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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
APOBEC1_chr12_7644400_7670908 | 7660375 | G | GGAAGGAA others(33): Show |
intron_variant | MODIFIER | HG01358.hp2 NA18612.hp1 NA18950.hp2 others(2): Show |
a0001a0002 | a0001c0002a0002c0001 | a0001c0002t0001a0002c0001t0001 | a0001c0002t0001g0340a0001c0002t0001g0341a0001c0002t0001g0343others(2): Show | 5 | 432 | 0.0116 | 40 | c.16+ others(55): Show |
APOBEC1 | ENSG00000111701.7 | transcript | ENST00000229304.5 | protein_coding | 1/4 | chr12 | TogoVar | ||||||
APOBEC1_chr12_7644400_7670908 | 7660375 | G | GGAAGGAA others(33): Show |
intron_variant | MODIFIER | HG00438.hp2 HG01261.hp2 HG01346.hp2 others(4): Show |
a0001 | a0001c0002a0001c0003 | a0001c0002t0001a0001c0003t0001 | a0001c0002t0001g0342a0001c0003t0001g0377a0001c0003t0001g0382others(4): Show | 7 | 432 | 0.0162 | 40 | c.16+ others(55): Show |
APOBEC1 | ENSG00000111701.7 | transcript | ENST00000229304.5 | protein_coding | 1/4 | chr12 | TogoVar | ||||||
APOBEC1_chr12_7644400_7670908 | 7660375 | G | GGAAGGAA others(33): Show |
intron_variant | MODIFIER | HG01070.hp2 HG02258.hp2 HG03579.hp1 others(1): Show |
a0001a0002 | a0001c0003a0002c0001 | a0001c0003t0001a0002c0001t0001a0002c0001t0002 | a0001c0003t0001g0331a0002c0001t0001g0394a0002c0001t0002g0399others(1): Show | 4 | 432 | 0.0093 | 40 | c.16+ others(55): Show |
APOBEC1 | ENSG00000111701.7 | transcript | ENST00000229304.5 | protein_coding | 1/4 | chr12 | TogoVar | ||||||
APOBEC1_chr12_7644400_7670908 | 7660375 | G | GGAAGGAC others(33): Show |
intron_variant | MODIFIER | HG00558.hp2 HG02572.hp1 NA19030.hp2 |
a0001a0002 | a0001c0003a0002c0001 | a0001c0003t0001a0002c0001t0001a0002c0001t0002 | a0001c0003t0001g0403a0002c0001t0001g0380a0002c0001t0002g0400 | 3 | 432 | 0.0069 | 40 | c.16+ others(55): Show |
APOBEC1 | ENSG00000111701.7 | transcript | ENST00000229304.5 | protein_coding | 1/4 | chr12 | TogoVar | ||||||
APOC1_chr19_44909608_44924346 | 44921918 | T | TGCGGCCG others(33): Show |
downstream_gene_variant | MODIFIER | HG03098.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0007 | 1 | 436 | 0.0023 | 40 | c.*26 others(51): Show |
APOC1 | ENSG00000130208.10 | transcript | ENST00000592535.6 | protein_coding | 2573 | chr19 | TogoVar | ||||||
APOH_chr17_66207033_66234415 | 66221266 | A | AAAGGAAG others(33): Show |
intron_variant | MODIFIER | HG03516.hp2 NA18522.hp1 |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0101a0002c0002t0001g0102 | 2 | 386 | 0.0052 | 40 | c.416 others(55): Show |
APOH | ENSG00000091583.11 | transcript | ENST00000205948.11 | protein_coding | 4/7 | chr17 | TogoVar | ||||||
APOL5_chr22_35712872_35734483 | 35717235 | A | AAAAAAAA others(33): Show |
upstream_gene_variant | MODIFIER | HG02257.hp2 HG02486.hp1 NA18971.hp1 |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0001a0002c0002t0001g0090a0002c0002t0001g0091 | 3 | 401 | 0.0075 | 40 | c.-63 others(49): Show |
APOL5 | ENSG00000128313.2 | transcript | ENST00000249044.2 | protein_coding | 636 | chr22 | TogoVar | ||||||
ARFIP1_chr4_152774954_152917357 | 152866723 | G | GCTCCTCA others(33): Show |
intron_variant | MODIFIER | HG02602.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0303 | 1 | 342 | 0.0029 | 40 | c.202 others(57): Show |
ARFIP1 | ENSG00000164144.16 | transcript | ENST00000353617.7 | protein_coding | 3/8 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARFRP1_chr20_63693647_63712976 | 63693729 | A | ACCACCTC others(33): Show |
downstream_gene_variant | MODIFIER | HG02630.hp2 | a0001 | a0001c0003 | a0001c0003t0004 | a0001c0003t0004g0014 | 1 | 296 | 0.0034 | 40 | c.*67 others(51): Show |
ARFRP1 | ENSG00000101246.20 | transcript | ENST00000622789.5 | protein_coding | 4917 | chr20 | TogoVar | ||||||
ARHGAP17_chr16_24914389_25020369 | 24961911 | T | TTATATAT others(33): Show |
intron_variant | MODIFIER | HG03486.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0119 | 1 | 240 | 0.0042 | 40 | c.574 others(57): Show |
ARHGAP17 | ENSG00000140750.17 | transcript | ENST00000289968.11 | protein_coding | 7/19 | chr16 | TogoVar | ||||||
ARHGAP20_chr11_110572043_110717437 | 110648172 | A | AATATATA others(33): Show |
