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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP26_chr5_142765377_143234007 | 143162314 | C | CACACACA others(3): Show |
intron_variant | MODIFIER | HG02735.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0142 | 1 | 198 | 0.0051 | 10 | c.198 others(31): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143168445 | C | CTTTTTTT others(3): Show |
intron_variant | MODIFIER | HG00438.hp1 HG00544.hp1 HG00558.hp2 others(16): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(11): Show | a0001c0001t0001g0141a0001c0001t0002g0013a0001c0001t0003g0015others(16): Show | 19 | 198 | 0.0960 | 10 | c.198 others(31): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP27_chr17_45388908_45437870 | 45399591 | C | CAAAGAAA others(3): Show |
intron_variant | MODIFIER | HG03540.hp2 | a0001 | a0001c0016 | a0001c0016t0015 | a0001c0016t0015g0300 | 1 | 347 | 0.0029 | 10 | c.174 others(29): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | TogoVar | ||||||
ARHGAP27_chr17_45388908_45437870 | 45411795 | T | TCACACAC others(3): Show |
intron_variant | MODIFIER | NA21309.hp2 | a0006 | a0006c0006 | a0006c0006t0014 | a0006c0006t0014g0181 | 1 | 347 | 0.0029 | 10 | c.658 others(27): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6729570 | G | GCACACAC others(3): Show |
upstream_gene_variant | MODIFIER | HG03579.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0072 | 1 | 248 | 0.0040 | 10 | c.-25 others(19): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 145 | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6729574 | G | GCACACAC others(3): Show |
upstream_gene_variant | MODIFIER | HG01891.hp1 HG02080.hp1 HG02155.hp1 others(14): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0009a0001c0003t0003others(4): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0121others(14): Show | 17 | 248 | 0.0686 | 10 | c.-24 others(19): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 141 | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6730219 | G | GTATATAT others(3): Show |
intron_variant | MODIFIER | HG02630.hp1 HG06807.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0022a0001c0003t0003 | a0001c0001t0022g0067a0001c0003t0003g0068 | 2 | 248 | 0.0081 | 10 | c.122 others(25): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6739645 | T | TTCTCTCT others(3): Show |
intron_variant | MODIFIER | HG01243.hp2 HG03471.hp2 |
a0001a0008 | a0001c0001a0008c0011 | a0001c0001t0001a0008c0011t0005 | a0001c0001t0001g0151a0008c0011t0005g0152 | 2 | 248 | 0.0081 | 10 | c.122 others(27): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6896899 | C | CTTTTATT others(3): Show |
intron_variant | MODIFIER | HG03041.hp1 HG03490.hp1 HG03492.hp1 |
a0003 | a0003c0013a0003c0023 | a0003c0013t0011a0003c0023t0001 | a0003c0013t0011g0062a0003c0013t0011g0063a0003c0023t0001g0120 | 3 | 248 | 0.0121 | 10 | c.203 others(27): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6908125 | G | GTTTTATT others(3): Show |
intron_variant | MODIFIER | HG00741.hp2 HG02723.hp1 NA19043.hp1 |
a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0027a0001c0003t0003g0085a0001c0003t0003g0122 | 3 | 248 | 0.0121 | 10 | c.203 others(27): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP29_chr1_94163905_94242584 | 94166813 | G | GCACACAC others(3): Show |
downstream_gene_variant | MODIFIER | HG02257.hp2 HG02723.hp2 HG03139.hp2 |
a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0288a0001c0001t0010g0299a0001c0001t0010g0304 | 3 | 356 | 0.0084 | 10 | c.*70 others(21): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2091 | chr1 | TogoVar | ||||||
ARHGAP29_chr1_94163905_94242584 | 94172612 | G | GATATATA others(3): Show |
3_prime_UTR_variant | MODIFIER | HG02717.hp2 NA18952.hp2 |
a0001 | a0001c0001 | a0001c0001t0021 | a0001c0001t0021g0260a0001c0001t0021g0310 | 2 | 356 | 0.0056 | 10 | c.*12 others(21): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 1256 | chr1 | TogoVar | |||||
ARHGAP29_chr1_94163905_94242584 | 94182811 | T | TAAAACAA others(3): Show |
intron_variant | MODIFIER | HG00741.hp1 HG01884.hp2 HG02109.hp1 others(19): Show |
a0001 | a0001c0001a0001c0009 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0156a0001c0001t0002g0223a0001c0001t0002g0236others(17): Show | 22 | 356 | 0.0618 | 10 | c.224 others(29): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161053462 | T | TTCTCTCT others(3): Show |
intron_variant | MODIFIER | HG00408.hp1 HG00544.hp1 HG00741.hp2 others(22): Show |
a0001a0002a0006 | a0001c0001a0002c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0001t0003a0002c0002t0001others(4): Show | a0001c0001t0001g0040a0001c0001t0001g0054a0001c0001t0001g0056others(22): Show | 25 | 390 | 0.0641 | 10 | c.537 others(23): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 5/11 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161053501 | T | TCTCTCTC others(3): Show |
intron_variant | MODIFIER | NA18942.hp1 NA19065.hp2 |
a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0137a0002c0003t0001g0138 | 2 | 390 | 0.0051 | 10 | c.537 others(25): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 5/11 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161055804 | T | TAATAAAA others(3): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00558.hp2 HG01243.hp2 others(8): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0044a0001c0001t0001g0063a0001c0001t0001g0073others(8): Show | 11 | 390 | 0.0282 | 10 | c.345 others(25): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 3/11 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161064779 | A | AAGAAAGA others(3): Show |
intron_variant | MODIFIER | HG03831.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0102 | 1 | 390 | 0.0026 | 10 | c.97+ others(25): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161064831 | G | GAAAGAAA others(3): Show |
intron_variant | MODIFIER | HG00639.hp1 HG02486.hp2 NA18994.hp1 others(1): Show |
a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0139a0002c0003t0001g0260a0002c0003t0001g0280others(1): Show | 4 | 390 | 0.0103 | 10 | c.97+ others(25): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119297909 | A | AACACACA others(3): Show |
intron_variant | MODIFIER | HG02647.hp2 HG03225.hp1 |
a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0019a0001c0005t0001g0020 | 2 | 310 | 0.0065 | 10 | c.100 others(27): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP31_chr3_119289383_119425714 | 119307940 | C | CAAAAAAA others(3): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG01071.hp2 others(23): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0005a0001c0001t0006a0001c0001t0011others(9): Show | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0006g0073others(23): Show | 26 | 310 | 0.0839 | 10 | c.100 others(29): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP31_chr3_119289383_119425714 | 119332604 | T | TTCTCTCT others(3): Show |
intron_variant | MODIFIER | HG02015.hp2 | a0001 | a0001c0005 | a0001c0005t0027 | a0001c0005t0027g0044 | 1 | 310 | 0.0032 | 10 | c.101 others(29): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP31_chr3_119289383_119425714 | 119388306 | T | TTACATAT others(3): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(29): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0005a0001c0001t0007a0001c0001t0011others(9): Show | a0001c0001t0005g0077a0001c0001t0005g0078a0001c0001t0005g0142others(29): Show | 32 | 310 | 0.1032 | 10 | c.683 others(27): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP32_chr11_128960060_129197325 | 128982474 | C | CGTGTGTG others(3): Show |
intron_variant | MODIFIER | HG00438.hp2 HG00609.hp2 HG01346.hp2 others(17): Show |
a0001a0007a0013 | a0001c0001a0001c0014a0007c0037others(1): Show | a0001c0001t0002a0001c0001t0004a0001c0014t0004others(2): Show | a0001c0001t0002g0113a0001c0001t0002g0156a0001c0001t0002g0166others(17): Show | 20 | 398 | 0.0503 | 10 | c.152 others(27): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 15/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 128985858 | G | GTATATAT others(3): Show |
intron_variant | MODIFIER | HG02630.hp1 HG02698.hp1 HG03195.hp1 others(9): Show |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0261a0001c0002t0001g0270a0001c0002t0001g0271others(9): Show | 12 | 398 | 0.0302 | 10 | c.152 others(27): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 15/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 128985858 | G | GTGTATAT others(3): Show |
intron_variant | MODIFIER | HG02723.hp1 NA18978.hp2 NA19055.hp2 |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0005a0001c0002t0006 | a0001c0002t0001g0301a0001c0002t0005g0291a0001c0002t0006g0304 | 3 | 398 | 0.0075 | 10 | c.152 others(27): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 15/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 128985858 | G | GTGTGTAT others(3): Show |
intron_variant | MODIFIER | HG00609.hp2 HG01258.hp2 HG02015.hp1 others(12): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0004a0001c0002t0001 | a0001c0001t0002g0158a0001c0001t0002g0166a0001c0001t0002g0169others(12): Show | 15 | 398 | 0.0377 | 10 | c.152 others(27): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 15/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 128985858 | G | GTGTGTGT others(3): Show |
intron_variant | MODIFIER | HG00438.hp2 HG03942.hp1 HG06807.hp2 others(3): Show |
a0001a0002 | a0001c0001a0002c0007 | a0001c0001t0004a0002c0007t0009 | a0001c0001t0004g0165a0001c0001t0004g0173a0001c0001t0004g0174others(3): Show | 6 | 398 | 0.0151 | 10 | c.152 others(27): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 15/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 128985858 | G | GTGTGTGT others(3): Show |
intron_variant | MODIFIER | HG02965.hp2 | a0002 | a0002c0007 | a0002c0007t0009 | a0002c0007t0009g0382 | 1 | 398 | 0.0025 | 10 | c.152 others(27): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 15/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 128989515 | T | TACACACA others(3): Show |
intron_variant | MODIFIER | HG02056.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0181 | 1 | 398 | 0.0025 | 10 | c.119 others(29): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 12/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 128989516 | T | TCACACAC others(3): Show |
intron_variant | MODIFIER | HG00423.hp1 HG00673.hp2 HG01074.hp2 others(29): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(4): Show | a0001c0001t0002g0002a0001c0001t0002g0096a0001c0001t0002g0098others(28): Show | 32 | 398 | 0.0804 | 10 | c.119 others(29): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 12/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 128989516 | T | TCTCACAC others(3): Show |
intron_variant | MODIFIER | HG02083.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0041 | 1 | 398 | 0.0025 | 10 | c.119 others(29): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 12/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129035173 | C | CCTCTCTC others(3): Show |
intron_variant | MODIFIER | HG02083.hp2 HG02735.hp1 HG03669.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0041a0001c0001t0002g0103a0001c0001t0002g0126others(1): Show | 4 | 398 | 0.0101 | 10 | c.104 others(29): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 11/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129143072 | C | CATATATA others(3): Show |
intron_variant | MODIFIER | HG00140.hp2 HG00423.hp2 HG00639.hp1 others(68): Show |
a0001a0002a0006others(3): Show | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0029others(16): Show | a0001c0001t0001g0330a0001c0001t0001g0331a0001c0001t0001g0350others(68): Show | 71 | 398 | 0.1784 | 10 | c.226 others(29): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 2/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129143088 | T | TATATATA others(3): Show |
intron_variant | MODIFIER | HG03239.hp2 HG03927.hp2 NA19078.hp2 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0001a0001c0003t0003 | a0001c0002t0001g0268a0001c0003t0003g0380a0001c0003t0003g0381 | 3 | 398 | 0.0075 | 10 | c.226 others(29): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 2/22 | chr11 | TogoVar | ||||||
ARHGAP33_chr19_35770564_35793822 | 35771989 | C | CTTTTTTT others(3): Show |
upstream_gene_variant | MODIFIER | NA18906.hp1 NA20300.hp2 |
a0006 | a0006c0016 | a0006c0016t0001 | a0006c0016t0001g0029 | 2 | 420 | 0.0048 | 10 | c.-36 others(21): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 3574 | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46869476 | T | TTGTGTGT others(3): Show |
intron_variant | MODIFIER | HG02615.hp2 HG03225.hp1 |
a0001 | a0001c0001 | a0001c0001t0007a0001c0001t0048 | a0001c0001t0007g0019a0001c0001t0048g0018 | 2 | 298 | 0.0067 | 10 | c.-18 others(29): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46888261 | A | AATATATA others(3): Show |
intron_variant | MODIFIER | HG01256.hp1 HG01258.hp1 homoSapiens_chm13v2.hp1 |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0008 | a0001c0001t0003g0098a0001c0001t0008g0097a0001c0001t0008g0108 | 3 | 298 | 0.0101 | 10 | c.-18 others(31): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46981825 | G | GTGTTTTG others(3): Show |
intron_variant | MODIFIER | HG02027.hp2 HG02055.hp2 HG02135.hp2 others(8): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0012a0001c0001t0021a0001c0001t0051others(2): Show | a0001c0001t0012g0113a0001c0001t0021g0254a0001c0001t0051g0229others(8): Show | 11 | 298 | 0.0369 | 10 | c.382 others(29): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 47003913 | G | GACACACA others(3): Show |
3_prime_UTR_variant | MODIFIER | NA19030.hp1 | a0001 | a0001c0001 | a0001c0001t0050 | a0001c0001t0050g0251 | 1 | 298 | 0.0034 | 10 | c.*32 others(21): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 7/7 | 3230 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||
ARHGAP35_chr19_46855997_47010077 | 47006267 | C | CTTTTTTT others(3): Show |
downstream_gene_variant | MODIFIER | HG02129.hp1 HG03139.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0007 | a0001c0001t0002g0200a0001c0001t0007g0015 | 2 | 298 | 0.0067 | 10 | c.*55 others(21): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1191 | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 47007073 | C | CTTTTTTT others(3): Show |
downstream_gene_variant | MODIFIER | HG01070.hp1 | a0001 | a0001c0001 | a0001c0001t0019 | a0001c0001t0019g0024 | 1 | 298 | 0.0034 | 10 | c.*63 others(21): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1997 | chr19 | TogoVar | ||||||
ARHGAP36_chrX_131053346_131094885 | 131075623 | A | ATGTGTGT others(3): Show |
intron_variant | MODIFIER | NA19066.hp1 NA21309.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0011 | a0001c0001t0001g0199a0001c0001t0011g0168 | 2 | 302 | 0.0066 | 10 | c.-14 others(29): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
ARHGAP36_chrX_131053346_131094885 | 131077764 | C | CATATATA others(3): Show |
intron_variant | MODIFIER | HG01081.hp1 HG02818.hp2 HG03130.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0004 | a0001c0001t0001g0036a0001c0001t0001g0062a0001c0001t0001g0063others(3): Show | 6 | 302 | 0.0199 | 10 | c.-14 others(29): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | |||||
ARHGAP39_chr8_144524179_144690846 | 144531575 | A | AATCCGGG others(3): Show |
intron_variant | MODIFIER | NA18967.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0143 | 1 | 246 | 0.0041 | 10 | c.298 others(27): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 10/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144669506 | C | CAAAAAAA others(3): Show |
intron_variant | MODIFIER | HG00408.hp1 HG02004.hp1 HG02080.hp1 others(22): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0011a0001c0001t0012others(2): Show | a0001c0001t0001g0029a0001c0001t0001g0030a0001c0001t0001g0031others(22): Show | 25 | 246 | 0.1016 | 10 | c.-82 others(29): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38630068 | C | CTTTCTTT others(3): Show |
intron_variant | MODIFIER | HG02886.hp2 HG02895.hp2 NA18906.hp1 |
a0005 | a0005c0006 | a0005c0006t0002 | a0005c0006t0002g0029a0005c0006t0002g0087 | 3 | 350 | 0.0086 | 10 | c.783 others(25): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100766222 | G | GGTGTGTG others(3): Show |
intron_variant | MODIFIER | HG00639.hp1 HG00741.hp1 HG01257.hp2 others(6): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0002c0004others(1): Show | a0001c0001t0001a0001c0001t0002a0002c0002t0004others(2): Show | a0001c0001t0001g0062a0001c0001t0001g0066a0001c0001t0001g0086others(6): Show | 9 | 286 | 0.0315 | 10 | c.155 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100779483 | T | TACACACA others(3): Show |
intron_variant | MODIFIER | NA19043.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0140 | 1 | 286 | 0.0035 | 10 | c.250 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100779485 | T | TATACACA others(3): Show |
intron_variant | MODIFIER | HG00408.hp1 HG00544.hp1 HG00597.hp1 others(35): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0014others(3): Show | a0001c0001t0001a0001c0001t0013a0001c0001t0041others(9): Show | a0001c0001t0001g0092a0001c0001t0001g0098a0001c0001t0001g0099others(35): Show | 38 | 286 | 0.1329 | 10 | c.250 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100837666 | C | CTTTTTTT others(3): Show |
intron_variant | MODIFIER | HG01256.hp2 HG01934.hp2 HG01975.hp2 others(9): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0004 | a0001c0001t0001a0001c0001t0013a0002c0002t0002others(3): Show | a0001c0001t0001g0069a0001c0001t0001g0084a0001c0001t0001g0088others(9): Show | 12 | 286 | 0.0420 | 10 | c.313 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |