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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP22_chr10_48441036_48610073 | 48539290 | C | CTTTTTTT others(13): Show |
intron_variant | MODIFIER | HG01884.hp2 HG03209.hp2 |
a0001 | a0001c0001 | a0001c0001t0008a0001c0001t0014 | a0001c0001t0008g0187 a0001c0001t0014g0256 |
2 | 103 | 0.0194 | 20 | c.322 others(39): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 3/9 | chr10 | TogoVar | |||||||
ARHGAP22_chr10_48441036_48610073 | 48539291 | A | ATTTTTTT others(13): Show |
intron_variant | MODIFIER | HG03139.hp2 | a0001 | a0001c0003 | a0001c0003t0003 | a0001c0003t0003g0241 | 1 | 70 | 0.0143 | 20 | c.322 others(39): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 3/9 | chr10 | TogoVar | |||||||
ARHGAP23_chr17_38423464_38517385 | 38426550 | C | CAAAAAAA others(13): Show |
upstream_gene_variant | MODIFIER | HG02809.hp2 NA19043.hp2 |
a0001 | a0001c0007a0001c0009 | a0001c0007t0013a0001c0009t0003 | a0001c0007t0013g0148 a0001c0009t0003g0172 |
2 | 129 | 0.0155 | 20 | c.-19 others(31): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1913 | chr17 | TogoVar | |||||||
ARHGAP23_chr17_38423464_38517385 | 38507276 | A | AAATAATA others(13): Show |
intron_variant | MODIFIER | NA18948.hp2 | a0001 | a0001c0006 | a0001c0006t0002 | a0001c0006t0002g0088 | 1 | 45 | 0.0222 | 20 | c.344 others(39): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38513074 | T | TTAAATAT others(13): Show |
downstream_gene_variant | MODIFIER | HG02109.hp1 HG02965.hp1 HG03453.hp2 others(2): Show |
a0001a0005a0006 | a0001c0001a0001c0004a0001c0037others(2): Show | a0001c0001t0001a0001c0004t0001a0001c0037t0003others(2): Show | a0001c0001t0001g0156 a0001c0004t0001g0131 a0001c0037t0003g0139 others(2): Show |
5 | 56 | 0.0893 | 20 | c.*21 others(31): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 690 | chr17 | TogoVar | |||||||
ARHGAP24_chr4_85470150_86007666 | 85655792 | T | TATATATA others(13): Show |
intron_variant | MODIFIER | NA20129.hp1 | a0001 | a0001c0005 | a0001c0005t0003 | a0001c0005t0003g0093 | 1 | 48 | 0.0208 | 20 | c.181 others(39): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85655812 | G | GAGAGAGA others(13): Show |
intron_variant | MODIFIER | HG02723.hp1 | a0005 | a0005c0010 | a0005c0010t0001 | a0005c0010t0001g0090 | 1 | 83 | 0.0120 | 20 | c.181 others(39): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85733060 | C | CTTTTTTT others(13): Show |
intron_variant | MODIFIER | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0002a0001c0003t0001 | a0001c0001t0001g0073 a0001c0002t0002g0004 a0001c0002t0002g0025 others(7): Show |
10 | 24 | 0.4167 | 20 | c.268 others(39): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85982373 | T | TTTTTGTT others(13): Show |
intron_variant | MODIFIER | HG00323.hp1 HG00423.hp1 HG00639.hp2 others(61): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(16): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(61): Show |
64 | 82 | 0.7805 | 20 | c.928 others(37): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 8/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP25_chr2_68729811_68831833 | 68743329 | A | ACAAGTGG others(13): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(251): Show |
a0001a0002a0003others(5): Show | a0001c0001a0002c0002a0002c0004others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(33): Show | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0017 others(245): Show |
254 | 366 | 0.6940 | 20 | c.61+ others(35): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | chr2 | TogoVar | |||||||
ARHGAP26_chr5_142765377_143234007 | 142949182 | A | AGAGAGAG others(13): Show |
intron_variant | MODIFIER | HG03491.hp1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0186 | 1 | 189 | 0.0053 | 20 | c.110 others(41): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142949190 | A | AGAGAGAG others(13): Show |
intron_variant | MODIFIER | HG01243.hp1 | a0001 | a0001c0001 | a0001c0001t0020 | a0001c0001t0020g0079 | 1 | 193 | 0.0052 | 20 | c.110 others(41): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142949221 | G | GAGGAGAG others(13): Show |
intron_variant | MODIFIER | HG03130.hp2 | a0001 | a0001c0001 | a0001c0001t0054 | a0001c0001t0054g0082 | 1 | 76 | 0.0132 | 20 | c.110 others(41): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | |||||||
ARHGAP26_chr5_142765377_143234007 | 142963194 | A | ATACATAT others(13): Show |
intron_variant | MODIFIER | HG02717.hp2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0045 | 1 | 188 | 0.0053 | 20 | c.110 others(41): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142980352 | C | CTTTATTT others(13): Show |
intron_variant | MODIFIER | HG00609.hp2 HG03098.hp2 NA18612.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(1): Show | a0001c0001t0001g0138 a0001c0001t0004g0002 a0001c0001t0005g0113 others(1): Show |
4 | 20 | 0.2000 | 20 | c.110 others(41): 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(13): Show |
intron_variant | MODIFIER | HG02056.hp2 | a0001 | a0001c0004 | a0001c0004t0007 | a0001c0004t0007g0054 | 1 | 171 | 0.0058 | 20 | c.110 others(39): 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(13): Show |
intron_variant | MODIFIER | HG02056.hp1 HG02074.hp1 HG02155.hp1 others(10): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(8): Show | a0001c0001t0001g0153 a0001c0001t0002g0195 a0001c0001t0004g0105 others(10): Show |
13 | 60 | 0.2167 | 20 | c.110 others(39): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143012576 | T | TATATATA others(13): Show |
intron_variant | MODIFIER | HG00438.hp1 HG00544.hp2 NA18944.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0002a0001c0001t0020a0001c0002t0004others(1): Show | a0001c0001t0002g0005 a0001c0001t0002g0006 a0001c0001t0002g0121 others(4): Show |
7 | 181 | 0.0387 | 20 | c.110 others(39): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | chr5 | TogoVar | |||||||
ARHGAP27_chr17_45388908_45437870 | 45399591 | C | CAAAGAAA others(13): Show |
intron_variant | MODIFIER | HG01891.hp1 HG02965.hp2 HG06807.hp1 others(2): Show |
a0002 | a0002c0002 | a0002c0002t0001a0002c0002t0005 | a0002c0002t0001g0093 a0002c0002t0001g0094 a0002c0002t0001g0095 others(2): Show |
5 | 41 | 0.1220 | 20 | c.174 others(39): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 12/19 | chr17 | TogoVar | |||||||
ARHGAP27_chr17_45388908_45437870 | 45433915 | T | TGGCTAAC others(13): Show |
upstream_gene_variant | MODIFIER | HG02257.hp2 HG02647.hp1 HG02647.hp2 others(7): Show |
a0001a0010 | a0001c0001a0001c0015a0010c0013 | a0001c0001t0001a0001c0001t0007a0001c0001t0022others(2): Show | a0001c0001t0001g0183 a0001c0001t0001g0184 a0001c0001t0001g0185 others(7): Show |
10 | 326 | 0.0307 | 20 | c.-14 others(31): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 1046 | chr17 | TogoVar | |||||||
ARHGAP28_chr18_6724716_6920716 | 6729574 | G | GCACACAC others(13): Show |
upstream_gene_variant | MODIFIER | HG02280.hp2 HG02922.hp2 HG03540.hp1 others(1): Show |
a0001a0002a0006 | a0001c0001a0001c0003a0002c0002others(1): Show | a0001c0001t0008a0001c0003t0003a0002c0002t0004others(1): Show | a0001c0001t0008g0143 a0001c0003t0003g0145 a0002c0002t0004g0147 others(1): Show |
4 | 163 | 0.0245 | 20 | c.-24 others(29): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 141 | chr18 | TogoVar | |||||||
ARHGAP28_chr18_6724716_6920716 | 6730216 | C | CATATATA others(13): Show |
intron_variant | MODIFIER | HG03139.hp2 | a0001 | a0001c0018 | a0001c0018t0020 | a0001c0018t0020g0007 | 1 | 245 | 0.0041 | 20 | c.122 others(35): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6730219 | G | GTATATAT others(13): Show |
intron_variant | MODIFIER | HG00099.hp1 HG02922.hp1 HG03130.hp2 others(4): Show |
a0001a0002a0008others(1): Show | a0001c0003a0001c0010a0002c0002others(3): Show | a0001c0003t0003a0001c0010t0003a0002c0002t0012others(3): Show | a0001c0003t0003g0087 a0001c0003t0003g0091 a0001c0010t0003g0089 others(4): Show |
7 | 127 | 0.0551 | 20 | c.122 others(35): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6730236 | T | TATATATA others(13): Show |
intron_variant | MODIFIER | HG01256.hp1 HG02965.hp1 HG03098.hp2 others(1): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0008a0001c0003t0003 | a0001c0001t0001g0075 a0001c0001t0008g0074 a0001c0003t0003g0076 others(1): Show |
4 | 243 | 0.0165 | 20 | c.122 others(35): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP29_chr1_94163905_94242584 | 94182811 | T | TAAAACAA others(13): Show |
intron_variant | MODIFIER | HG02895.hp2 HG02897.hp2 |
a0001 | a0001c0001 | a0001c0001t0018 | a0001c0001t0018g0234 a0001c0001t0018g0235 |
2 | 164 | 0.0122 | 20 | c.224 others(39): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161053462 | T | TTCTCTCT others(13): Show |
intron_variant | MODIFIER | HG03834.hp1 NA18988.hp1 |
a0002 | a0002c0002a0002c0003 | a0002c0002t0001a0002c0003t0001 | a0002c0002t0001g0326 a0002c0003t0001g0299 |
2 | 29 | 0.0690 | 20 | c.537 others(33): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 5/11 | chr1 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161064777 | G | GAGAAAGA others(13): Show |
intron_variant | MODIFIER | HG02970.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0136 | 1 | 372 | 0.0027 | 20 | c.97+ others(35): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | |||||||
ARHGAP31_chr3_119289383_119425714 | 119293703 | A | AGTGTGTG others(13): Show |
upstream_gene_variant | MODIFIER | HG01255.hp2 HG02280.hp2 HG02559.hp2 others(5): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0004others(4): Show | a0001c0001t0020a0001c0002t0001a0001c0004t0003others(5): Show | a0001c0001t0020g0044 a0001c0002t0001g0008 a0001c0004t0003g0025 others(5): Show |
8 | 208 | 0.0385 | 20 | c.-12 others(31): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 679 | chr3 | TogoVar | |||||||
ARHGAP31_chr3_119289383_119425714 | 119307940 | C | CAAAAAAA others(13): Show |
intron_variant | MODIFIER | HG00323.hp1 HG00408.hp1 HG00609.hp1 others(29): Show |
a0001a0002a0015 | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0005a0001c0001t0006a0001c0001t0020others(11): Show | a0001c0001t0005g0097 a0001c0001t0005g0129 a0001c0001t0005g0169 others(29): Show |
32 | 39 | 0.8205 | 20 | c.100 others(39): 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(13): Show |
intron_variant | MODIFIER | HG00408.hp2 HG00438.hp2 HG00609.hp2 others(36): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(18): Show | a0001c0001t0005g0129 a0001c0001t0006g0095 a0001c0001t0006g0104 others(35): Show |
39 | 137 | 0.2847 | 20 | c.683 others(37): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 6/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 129143072 | C | CATATATA others(13): Show |
intron_variant | MODIFIER | HG02056.hp1 HG02080.hp2 HG02615.hp1 others(7): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0016others(1): Show | a0001c0001t0002a0001c0001t0004a0001c0003t0006others(3): Show | a0001c0001t0002g0099 a0001c0001t0002g0102 a0001c0001t0002g0139 others(7): Show |
10 | 112 | 0.0893 | 20 | c.226 others(39): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 2/22 | chr11 | TogoVar | |||||||
ARHGAP35_chr19_46855997_47010077 | 46879587 | A | AAAATAAA others(13): Show |
intron_variant | MODIFIER | HG00280.hp1 HG00558.hp2 HG01070.hp1 others(34): Show |
a0001a0006 | a0001c0001a0001c0002a0006c0008 | a0001c0001t0001a0001c0001t0004a0001c0001t0016others(9): Show | a0001c0001t0001g0170 a0001c0001t0001g0171 a0001c0001t0001g0172 others(34): Show |
37 | 125 | 0.2960 | 20 | c.-18 others(41): 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(13): Show |
intron_variant | MODIFIER | HG03471.hp1 NA19030.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0035 a0001c0001t0003g0188 |
2 | 6 | 0.3333 | 20 | c.-14 others(39): Show |
ARHGAP36 | ENSG00000147256.12 | transcript | ENST00000276211.10 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chrX | TogoVar | ||||||
ARHGAP39_chr8_144524179_144690846 | 144561457 | T | TTCCATCA others(13): Show |
intron_variant | MODIFIER | HG03225.hp2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0124 | 1 | 239 | 0.0042 | 20 | c.513 others(37): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144561941 | C | CACTCCAG others(13): Show |
intron_variant | MODIFIER | HG02300.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0112 | 1 | 243 | 0.0041 | 20 | c.513 others(37): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144562445 | G | GACTCCAG others(13): Show |
intron_variant | MODIFIER | NA19091.hp1 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0031 | 1 | 202 | 0.0050 | 20 | c.513 others(37): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144562529 | G | GACTCCAG others(13): Show |
intron_variant | MODIFIER | HG02257.hp1 HG02622.hp1 HG03195.hp2 |
a0001a0004 | a0001c0007a0004c0013 | a0001c0007t0003a0001c0007t0017a0004c0013t0002 | a0001c0007t0003g0074 a0001c0007t0017g0015 a0004c0013t0002g0194 |
3 | 234 | 0.0128 | 20 | c.513 others(37): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 3/11 | chr8 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144601510 | A | ATGTGTGT others(13): Show |
intron_variant | MODIFIER | HG02055.hp2 HG02809.hp2 HG02886.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0157 a0001c0001t0004g0149 a0001c0001t0004g0150 others(5): Show |
8 | 244 | 0.0328 | 20 | c.80+ others(35): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 2/11 | chr8 | TogoVar | |||||||
ARHGAP40_chr20_38596809_38655653 | 38627633 | G | GGGTGTGT others(13): Show |
intron_variant | MODIFIER | HG00558.hp1 HG00639.hp2 HG00673.hp1 others(71): Show |
a0001a0004a0007others(6): Show | a0001c0002a0001c0008a0004c0011others(8): Show | a0001c0002t0001a0001c0002t0002a0001c0002t0003others(17): Show | a0001c0002t0001g0024 a0001c0002t0001g0124 a0001c0002t0001g0125 others(67): Show |
74 | 343 | 0.2157 | 20 | c.558 others(35): Show |
ARHGAP40 | ENSG00000124143.11 | transcript | ENST00000373345.9 | protein_coding | 3/14 | INFO_REALIGN_3_PRIME | chr20 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100837926 | T | TTTTTATT others(13): Show |
intron_variant | MODIFIER | HG00639.hp1 HG00733.hp2 HG00738.hp2 others(23): Show |
a0001a0002a0003 | a0001c0001a0001c0008a0002c0002others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0008t0001others(10): Show | a0001c0001t0001g0021 a0001c0001t0001g0023 a0001c0001t0001g0160 others(23): Show |
26 | 47 | 0.5532 | 20 | c.313 others(39): 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(13): Show |
intron_variant | MODIFIER | HG01261.hp2 HG02004.hp1 |
a0003 | a0003c0007 | a0003c0007t0005 | a0003c0007t0005g0058 a0003c0007t0005g0064 |
2 | 41 | 0.0488 | 20 | c.385 others(39): 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(13): Show |
intron_variant | MODIFIER | HG01192.hp2 HG01257.hp2 HG02083.hp2 others(8): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0008 | a0001c0001t0001g0069 a0001c0001t0001g0073 a0001c0001t0001g0079 others(8): Show |
11 | 50 | 0.2200 | 20 | c.385 others(39): 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(13): Show |
intron_variant | MODIFIER | NA19075.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0065 | 1 | 68 | 0.0147 | 20 | c.385 others(37): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100980559 | C | CTTCTTTT others(13): Show |
intron_variant | MODIFIER | HG02818.hp2 HG03492.hp2 |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0008 | a0001c0001t0001g0152 a0002c0002t0008g0005 |
2 | 25 | 0.0800 | 20 | c.245 others(39): 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(13): Show |
intron_variant | MODIFIER | NA19084.hp2 | a0006 | a0006c0017 | a0006c0017t0001 | a0006c0017t0001g0183 | 1 | 24 | 0.0417 | 20 | c.245 others(39): 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(13): Show |
downstream_gene_variant | MODIFIER | HG00735.hp2 HG03139.hp2 |
a0002 | a0002c0002a0002c0005 | a0002c0002t0012a0002c0005t0016 | a0002c0002t0012g0027 a0002c0005t0016g0032 |
2 | 20 | 0.1000 | 20 | c.*68 others(31): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 1715 | chr11 | TogoVar | |||||||
ARHGAP44_chr17_12784498_12996643 | 12841594 | T | TCTCTCTC others(13): Show |
intron_variant | MODIFIER | HG02109.hp1 HG03209.hp2 HG03491.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0017 a0001c0001t0003g0074 a0001c0001t0003g0075 |
3 | 126 | 0.0238 | 20 | c.53+ others(37): 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(13): Show |
intron_variant | MODIFIER | HG02071.hp2 HG02257.hp2 HG03831.hp2 others(2): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0012 a0001c0001t0001g0015 a0001c0001t0002g0019 others(2): Show |
5 | 128 | 0.0391 | 20 | c.53+ others(37): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 1/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12931841 | T | TACACACA others(13): Show |
intron_variant | MODIFIER | NA18968.hp2 | a0001 | a0001c0001 | a0001c0001t0011 | a0001c0001t0011g0059 | 1 | 40 | 0.0250 | 20 | c.582 others(37): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 7/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP44_chr17_12784498_12996643 | 12948723 | T | TACACACA others(13): Show |
intron_variant | MODIFIER | HG02622.hp2 HG04228.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0024 | a0001c0001t0001g0026 a0001c0001t0024g0006 |
2 | 44 | 0.0455 | 20 | c.862 others(35): Show |
ARHGAP44 | ENSG00000006740.18 | transcript | ENST00000379672.10 | protein_coding | 10/20 | INFO_REALIGN_3_PRIME | chr17 | TogoVar |