intron_variant | MODIFIER | HG01169.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0078 | 1 | 226 | 0.0044 | 40 | c.189 others(59): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38513074 | T | TTAAATAT others(33): Show |
downstream_gene_variant | MODIFIER | HG00280.hp2 HG00597.hp1 HG01081.hp2 others(6): Show |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0001 | a0001c0001t0001g0002a0001c0001t0001g0005a0001c0001t0001g0019others(5): Show | 9 | 309 | 0.0291 | 40 | c.*21 others(51): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 690 | chr17 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85632600 | C | CGTGTATA others(33): Show |
intron_variant | MODIFIER | HG02055.hp2 HG02717.hp1 HG03130.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0062a0001c0001t0001g0065a0001c0001t0001g0069 | 3 | 108 | 0.0278 | 40 | c.180 others(59): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142949165 | C | CAGAGAGA others(33): Show |
intron_variant | MODIFIER | HG02818.hp2 | a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0039 | 1 | 198 | 0.0051 | 40 | c.110 others(61): 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(33): Show |
intron_variant | MODIFIER | HG00408.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0161 | 1 | 198 | 0.0051 | 40 | c.110 others(61): 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(33): Show |
intron_variant | MODIFIER | NA19240.hp2 | a0001 | a0001c0001 | a0001c0001t0016 | a0001c0001t0016g0040 | 1 | 198 | 0.0051 | 40 | c.110 others(59): 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(33): Show |
intron_variant | MODIFIER | HG00408.hp2 NA18948.hp1 |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0004 | a0001c0002t0001g0161a0001c0002t0004g0061 | 2 | 198 | 0.0101 | 40 | c.110 others(59): 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(33): Show |
intron_variant | MODIFIER | HG02818.hp1 HG03669.hp2 NA18982.hp1 others(1): Show |
a0002a0003a0011 | a0002c0002a0003c0003a0011c0012 | a0002c0002t0001a0003c0003t0001a0011c0012t0001 | a0002c0002t0001g0151a0003c0003t0001g0090a0003c0003t0001g0133others(1): Show | 4 | 347 | 0.0115 | 40 | c.174 others(59): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6730219 | G | GTATGTAT others(33): Show |
intron_variant | MODIFIER | HG00544.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0139 | 1 | 248 | 0.0040 | 40 | c.122 others(55): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP31_chr3_119289383_119425714 | 119422123 | C | CTAGAGGA others(33): Show |
downstream_gene_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00609.hp1 others(44): Show |
a0001a0011 | a0001c0001a0011c0019 | a0001c0001t0005a0001c0001t0007a0001c0001t0011others(3): Show | a0001c0001t0005g0022a0001c0001t0005g0058a0001c0001t0005g0077others(43): Show | 47 | 310 | 0.1516 | 40 | c.*58 others(51): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1410 | chr3 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129129166 | A | AGAAGTGA others(33): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(60): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0002a0001c0001t0004a0001c0001t0022others(5): Show | a0001c0001t0002g0002a0001c0001t0002g0094a0001c0001t0002g0096others(59): Show | 63 | 398 | 0.1583 | 40 | c.226 others(57): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 2/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129129315 | T | TGCCCCGT others(33): Show |
intron_variant | MODIFIER | HG03471.hp1 | a0014 | a0014c0036 | a0014c0036t0020 | a0014c0036t0020g0193 | 1 | 398 | 0.0025 | 40 | c.226 others(57): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 2/22 | chr11 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129143072 | C | CATATATA others(33): Show |
intron_variant | MODIFIER | NA18942.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0164 | 1 | 398 | 0.0025 | 40 | c.226 others(59): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 2/22 | chr11 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 47009845 | G | GCCGCCCC others(33): Show |
downstream_gene_variant | MODIFIER | HG00408.hp1 HG00438.hp2 HG00558.hp1 others(89): Show |
a0001a0003a0006 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(24): Show | a0001c0001t0001g0171a0001c0001t0001g0205a0001c0001t0004g0022others(89): Show | 92 | 298 | 0.3087 | 40 | c.*91 others(51): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 4769 | chr19 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144562288 | T | TCCAGTGG others(33): Show |
intron_variant | MODIFIER | HG03195.hp2 | a0001 | a0001c0007 | a0001c0007t0017 | a0001c0007t0017g0019 | 1 | 246 | 0.0041 | 40 | c.513 others(57): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144562324 | A | ACGCTCCA others(33): Show |
intron_variant | MODIFIER | HG02257.hp1 | a0001 | a0001c0007 | a0001c0007t0003 | a0001c0007t0003g0078 | 1 | 246 | 0.0041 | 40 | c.513 others(57): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144562509 | C | CACTCCAG others(33): Show |
intron_variant | MODIFIER | HG02622.hp1 | a0005 | a0005c0013 | a0005c0013t0002 | a0005c0013t0002g0195 | 1 | 246 | 0.0041 | 40 | c.513 others(57): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144620226 | T | TGTGTGTG others(33): Show |
intron_variant | MODIFIER | HG00323.hp2 HG01975.hp1 HG02559.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0005a0001c0002t0001 | a0001c0001t0001g0016a0001c0001t0001g0132a0001c0001t0005g0243others(3): Show | 6 | 246 | 0.0244 | 40 | c.-81 others(59): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100837926 | T | TTTTTATT others(33): Show |
intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(70): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0001c0008others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(16): Show | a0001c0001t0001g0007a0001c0001t0001g0047a0001c0001t0001g0070others(70): Show | 73 | 286 | 0.2552 | 40 | c.313 others(59): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTCTTTT others(33): Show |
intron_variant | MODIFIER | NA18906.hp1 | a0002 | a0002c0002 | a0002c0002t0009 | a0002c0002t0009g0035 | 1 | 286 | 0.0035 | 40 | c.245 others(59): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12948723 | T | TACACACA others(33): Show |
intron_variant | MODIFIER | NA18906.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0090 | 1 | 230 | 0.0044 | 40 | c.862 others(55): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP4_chrX_153902378_153931264 | 153925252 | A | AATGATGT others(33): Show |
intron_variant | MODIFIER | NA19010.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0050 | 1 | 308 | 0.0033 | 40 | c.67+ others(53): Show |
ARHGAP4 | ENSG00000089820.17 | transcript | ENST00000350060.10 | protein_coding | 1/21 | chrX | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44863968 | G | GTACAGGG others(33): Show |
downstream_gene_variant | MODIFIER | NA18947.hp1 | a0002 | a0002c0016 | a0002c0016t0004 | a0002c0016t0004g0199 | 1 | 390 | 0.0026 | 40 | c.*13 others(51): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 1185 | chr22 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1824019 | G | GGCGGGGG others(33): Show |
5_prime_UTR_variant | MODIFIER | HG00438.hp1 | a0001 | a0001c0120 | a0001c0120t0057 | a0001c0120t0057g0134 | 1 | 363 | 0.0028 | 40 | c.-11 others(48): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/29 | 19318 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||
ARHGEF10_chr8_1818926_1963641 | 1825200 | T | TCCCCCCT others(33): Show |
intron_variant | MODIFIER | HG00621.hp1 HG00735.hp2 |
a0001a0002 | a0001c0013a0002c0078 | a0001c0013t0001a0002c0078t0002 | a0001c0013t0001g0029a0002c0078t0002g0036 | 2 | 363 | 0.0055 | 40 | c.-48 others(57): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1858850 | T | TCTCTCTG others(33): Show |
intron_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00423.hp1 others(109): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0002a0001c0003others(56): Show | a0001c0001t0002a0001c0002t0001a0001c0003t0001others(87): Show | a0001c0001t0002g0239a0001c0002t0001g0274a0001c0003t0001g0026others(108): Show | 112 | 363 | 0.3085 | 40 | c.193 others(55): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 3/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1920031 | T | TATGGGTG others(33): Show |
intron_variant | MODIFIER | HG02293.hp1 HG04204.hp2 |
a0001 | a0001c0003a0001c0019 | a0001c0003t0007a0001c0019t0001 | a0001c0003t0007g0102a0001c0019t0001g0215 | 2 | 363 | 0.0055 | 40 | c.214 others(59): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1920051 | C | CGTGGGTG others(33): Show |
intron_variant | MODIFIER | NA18959.hp1 NA19002.hp1 |
a0001 | a0001c0018a0001c0050 | a0001c0018t0025a0001c0050t0006 | a0001c0018t0025g0296a0001c0050t0006g0127 | 2 | 363 | 0.0055 | 40 | c.214 others(59): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 18/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF11_chr1_156929840_157050742 | 157013259 | T | TCACACAC others(33): Show |
intron_variant | MODIFIER | NA18981.hp2 | a0003 | a0003c0003 | a0003c0003t0003 | a0003c0003t0003g0264 | 1 | 362 | 0.0028 | 40 | c.33- others(57): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 1/40 | chr1 | TogoVar | ||||||
ARHGEF12_chr11_120331413_120494937 | 120347183 | C | CCTTCCTT others(33): Show |
intron_variant | MODIFIER | HG02056.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0191 | 1 | 308 | 0.0033 | 40 | c.32+ others(55): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120347183 | C | CCTTCCTT others(33): Show |
intron_variant | MODIFIER | NA20752.hp1 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0195 | 1 | 308 | 0.0033 | 40 | c.32+ others(55): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120347183 | C | CCTTCCTT others(33): Show |
intron_variant | MODIFIER | HG03209.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0212 | 1 | 308 | 0.0033 | 40 | c.32+ others(55): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF12_chr11_120331413_120494937 | 120399321 | C | CAAAAAAA others(33): Show |
intron_variant | MODIFIER | HG00733.hp1 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0129 | 1 | 308 | 0.0033 | 40 | c.33- others(55): Show |
ARHGEF12 | ENSG00000196914.9 | transcript | ENST00000397843.7 | protein_coding | 1/40 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGEF18_chr19_7343937_7477478 | 7367882 | A | ACACATAT others(33): Show |
intron_variant | MODIFIER | HG02976.hp1 | a0033 | a0033c0030 | a0033c0030t0006 | a0033c0030t0006g0255 | 1 | 298 | 0.0034 | 40 | c.16- others(55): Show |
ARHGEF18 | ENSG00000104880.19 | transcript | ENST00000668164.2 | protein_coding | 2/28 | chr19 | TogoVar | ||||||
ARHGEF28_chr5_73621196_73946990 | 73737439 | C | CTTCTTTT others(33): Show |
intron_variant | MODIFIER | HG00621.hp2 HG01074.hp2 NA18906.hp2 others(6): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0023a0002c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0023t0001others(5): Show | a0001c0001t0001g0036a0001c0001t0002g0050a0001c0001t0002g0077others(6): Show | 9 | 188 | 0.0479 | 40 | c.34- others(57): Show |
ARHGEF28 | ENSG00000214944.10 | transcript | ENST00000513042.7 | protein_coding | 2/35 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF35_chr7_144181083_144200833 | 144182532 | A | ATTGTCTA others(33): Show |
downstream_gene_variant | MODIFIER | HG03654.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0149 | 1 | 383 | 0.0026 | 40 | c.*43 others(51): Show |
ARHGEF35 | ENSG00000213214.6 | transcript | ENST00000378115.3 | protein_coding | 3550 | chr7 | TogoVar | ||||||
ARHGEF37_chr5_149576498_149639968 | 149599434 | C | CTTATTTA others(33): Show |
intron_variant | MODIFIER | NA18960.hp2 NA18998.hp1 NA19074.hp2 |
a0003 | a0003c0003 | a0003c0003t0002a0003c0003t0008 | a0003c0003t0002g0303a0003c0003t0002g0307a0003c0003t0008g0296 | 3 | 394 | 0.0076 | 40 | c.186 others(57): Show |
ARHGEF37 | ENSG00000183111.12 | transcript | ENST00000333677.7 | protein_coding | 2/12 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGEF38_chr4_105547620_105685914 | 105561424 | G | GGAATAGA others(33): Show |
intron_variant | MODIFIER | HG02523.hp2 | a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0110 | 1 | 186 | 0.0054 | 40 | c.196 others(57): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGEF38_chr4_105547620_105685914 | 105561424 | G | GGAATGGA others(33): Show |
intron_variant | MODIFIER | HG03471.hp2 | a0001 | a0001c0009 | a0001c0009t0015 | a0001c0009t0015g0106 | 1 | 186 | 0.0054 | 40 | c.196 others(57): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGEF38_chr4_105547620_105685914 | 105561439 | A | AGAATGGA others(33): Show |
intron_variant | MODIFIER | NA19240.hp2 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0173 | 1 | 186 | 0.0054 | 40 | c.196 others(57): Show |
ARHGEF38 | ENSG00000236699.9 | transcript | ENST00000420470.3 | protein_coding | 1/13 | INFO_REALIGN_3_PRIME | chr4 | TogoVar |