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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP30_chr1_161041946_161074891 | 161055910 | TAAAATAA others(4): Show |
T | intron_variant | MODIFIER | HG01106.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0178 | 1 | 390 | 0.0026 | -11 | c.345 others(26): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 3/11 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161055915 | TAAAATAA others(4): Show |
T | intron_variant | MODIFIER | HG03195.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0184 | 1 | 390 | 0.0026 | -11 | c.345 others(26): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 3/11 | chr1 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119382674 | GCCTTTAT others(4): Show |
G | intron_variant | MODIFIER | HG03098.hp1 | a0002 | a0002c0003 | a0002c0003t0009 | a0002c0003t0009g0220 | 1 | 310 | 0.0032 | -11 | c.539 others(26): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 5/11 | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119407367 | GAAAAAAA others(4): Show |
G | intron_variant | MODIFIER | HG02486.hp1 | a0001 | a0001c0001 | a0001c0001t0061 | a0001c0001t0061g0057 | 1 | 310 | 0.0032 | -11 | c.164 others(30): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP33_chr19_35770564_35793822 | 35773965 | CTTTTTTT others(4): Show |
C | upstream_gene_variant | MODIFIER | NA19078.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0002 | 1 | 420 | 0.0024 | -11 | c.-16 others(22): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 1598 | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 46868893 | ATTTTTTT others(4): Show |
A | intron_variant | MODIFIER | HG00558.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0072 | 1 | 298 | 0.0034 | -11 | c.-18 others(30): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 46983606 | CTTTTTTT others(4): Show |
C | intron_variant | MODIFIER | HG02622.hp1 | a0001 | a0001c0001 | a0001c0001t0024 | a0001c0001t0024g0032 | 1 | 298 | 0.0034 | -11 | c.382 others(30): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 3/6 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP35_chr19_46855997_47010077 | 47006267 | CTTTTTTT others(4): Show |
C | downstream_gene_variant | MODIFIER | HG00099.hp1 | a0001 | a0001c0001 | a0001c0001t0009 | a0001c0001t0009g0143 | 1 | 298 | 0.0034 | -11 | c.*55 others(22): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1191 | chr19 | TogoVar | ||||||
ARHGAP35_chr19_46855997_47010077 | 47007073 | CTTTTTTT others(4): Show |
C | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(95): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0007a0001c0009others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | a0001c0001t0001g0068a0001c0001t0001g0119a0001c0001t0001g0153others(95): Show | 98 | 298 | 0.3289 | -11 | c.*63 others(22): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1997 | chr19 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144543810 | TGGCCCAA others(4): Show |
T | intron_variant | MODIFIER | HG01891.hp1 HG02055.hp2 HG02109.hp2 others(12): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0004a0001c0001t0016others(1): Show | a0001c0001t0003g0063a0001c0001t0003g0068a0001c0001t0003g0071others(12): Show | 15 | 246 | 0.0610 | -11 | c.252 others(30): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 6/11 | chr8 | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144608156 | CAAAAAAA others(4): Show |
C | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(71): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0007others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(8): Show | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0097others(71): Show | 74 | 246 | 0.3008 | -11 | c.-81 others(28): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | ||||||
ARHGAP40_chr20_38596809_38655653 | 38627673 | GGTGTGTG others(4): Show |
G | intron_variant | MODIFIER | HG02486.hp1 | a0001 | a0001c0004 | a0001c0004t0016 | a0001c0004t0016g0231 | 1 | 350 | 0.0029 | -11 | c.558 others(26): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100705977 | CTTTTTTT others(4): Show |
C | intron_variant | MODIFIER | HG00673.hp1 | a0001 | a0001c0001 | a0001c0001t0019 | a0001c0001t0019g0180 | 1 | 286 | 0.0035 | -11 | c.154 others(30): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921239 | ATATATAT others(4): Show |
A | intron_variant | MODIFIER | NA21309.hp1 | a0002 | a0002c0002 | a0002c0002t0025 | a0002c0002t0025g0247 | 1 | 286 | 0.0035 | -11 | c.487 others(26): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100921245 | ATTTTTTT others(4): Show |
A | intron_variant | MODIFIER | HG00733.hp1 | a0001 | a0001c0003 | a0001c0003t0006 | a0001c0003t0006g0112 | 1 | 286 | 0.0035 | -11 | c.487 others(26): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 5/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | CTTTTTTT others(4): Show |
C | intron_variant | MODIFIER | HG01891.hp1 HG02055.hp2 HG03098.hp2 others(4): Show |
a0002 | a0002c0005 | a0002c0005t0010a0002c0005t0016 | a0002c0005t0010g0030a0002c0005t0010g0044a0002c0005t0010g0056others(4): Show | 7 | 286 | 0.0245 | -11 | c.245 others(30): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 22/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12802956 | TATATATA others(4): Show |
T | intron_variant | MODIFIER | HG00423.hp1 NA18959.hp2 NA18994.hp1 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0004a0001c0001t0019a0001c0004t0002 | a0001c0001t0004g0217a0001c0001t0019g0210a0001c0004t0002g0218 | 3 | 230 | 0.0130 | -11 | c.53+ others(28): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12802958 | TATATATA others(4): Show |
T | intron_variant | MODIFIER | HG00733.hp1 HG01070.hp2 HG01167.hp1 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(2): Show | a0001c0001t0001g0144a0001c0001t0001g0202a0001c0001t0001g0204others(10): Show | 13 | 230 | 0.0565 | -11 | c.53+ others(28): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12802959 | ATATATAT others(4): Show |
A | intron_variant | MODIFIER | HG01978.hp1 HG02622.hp1 HG02717.hp2 others(5): Show |
a0001 | a0001c0001a0001c0005a0001c0006 | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(2): Show | a0001c0001t0001g0140a0001c0001t0001g0185a0001c0001t0002g0199others(5): Show | 8 | 230 | 0.0348 | -11 | c.53+ others(28): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12802961 | ATATATAT others(4): Show |
A | intron_variant | MODIFIER | HG00099.hp1 HG00733.hp2 HG01255.hp2 |
a0001 | a0001c0001 | a0001c0001t0006 | a0001c0001t0006g0097a0001c0001t0006g0129a0001c0001t0006g0196 | 3 | 230 | 0.0130 | -11 | c.53+ others(28): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12802963 | ATATATAT others(4): Show |
A | intron_variant | MODIFIER | HG03492.hp1 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0120 | 1 | 230 | 0.0044 | -11 | c.53+ others(28): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12860856 | CTTTTTTT others(4): Show |
C | intron_variant | MODIFIER | HG03540.hp2 | a0001 | a0001c0001 | a0001c0001t0008 | a0001c0001t0008g0042 | 1 | 230 | 0.0044 | -11 | c.54- others(28): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12903108 | GAGAGAGA others(4): Show |
G | intron_variant | MODIFIER | NA20300.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0138 | 1 | 230 | 0.0044 | -11 | c.199 others(28): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12903110 | GAGAGAGA others(4): Show |
G | intron_variant | MODIFIER | NA21309.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0176 | 1 | 230 | 0.0044 | -11 | c.199 others(28): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12903112 | GAGAGAGA others(4): Show |
G | intron_variant | MODIFIER | HG03486.hp1 NA18951.hp2 |
a0001 | a0001c0001a0001c0006 | a0001c0001t0002a0001c0006t0003 | a0001c0001t0002g0108a0001c0006t0003g0091 | 2 | 230 | 0.0087 | -11 | c.199 others(28): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 3/20 | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12952722 | CTTTTTTT others(4): Show |
C | intron_variant | MODIFIER | NA18951.hp1 | a0001 | a0001c0001 | a0001c0001t0003 | a0001c0001t0003g0049 | 1 | 230 | 0.0044 | -11 | c.113 others(28): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 13/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12989101 | CAAAAAAA others(4): Show |
C | intron_variant | MODIFIER | HG00733.hp1 HG01109.hp1 HG03239.hp2 others(1): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0018a0001c0003t0001 | a0001c0001t0018g0103a0001c0003t0001g0160a0001c0003t0001g0207others(1): Show | 4 | 230 | 0.0174 | -11 | c.231 others(28): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 20/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP44_chr17_12784498_12996643 | 12993961 | CTCCGTAG others(4): Show |
C | downstream_gene_variant | MODIFIER | HG03209.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0035 | 1 | 230 | 0.0044 | -11 | c.*37 others(22): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 2319 | chr17 | TogoVar | ||||||
ARHGAP45_chr19_1062167_1091628 | 1067039 | GCCCGCCA others(4): Show |
G | upstream_gene_variant | MODIFIER | NA19054.hp1 | a0003 | a0003c0003 | a0003c0003t0002 | a0003c0003t0002g0300 | 1 | 418 | 0.0024 | -11 | c.-36 others(20): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 127 | chr19 | TogoVar | ||||||
ARHGAP45_chr19_1062167_1091628 | 1076481 | GTCTTTTT others(4): Show |
G | intron_variant | MODIFIER | HG02723.hp2 HG02886.hp2 HG03471.hp2 |
a0001a0004 | a0001c0004a0004c0029a0004c0058 | a0001c0004t0017a0004c0029t0009a0004c0058t0020 | a0001c0004t0017g0206a0004c0029t0009g0173a0004c0058t0020g0176 | 3 | 418 | 0.0072 | -11 | c.118 others(30): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP45_chr19_1062167_1091628 | 1076483 | CTTTTTTT others(4): Show |
C | intron_variant | MODIFIER | HG01496.hp1 NA19060.hp1 |
a0002 | a0002c0001a0002c0021 | a0002c0001t0005a0002c0021t0003 | a0002c0001t0005g0287a0002c0021t0003g0128 | 2 | 418 | 0.0048 | -11 | c.118 others(30): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr19 | TogoVar | |||||
ARHGAP45_chr19_1062167_1091628 | 1088536 | CAGGTGAA others(4): Show |
C | downstream_gene_variant | MODIFIER | HG01243.hp2 HG01978.hp2 HG02258.hp1 others(4): Show |
a0001 | a0001c0004a0001c0017 | a0001c0004t0006a0001c0017t0006 | a0001c0004t0006g0015a0001c0004t0006g0016a0001c0004t0006g0216others(3): Show | 7 | 418 | 0.0168 | -11 | c.*25 others(22): Show |
ARHGAP45 | ENSG00000180448.11 | transcript | ENST00000313093.7 | protein_coding | 1909 | chr19 | TogoVar | ||||||
ARHGAP5_chr14_32072304_32164728 | 32153406 | CAAAAAAA others(4): Show |
C | intron_variant | MODIFIER | HG00609.hp2 HG01243.hp1 HG02258.hp2 others(2): Show |
a0001a0009 | a0001c0002a0009c0014 | a0001c0002t0005a0009c0014t0015 | a0001c0002t0005g0004a0001c0002t0005g0168a0001c0002t0005g0169others(1): Show | 5 | 186 | 0.0269 | -11 | c.418 others(28): Show |
ARHGAP5 | ENSG00000100852.14 | transcript | ENST00000345122.8 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr14 | TogoVar | |||||
ARHGAP6_chrX_11132544_11670920 | 11176337 | ATATATAT others(4): Show |
A | intron_variant | MODIFIER | HG03688.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0078 | 1 | 144 | 0.0069 | -11 | c.162 others(30): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 8/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11327930 | AAGGTACT others(4): Show |
A | intron_variant | MODIFIER | HG02451.hp1 HG02698.hp1 HG02922.hp2 others(10): Show |
a0001a0002a0005 | a0001c0001a0002c0002a0005c0006 | a0001c0001t0001a0001c0001t0002a0002c0002t0003others(3): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0056others(10): Show | 13 | 144 | 0.0903 | -11 | c.589 others(30): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11358474 | TTTCTTTC others(4): Show |
T | intron_variant | MODIFIER | HG01243.hp1 | a0001 | a0001c0004 | a0001c0004t0005 | a0001c0004t0005g0015 | 1 | 144 | 0.0069 | -11 | c.589 others(32): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11651284 | CCTCCCAC others(4): Show |
C | intron_variant | MODIFIER | HG00280.hp1 HG01515.hp1 HG02698.hp1 others(7): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0003a0002c0002t0016 | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0008others(7): Show | 10 | 144 | 0.0694 | -11 | c.588 others(30): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP6_chrX_11132544_11670920 | 11660530 | CAAAAAAA others(4): Show |
C | intron_variant | MODIFIER | HG01243.hp1 HG02451.hp2 HG02622.hp2 others(6): Show |
a0001 | a0001c0001a0001c0004a0001c0007 | a0001c0001t0001a0001c0001t0007a0001c0004t0005others(1): Show | a0001c0001t0001g0014a0001c0001t0001g0020a0001c0001t0001g0044others(6): Show | 9 | 144 | 0.0625 | -11 | c.588 others(28): Show |
ARHGAP6 | ENSG00000047648.23 | transcript | ENST00000337414.9 | protein_coding | 1/12 | chrX | TogoVar | ||||||
ARHGAP8_chr22_44747575_44867784 | 44800486 | TCTCAAGG others(4): Show |
T | intron_variant | MODIFIER | HG01192.hp2 | a0008 | a0008c0014 | a0008c0014t0005 | a0008c0014t0005g0287 | 1 | 390 | 0.0026 | -11 | c.80- others(26): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 2/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44829118 | CAAAAAAA others(4): Show |
C | intron_variant | MODIFIER | HG02257.hp2 NA18522.hp2 |
a0012 | a0012c0038a0012c0056 | a0012c0038t0005a0012c0056t0005 | a0012c0038t0005g0318a0012c0056t0005g0323 | 2 | 390 | 0.0051 | -11 | c.596 others(28): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 7/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44854024 | CAAAAAAA others(4): Show |
C | intron_variant | MODIFIER | HG00099.hp2 HG01081.hp1 HG01192.hp2 others(15): Show |
a0001a0002a0003others(4): Show | a0001c0001a0002c0003a0002c0011others(8): Show | a0001c0001t0009a0002c0003t0004a0002c0011t0005others(8): Show | a0001c0001t0009g0173a0001c0001t0009g0321a0002c0003t0004g0142others(15): Show | 18 | 390 | 0.0462 | -11 | c.877 others(28): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGAP8_chr22_44747575_44867784 | 44856254 | CTTTTTTT others(4): Show |
C | intron_variant | MODIFIER | HG02165.hp2 HG04199.hp2 NA18954.hp2 others(3): Show |
a0001a0002a0010 | a0001c0001a0002c0011a0002c0013others(2): Show | a0001c0001t0010a0002c0011t0007a0002c0013t0007others(2): Show | a0001c0001t0010g0198a0002c0011t0007g0031a0002c0011t0007g0182others(3): Show | 6 | 390 | 0.0154 | -11 | c.878 others(28): Show |
ARHGAP8 | ENSG00000241484.10 | transcript | ENST00000356099.11 | protein_coding | 10/11 | INFO_REALIGN_3_PRIME | chr22 | TogoVar | |||||
ARHGDIG_chr16_275591_288010 | 285914 | CCCCGCGG others(4): Show |
C | downstream_gene_variant | MODIFIER | HG03098.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 | 1 | 442 | 0.0023 | -11 | c.*31 others(22): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 2905 | chr16 | TogoVar | ||||||
ARHGDIG_chr16_275591_288010 | 285955 | CCCCGCGG others(4): Show |
C | downstream_gene_variant | MODIFIER | NA18947.hp1 NA18984.hp2 NA18999.hp2 others(3): Show |
a0001a0005 | a0001c0001a0005c0008 | a0001c0001t0002a0005c0008t0002 | a0001c0001t0002g0001a0001c0001t0002g0002a0005c0008t0002g0002 | 6 | 442 | 0.0136 | -11 | c.*31 others(22): Show |
ARHGDIG | ENSG00000242173.10 | transcript | ENST00000219409.8 | protein_coding | 2946 | chr16 | TogoVar | ||||||
ARHGEF10L_chr1_17534698_17702869 | 17665318 | GCAGCTGT others(4): Show |
G | intron_variant | MODIFIER | HG01884.hp1 HG02622.hp2 HG02630.hp1 others(2): Show |
a0001a0010 | a0001c0017a0001c0043a0001c0044others(1): Show | a0001c0017t0002a0001c0043t0002a0001c0044t0004others(1): Show | a0001c0017t0002g0113a0001c0017t0002g0148a0001c0043t0002g0051others(2): Show | 5 | 168 | 0.0298 | -11 | c.300 others(28): Show |
ARHGEF10L | ENSG00000074964.17 | transcript | ENST00000361221.8 | protein_coding | 26/28 | INFO_REALIGN_3_PRIME | chr1 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1824008 | CGGCGGGG others(4): Show |
C | 5_prime_UTR_variant | MODIFIER | HG00741.hp2 | a0005 | a0005c0039 | a0005c0039t0030 | a0005c0039t0030g0139 | 1 | 363 | 0.0028 | -11 | c.-15 others(20): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 1/29 | 19380 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||
ARHGEF10_chr8_1818926_1963641 | 1851200 | TCATTACA others(4): Show |
T | intron_variant | MODIFIER | HG02615.hp2 HG02622.hp2 HG02647.hp2 others(2): Show |
a0001a0003a0010 | a0001c0002a0003c0038a0010c0097others(1): Show | a0001c0002t0001a0003c0038t0019a0010c0097t0014others(1): Show | a0001c0002t0001g0211a0001c0002t0001g0267a0003c0038t0019g0266others(2): Show | 5 | 363 | 0.0138 | -11 | c.38- others(26): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | chr8 | TogoVar | ||||||
ARHGEF10_chr8_1818926_1963641 | 1854597 | CCCAAGCC others(4): Show |
C | intron_variant | MODIFIER | HG01884.hp2 HG02280.hp1 HG03486.hp1 |
a0001a0004 | a0001c0003a0001c0004a0004c0064 | a0001c0003t0051a0001c0004t0048a0004c0064t0071 | a0001c0003t0051g0118a0001c0004t0048g0104a0004c0064t0071g0189 | 3 | 363 | 0.0083 | -11 | c.38- others(26): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 2/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF10_chr8_1818926_1963641 | 1886675 | TGCTCTGT others(4): Show |
T | intron_variant | MODIFIER | HG00140.hp2 HG01070.hp2 HG03942.hp2 others(1): Show |
a0002 | a0002c0017a0002c0024 | a0002c0017t0002a0002c0017t0006a0002c0024t0001 | a0002c0017t0002g0041a0002c0017t0002g0042a0002c0017t0006g0114others(1): Show | 4 | 363 | 0.0110 | -11 | c.118 others(28): Show |
ARHGEF10 | ENSG00000104728.16 | transcript | ENST00000349830.8 | protein_coding | 11/28 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ARHGEF11_chr1_156929840_157050742 | 156939453 | CAGGGGGA others(4): Show |
C | intron_variant | MODIFIER | HG02572.hp1 HG03139.hp2 |
a0002 | a0002c0004 | a0002c0004t0021 | a0002c0004t0021g0174a0002c0004t0021g0175 | 2 | 362 | 0.0055 | -11 | c.409 others(26): Show |
ARHGEF11 | ENSG00000132694.19 | transcript | ENST00000368194.8 | protein_coding | 37/40 | chr1 | TogoVar |