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 | 142963198 | A | ATGTGTGT others(9): Show |
intron_variant | MODIFIER | HG01167.hp1 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0088 | 1 | 144 | 0.0069 | 16 | c.110 others(37): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143012548 | C | CATATATA others(9): Show |
intron_variant | MODIFIER | HG02615.hp2 | a0001 | a0001c0001 | a0001c0001t0019 | a0001c0001t0019g0049 | 1 | 171 | 0.0058 | 16 | 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(9): Show |
intron_variant | MODIFIER | HG00597.hp1 NA18960.hp1 NA19087.hp2 |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0002a0001c0002t0005 | a0001c0002t0001g0147 a0001c0002t0002g0030 a0001c0002t0005g0062 |
3 | 50 | 0.0600 | 16 | 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 | 143087636 | C | CTTTTTTT others(9): Show |
intron_variant | MODIFIER | HG02074.hp1 HG02886.hp2 NA20300.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0023 | a0001c0001t0002g0117 a0001c0001t0002g0195 a0001c0001t0023g0112 |
3 | 48 | 0.0625 | 16 | c.153 others(37): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143168445 | C | CTTTTTTT others(9): Show |
intron_variant | MODIFIER | HG00408.hp2 HG03710.hp2 |
a0001 | a0001c0003 | a0001c0003t0001a0001c0003t0035 | a0001c0003t0001g0161 a0001c0003t0035g0175 |
2 | 26 | 0.0769 | 16 | c.198 others(37): 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(9): Show |
downstream_gene_variant | MODIFIER | HG00323.hp2 HG00438.hp1 HG00544.hp1 others(46): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(26): Show | a0001c0001t0001g0012 a0001c0001t0001g0020 a0001c0001t0001g0029 others(46): Show |
49 | 78 | 0.6282 | 16 | c.*10 others(29): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 3624 | chr5 | TogoVar | |||||||
ARHGAP28_chr18_6724716_6920716 | 6729570 | G | GCACACAC others(9): Show |
upstream_gene_variant | MODIFIER | HG02451.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0100 | 1 | 233 | 0.0043 | 16 | c.-25 others(25): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 145 | chr18 | TogoVar | |||||||
ARHGAP28_chr18_6724716_6920716 | 6729574 | G | GCACACAC others(9): Show |
upstream_gene_variant | MODIFIER | HG01099.hp1 HG01943.hp1 HG03669.hp1 others(2): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0002c0002others(1): Show | a0001c0001t0001a0001c0003t0003a0002c0002t0002others(1): Show | a0001c0001t0001g0097 a0001c0001t0001g0102 a0001c0003t0003g0110 others(2): Show |
5 | 164 | 0.0305 | 16 | c.-24 others(25): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 141 | chr18 | TogoVar | |||||||
ARHGAP28_chr18_6724716_6920716 | 6730219 | G | GTATATAT others(9): Show |
intron_variant | MODIFIER | HG03579.hp1 NA20129.hp1 |
a0001 | a0001c0001a0001c0019 | a0001c0001t0001a0001c0019t0021 | a0001c0001t0001g0072 a0001c0019t0021g0073 |
2 | 122 | 0.0164 | 16 | 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 | 6730219 | G | GTATGTAT others(9): Show |
intron_variant | MODIFIER | HG01884.hp1 | a0004 | a0004c0007 | a0004c0007t0004 | a0004c0007t0004g0115 | 1 | 121 | 0.0083 | 16 | 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 | 6739645 | T | TTCTCTCT others(9): Show |
intron_variant | MODIFIER | HG02922.hp2 NA18906.hp2 |
a0001a0006 | a0001c0003a0006c0008 | a0001c0003t0003a0006c0008t0002 | a0001c0003t0003g0145 a0006c0008t0002g0146 |
2 | 127 | 0.0157 | 16 | c.122 others(33): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6831488 | C | CTTTTTTT others(9): Show |
intron_variant | MODIFIER | HG01106.hp1 HG03471.hp1 NA19043.hp1 others(1): Show |
a0001a0010 | a0001c0003a0010c0014 | a0001c0003t0003a0010c0014t0001 | a0001c0003t0003g0002 a0001c0003t0003g0085 a0001c0003t0003g0104 others(1): Show |
4 | 243 | 0.0165 | 16 | c.326 others(33): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6841203 | C | CTCTCTCT others(9): Show |
intron_variant | MODIFIER | HG02647.hp1 HG03041.hp2 |
a0001a0007 | a0001c0001a0007c0009 | a0001c0001t0001a0007c0009t0003 | a0001c0001t0001g0106 a0007c0009t0003g0162 |
2 | 161 | 0.0124 | 16 | c.543 others(33): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161053462 | T | TTCTCTCT others(9): Show |
intron_variant | MODIFIER | HG00140.hp2 HG03654.hp2 NA18967.hp1 others(4): Show |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0030 a0002c0002t0001g0031 a0002c0002t0001g0267 others(4): Show |
7 | 34 | 0.2059 | 16 | c.537 others(29): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 5/11 | chr1 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161064777 | G | GAGAAAGA others(9): Show |
intron_variant | MODIFIER | HG03669.hp2 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0089 | 1 | 372 | 0.0027 | 16 | c.97+ others(31): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161064779 | A | AAAAGAAA others(9): Show |
intron_variant | MODIFIER | NA19064.hp1 NA19085.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0004 a0002c0002t0001g0060 |
2 | 308 | 0.0065 | 16 | c.97+ others(31): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | |||||||
ARHGAP31_chr3_119289383_119425714 | 119293703 | A | AGTGTGTG others(9): Show |
upstream_gene_variant | MODIFIER | NA18906.hp2 | a0001 | a0001c0005 | a0001c0005t0001 | a0001c0005t0001g0166 | 1 | 201 | 0.0050 | 16 | c.-12 others(27): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 679 | chr3 | TogoVar | |||||||
ARHGAP31_chr3_119289383_119425714 | 119297909 | A | AACACACA others(9): Show |
intron_variant | MODIFIER | HG01099.hp2 HG02486.hp1 HG02486.hp2 others(1): Show |
a0001a0007 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0060a0001c0002t0001a0001c0004t0058others(1): Show | a0001c0001t0060g0058 a0001c0002t0001g0015 a0001c0004t0058g0016 others(1): Show |
4 | 120 | 0.0333 | 16 | c.100 others(33): 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(9): Show |
intron_variant | MODIFIER | HG00738.hp2 HG01106.hp2 HG02055.hp2 others(23): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0005others(4): Show | a0001c0001t0005a0001c0001t0006a0001c0001t0020others(12): Show | a0001c0001t0005g0118 a0001c0001t0006g0066 a0001c0001t0006g0067 others(23): Show |
26 | 124 | 0.2097 | 16 | c.683 others(33): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 128985858 | G | GTGTATAT others(9): Show |
intron_variant | MODIFIER | HG02280.hp2 | a0001 | a0001c0002 | a0001c0002t0005 | a0001c0002t0005g0250 | 1 | 140 | 0.0071 | 16 | c.152 others(33): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 15/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 128985858 | G | GTGTGTGT others(9): Show |
intron_variant | MODIFIER | NA18990.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0159 | 1 | 140 | 0.0071 | 16 | c.152 others(33): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 15/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129143072 | C | CATATATA others(9): Show |
intron_variant | MODIFIER | HG01109.hp2 HG01891.hp1 HG02451.hp1 others(9): Show |
a0001a0002a0013 | a0001c0003a0001c0015a0002c0004others(1): Show | a0001c0003t0006a0001c0015t0035a0001c0015t0036others(4): Show | a0001c0003t0006g0202 a0001c0003t0006g0203 a0001c0003t0006g0204 others(9): Show |
12 | 114 | 0.1053 | 16 | c.226 others(35): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 2/22 | chr11 | TogoVar | |||||||
ARHGAP32_chr11_128960060_129197325 | 129193551 | T | TATATATA others(9): Show |
upstream_gene_variant | MODIFIER | HG02257.hp1 | a0002 | a0002c0007 | a0002c0007t0001 | a0002c0007t0001g0391 | 1 | 396 | 0.0025 | 16 | c.-13 others(27): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 1227 | chr11 | TogoVar | |||||||
ARHGAP33_chr19_35770564_35793822 | 35771989 | C | CTTTTTTT others(9): Show |
upstream_gene_variant | MODIFIER | HG01975.hp1 HG03041.hp2 NA19063.hp1 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0001 a0001c0002t0001g0028 |
3 | 4 | 0.7500 | 16 | c.-36 others(27): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 3574 | chr19 | TogoVar | |||||||
ARHGAP35_chr19_46855997_47010077 | 46879587 | A | AAAATAAA others(9): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00639.hp2 HG00733.hp2 others(64): Show |
a0001a0004 | a0001c0001a0004c0012 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(7): Show | a0001c0001t0001g0118 a0001c0001t0001g0131 a0001c0001t0001g0132 others(64): Show |
67 | 155 | 0.4323 | 16 | c.-18 others(37): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | ||||||
ARHGAP36_chrX_131053346_131094885 | 131077764 | C | CATATATA others(9): Show |
intron_variant | MODIFIER | HG02559.hp2 HG02630.hp1 HG03490.hp1 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0016 a0001c0001t0002g0043 a0001c0001t0002g0066 others(2): Show |
6 | 10 | 0.6000 | 16 | c.-14 others(35): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144526964 | C | CGCTCCCG others(9): Show |
downstream_gene_variant | MODIFIER | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(2): Show |
a0001 | a0001c0004 | a0001c0004t0006 | a0001c0004t0006g0064 a0001c0004t0006g0065 a0001c0004t0006g0068 others(2): Show |
5 | 244 | 0.0205 | 16 | c.*34 others(27): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2214 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144669506 | C | CAAAAAAA others(9): Show |
intron_variant | MODIFIER | HG02886.hp1 HG02922.hp2 HG02965.hp2 others(1): Show |
a0001 | a0001c0004 | a0001c0004t0006 | a0001c0004t0006g0064 a0001c0004t0006g0068 a0001c0004t0006g0069 others(1): Show |
4 | 9 | 0.4444 | 16 | c.-82 others(35): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | |||||||
ARHGAP40_chr20_38596809_38655653 | 38603451 | A | ATCTATCT others(9): Show |
intron_variant | MODIFIER | HG01952.hp1 | a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0114 | 1 | 146 | 0.0068 | 16 | c.137 others(33): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38616935 | C | CTTTATTT others(9): Show |
intron_variant | MODIFIER | HG01106.hp1 HG01175.hp2 HG01993.hp2 others(3): Show |
a0001a0021 | a0001c0001a0001c0002a0001c0008others(2): Show | a0001c0001t0002a0001c0002t0002a0001c0008t0004others(2): Show | a0001c0001t0002g0011 a0001c0002t0002g0062 a0001c0008t0004g0305 others(2): Show |
6 | 60 | 0.1000 | 16 | c.138 others(33): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 1/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100806837 | G | GTTTATTT others(9): Show |
intron_variant | MODIFIER | HG03579.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002 | 1 | 64 | 0.0156 | 16 | c.312 others(35): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100837666 | C | CTTTTTTT others(9): Show |
intron_variant | MODIFIER | HG01928.hp1 HG02145.hp1 NA18940.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0004 | a0001c0001t0001g0099 a0001c0001t0001g0155 a0001c0001t0001g0157 others(3): Show |
6 | 39 | 0.1538 | 16 | c.313 others(35): 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(9): Show |
intron_variant | MODIFIER | HG00741.hp2 HG01069.hp1 HG02074.hp2 others(1): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0004 | a0001c0001t0001g0179 a0001c0001t0001g0204 a0002c0002t0004g0114 others(1): Show |
4 | 159 | 0.0252 | 16 | 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 | 100903117 | G | GCACACAC others(9): Show |
intron_variant | MODIFIER | HG03195.hp2 HG03669.hp1 NA19043.hp1 others(1): Show |
a0002 | a0002c0002 | a0002c0002t0002a0002c0002t0006a0002c0002t0025others(1): Show | a0002c0002t0002g0252 a0002c0002t0006g0057 a0002c0002t0025g0250 others(1): Show |
4 | 43 | 0.0930 | 16 | c.385 others(35): 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(9): Show |
intron_variant | MODIFIER | HG00323.hp2 HG00544.hp1 HG00544.hp2 others(28): Show |
a0001 | a0001c0001a0001c0012a0001c0015 | a0001c0001t0001a0001c0001t0006a0001c0001t0013others(5): Show | a0001c0001t0001g0007 a0001c0001t0001g0022 a0001c0001t0001g0065 others(28): Show |
31 | 70 | 0.4429 | 16 | c.385 others(35): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100903117 | G | GTGCACAC others(9): Show |
intron_variant | MODIFIER | HG01934.hp1 | a0001 | a0001c0001 | a0001c0001t0036 | a0001c0001t0036g0070 | 1 | 40 | 0.0250 | 16 | c.385 others(35): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | chr11 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100903709 | A | AAAAAAAA others(9): Show |
intron_variant | MODIFIER | HG01175.hp1 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0024 | 1 | 68 | 0.0147 | 16 | 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 | 100903709 | A | AAAAAAAA others(9): Show |
intron_variant | MODIFIER | HG01175.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0063 | 1 | 68 | 0.0147 | 16 | 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 | 100903709 | A | AAAAAAAA others(9): Show |
intron_variant | MODIFIER | HG01074.hp2 | a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0244 | 1 | 68 | 0.0147 | 16 | 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 | 100903709 | A | AATATATA others(9): Show |
intron_variant | MODIFIER | HG00738.hp1 HG02132.hp1 HG03017.hp1 others(1): Show |
a0001a0002 | a0001c0001a0002c0004 | a0001c0001t0001a0002c0004t0007 | a0001c0001t0001g0067 a0001c0001t0001g0137 a0001c0001t0001g0140 others(1): Show |
4 | 71 | 0.0563 | 16 | 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 | 100972516 | T | TTGGATGG others(9): Show |
intron_variant | MODIFIER | HG03688.hp1 | a0002 | a0002c0004 | a0002c0004t0007 | a0002c0004t0007g0122 | 1 | 147 | 0.0068 | 16 | c.155 others(33): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTCTTTT others(9): Show |
intron_variant | MODIFIER | HG01081.hp2 NA20129.hp2 |
a0002 | a0002c0002 | a0002c0002t0002a0002c0002t0020 | a0002c0002t0002g0083 a0002c0002t0020g0112 |
2 | 25 | 0.0800 | 16 | c.245 others(35): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTTTTTT others(9): Show |
intron_variant | MODIFIER | HG03831.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0186 | 1 | 24 | 0.0417 | 16 | c.245 others(35): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100995655 | G | GAATAAAT others(9): Show |
downstream_gene_variant | MODIFIER | HG00733.hp2 HG01123.hp1 HG01346.hp1 others(20): Show |
a0001a0002a0004others(1): Show | a0001c0001a0002c0002a0002c0005others(3): Show | a0001c0001t0001a0001c0001t0031a0001c0001t0037others(10): Show | a0001c0001t0001g0046 a0001c0001t0031g0249 a0001c0001t0037g0041 others(20): Show |
23 | 41 | 0.5610 | 16 | c.*68 others(27): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1715 | chr11 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12796136 | A | ATATCTAT others(9): Show |
intron_variant | MODIFIER | HG02451.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0174 | 1 | 2 | 0.5000 | 16 | c.53+ others(31): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12841585 | G | GTCTCTCT others(9): Show |
intron_variant | MODIFIER | HG03471.hp2 HG03579.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0226 a0001c0001t0001g0227 |
2 | 190 | 0.0105 | 16 | c.53+ others(33): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12841594 | T | TCTCTCTC others(9): Show |
intron_variant | MODIFIER | NA18989.hp2 | a0001 | a0001c0002 | a0001c0002t0030 | a0001c0002t0030g0065 | 1 | 124 | 0.0081 | 16 | c.53+ others(33): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12841594 | T | TCTCTCTC others(9): Show |
intron_variant | MODIFIER | HG01167.hp2 HG01169.hp2 HG01891.hp1 others(6): Show |
a0001a0002a0005 | a0001c0001a0001c0004a0002c0007others(1): Show | a0001c0001t0003a0001c0001t0005a0001c0001t0011others(4): Show | a0001c0001t0003g0063 a0001c0001t0003g0084 a0001c0001t0005g0052 others(6): Show |
9 | 132 | 0.0682 | 16 | c.53+ others(33): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12841594 | T | TCTCTCTC others(9): Show |
intron_variant | MODIFIER | HG00735.hp1 HG03486.hp1 |
a0001 | a0001c0001a0001c0006 | a0001c0001t0003a0001c0006t0003 | a0001c0001t0003g0046 a0001c0006t0003g0091 |
2 | 125 | 0.0160 | 16 | c.53+ others(33): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12841594 | T | TGTCTCTC others(9): Show |
intron_variant | MODIFIER | HG02922.hp2 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0045 | 1 | 124 | 0.0081 | 16 | c.53+ others(33): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar |