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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP26_chr5_142765377_143234007 | 142963194 | A | ATGTGTGT others(7): Show |
intron_variant | MODIFIER | HG02647.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0111 | 1 | 188 | 0.0053 | 14 | c.110 others(35): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142963198 | A | ATGTGTGT others(7): Show |
intron_variant | MODIFIER | HG02257.hp2 HG02970.hp1 NA19240.hp2 |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0016a0001c0001t0028 | a0001c0001t0006g0104 a0001c0001t0016g0040 a0001c0001t0028g0085 |
3 | 146 | 0.0205 | 14 | c.110 others(35): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143012552 | C | CATATATA others(7): Show |
intron_variant | MODIFIER | HG00609.hp2 HG02615.hp1 HG02717.hp1 others(5): Show |
a0001a0002 | a0001c0001a0002c0007 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(3): Show | a0001c0001t0001g0012 a0001c0001t0001g0029 a0001c0001t0002g0036 others(5): Show |
8 | 55 | 0.1455 | 14 | c.110 others(33): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143012556 | T | TATATATA others(7): Show |
intron_variant | MODIFIER | HG02572.hp2 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0094 | 1 | 195 | 0.0051 | 14 | c.110 others(33): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143087636 | C | CTTTTTTT others(7): Show |
intron_variant | MODIFIER | HG03491.hp1 HG03579.hp2 NA18978.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0002a0001c0001t0006a0001c0002t0007others(1): Show | a0001c0001t0002g0013 a0001c0001t0006g0064 a0001c0002t0007g0067 others(1): Show |
4 | 49 | 0.0816 | 14 | c.153 others(35): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143115321 | G | GAAACTTA others(7): Show |
intron_variant | MODIFIER | HG02572.hp2 HG03209.hp2 |
a0001 | a0001c0001 | a0001c0001t0011a0001c0001t0031 | a0001c0001t0011g0094 a0001c0001t0031g0051 |
2 | 196 | 0.0102 | 14 | c.153 others(33): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143167482 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG02723.hp2 HG02922.hp1 |
a0001 | a0001c0003 | a0001c0003t0002a0001c0003t0012 | a0001c0003t0002g0044 a0001c0003t0012g0093 |
2 | 34 | 0.0588 | 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 | C | CTTTTTTT others(7): Show |
intron_variant | MODIFIER | HG01071.hp1 NA18945.hp1 |
a0001 | a0001c0002a0001c0003 | a0001c0002t0008a0001c0003t0003 | a0001c0002t0008g0009 a0001c0003t0003g0198 |
2 | 26 | 0.0769 | 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 | 143232630 | C | CTTTTTTT others(7): Show |
downstream_gene_variant | MODIFIER | HG00738.hp2 HG02818.hp2 HG02897.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0009a0001c0001t0011others(2): Show | a0001c0001t0002g0001 a0001c0001t0009g0026 a0001c0001t0009g0039 others(5): Show |
8 | 37 | 0.2162 | 14 | c.*10 others(27): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 3624 | chr5 | TogoVar | |||||||
ARHGAP27_chr17_45388908_45437870 | 45411795 | T | TCACACAC others(7): Show |
intron_variant | MODIFIER | HG02647.hp1 | a0001 | a0001c0015 | a0001c0015t0009 | a0001c0015t0009g0190 | 1 | 289 | 0.0035 | 14 | c.658 others(31): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | TogoVar | |||||||
ARHGAP28_chr18_6724716_6920716 | 6729574 | G | GCACACAC others(7): Show |
upstream_gene_variant | MODIFIER | HG00099.hp1 HG00621.hp2 HG02523.hp1 others(8): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0002c0002others(4): Show | a0001c0001t0001a0001c0001t0019a0001c0003t0003others(5): Show | a0001c0001t0001g0082 a0001c0001t0019g0008 a0001c0003t0003g0079 others(8): Show |
11 | 170 | 0.0647 | 14 | c.-24 others(23): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 141 | chr18 | TogoVar | |||||||
ARHGAP28_chr18_6724716_6920716 | 6729574 | G | GCGCACAC others(7): Show |
upstream_gene_variant | MODIFIER | HG02602.hp1 | a0001 | a0001c0001 | a0001c0001t0017 | a0001c0001t0017g0118 | 1 | 160 | 0.0063 | 14 | c.-24 others(23): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 141 | chr18 | TogoVar | |||||||
ARHGAP28_chr18_6724716_6920716 | 6730219 | G | GTATATAT others(7): Show |
intron_variant | MODIFIER | HG00280.hp1 HG03209.hp1 HG03669.hp2 |
a0001a0006 | a0001c0001a0006c0008 | a0001c0001t0001a0006c0008t0002 | a0001c0001t0001g0070 a0001c0001t0001g0071 a0006c0008t0002g0069 |
3 | 123 | 0.0244 | 14 | c.122 others(29): 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(7): Show |
intron_variant | MODIFIER | HG01346.hp1 HG02280.hp2 HG02615.hp1 others(3): Show |
a0001a0002a0007 | a0001c0001a0002c0002a0007c0009 | a0001c0001t0001a0001c0001t0008a0002c0002t0002others(2): Show | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0008g0143 others(3): Show |
6 | 131 | 0.0458 | 14 | c.122 others(31): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6841208 | C | CCTCTCTC others(7): Show |
intron_variant | MODIFIER | HG00280.hp2 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0235 | 1 | 165 | 0.0061 | 14 | c.543 others(31): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6854742 | G | GCTGCAGC others(7): Show |
intron_variant | MODIFIER | HG02895.hp2 | a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0245 | 1 | 179 | 0.0056 | 14 | c.636 others(31): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6909301 | T | TTTTCTTT others(7): Show |
intron_variant | MODIFIER | HG01175.hp1 HG01243.hp1 HG03669.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0097 a0001c0001t0001g0107 a0001c0001t0001g0222 |
3 | 193 | 0.0155 | 14 | c.209 others(31): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 17/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP29_chr1_94163905_94242584 | 94166813 | G | GCACGCAC others(7): Show |
downstream_gene_variant | MODIFIER | HG02922.hp1 NA18522.hp1 |
a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0016 | 2 | 226 | 0.0088 | 14 | c.*70 others(25): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2091 | chr1 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161053462 | T | TTCTCTCT others(7): Show |
intron_variant | MODIFIER | HG00438.hp2 HG00621.hp1 HG01074.hp2 others(2): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0003a0002c0002t0001 | a0001c0001t0001g0129 a0001c0001t0003g0154 a0002c0002t0001g0023 others(2): Show |
5 | 32 | 0.1563 | 14 | c.537 others(27): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 5/11 | chr1 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161064761 | G | GAAAGAAA others(7): Show |
intron_variant | MODIFIER | NA19004.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0051 | 1 | 388 | 0.0026 | 14 | c.97+ others(29): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161064831 | G | GAAAGAAA others(7): Show |
intron_variant | MODIFIER | HG00642.hp1 HG02572.hp1 HG04115.hp1 others(1): Show |
a0002 | a0002c0003 | a0002c0003t0001 | a0002c0003t0001g0029 a0002c0003t0001g0151 a0002c0003t0001g0255 others(1): Show |
4 | 338 | 0.0118 | 14 | c.97+ others(29): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | |||||||
ARHGAP31_chr3_119289383_119425714 | 119297909 | A | AACACACA others(7): Show |
intron_variant | MODIFIER | HG01884.hp1 HG02896.hp1 HG02897.hp2 others(1): Show |
a0001a0004 | a0001c0001a0001c0002a0004c0007 | a0001c0001t0059a0001c0002t0028a0004c0007t0015 | a0001c0001t0059g0027 a0001c0002t0028g0018 a0001c0002t0028g0019 others(1): Show |
4 | 120 | 0.0333 | 14 | c.100 others(31): 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(7): Show |
intron_variant | MODIFIER | HG01071.hp2 HG01884.hp2 HG02148.hp1 others(15): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0005others(2): Show | a0001c0001t0008a0001c0001t0039a0001c0001t0040others(10): Show | a0001c0001t0008g0194 a0001c0001t0039g0259 a0001c0001t0040g0254 others(15): Show |
18 | 116 | 0.1552 | 14 | c.683 others(31): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 128976078 | C | CATATATA others(7): Show |
intron_variant | MODIFIER | HG06807.hp1 | a0001 | a0001c0003 | a0001c0003t0005 | a0001c0003t0005g0188 | 1 | 177 | 0.0056 | 14 | c.219 others(31): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 20/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 128982474 | C | CGTGTGTG others(7): Show |
intron_variant | MODIFIER | HG01261.hp1 NA18955.hp2 NA19002.hp1 |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0183 a0001c0001t0004g0184 a0001c0001t0004g0369 |
3 | 129 | 0.0233 | 14 | c.152 others(31): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 15/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 128985858 | G | GTATATAT others(7): Show |
intron_variant | MODIFIER | HG02280.hp1 HG02615.hp2 |
a0001 | a0001c0002a0001c0010 | a0001c0002t0001a0001c0010t0014 | a0001c0002t0001g0246 a0001c0010t0014g0200 |
2 | 141 | 0.0142 | 14 | c.152 others(31): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 15/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 128985858 | G | GTGTATAT others(7): Show |
intron_variant | MODIFIER | HG01496.hp2 HG02055.hp2 |
a0001 | a0001c0016a0001c0022 | a0001c0016t0014a0001c0022t0001 | a0001c0016t0014g0191 a0001c0022t0001g0249 |
2 | 141 | 0.0142 | 14 | c.152 others(31): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 15/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 128985858 | G | GTGTGTAT others(7): Show |
intron_variant | MODIFIER | NA18994.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0156 | 1 | 140 | 0.0071 | 14 | c.152 others(31): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 15/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 128985858 | G | GTGTGTGT others(7): Show |
intron_variant | MODIFIER | NA19078.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0179 | 1 | 140 | 0.0071 | 14 | c.152 others(31): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 15/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 128989516 | T | TCACACAC others(7): Show |
intron_variant | MODIFIER | HG00741.hp2 HG01496.hp2 HG02004.hp2 others(6): Show |
a0001 | a0001c0001a0001c0010a0001c0016others(1): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(4): Show | a0001c0001t0002g0115 a0001c0001t0002g0118 a0001c0001t0002g0390 others(6): Show |
9 | 139 | 0.0647 | 14 | c.119 others(33): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 12/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129035173 | C | CCTCTCTC others(7): Show |
intron_variant | MODIFIER | HG03130.hp1 | a0001 | a0001c0001 | a0001c0001t0022 | a0001c0001t0022g0148 | 1 | 324 | 0.0031 | 14 | c.104 others(33): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 11/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129143072 | C | CATATATA others(7): Show |
intron_variant | MODIFIER | HG00558.hp2 HG04204.hp2 NA18939.hp1 others(7): Show |
a0001a0016 | a0001c0002a0016c0029 | a0001c0002t0001a0001c0002t0005a0016c0029t0023 | a0001c0002t0001g0263 a0001c0002t0001g0271 a0001c0002t0001g0273 others(7): Show |
10 | 112 | 0.0893 | 14 | c.226 others(33): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 2/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129193703 | A | ATATATAT others(7): Show |
upstream_gene_variant | MODIFIER | HG01952.hp1 NA18952.hp2 |
a0002a0010 | a0002c0004a0010c0027 | a0002c0004t0013a0010c0027t0001 | a0002c0004t0013g0395 a0010c0027t0001g0236 |
2 | 217 | 0.0092 | 14 | c.-15 others(25): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 1379 | chr11 | TogoVar | |||||||
ARHGAP33_chr19_35770564_35793822 | 35771989 | C | CTTTTTTT others(7): Show |
upstream_gene_variant | MODIFIER | HG02055.hp1 HG02630.hp2 HG03041.hp1 others(2): Show |
a0001 | a0001c0002a0001c0006 | a0001c0002t0001a0001c0006t0001 | a0001c0002t0001g0001 a0001c0002t0001g0018 a0001c0002t0001g0050 others(1): Show |
5 | 6 | 0.8333 | 14 | c.-36 others(25): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 3574 | chr19 | TogoVar | |||||||
ARHGAP35_chr19_46855997_47010077 | 46983054 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG02027.hp1 | a0002 | a0002c0004 | a0002c0004t0002 | a0002c0004t0002g0008 | 1 | 59 | 0.0169 | 14 | c.382 others(33): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP36_chrX_131053346_131094885 | 131075623 | A | ATGTGTGT others(7): Show |
intron_variant | MODIFIER | HG01167.hp1 HG01169.hp1 HG02630.hp1 |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0032 a0001c0001t0004g0034 |
3 | 12 | 0.2500 | 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 | C | CATATATA others(7): Show |
intron_variant | MODIFIER | HG01167.hp1 HG01169.hp1 HG02109.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0004 | a0001c0001t0001g0018 a0001c0001t0001g0204 a0001c0001t0003g0017 others(2): Show |
8 | 12 | 0.6667 | 14 | c.-14 others(33): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144669506 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG03209.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0020 | 1 | 6 | 0.1667 | 14 | c.-82 others(33): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | |||||||
ARHGAP40_chr20_38596809_38655653 | 38630082 | T | TTCTTTCT others(7): Show |
intron_variant | MODIFIER | HG02896.hp1 HG02897.hp1 |
a0008 | a0008c0006 | a0008c0006t0002 | a0008c0006t0002g0105 a0008c0006t0002g0107 |
2 | 341 | 0.0059 | 14 | c.783 others(29): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 5/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100779485 | T | TATATATA others(7): Show |
intron_variant | MODIFIER | NA18970.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0143 | 1 | 132 | 0.0076 | 14 | c.250 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 2/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100794075 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG02559.hp2 | a0002 | a0002c0011 | a0002c0011t0017 | a0002c0011t0017g0209 | 1 | 14 | 0.0714 | 14 | c.251 others(30): 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(7): Show |
intron_variant | MODIFIER | HG00423.hp2 HG01081.hp1 HG02257.hp2 others(4): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0005 | a0001c0001t0001a0001c0001t0019a0002c0002t0008others(1): Show | a0001c0001t0001g0109 a0001c0001t0001g0131 a0001c0001t0019g0078 others(4): Show |
7 | 40 | 0.1750 | 14 | c.313 others(33): 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(7): Show |
intron_variant | MODIFIER | HG02083.hp1 HG02165.hp1 HG02602.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0034 | a0001c0001t0001g0066 a0001c0001t0001g0092 a0001c0001t0001g0265 others(1): Show |
4 | 124 | 0.0323 | 14 | c.313 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100858117 | G | GTGTGTGT others(7): Show |
intron_variant | MODIFIER | HG01106.hp2 HG01515.hp1 HG01978.hp1 others(7): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0007 | a0001c0001t0001a0001c0001t0030a0002c0002t0004others(2): Show | a0001c0001t0001g0123 a0001c0001t0001g0180 a0001c0001t0001g0187 others(7): Show |
10 | 165 | 0.0606 | 14 | c.313 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100893158 | G | GGTGTGTG others(7): Show |
intron_variant | MODIFIER | HG01346.hp1 HG01358.hp1 HG02486.hp1 others(2): Show |
a0001a0002 | a0001c0001a0001c0010a0002c0002 | a0001c0001t0001a0001c0010t0001a0002c0002t0002 | a0001c0001t0001g0002 a0001c0001t0001g0023 a0001c0001t0001g0074 others(2): Show |
5 | 34 | 0.1471 | 14 | c.385 others(33): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903117 | G | GCACACAC others(7): Show |
intron_variant | MODIFIER | HG01106.hp2 HG03490.hp2 HG03492.hp1 others(2): Show |
a0002a0003a0005 | a0002c0002a0002c0006a0003c0007others(1): Show | a0002c0002t0012a0002c0006t0008a0003c0007t0005others(1): Show | a0002c0002t0012g0049 a0002c0002t0012g0050 a0002c0006t0008g0243 others(2): Show |
5 | 44 | 0.1136 | 14 | c.385 others(33): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903117 | G | GCGCACAC others(7): Show |
intron_variant | MODIFIER | HG01346.hp2 HG02056.hp1 HG02129.hp2 others(9): Show |
a0001 | a0001c0001a0001c0014 | a0001c0001t0001a0001c0014t0001 | a0001c0001t0001g0080 a0001c0001t0001g0129 a0001c0001t0001g0132 others(9): Show |
12 | 51 | 0.2353 | 14 | c.385 others(33): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903117 | G | GCGCGCAC others(7): Show |
intron_variant | MODIFIER | NA19002.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0225 | 1 | 40 | 0.0250 | 14 | c.385 others(33): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903706 | C | CAAAAAAA others(7): Show |
intron_variant | MODIFIER | HG01257.hp1 HG01258.hp1 |
a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0019 a0002c0002t0002g0026 |
2 | 263 | 0.0076 | 14 | c.385 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903709 | A | AATATATA others(7): Show |
intron_variant | MODIFIER | HG03492.hp2 NA18957.hp1 NA18957.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0152 a0001c0001t0001g0208 a0001c0001t0001g0279 |
3 | 70 | 0.0429 | 14 | c.385 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |