view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | 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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP28_chr18_6724716_6920716 | 6730219 | G | GTATATAT others(3): Show |
intron_variant | MODIFIER | HG02630.hp1 HG06807.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0022a0001c0003t0003 | a0001c0001t0022g0067 a0001c0003t0003g0068 |
2 | 122 | 0.0164 | 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 | a0001c0001t0001g0151 a0008c0011t0005g0152 |
2 | 127 | 0.0157 | 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 | a0003c0013t0011g0062 a0003c0013t0011g0063 a0003c0023t0001g0120 |
3 | 243 | 0.0123 | 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 | a0001c0003t0003g0027 a0001c0003t0003g0085 a0001c0003t0003g0122 |
3 | 208 | 0.0144 | 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 | a0001c0001t0010g0136 a0001c0001t0010g0238 a0001c0001t0010g0303 |
3 | 227 | 0.0132 | 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 | a0001c0001t0021g0089 a0001c0001t0021g0309 |
2 | 21 | 0.0952 | 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(18): Show |
a0001 | a0001c0001a0001c0009 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0239 a0001c0001t0002g0043 a0001c0001t0002g0064 others(16): Show |
21 | 183 | 0.1148 | 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 |
a0001a0002a0011 | a0001c0001a0002c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0001t0003a0002c0002t0001others(4): Show | a0001c0001t0001g0004 a0001c0001t0001g0073 a0001c0001t0001g0074 others(21): Show |
25 | 52 | 0.4808 | 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 | a0002c0003t0001g0012 | 2 | 386 | 0.0052 | 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 | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0090 others(8): Show |
11 | 367 | 0.0300 | 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 | a0001c0001t0001g0113 | 1 | 307 | 0.0033 | 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 | a0002c0003t0001g0147 a0002c0003t0001g0256 a0002c0003t0001g0302 others(1): Show |
4 | 338 | 0.0118 | 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 | a0001c0005t0001g0020 a0001c0005t0001g0021 |
2 | 118 | 0.0169 | 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 | a0001c0001t0005g0084 a0001c0001t0005g0085 a0001c0001t0006g0074 others(23): Show |
26 | 33 | 0.7879 | 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 | a0001c0005t0027g0045 | 1 | 285 | 0.0035 | 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 | a0001c0001t0005g0084 a0001c0001t0005g0085 a0001c0001t0005g0143 others(29): Show |
32 | 130 | 0.2462 | 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(16): Show |
a0001a0011a0018 | a0001c0001a0001c0014a0011c0037others(1): Show | a0001c0001t0002a0001c0001t0004a0001c0014t0004others(2): Show | a0001c0001t0002g0113 a0001c0001t0002g0156 a0001c0001t0002g0166 others(16): Show |
19 | 145 | 0.1310 | 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 | a0001c0002t0001g0263 a0001c0002t0001g0272 a0001c0002t0001g0273 others(9): Show |
12 | 151 | 0.0795 | 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 | a0001c0002t0001g0303 a0001c0002t0005g0293 a0001c0002t0006g0306 |
3 | 142 | 0.0211 | 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(11): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0004a0001c0002t0001 | a0001c0001t0002g0158 a0001c0001t0002g0166 a0001c0001t0002g0169 others(11): Show |
14 | 153 | 0.0915 | 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 | a0001c0001t0004g0165 a0001c0001t0004g0173 a0001c0001t0004g0174 others(3): Show |
6 | 145 | 0.0414 | 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 | a0002c0007t0009g0384 | 1 | 140 | 0.0071 | 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 | 372 | 0.0027 | 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 | a0001c0001t0002g0002 a0001c0001t0002g0096 a0001c0001t0002g0098 others(28): Show |
32 | 162 | 0.1975 | 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 | 131 | 0.0076 | 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 | a0001c0001t0002g0041 a0001c0001t0002g0103 a0001c0001t0002g0126 others(1): Show |
4 | 327 | 0.0122 | 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 | a0001c0001t0001g0332 a0001c0001t0001g0333 a0001c0001t0001g0352 others(68): Show |
71 | 173 | 0.4104 | 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 | a0001c0002t0001g0270 a0001c0003t0003g0382 a0001c0003t0003g0383 |
3 | 395 | 0.0076 | 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 | 3 | 0.6667 | 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 | a0001c0001t0002a0001c0001t0042 | a0001c0001t0002g0019 a0001c0001t0042g0018 |
2 | 135 | 0.0148 | 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 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0010 | a0001c0001t0002g0098 a0001c0001t0010g0097 |
2 | 34 | 0.0588 | 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 | a0001c0001t0009a0001c0001t0017a0001c0001t0045others(2): Show | a0001c0001t0009g0111 a0001c0001t0017g0254 a0001c0001t0045g0229 others(8): Show |
11 | 50 | 0.2200 | 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 | a0001c0001t0044 | a0001c0001t0044g0251 | 1 | 248 | 0.0040 | 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 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0202 a0001c0001t0002g0015 |
2 | 27 | 0.0741 | 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 | a0001c0001t0016 | a0001c0001t0016g0024 | 1 | 66 | 0.0152 | 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 | a0001c0001t0001a0001c0001t0010 | a0001c0001t0001g0182 a0001c0001t0010g0154 |
2 | 11 | 0.1818 | 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 | a0001c0001t0001g0037 a0001c0001t0001g0073 a0001c0001t0001g0074 others(3): Show |
6 | 10 | 0.6000 | 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 | a0001c0001t0001g0141 | 1 | 244 | 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 | a0001c0001t0001g0024 a0001c0001t0001g0025 a0001c0001t0001g0026 others(22): Show |
25 | 30 | 0.8333 | 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 |
a0008 | a0008c0006 | a0008c0006t0002 | a0008c0006t0002g0028 a0008c0006t0002g0086 |
3 | 339 | 0.0088 | 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 | a0001c0001t0001g0062 a0001c0001t0001g0073 a0001c0001t0001g0088 others(6): Show |
9 | 194 | 0.0464 | 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 | a0001c0001t0001g0142 | 1 | 253 | 0.0040 | 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 | a0001c0001t0001g0092 a0001c0001t0001g0098 a0001c0001t0001g0099 others(35): Show |
38 | 169 | 0.2249 | 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 | a0001c0001t0001g0068 a0001c0001t0001g0069 a0001c0001t0001g0077 others(9): Show |
12 | 45 | 0.2667 | 10 | c.313 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100858086 | G | GGGGTGTG others(3): Show |
intron_variant | MODIFIER | HG03492.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0152 | 1 | 121 | 0.0083 | 10 | c.313 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100858086 | G | GGTGTGTG others(3): Show |
intron_variant | MODIFIER | HG00597.hp1 HG00735.hp1 HG00738.hp1 others(12): Show |
a0001a0002 | a0001c0001a0001c0014a0002c0004 | a0001c0001t0001a0001c0001t0041a0001c0014t0001others(1): Show | a0001c0001t0001g0065 a0001c0001t0001g0067 a0001c0001t0001g0068 others(12): Show |
15 | 135 | 0.1111 | 10 | c.313 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100858086 | G | GTTGTGTG others(3): Show |
intron_variant | MODIFIER | NA19091.hp1 | a0001 | a0001c0012 | a0001c0012t0001 | a0001c0012t0001g0133 | 1 | 121 | 0.0083 | 10 | c.313 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | chr11 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100858117 | G | GTGTGTGT others(3): Show |
intron_variant | MODIFIER | HG00423.hp1 HG02004.hp2 HG02738.hp1 others(3): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0006a0001c0003t0026 | a0001c0001t0001g0062 a0001c0001t0001g0088 a0001c0003t0006g0164 others(3): Show |
6 | 161 | 0.0373 | 10 | c.313 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100875073 | G | GTCTCTCT others(3): Show |
intron_variant | MODIFIER | HG02818.hp2 | a0002 | a0002c0002 | a0002c0002t0008 | a0002c0002t0008g0005 | 1 | 257 | 0.0039 | 10 | c.384 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100893158 | G | GGTGTGTG others(3): Show |
intron_variant | MODIFIER | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(80): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0003a0001c0012others(4): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0013others(14): Show | a0001c0001t0001g0007 a0001c0001t0001g0011 a0001c0001t0001g0022 others(80): Show |
83 | 112 | 0.7411 | 10 | c.385 others(29): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |