(29): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161064817 | AAGAAAGA others(7): Show |
A | intron_variant | MODIFIER | HG00597.hp2 HG01433.hp2 HG01952.hp2 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0016a0001c0001t0001g0121a0001c0001t0001g0127others(12): Show | 15 | 390 | 0.0385 | -14 | c.97+ others(29): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119332625 | TCTCTCTC others(7): Show |
T | intron_variant | MODIFIER | HG02257.hp2 | a0001 | a0001c0002 | a0001c0002t0012 | a0001c0002t0012g0206 | 1 | 310 | 0.0032 | -14 | c.101 others(33): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP31_chr3_119289383_119425714 | 119332633 | TCTCACAC others(7): Show |
T | intron_variant | MODIFIER | HG01106.hp2 HG02280.hp1 HG02572.hp1 others(7): Show |
a0001a0003a0004 | a0001c0005a0003c0006a0003c0009others(1): Show | a0001c0005t0001a0003c0006t0001a0003c0009t0012others(1): Show | a0001c0005t0001g0029a0001c0005t0001g0034a0001c0005t0001g0035others(7): Show | 10 | 310 | 0.0323 | -14 | c.101 others(33): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP32_chr11_128960060_129197325 | 128984795 | AATAGTGT others(7): Show |
A | intron_variant | MODIFIER | HG02056.hp1 HG02080.hp2 NA18942.hp1 others(12): Show |
a0002 | a0002c0004 | a0002c0004t0001a0002c0004t0005a0002c0004t0013others(3): Show | a0002c0004t0001g0205a0002c0004t0001g0209a0002c0004t0001g0214others(12): Show | 15 | 398 | 0.0377 | -14 | c.152 others(33): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 15/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129029801 | CAAAAAAA others(7): Show |
C | intron_variant | MODIFIER | NA18956.hp1 | a0001 | a0001c0032 | a0001c0032t0001 | a0001c0032t0001g0185 | 1 | 398 | 0.0025 | -14 | c.104 others(35): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 11/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129036380 | CAAAAAAA others(7): Show |
C | intron_variant | MODIFIER | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(94): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0005a0001c0032others(3): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(12): Show | a0001c0001t0001g0001a0001c0001t0001g0005a0001c0001t0001g0006others(93): Show | 97 | 398 | 0.2437 | -14 | c.104 others(33): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 11/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129058209 | ACACACAC others(7): Show |
A | intron_variant | MODIFIER | HG03831.hp2 | a0001 | a0001c0001 | a0001c0001t0016 | a0001c0001t0016g0197 | 1 | 398 | 0.0025 | -14 | c.963 others(31): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 10/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129193689 | TTATATAA others(7): Show |
T | upstream_gene_variant | MODIFIER | HG02258.hp2 HG02559.hp2 HG02818.hp1 others(1): Show |
a0001a0011 | a0001c0002a0011c0021 | a0001c0002t0001a0011c0021t0006 | a0001c0002t0001g0224a0001c0002t0001g0225a0001c0002t0001g0226others(1): Show | 4 | 398 | 0.0101 | -14 | c.-15 others(25): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 1365 | chr11 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46888261 | AATATATA others(7): Show |
A | intron_variant | MODIFIER | HG01255.hp2 HG01496.hp2 HG02559.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0007a0001c0001t0014others(2): Show | a0001c0001t0001g0175a0001c0001t0001g0176a0001c0001t0001g0183others(4): Show | 7 | 298 | 0.0235 | -14 | c.-18 others(35): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46978893 | GGGGGTGT others(7): Show |
G | intron_variant | MODIFIER | HG02074.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0295 | 1 | 298 | 0.0034 | -14 | c.382 others(33): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 47006267 | CTTTTTTT others(7): Show |
C | downstream_gene_variant | MODIFIER | HG00642.hp1 HG01243.hp2 HG02055.hp2 others(11): Show |
a0001 | a0001c0002a0001c0005a0001c0006 | a0001c0002t0006a0001c0002t0036a0001c0005t0006others(1): Show | a0001c0002t0006g0207a0001c0002t0006g0209a0001c0002t0006g0211others(11): Show | 14 | 298 | 0.0470 | -14 | c.*55 others(25): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1191 | chr19 | TogoVar | ||||||
ARHGAP36_chrX_131053346_131094885 | 131063708 | TCCACCAC others(7): Show |
T | intron_variant | MODIFIER | HG01123.hp1 HG01891.hp2 HG02258.hp1 others(9): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(2): Show | a0001c0001t0001g0152a0001c0001t0001g0154a0001c0001t0001g0155others(8): Show | 12 | 302 | 0.0397 | -14 | c.-14 others(33): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
ARHGAP36_chrX_131053346_131094885 | 131077764 | CATATATA others(7): Show |
C | intron_variant | MODIFIER | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(57): Show |
a0000a0001 | a0000c0003a0001c0001a0001c0004 | a0000c0003t0007a0001c0001t0001a0001c0001t0002others(3): Show | a0000c0003t0007g0096a0001c0001t0001g0014a0001c0001t0001g0091others(34): Show | 60 | 302 | 0.1987 | -14 | c.-14 others(33): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
ARHGAP36_chrX_131053346_131094885 | 131079537 | GTTTGTTT others(7): Show |
G | intron_variant | MODIFIER | HG00733.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0105 | 1 | 302 | 0.0033 | -14 | c.-14 others(33): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
ARHGAP40_chr20_38596809_38655653 | 38627594 | GGTGTGCG others(7): Show |
G | intron_variant | MODIFIER | HG00558.hp2 NA18965.hp2 NA18975.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0188others(1): Show | 4 | 350 | 0.0114 | -14 | c.558 others(29): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ARHGAP40_chr20_38596809_38655653 | 38630068 | CTTTCTTT others(7): Show |
C | intron_variant | MODIFIER | HG00738.hp2 HG01167.hp2 HG01169.hp1 others(6): Show |
a0001a0004a0017others(1): Show | a0001c0001a0004c0011a0004c0014others(2): Show | a0001c0001t0006a0004c0011t0004a0004c0011t0007others(3): Show | a0001c0001t0006g0083a0001c0001t0006g0091a0001c0001t0006g0092others(5): Show | 9 | 350 | 0.0257 | -14 | c.783 others(29): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ARHGAP40_chr20_38596809_38655653 | 38632401 | ACAGGCGC others(7): Show |
A | intron_variant | MODIFIER | HG00140.hp2 HG01361.hp1 HG02735.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0140a0001c0001t0001g0182a0001c0001t0001g0275 | 3 | 350 | 0.0086 | -14 | c.784 others(31): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100699498 | ATATATAT others(7): Show |
A | intron_variant | MODIFIER | HG02074.hp1 NA18989.hp1 NA19000.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0013a0001c0003t0033 | a0001c0001t0001g0276a0001c0001t0013g0283a0001c0003t0033g0284 | 3 | 286 | 0.0105 | -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 | 100699500 | ATATATAT others(7): Show |
A | intron_variant | MODIFIER | HG01070.hp1 HG01071.hp2 HG01192.hp1 others(3): Show |
a0001a0002 | a0001c0003a0002c0002 | a0001c0003t0006a0002c0002t0004 | a0001c0003t0006g0259a0001c0003t0006g0260a0001c0003t0006g0261others(3): Show | 6 | 286 | 0.0210 | -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 | 100699502 | ATATATTT others(7): Show |
A | intron_variant | MODIFIER | HG02615.hp2 HG02970.hp2 HG03225.hp1 others(2): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0004 | a0001c0001t0001a0002c0002t0001a0002c0002t0002others(1): Show | a0001c0001t0001g0011a0002c0002t0001g0015a0002c0002t0001g0017others(2): Show | 5 | 286 | 0.0175 | -14 | c.154 others(33): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |