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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARFGEF3_chr6_138156939_138349663 | 138343453 | GGGTGTTT others(6): Show |
G | 3_prime_UTR_variant | MODIFIER | HG02055.hp2 HG02451.hp1 HG02559.hp2 others(6): Show |
a0001a0002 | a0001c0001a0001c0005a0001c0015others(3): Show | a0001c0001t0008a0001c0005t0008a0001c0015t0021others(4): Show | a0001c0001t0008g0119a0001c0001t0008g0179a0001c0001t0008g0184others(6): Show | 9 | 190 | 0.0474 | -13 | c.*69 others(24): Show |
ARFGEF3 | ENSG00000112379.9 | transcript | ENST00000251691.5 | protein_coding | 34/34 | 6971 | INFO_REALIGN_3_PRIME | chr6 | TogoVar | ||||
ARFGEF3_chr6_138156939_138349663 | 138345449 | AATTATAT others(6): Show |
A | downstream_gene_variant | MODIFIER | NA18906.hp1 | a0002 | a0002c0011 | a0002c0011t0005 | a0002c0011t0005g0013 | 1 | 190 | 0.0053 | -13 | c.*89 others(24): Show |
ARFGEF3 | ENSG00000112379.9 | transcript | ENST00000251691.5 | protein_coding | 787 | chr6 | TogoVar | ||||||
ARFIP1_chr4_152774954_152917357 | 152795820 | ATTTTTTT others(6): Show |
A | intron_variant | MODIFIER | HG01257.hp1 HG02074.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0083a0001c0001t0003g0127 | 2 | 342 | 0.0059 | -13 | c.-10 others(32): Show |
ARFIP1 | ENSG00000164144.16 | transcript | ENST00000353617.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARFIP1_chr4_152774954_152917357 | 152808283 | ATTTTTTT others(6): Show |
A | intron_variant | MODIFIER | HG02976.hp2 HG03516.hp2 |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0322a0001c0001t0004g0337 | 2 | 342 | 0.0059 | -13 | c.-9- others(30): Show |
ARFIP1 | ENSG00000164144.16 | transcript | ENST00000353617.7 | protein_coding | 1/8 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARFRP1_chr20_63693647_63712976 | 63698624 | TTTTTTAA others(6): Show |
T | downstream_gene_variant | MODIFIER | HG00438.hp1 NA19067.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0007a0001c0001t0001g0010 | 2 | 296 | 0.0068 | -13 | c.*18 others(24): Show |
ARFRP1 | ENSG00000101246.20 | transcript | ENST00000622789.5 | protein_coding | 22 | chr20 | TogoVar | ||||||
ARG1_chr6_131568226_131589329 | 131569420 | TTTTTTTT others(6): Show |
T | upstream_gene_variant | MODIFIER | HG01891.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0030 | 1 | 420 | 0.0024 | -13 | c.-38 others(24): Show |
ARG1 | ENSG00000118520.16 | transcript | ENST00000368087.8 | protein_coding | 3805 | chr6 | TogoVar | ||||||
ARG2_chr14_67614920_67656708 | 67637410 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG02257.hp1 HG02559.hp2 HG02723.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0222a0001c0001t0002g0022a0001c0001t0002g0147others(1): Show | 5 | 438 | 0.0114 | -13 | c.185 others(30): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 2/7 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
ARG2_chr14_67614920_67656708 | 67643852 | TAAAAAAA others(6): Show |
T | intron_variant | MODIFIER | HG01192.hp1 HG01261.hp2 HG01433.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0088a0001c0001t0001g0272a0001c0001t0001g0294others(2): Show | 5 | 438 | 0.0114 | -13 | c.362 others(30): Show |
ARG2 | ENSG00000081181.8 | transcript | ENST00000261783.4 | protein_coding | 3/7 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
ARGFX_chr3_121562949_121595622 | 121576706 | TTTTTCTT others(6): Show |
T | intron_variant | MODIFIER | HG02615.hp1 | a0002 | a0002c0002 | a0002c0002t0019 | a0002c0002t0019g0391 | 1 | 410 | 0.0024 | -13 | c.104 others(26): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARGFX_chr3_121562949_121595622 | 121577240 | TATATATA others(6): Show |
T | intron_variant | MODIFIER | NA19030.hp1 | a0003 | a0003c0003 | a0003c0003t0023 | a0003c0003t0023g0387 | 1 | 410 | 0.0024 | -13 | c.220 others(28): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | chr3 | TogoVar | ||||||
ARGFX_chr3_121562949_121595622 | 121577242 | TATATATA others(6): Show |
T | intron_variant | MODIFIER | HG02258.hp2 HG02280.hp1 HG02615.hp2 others(3): Show |
a0003 | a0003c0003 | a0003c0003t0008a0003c0003t0041a0003c0003t0042 | a0003c0003t0008g0013a0003c0003t0008g0345a0003c0003t0008g0353others(3): Show | 6 | 410 | 0.0146 | -13 | c.220 others(28): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | chr3 | TogoVar | ||||||
ARGFX_chr3_121562949_121595622 | 121579935 | CTTTTCTT others(6): Show |
C | intron_variant | MODIFIER | HG01975.hp2 HG02615.hp1 NA18973.hp2 |
a0001a0002a0004 | a0001c0001a0002c0002a0004c0004 | a0001c0001t0002a0002c0002t0019a0004c0004t0002 | a0001c0001t0002g0045a0002c0002t0019g0391a0004c0004t0002g0052 | 3 | 410 | 0.0073 | -13 | c.220 others(30): Show |
ARGFX | ENSG00000186103.5 | transcript | ENST00000334384.5 | protein_coding | 3/4 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP10_chr4_147727088_148077776 | 148039368 | ATTTTTTT others(6): Show |
A | intron_variant | MODIFIER | NA18906.hp1 | a0004 | a0004c0010 | a0004c0010t0001 | a0004c0010t0001g0048 | 1 | 106 | 0.0094 | -13 | c.186 others(32): Show |
ARHGAP10 | ENSG00000071205.12 | transcript | ENST00000336498.8 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP11B_chr15_30621128_30643810 | 30624418 | CAAAAAAA others(6): Show |
C | upstream_gene_variant | MODIFIER | NA18975.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0022 | 1 | 247 | 0.0041 | -13 | c.-24 others(24): Show |
ARHGAP11B | ENSG00000285077.4 | transcript | ENST00000697964.2 | protein_coding | 1709 | chr15 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31841043 | GAATAAAA others(6): Show |
G | intron_variant | MODIFIER | HG02572.hp1 HG02896.hp2 |
a0001 | a0001c0007 | a0001c0007t0028 | a0001c0007t0028g0239a0001c0007t0028g0240 | 2 | 322 | 0.0062 | -13 | c.129 others(32): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 7/19 | chr10 | TogoVar | ||||||
ARHGAP12_chr10_31800398_31933831 | 31922180 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG02615.hp1 HG03098.hp2 HG03516.hp2 |
a0001 | a0001c0003 | a0001c0003t0010 | a0001c0003t0010g0006a0001c0003t0010g0017a0001c0003t0010g0018 | 3 | 322 | 0.0093 | -13 | c.-11 others(32): Show |
ARHGAP12 | ENSG00000165322.18 | transcript | ENST00000344936.7 | protein_coding | 1/19 | chr10 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143239990 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG03490.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0090 | 1 | 162 | 0.0062 | -13 | c.385 others(32): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 5/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143416816 | CCACCACC others(6): Show |
C | intron_variant | MODIFIER | NA18948.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0081 | 1 | 162 | 0.0062 | -13 | c.475 others(32): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 6/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143605858 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG00642.hp1 NA19043.hp1 NA19240.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0005a0001c0001t0001g0107a0001c0001t0001g0122 | 3 | 162 | 0.0185 | -13 | c.100 others(34): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP15_chr2_143124419_143773352 | 143606058 | AAAAAAAA others(6): Show |
A | intron_variant | MODIFIER | HG01255.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0030 | 1 | 162 | 0.0062 | -13 | c.100 others(34): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 11/13 | chr2 | TogoVar | ||||||
ARHGAP15_chr2_143124419_143773352 | 143686383 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG03654.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0070 | 1 | 162 | 0.0062 | -13 | c.113 others(34): Show |
ARHGAP15 | ENSG00000075884.14 | transcript | ENST00000295095.11 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP18_chr6_129571132_129715177 | 129619345 | CAGGGGGA others(6): Show |
C | intron_variant | MODIFIER | HG02622.hp1 HG02965.hp2 HG03225.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0004a0001c0001t0013 | a0001c0001t0004g0123a0001c0001t0004g0134a0001c0001t0004g0139others(1): Show | 4 | 238 | 0.0168 | -13 | c.787 others(28): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129625143 | TATATATT others(6): Show |
T | intron_variant | MODIFIER | HG03710.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0066 | 1 | 238 | 0.0042 | -13 | c.786 others(30): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129625781 | ATATAATA others(6): Show |
A | intron_variant | MODIFIER | NA18994.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0107 | 1 | 238 | 0.0042 | -13 | c.786 others(30): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129625942 | ATATATTT others(6): Show |
A | intron_variant | MODIFIER | HG00544.hp2 HG00621.hp1 HG00639.hp2 others(49): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0017others(1): Show | a0001c0001t0001g0001a0001c0001t0001g0090a0001c0001t0001g0094others(48): Show | 52 | 238 | 0.2185 | -13 | c.786 others(30): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 5/14 | chr6 | TogoVar | ||||||
ARHGAP18_chr6_129571132_129715177 | 129676915 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | HG02615.hp1 HG02615.hp2 HG02630.hp2 others(1): Show |
a0001a0007 | a0001c0001a0007c0008 | a0001c0001t0003a0001c0001t0011a0007c0008t0004 | a0001c0001t0003g0075a0001c0001t0003g0225a0001c0001t0011g0141others(1): Show | 4 | 238 | 0.0168 | -13 | c.113 others(32): Show |
ARHGAP18 | ENSG00000146376.11 | transcript | ENST00000368149.3 | protein_coding | 1/14 | chr6 | TogoVar | ||||||
ARHGAP19_chr10_97217179_97297637 | 97231059 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG00558.hp2 HG02135.hp1 |
a0002 | a0002c0004 | a0002c0004t0002 | a0002c0004t0002g0072a0002c0004t0002g0089 | 2 | 242 | 0.0083 | -13 | c.128 others(32): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 9/11 | chr10 | TogoVar | ||||||
ARHGAP19_chr10_97217179_97297637 | 97239547 | AGAGGGTG others(6): Show |
A | intron_variant | MODIFIER | NA18969.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0212 | 1 | 242 | 0.0041 | -13 | c.118 others(32): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | TogoVar | ||||||
ARHGAP19_chr10_97217179_97297637 | 97239548 | GAGGGTGT others(6): Show |
G | intron_variant | MODIFIER | NA18986.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0162 | 1 | 242 | 0.0041 | -13 | c.118 others(32): Show |
ARHGAP19 | ENSG00000213390.11 | transcript | ENST00000358531.9 | protein_coding | 8/11 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24580886 | CAAAAAAA others(6): Show |
C | downstream_gene_variant | MODIFIER | NA18957.hp1 NA18992.hp1 NA19005.hp2 others(2): Show |
a0006 | a0006c0006 | a0006c0006t0002a0006c0006t0003 | a0006c0006t0002g0348a0006c0006t0002g0349a0006c0006t0002g0350others(2): Show | 5 | 352 | 0.0142 | -13 | c.*35 others(24): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2727 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24587466 | AAATTTAG others(6): Show |
A | intron_variant | MODIFIER | HG00140.hp1 HG00323.hp1 HG00423.hp2 others(31): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0169a0001c0001t0001g0170a0001c0001t0001g0176others(31): Show | 34 | 352 | 0.0966 | -13 | c.418 others(32): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 25/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24625299 | GAAAAAAA others(6): Show |
G | intron_variant | MODIFIER | HG02257.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0192 | 1 | 352 | 0.0028 | -13 | c.496 others(30): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24695050 | CAAAAAAA others(6): Show |
C | intron_variant | MODIFIER | HG00408.hp2 HG01952.hp1 HG02083.hp2 others(13): Show |
a0001a0003a0006others(1): Show | a0001c0001a0003c0003a0006c0006others(1): Show | a0001c0001t0001a0003c0003t0001a0006c0006t0003others(2): Show | a0001c0001t0001g0160a0001c0001t0001g0170a0001c0001t0001g0199others(13): Show | 16 | 352 | 0.0455 | -13 | c.64- others(30): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | TogoVar | ||||||
ARHGAP22_chr10_48441036_48610073 | 48545884 | CCATTCTA others(6): Show |
C | intron_variant | MODIFIER | HG02965.hp2 | a0001 | a0001c0002 | a0001c0002t0007 | a0001c0002t0007g0160 | 1 | 270 | 0.0037 | -13 | c.322 others(30): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 3/9 | chr10 | TogoVar | ||||||
ARHGAP22_chr10_48441036_48610073 | 48555373 | GAGGAGTG others(6): Show |
G | intron_variant | MODIFIER | HG00558.hp2 HG01074.hp2 HG01081.hp2 others(31): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0078others(31): Show | 34 | 270 | 0.1259 | -13 | c.322 others(26): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 3/9 | chr10 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38504978 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | HG00735.hp2 HG01106.hp1 HG01169.hp1 others(32): Show |
a0001a0008 | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0002others(13): Show | a0001c0001t0001g0006a0001c0001t0001g0064a0001c0001t0001g0077others(32): Show | 35 | 309 | 0.1133 | -13 | c.344 others(32): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85485375 | AAATATAT others(6): Show |
A | intron_variant | MODIFIER | HG03579.hp2 NA20129.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0007 | a0001c0001t0001g0104a0001c0002t0007g0100 | 2 | 108 | 0.0185 | -13 | c.-21 others(30): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85485377 | ATATATAT others(6): Show |
A | intron_variant | MODIFIER | HG02615.hp1 NA18906.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0067a0001c0001t0001g0102 | 2 | 108 | 0.0185 | -13 | c.-21 others(30): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85570366 | CTTTCTTT others(6): Show |
C | intron_variant | MODIFIER | NA18906.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0102 | 1 | 108 | 0.0093 | -13 | c.-20 others(28): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85690202 | TGATATTC others(6): Show |
T | intron_variant | MODIFIER | HG00423.hp2 HG01070.hp1 HG01071.hp1 others(18): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0002t0002a0001c0003t0001others(5): Show | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0048others(18): Show | 21 | 108 | 0.1944 | -13 | c.181 others(32): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85690210 | TTCAGAGA others(6): Show |
T | intron_variant | MODIFIER | HG01516.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0019 | 1 | 108 | 0.0093 | -13 | c.181 others(32): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85875585 | TATTTTAT others(6): Show |
T | intron_variant | MODIFIER | HG01243.hp1 HG02145.hp2 HG02451.hp1 others(3): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0006 | a0001c0001t0001a0001c0001t0005a0001c0003t0001others(1): Show | a0001c0001t0001g0090a0001c0001t0005g0036a0001c0001t0005g0074others(3): Show | 6 | 108 | 0.0556 | -13 | c.269 others(32): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85897191 | CTGGCCCT others(6): Show |
C | intron_variant | MODIFIER | HG02145.hp1 HG03130.hp2 |
a0002 | a0002c0006 | a0002c0006t0006a0002c0006t0018 | a0002c0006t0006g0031a0002c0006t0018g0040 | 2 | 108 | 0.0185 | -13 | c.269 others(32): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142890146 | AAAAAAAT others(6): Show |
A | intron_variant | MODIFIER | HG03710.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0174 | 1 | 198 | 0.0051 | -13 | c.487 others(30): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143056316 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | HG03195.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0022 | 1 | 198 | 0.0051 | -13 | c.143 others(30): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 16/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143177987 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | HG02622.hp1 HG03471.hp2 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0033a0001c0002t0004 | a0001c0001t0033g0053a0001c0002t0004g0100 | 2 | 198 | 0.0101 | -13 | c.198 others(34): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143191924 | TACCGTTT others(6): Show |
T | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0004a0001c0001t0010a0001c0001t0019others(3): Show | a0001c0001t0004g0002a0001c0001t0010g0080a0001c0001t0019g0010others(4): Show | 7 | 198 | 0.0354 | -13 | c.198 others(34): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP27_chr17_45388908_45437870 | 45402173 | AGGGAAAG others(6): Show |
A | intron_variant | MODIFIER | HG00673.hp2 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0257 | 1 | 347 | 0.0029 | -13 | c.174 others(30): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | TogoVar | ||||||
ARHGAP27_chr17_45388908_45437870 | 45412962 | CTTTTTTT others(6): Show |
C | intron_variant | MODIFIER | HG02257.hp2 HG02647.hp2 HG02717.hp2 others(9): Show |
a0001a0002a0004others(3): Show | a0001c0001a0002c0002a0004c0004others(3): Show | a0001c0001t0001a0001c0001t0007a0002c0002t0001others(4): Show | a0001c0001t0001g0172a0001c0001t0001g0173a0001c0001t0001g0174others(9): Show | 12 | 347 | 0.0346 | -13 | c.658 others(30): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | TogoVar | ||||||
ARHGAP27_chr17_45388908_45437870 | 45414537 | AAGCAATC others(6): Show |
A | intron_variant | MODIFIER | NA18992.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0277 | 1 | 347 | 0.0029 | -13 | c.658 others(30): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | TogoVar |