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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP20_chr11_110572043_110717437 | 110660069 | A | AAAAAACA others(4): Show |
intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG02015.hp1 others(7): Show |
a0001a0009 | a0001c0001a0001c0002a0009c0021 | a0001c0001t0001a0001c0001t0003a0001c0002t0005others(1): Show | a0001c0001t0001g0207 a0001c0001t0003g0209 a0001c0002t0005g0206 others(7): Show |
10 | 157 | 0.0637 | 11 | c.189 others(30): Show |
ARHGAP20 | ENSG00000137727.13 | transcript | ENST00000683387.1 | protein_coding | 2/14 | chr11 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24580886 | C | CAAAAAAA others(4): Show |
downstream_gene_variant | MODIFIER | HG02451.hp1 HG02630.hp2 HG03130.hp1 others(1): Show |
a0001a0005 | a0001c0001a0005c0005 | a0001c0001t0001a0001c0001t0013a0005c0005t0001 | a0001c0001t0001g0254 a0001c0001t0013g0255 a0005c0005t0001g0103 others(1): Show |
4 | 30 | 0.1333 | 11 | c.*35 others(22): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2727 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24624337 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG01891.hp2 HG02559.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0167 a0001c0001t0001g0172 |
2 | 142 | 0.0141 | 11 | c.496 others(28): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24625050 | T | TGGGGGGG others(4): Show |
intron_variant | MODIFIER | HG03195.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0194 | 1 | 140 | 0.0071 | 11 | c.496 others(28): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24625062 | G | GGGGGGGG others(4): Show |
intron_variant | MODIFIER | NA18959.hp1 NA19002.hp2 NA19004.hp1 |
a0003a0008 | a0003c0003a0008c0009 | a0003c0003t0001a0008c0009t0005 | a0003c0003t0001g0199 a0003c0003t0001g0225 a0008c0009t0005g0003 |
3 | 277 | 0.0108 | 11 | c.496 others(28): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24628982 | A | ATATATAT others(4): Show |
intron_variant | MODIFIER | HG02738.hp1 HG02965.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0014 a0001c0001t0001g0258 |
2 | 141 | 0.0142 | 11 | c.495 others(28): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24628982 | A | ATATATAT others(4): Show |
intron_variant | MODIFIER | HG04199.hp1 HG04228.hp1 NA18982.hp2 others(2): Show |
a0001a0003a0005 | a0001c0001a0003c0003a0005c0005 | a0001c0001t0001a0003c0003t0001a0005c0005t0001 | a0001c0001t0001g0170 a0001c0001t0001g0230 a0001c0001t0001g0245 others(2): Show |
5 | 144 | 0.0347 | 11 | c.495 others(28): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24628982 | A | ATATATAT others(4): Show |
intron_variant | MODIFIER | HG01109.hp2 HG02615.hp1 HG02717.hp2 others(1): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0179 a0001c0001t0001g0224 a0001c0001t0001g0243 others(1): Show |
4 | 143 | 0.0280 | 11 | c.495 others(28): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24628982 | A | ATATATTT others(4): Show |
intron_variant | MODIFIER | NA18975.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0233 | 1 | 140 | 0.0071 | 11 | c.495 others(28): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24628982 | A | ATATTTTT others(4): Show |
intron_variant | MODIFIER | HG02257.hp2 HG02258.hp2 |
a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0135 a0002c0002t0001g0136 |
2 | 141 | 0.0142 | 11 | c.495 others(28): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | |||||||
ARHGAP21_chr10_24578614_24728887 | 24628983 | T | TATATATA others(4): Show |
intron_variant | MODIFIER | HG01261.hp1 HG02080.hp1 HG02486.hp1 others(2): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0145 a0001c0001t0001g0177 a0002c0002t0001g0051 others(2): Show |
5 | 299 | 0.0167 | 11 | c.495 others(28): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 7/25 | chr10 | TogoVar | |||||||
ARHGAP22_chr10_48441036_48610073 | 48524467 | A | AGGGGGCG others(4): Show |
intron_variant | MODIFIER | HG00323.hp1 HG00558.hp2 HG00642.hp2 others(65): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(18): Show | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0088 others(64): Show |
68 | 268 | 0.2537 | 11 | c.322 others(30): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 3/9 | chr10 | TogoVar | |||||||
ARHGAP22_chr10_48441036_48610073 | 48577786 | A | AACTGCTC others(4): Show |
intron_variant | MODIFIER | HG00280.hp2 HG00544.hp1 HG00544.hp2 others(82): Show |
a0001a0004a0005others(3): Show | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(14): Show | a0001c0001t0001g0018 a0001c0001t0001g0019 a0001c0001t0001g0044 others(82): Show |
85 | 268 | 0.3172 | 11 | c.234 others(28): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 2/9 | chr10 | TogoVar | |||||||
ARHGAP22_chr10_48441036_48610073 | 48577801 | G | GTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG00544.hp1 HG01106.hp2 HG01168.hp2 others(32): Show |
a0001a0008 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0018 a0001c0001t0001g0051 a0001c0001t0001g0057 others(32): Show |
35 | 103 | 0.3398 | 11 | c.234 others(28): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 2/9 | chr10 | TogoVar | |||||||
ARHGAP23_chr17_38423464_38517385 | 38426550 | C | CAAAAAAA others(4): Show |
upstream_gene_variant | MODIFIER | HG03098.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0079 | 1 | 128 | 0.0078 | 11 | c.-19 others(22): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1913 | chr17 | TogoVar | |||||||
ARHGAP23_chr17_38423464_38517385 | 38447437 | G | GAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG01169.hp1 HG03017.hp2 HG03492.hp1 others(7): Show |
a0001a0008 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0002a0001c0003t0001others(2): Show | a0001c0001t0001g0095 a0001c0002t0002g0015 a0001c0002t0002g0110 others(7): Show |
10 | 173 | 0.0578 | 11 | c.64- others(28): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85497550 | A | AGTGGCTC others(4): Show |
intron_variant | MODIFIER | NA21309.hp1 | a0001 | a0001c0002 | a0001c0002t0002 | a0001c0002t0002g0060 | 1 | 108 | 0.0093 | 11 | c.-21 others(30): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85541142 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG00735.hp2 | a0003 | a0003c0012 | a0003c0012t0001 | a0003c0012t0001g0027 | 1 | 40 | 0.0250 | 11 | c.-20 others(30): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85610451 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG02717.hp1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0063 | 1 | 14 | 0.0714 | 11 | c.180 others(30): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85655810 | G | GAGAGAGA others(4): Show |
intron_variant | MODIFIER | HG03486.hp2 | a0001 | a0001c0005 | a0001c0005t0004 | a0001c0005t0004g0037 | 1 | 98 | 0.0102 | 11 | c.181 others(30): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85660794 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG00639.hp2 HG01069.hp1 HG01074.hp2 others(6): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0020others(3): Show | a0001c0001t0001g0014 a0001c0001t0001g0039 a0001c0001t0001g0081 others(6): Show |
9 | 12 | 0.7500 | 11 | c.181 others(30): 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(4): Show |
intron_variant | MODIFIER | HG00323.hp2 HG00423.hp1 HG00735.hp1 others(16): Show |
a0001a0003a0005 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0020a0001c0002t0002others(6): Show | a0001c0001t0001g0003 a0001c0001t0001g0010 a0001c0001t0001g0021 others(16): Show |
19 | 33 | 0.5758 | 11 | c.268 others(30): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85875698 | T | TATAAAAT others(4): Show |
intron_variant | MODIFIER | HG02258.hp1 HG02897.hp2 HG03471.hp1 others(2): Show |
a0001 | a0001c0002 | a0001c0002t0002a0001c0002t0008 | a0001c0002t0002g0004 a0001c0002t0002g0041 a0001c0002t0002g0069 others(2): Show |
5 | 108 | 0.0463 | 11 | c.269 others(30): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | chr4 | TogoVar | |||||||
ARHGAP24_chr4_85470150_86007666 | 85973833 | G | GTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG02055.hp2 NA19240.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0024 a0001c0001t0001g0066 |
2 | 33 | 0.0606 | 11 | c.733 others(28): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142890136 | T | TAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG02615.hp1 HG03654.hp2 NA19010.hp2 others(1): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0007 | a0001c0001t0007a0001c0001t0033a0001c0002t0001others(1): Show | a0001c0001t0007g0106 a0001c0001t0033g0192 a0001c0002t0001g0197 others(1): Show |
4 | 154 | 0.0260 | 11 | c.487 others(28): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142890151 | A | AAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG02572.hp1 NA18952.hp1 NA18995.hp1 |
a0001 | a0001c0001a0001c0008 | a0001c0001t0001a0001c0001t0002a0001c0008t0019 | a0001c0001t0001g0020 a0001c0001t0002g0001 a0001c0008t0019g0177 |
3 | 118 | 0.0254 | 11 | c.487 others(28): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142890151 | A | AAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG03017.hp1 | a0001 | a0001c0001 | a0001c0001t0007 | a0001c0001t0007g0107 | 1 | 116 | 0.0086 | 11 | c.487 others(28): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142890151 | A | AAAAATAT others(4): Show |
intron_variant | MODIFIER | HG02647.hp2 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0111 | 1 | 116 | 0.0086 | 11 | c.487 others(28): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142949190 | A | AGAGAGAG others(4): Show |
intron_variant | MODIFIER | HG03453.hp1 | a0001 | a0001c0001 | a0001c0001t0026 | a0001c0001t0026g0097 | 1 | 193 | 0.0052 | 11 | c.110 others(32): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142980352 | C | CTTTTATT others(4): Show |
intron_variant | MODIFIER | HG03130.hp1 | a0001 | a0001c0001 | a0001c0001t0022 | a0001c0001t0022g0055 | 1 | 17 | 0.0588 | 11 | c.110 others(32): 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(4): Show |
intron_variant | MODIFIER | HG02965.hp1 NA18960.hp2 NA19081.hp2 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0004 | a0001c0001t0002g0121 a0001c0001t0002g0128 a0001c0001t0004g0105 |
3 | 48 | 0.0625 | 11 | c.153 others(32): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143109154 | G | GTAACTCA others(4): Show |
intron_variant | MODIFIER | HG00323.hp1 HG00408.hp1 HG00438.hp1 others(105): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(44): Show | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0034 others(105): Show |
108 | 196 | 0.5510 | 11 | c.153 others(32): 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(4): Show |
intron_variant | MODIFIER | HG00408.hp1 HG03710.hp1 NA18990.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0007others(4): Show | a0001c0001t0001g0131 a0001c0001t0003g0174 a0001c0001t0007g0068 others(4): Show |
7 | 31 | 0.2258 | 11 | c.198 others(32): 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(4): Show |
downstream_gene_variant | MODIFIER | HG01934.hp1 HG02451.hp2 HG02615.hp1 others(11): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0007 | a0001c0001t0002a0001c0001t0004a0001c0001t0005others(5): Show | a0001c0001t0002g0008 a0001c0001t0002g0022 a0001c0001t0002g0036 others(11): Show |
14 | 43 | 0.3256 | 11 | c.*10 others(24): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 3624 | chr5 | TogoVar | |||||||
ARHGAP27_chr17_45388908_45437870 | 45412962 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG03579.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0194 | 1 | 81 | 0.0123 | 11 | c.658 others(28): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | TogoVar | |||||||
ARHGAP27_chr17_45388908_45437870 | 45434445 | A | ATTTTCTT others(4): Show |
upstream_gene_variant | MODIFIER | NA20129.hp1 | a0002 | a0002c0002 | a0002c0002t0005 | a0002c0002t0005g0051 | 1 | 346 | 0.0029 | 11 | c.-19 others(22): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 1576 | chr17 | TogoVar | |||||||
ARHGAP28_chr18_6724716_6920716 | 6841184 | T | TTTCTCTC others(4): Show |
intron_variant | MODIFIER | NA18956.hp1 | a0003 | a0003c0004 | a0003c0004t0001 | a0003c0004t0001g0045 | 1 | 242 | 0.0041 | 11 | c.543 others(28): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | TogoVar | |||||||
ARHGAP28_chr18_6724716_6920716 | 6841208 | C | CTCTCTCT others(4): Show |
intron_variant | MODIFIER | HG06807.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0228 | 1 | 165 | 0.0061 | 11 | c.543 others(28): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161064828 | A | AAAGAAAG others(4): Show |
intron_variant | MODIFIER | HG02056.hp2 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0056 | 1 | 385 | 0.0026 | 11 | c.97+ others(26): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161064834 | A | AGAAAGAA others(4): Show |
intron_variant | MODIFIER | NA19060.hp1 | a0011 | a0011c0009 | a0011c0009t0001 | a0011c0009t0001g0058 | 1 | 387 | 0.0026 | 11 | c.97+ others(26): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | |||||||
ARHGAP31_chr3_119289383_119425714 | 119307940 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG00621.hp2 HG02257.hp1 HG02300.hp2 others(4): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0029a0001c0002t0001a0001c0002t0012others(4): Show | a0001c0001t0029g0055 a0001c0002t0001g0083 a0001c0002t0012g0175 others(4): Show |
7 | 14 | 0.5000 | 11 | c.100 others(30): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP32_chr11_128960060_129197325 | 128982507 | G | GTGTGTGT others(4): Show |
intron_variant | MODIFIER | NA19078.hp1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0179 | 1 | 396 | 0.0025 | 11 | c.152 others(28): Show |
ARHGAP32 | ENSG00000134909.19 | transcript | ENST00000682385.1 | protein_coding | 15/22 | chr11 | TogoVar | |||||||
ARHGAP33_chr19_35770564_35793822 | 35771081 | C | CTCCTCCT others(4): Show |
upstream_gene_variant | MODIFIER | NA19062.hp1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0005 | 1 | 418 | 0.0024 | 11 | c.-45 others(22): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 4482 | chr19 | TogoVar | |||||||
ARHGAP33_chr19_35770564_35793822 | 35771989 | C | CTTTTTTT others(4): Show |
upstream_gene_variant | MODIFIER | HG02109.hp1 HG02258.hp1 HG02630.hp1 others(1): Show |
a0001a0005 | a0001c0001a0001c0006a0005c0015 | a0001c0001t0001a0001c0006t0001a0005c0015t0001 | a0001c0001t0001g0025 a0001c0006t0001g0001 a0005c0015t0001g0025 others(1): Show |
4 | 5 | 0.8000 | 11 | c.-36 others(22): Show |
ARHGAP33 | ENSG00000004777.19 | transcript | ENST00000007510.9 | protein_coding | 3574 | chr19 | TogoVar | |||||||
ARHGAP35_chr19_46855997_47010077 | 47007073 | C | CTTTTTTT others(4): Show |
downstream_gene_variant | MODIFIER | HG01071.hp2 HG02145.hp1 |
a0001 | a0001c0001 | a0001c0001t0016a0001c0001t0024 | a0001c0001t0016g0219 a0001c0001t0024g0025 |
2 | 67 | 0.0299 | 11 | c.*63 others(22): Show |
ARHGAP35 | ENSG00000160007.20 | transcript | ENST00000672722.1 | protein_coding | 1997 | chr19 | TogoVar | |||||||
ARHGAP39_chr8_144524179_144690846 | 144669506 | C | CAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG00438.hp1 HG02135.hp1 HG02293.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0014 | a0001c0001t0001g0048 a0001c0001t0001g0051 a0001c0001t0014g0049 |
3 | 8 | 0.3750 | 11 | c.-82 others(30): Show |
ARHGAP39 | ENSG00000147799.12 | transcript | ENST00000377307.7 | protein_coding | 1/11 | chr8 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100837666 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG00642.hp1 HG01123.hp2 HG01515.hp2 others(13): Show |
a0001a0002 | a0001c0001a0001c0014a0001c0015others(1): Show | a0001c0001t0001a0001c0001t0034a0001c0014t0001others(2): Show | a0001c0001t0001g0011 a0001c0001t0001g0079 a0001c0001t0001g0098 others(13): Show |
16 | 49 | 0.3265 | 11 | c.313 others(30): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100893158 | G | GTGTGTGT others(4): Show |
intron_variant | MODIFIER | HG01192.hp1 | a0001 | a0001c0003 | a0001c0003t0006 | a0001c0003t0006g0286 | 1 | 30 | 0.0333 | 11 | c.385 others(30): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | chr11 | TogoVar | |||||||
ARHGAP42_chr11_100682288_100998941 | 100903709 | A | AAAAAAAA others(4): Show |
intron_variant | MODIFIER | HG01433.hp1 | a0002 | a0002c0002 | a0002c0002t0001 | a0002c0002t0001g0015 | 1 | 68 | 0.0147 | 11 | c.385 others(28): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 4/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar | ||||||
ARHGAP42_chr11_100682288_100998941 | 100952734 | C | CTTTTTTT others(4): Show |
intron_variant | MODIFIER | HG00738.hp1 HG00741.hp1 HG01243.hp2 others(21): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(5): Show | a0001c0001t0001g0062 a0001c0001t0001g0109 a0001c0001t0001g0152 others(21): Show |
24 | 43 | 0.5581 | 11 | c.116 others(30): Show |
ARHGAP42 | ENSG00000165895.19 | transcript | ENST00000298815.13 | protein_coding | 12/23 | INFO_REALIGN_3_PRIME | chr11 | TogoVar |