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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARFGEF2_chr20_48916711_49041693 | 48918076 | T | TATATACA others(23): Show |
upstream_gene_variant | MODIFIER | HG00558.hp2 HG00642.hp1 HG01243.hp1 others(16): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0002a0001c0003t0001a0001c0003t0009 | a0001c0001t0002g0116 a0001c0003t0001g0031 a0001c0003t0001g0035 others(16): Show |
19 | 133 | 0.1429 | 30 | c.-38 others(41): Show |
ARFGEF2 | ENSG00000124198.10 | transcript | ENST00000371917.5 | protein_coding | 3634 | chr20 | TogoVar | |||||||
ARFIP1_chr4_152774954_152917357 | 152804089 | C | CATGTATT others(23): Show |
intron_variant | MODIFIER | HG02602.hp2 HG03710.hp2 NA20752.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0003 | a0001c0001t0002g0217 a0001c0001t0003g0268 a0001c0001t0003g0320 |
3 | 244 | 0.0123 | 30 | c.-10 others(49): Show |
ARFIP1 | ENSG00000164144.16 | transcript | ENST00000353617.7 | protein_coding | 1/8 | chr4 | TogoVar | |||||||
ARFRP1_chr20_63693647_63712976 | 63693675 | A | ACCTCCAC others(23): Show |
downstream_gene_variant | MODIFIER | HG01891.hp2 HG01952.hp2 NA18984.hp1 |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0001 a0001c0002t0002g0095 |
3 | 157 | 0.0191 | 30 | c.*67 others(41): Show |
ARFRP1 | ENSG00000101246.20 | transcript | ENST00000622789.5 | protein_coding | 4971 | chr20 | TogoVar | |||||||
ARFRP1_chr20_63693647_63712976 | 63693699 | A | ACCACCTC others(23): Show |
downstream_gene_variant | MODIFIER | NA18943.hp2 NA18979.hp1 NA18990.hp1 others(3): Show |
a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0001 a0001c0002t0002g0009 a0001c0002t0002g0011 others(2): Show |
6 | 194 | 0.0309 | 30 | c.*67 others(41): Show |
ARFRP1 | ENSG00000101246.20 | transcript | ENST00000622789.5 | protein_coding | 4947 | chr20 | TogoVar | |||||||
ARHGAP10_chr4_147727088_148077776 | 148017680 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | HG02145.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0061 | 1 | 66 | 0.0152 | 30 | c.171 others(49): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148043724 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | NA18979.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0066 | 1 | 104 | 0.0096 | 30 | c.186 others(49): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP10_chr4_147727088_148077776 | 148064647 | T | TGCGTTAG others(23): Show |
intron_variant | MODIFIER | HG01070.hp1 HG01167.hp2 HG02145.hp1 others(8): Show |
a0001 | a0001c0001a0001c0008 | a0001c0001t0001a0001c0001t0002a0001c0008t0001 | a0001c0001t0001g0016 a0001c0001t0001g0035 a0001c0001t0001g0047 others(8): Show |
11 | 104 | 0.1058 | 30 | c.227 others(47): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143413966 | T | TGTGTGTG others(23): Show |
intron_variant | MODIFIER | HG01243.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0007 | 1 | 22 | 0.0455 | 30 | c.475 others(49): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143542737 | T | TATATATG others(23): Show |
intron_variant | MODIFIER | HG01358.hp1 NA18953.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0072 a0001c0001t0001g0080 |
2 | 160 | 0.0125 | 30 | c.926 others(49): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 10/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143656934 | G | GGTGTGTG others(23): Show |
intron_variant | MODIFIER | NA19085.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0051 | 1 | 10 | 0.1000 | 30 | c.113 others(51): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143673758 | G | GTGTGTGT others(23): Show |
intron_variant | MODIFIER | HG02148.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0073 | 1 | 18 | 0.0556 | 30 | c.113 others(51): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143673758 | G | GTGTGTGT others(23): Show |
intron_variant | MODIFIER | NA18991.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0086 | 1 | 18 | 0.0556 | 30 | c.113 others(51): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129625420 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | HG00423.hp1 HG02155.hp2 HG02615.hp2 others(9): Show |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0008 | a0001c0001t0001a0001c0001t0002a0002c0002t0001others(1): Show | a0001c0001t0001g0075 a0001c0001t0001g0084 a0001c0001t0001g0091 others(9): Show |
12 | 220 | 0.0545 | 30 | c.786 others(47): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | |||||||
ARHGAP18_chr6_129571132_129715177 | 129625607 | T | TTATTATA others(23): Show |
intron_variant | MODIFIER | HG00140.hp2 HG00639.hp1 HG00642.hp1 others(8): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001a0002c0002t0018 | a0001c0001t0001g0080 a0001c0001t0001g0108 a0001c0001t0001g0109 others(8): Show |
11 | 235 | 0.0468 | 30 | c.786 others(47): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | |||||||
ARHGAP20_chr11_110572043_110717437 | 110687035 | C | CATATATA others(23): Show |
intron_variant | MODIFIER | HG01074.hp1 HG01891.hp2 HG02040.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0150 a0001c0001t0002g0156 a0001c0001t0002g0157 others(2): Show |
5 | 130 | 0.0385 | 30 | c.188 others(47): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24628810 | T | TATATATA others(23): Show |
intron_variant | MODIFIER | HG01496.hp1 HG01516.hp2 HG02027.hp2 others(7): Show |
a0002 | a0002c0002a0002c0017 | a0002c0002t0001a0002c0002t0014a0002c0017t0001 | a0002c0002t0001g0020 a0002c0002t0001g0114 a0002c0002t0001g0115 others(7): Show |
10 | 346 | 0.0289 | 30 | c.495 others(47): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24628982 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | HG03471.hp2 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0134 | 1 | 140 | 0.0071 | 30 | c.495 others(47): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | |||||||
ARHGAP22_chr10_48441036_48610073 | 48577793 | C | CTTTTACT others(23): Show |
intron_variant | MODIFIER | HG00597.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0199 | 1 | 237 | 0.0042 | 30 | c.234 others(47): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 2/9 | chr10 | TogoVar | |||||||
ARHGAP23_chr17_38423464_38517385 | 38513074 | T | TTAAATAT others(23): Show |
downstream_gene_variant | MODIFIER | HG00323.hp1 HG01109.hp1 HG01243.hp1 others(20): Show |
a0001 | a0001c0001a0001c0003a0001c0004others(5): Show | a0001c0001t0001a0001c0001t0003a0001c0003t0001others(6): Show | a0001c0001t0001g0002 a0001c0001t0001g0019 a0001c0001t0001g0034 others(20): Show |
23 | 74 | 0.3108 | 30 | c.*21 others(41): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 690 | chr17 | TogoVar | |||||||
ARHGAP23_chr17_38423464_38517385 | 38513074 | T | TTAAATAT others(23): Show |
downstream_gene_variant | MODIFIER | NA18995.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0077 | 1 | 52 | 0.0192 | 30 | c.*21 others(41): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 690 | chr17 | TogoVar | |||||||
ARHGAP24_chr4_85470150_86007666 | 85733060 | C | CTTTTTTT others(23): Show |
intron_variant | MODIFIER | HG01109.hp2 NA21309.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0030 a0001c0002t0002g0060 |
2 | 16 | 0.1250 | 30 | c.268 others(49): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142949200 | A | AGAGGAGA others(23): Show |
intron_variant | MODIFIER | HG03453.hp2 | a0001 | a0001c0001 | a0001c0001t0029 | a0001c0001t0029g0102 | 1 | 181 | 0.0055 | 30 | c.110 others(51): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142949202 | A | AGAGGAGA others(23): Show |
intron_variant | MODIFIER | HG00408.hp2 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0161 | 1 | 178 | 0.0056 | 30 | c.110 others(51): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142949221 | G | GAGAGAGA others(23): Show |
intron_variant | MODIFIER | HG02155.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0019 | 1 | 76 | 0.0132 | 30 | c.110 others(51): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | |||||||
ARHGAP26_chr5_142765377_143234007 | 142949221 | G | GAGAGAGG others(23): Show |
intron_variant | MODIFIER | HG02647.hp2 HG03098.hp1 NA19043.hp1 |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0014a0001c0001t0021 | a0001c0001t0004g0111 a0001c0001t0014g0041 a0001c0001t0021g0081 |
3 | 78 | 0.0385 | 30 | c.110 others(51): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | |||||||
ARHGAP26_chr5_142765377_143234007 | 142963198 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | NA19009.hp1 | a0001 | a0001c0003 | a0001c0003t0005 | a0001c0003t0005g0060 | 1 | 144 | 0.0069 | 30 | c.110 others(51): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142963198 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | HG02280.hp2 | a0001 | a0001c0001 | a0001c0001t0024 | a0001c0001t0024g0103 | 1 | 144 | 0.0069 | 30 | c.110 others(51): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142963198 | A | ATATATAT others(23): Show |
intron_variant | MODIFIER | NA19083.hp2 | a0001 | a0001c0009 | a0001c0009t0003 | a0001c0009t0003g0014 | 1 | 144 | 0.0069 | 30 | c.110 others(51): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143012552 | C | CATACATA others(23): Show |
intron_variant | MODIFIER | HG02647.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0111 | 1 | 48 | 0.0208 | 30 | c.110 others(49): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143012552 | C | CATACATA others(23): Show |
intron_variant | MODIFIER | HG02280.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0087 | 1 | 48 | 0.0208 | 30 | c.110 others(49): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143012552 | C | CATACATA others(23): Show |
intron_variant | MODIFIER | HG02647.hp1 HG03710.hp1 NA18957.hp2 others(1): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0003a0001c0001t0010others(1): Show | a0001c0001t0001g0017 a0001c0001t0003g0174 a0001c0001t0010g0080 others(1): Show |
4 | 51 | 0.0784 | 30 | c.110 others(49): 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(23): Show |
intron_variant | MODIFIER | HG02109.hp1 | a0001 | a0001c0001 | a0001c0001t0015 | a0001c0001t0015g0123 | 1 | 48 | 0.0208 | 30 | c.110 others(49): 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(23): Show |
intron_variant | MODIFIER | HG02523.hp2 NA18995.hp2 NA19043.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0021a0001c0002t0002a0001c0002t0003 | a0001c0001t0021g0081 a0001c0002t0002g0129 a0001c0002t0003g0168 |
3 | 50 | 0.0600 | 30 | c.110 others(49): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP27_chr17_45388908_45437870 | 45399591 | C | CAAAGAAA others(23): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00621.hp2 HG00639.hp2 others(54): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0002a0002c0010others(6): Show | a0001c0001t0001a0002c0002t0001a0002c0002t0002others(10): Show | a0001c0001t0001g0183 a0001c0001t0001g0206 a0001c0001t0001g0214 others(50): Show |
57 | 93 | 0.6129 | 30 | c.174 others(49): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | TogoVar | |||||||
ARHGAP28_chr18_6724716_6920716 | 6730219 | G | GTATATAT others(23): Show |
intron_variant | MODIFIER | HG01081.hp2 | a0001 | a0001c0010 | a0001c0010t0003 | a0001c0010t0003g0114 | 1 | 121 | 0.0083 | 30 | c.122 others(45): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6730219 | G | GTATGTAT others(23): Show |
intron_variant | MODIFIER | HG03579.hp2 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0119 | 1 | 121 | 0.0083 | 30 | c.122 others(45): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6730219 | G | GTATGTAT others(23): Show |
intron_variant | MODIFIER | HG02155.hp1 | a0003 | a0003c0004 | a0003c0004t0001 | a0003c0004t0001g0125 | 1 | 121 | 0.0083 | 30 | c.122 others(45): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6841156 | T | TCTCACTG others(23): Show |
intron_variant | MODIFIER | HG04184.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0011 | 1 | 246 | 0.0041 | 30 | c.543 others(47): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | TogoVar | |||||||
ARHGAP31_chr3_119289383_119425714 | 119293703 | A | AGTGTGTG others(23): Show |
upstream_gene_variant | MODIFIER | HG00639.hp1 HG02055.hp1 HG02129.hp1 others(21): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0004others(6): Show | a0001c0001t0006a0001c0001t0011a0001c0001t0017others(15): Show | a0001c0001t0006g0026 a0001c0001t0011g0300 a0001c0001t0017g0176 others(21): Show |
24 | 224 | 0.1071 | 30 | c.-12 others(41): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 679 | chr3 | TogoVar | |||||||
ARHGAP31_chr3_119289383_119425714 | 119307940 | C | CAAAAAAA others(23): Show |
intron_variant | MODIFIER | NA18962.hp2 | a0001 | a0001c0001 | a0001c0001t0005 | a0001c0001t0005g0170 | 1 | 8 | 0.1250 | 30 | c.100 others(49): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119321279 | C | CTATATAT others(23): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00621.hp2 others(18): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0005a0001c0001t0006a0001c0002t0001others(7): Show | a0001c0001t0005g0084 a0001c0001t0005g0085 a0001c0001t0006g0074 others(18): Show |
21 | 193 | 0.1088 | 30 | c.100 others(49): 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(23): Show |
intron_variant | MODIFIER | HG03239.hp2 HG04228.hp1 NA18971.hp2 others(4): Show |
a0001a0012 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0008a0001c0001t0018a0001c0001t0020others(4): Show | a0001c0001t0008g0171 a0001c0001t0018g0209 a0001c0001t0020g0065 others(4): Show |
7 | 105 | 0.0667 | 30 | c.683 others(47): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129143072 | C | CATATATA others(23): Show |
intron_variant | MODIFIER | HG01258.hp2 HG02129.hp2 NA18943.hp2 others(2): Show |
a0001a0018 | a0001c0001a0018c0031 | a0001c0001t0002a0001c0001t0004a0018c0031t0004 | a0001c0001t0002g0117 a0001c0001t0004g0154 a0001c0001t0004g0175 others(2): Show |
5 | 107 | 0.0467 | 30 | c.226 others(49): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 2/22 | chr11 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144556598 | A | AGGCAAAG others(23): Show |
intron_variant | MODIFIER | HG00280.hp1 HG00408.hp2 HG00639.hp1 others(6): Show |
a0001a0003 | a0001c0003a0001c0005a0001c0010others(1): Show | a0001c0003t0001a0001c0003t0009a0001c0005t0001others(3): Show | a0001c0003t0001g0004 a0001c0003t0001g0011 a0001c0003t0001g0095 others(6): Show |
9 | 244 | 0.0369 | 30 | c.513 others(45): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144617425 | A | ACAAACCA others(23): Show |
intron_variant | MODIFIER | HG02630.hp1 | a0005 | a0005c0011 | a0005c0011t0001 | a0005c0011t0001g0067 | 1 | 244 | 0.0041 | 30 | c.-81 others(49): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100751277 | G | GTTTTTTT others(23): Show |
intron_variant | MODIFIER | HG02818.hp1 | a0002 | a0002c0006 | a0002c0006t0008 | a0002c0006t0008g0240 | 1 | 267 | 0.0037 | 30 | c.155 others(49): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100837926 | T | TTTTTATT others(23): Show |
intron_variant | MODIFIER | HG01261.hp1 HG02056.hp1 HG02896.hp1 others(3): Show |
a0001a0002 | a0001c0001a0001c0014a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0014t0001others(1): Show | a0001c0001t0001g0002 a0001c0001t0001g0171 a0001c0001t0002g0096 others(3): Show |
6 | 27 | 0.2222 | 30 | c.313 others(49): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903117 | G | GCGCGCAC others(23): Show |
intron_variant | MODIFIER | HG02055.hp2 | a0002 | a0002c0005 | a0002c0005t0010 | a0002c0005t0010g0030 | 1 | 40 | 0.0250 | 30 | c.385 others(49): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTCTTTT others(23): Show |
intron_variant | MODIFIER | HG02129.hp2 HG03834.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0088 a0001c0001t0001g0129 |
2 | 25 | 0.0800 | 30 | c.245 others(49): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12841594 | T | TCTCTCTC others(23): Show |
intron_variant | MODIFIER | NA20129.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0030 | 1 | 124 | 0.0081 | 30 | c.53+ others(47): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar |