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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP26_chr5_142765377_143234007 | 142963198 | A | ATATGTGT others(9): Show |
intron_variant | MODIFIER | HG02809.hp2 | a0001 | a0001c0001 | a0001c0001t0050 | a0001c0001t0050g0074 | 1 | 198 | 0.0051 | 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 | 142963198 | A | ATGTGTGT others(9): Show |
intron_variant | MODIFIER | HG01167.hp1 | a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0088 | 1 | 198 | 0.0051 | 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 | a0001c0001t0020 | a0001c0001t0020g0049 | 1 | 198 | 0.0051 | 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 | a0001c0003 | a0001c0003t0001a0001c0003t0002a0001c0003t0005 | a0001c0003t0001g0147a0001c0003t0002g0030a0001c0003t0005g0062 | 3 | 198 | 0.0152 | 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 | a0001c0001t0002a0001c0001t0024 | a0001c0001t0002g0117a0001c0001t0002g0195a0001c0001t0024g0112 | 3 | 198 | 0.0152 | 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 | a0001c0002 | a0001c0002t0001a0001c0002t0017 | a0001c0002t0001g0161a0001c0002t0017g0175 | 2 | 198 | 0.0101 | 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 | a0001c0001t0001g0012a0001c0001t0001g0020a0001c0001t0001g0029others(46): Show | 49 | 198 | 0.2475 | 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 | 248 | 0.0040 | 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 | a0001c0001t0001g0097a0001c0001t0001g0102a0001c0003t0003g0110others(2): Show | 5 | 248 | 0.0202 | 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 | a0001c0001t0001g0072a0001c0019t0021g0073 | 2 | 248 | 0.0081 | 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 | 248 | 0.0040 | 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 |
a0001a0007 | a0001c0003a0007c0008 | a0001c0003t0003a0007c0008t0002 | a0001c0003t0003g0145a0007c0008t0002g0146 | 2 | 248 | 0.0081 | 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 | a0001c0003t0003g0002a0001c0003t0003g0085a0001c0003t0003g0104others(1): Show | 4 | 248 | 0.0161 | 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 |
a0001a0006 | a0001c0001a0006c0009 | a0001c0001t0001a0006c0009t0003 | a0001c0001t0001g0106a0006c0009t0003g0162 | 2 | 248 | 0.0081 | 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 | a0002c0002t0001g0277a0002c0002t0001g0309a0002c0002t0001g0313others(4): Show | 7 | 390 | 0.0180 | 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 | a0001c0001t0003g0072 | 1 | 390 | 0.0026 | 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 | a0001c0001t0001g0035a0002c0002t0001g0034 | 2 | 390 | 0.0051 | 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 | a0001c0005t0001g0165 | 1 | 310 | 0.0032 | 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 |
a0001a0014 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0061a0001c0002t0001a0001c0004t0059others(1): Show | a0001c0001t0061g0057a0001c0002t0001g0014a0001c0004t0059g0015others(1): Show | 4 | 310 | 0.0129 | 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 | a0001c0001t0005g0117a0001c0001t0006g0065a0001c0001t0006g0066others(23): Show | 26 | 310 | 0.0839 | 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 | a0001c0002t0005g0248 | 1 | 398 | 0.0025 | 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 | 398 | 0.0025 | 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 |
a0001a0002a0011 | a0001c0003a0001c0015a0002c0004others(1): Show | a0001c0003t0006a0001c0015t0035a0001c0015t0036others(4): Show | a0001c0003t0006g0200a0001c0003t0006g0201a0001c0003t0006g0202others(9): Show | 12 | 398 | 0.0302 | 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 | 398 | 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 | a0001c0002t0001g0001a0001c0002t0001g0028 | 3 | 420 | 0.0071 | 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(65): Show |
a0001a0005 | a0001c0001a0005c0012 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0119a0001c0001t0001g0134a0001c0001t0001g0142others(65): Show | 68 | 298 | 0.2282 | 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 | a0001c0001t0001g0060a0001c0001t0001g0070a0001c0001t0002g0038others(3): Show | 6 | 302 | 0.0199 | 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 | a0001c0004t0006g0069a0001c0004t0006g0070a0001c0004t0006g0073others(2): Show | 5 | 246 | 0.0203 | 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 | a0001c0004t0006g0069a0001c0004t0006g0073a0001c0004t0006g0074others(1): Show | 4 | 246 | 0.0163 | 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 | a0001c0001t0009g0115 | 1 | 350 | 0.0029 | 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 |
a0001a0019 | a0001c0001a0001c0002a0001c0008others(2): Show | a0001c0001t0002a0001c0002t0002a0001c0008t0004others(2): Show | a0001c0001t0002g0009a0001c0002t0002g0063a0001c0008t0004g0309others(2): Show | 6 | 350 | 0.0171 | 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 | 100751277 | G | GTTTTTTT others(9): Show |
intron_variant | MODIFIER | homoSapiens_chm13v2.hp1 | a0002 | a0002c0006 | a0002c0006t0012 | a0002c0006t0012g0176 | 1 | 286 | 0.0035 | 16 | c.155 others(35): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100806837 | G | GTTTATTT others(9): Show |
intron_variant | MODIFIER | HG03579.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002 | 1 | 286 | 0.0035 | 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 | a0001c0001t0001g0099a0001c0001t0001g0164a0001c0001t0001g0165others(3): Show | 6 | 286 | 0.0210 | 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 | a0001c0001t0001g0178a0001c0001t0001g0203a0002c0002t0004g0108others(1): Show | 4 | 286 | 0.0140 | 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 | a0002c0002t0002g0252a0002c0002t0006g0057a0002c0002t0025g0247others(1): Show | 4 | 286 | 0.0140 | 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 | a0001c0001t0001g0007a0001c0001t0001g0023a0001c0001t0001g0066others(28): Show | 31 | 286 | 0.1084 | 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 | a0001c0001t0036g0090 | 1 | 286 | 0.0035 | 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 | a0002c0002t0002g0019 | 1 | 286 | 0.0035 | 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 | a0002c0002t0002g0085 | 1 | 286 | 0.0035 | 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 | 286 | 0.0035 | 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 | a0001c0001t0001g0080a0001c0001t0001g0134a0001c0001t0001g0136others(1): Show | 4 | 286 | 0.0140 | 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 | a0002c0004t0007g0125 | 1 | 286 | 0.0035 | 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 | a0002c0002t0002g0073a0002c0002t0020g0106 | 2 | 286 | 0.0070 | 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 | a0001c0001t0001g0184 | 1 | 286 | 0.0035 | 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 | a0001c0001t0001g0047a0001c0001t0031g0251a0001c0001t0037g0041others(20): Show | 23 | 286 | 0.0804 | 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 | 230 | 0.0044 | 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 | a0001c0001t0001g0227a0001c0001t0001g0228 | 2 | 230 | 0.0087 | 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 | a0001c0002t0030g0060 | 1 | 230 | 0.0044 | 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 |
a0001a0002a0006 | a0001c0001a0001c0004a0002c0007others(1): Show | a0001c0001t0003a0001c0001t0005a0001c0001t0011others(4): Show | a0001c0001t0003g0056a0001c0001t0003g0059a0001c0001t0005g0080others(6): Show | 9 | 230 | 0.0391 | 16 | c.53+ others(33): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar |