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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP25_chr2_68729811_68831833 | 68821906 | GTTT | G | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(120): Show |
a0001a0002a0007others(1): Show | a0001c0001a0002c0008a0007c0013others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(108): Show |
123 | 222 | 0.5541 | -3 | c.120 others(20): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP25_chr2_68729811_68831833 | 68827485 | CAGA | C | downstream_gene_variant | MODIFIER | HG02622.hp1 HG02809.hp2 NA19043.hp2 |
a0002 | a0002c0002 | a0002c0002t0001a0002c0002t0003 | a0002c0002t0001g0263 a0002c0002t0003g0056 a0002c0002t0003g0338 |
3 | 366 | 0.0082 | -3 | c.*12 others(14): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 653 | chr2 | TogoVar | |||||||
ARHGAP26_chr5_142765377_143234007 | 142779178 | TAGC | T | intron_variant | MODIFIER | HG01934.hp1 HG02451.hp2 HG02717.hp2 others(2): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0002a0001c0001t0043a0001c0003t0002 | a0001c0001t0002g0043 a0001c0001t0002g0045 a0001c0001t0002g0046 others(2): Show |
5 | 196 | 0.0255 | -3 | c.154 others(20): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142795037 | ATCT | A | intron_variant | MODIFIER | HG00544.hp2 HG00597.hp1 HG00609.hp2 others(48): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(29): Show | a0001c0001t0001g0029 a0001c0001t0001g0034 a0001c0001t0001g0141 others(48): Show |
51 | 196 | 0.2602 | -3 | c.154 others(22): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142808236 | GAAA | G | intron_variant | MODIFIER | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(22): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(14): Show | a0001c0001t0001g0153 a0001c0001t0001g0158 a0001c0001t0003g0176 others(22): Show |
25 | 27 | 0.9259 | -3 | c.154 others(22): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142821300 | GTTT | G | intron_variant | MODIFIER | HG00558.hp2 HG02132.hp1 HG03041.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0196 a0001c0001t0002g0128 a0001c0001t0003g0165 others(5): Show |
8 | 83 | 0.0964 | -3 | c.154 others(22): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142838677 | ATTG | A | intron_variant | MODIFIER | HG02615.hp2 HG02809.hp1 |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0019 | a0001c0001t0006g0084 a0001c0001t0019g0049 |
2 | 196 | 0.0102 | -3 | c.155 others(22): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142865478 | GTTT | G | intron_variant | MODIFIER | HG00438.hp1 HG00544.hp1 HG00544.hp2 others(38): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(21): Show | a0001c0001t0001g0029 a0001c0001t0001g0131 a0001c0001t0001g0138 others(38): Show |
41 | 131 | 0.3130 | -3 | c.155 others(20): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142876776 | CAAA | C | intron_variant | MODIFIER | HG00408.hp1 HG00597.hp1 HG02056.hp1 others(17): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(10): Show | a0001c0001t0002g0190 a0001c0001t0002g0195 a0001c0001t0004g0105 others(17): Show |
20 | 85 | 0.2353 | -3 | c.312 others(20): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 3/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142890152 | ATAT | A | intron_variant | MODIFIER | HG02886.hp1 HG03490.hp1 NA19043.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0044a0001c0003t0001a0001c0003t0050 | a0001c0001t0044g0052 a0001c0003t0001g0149 a0001c0003t0050g0089 |
3 | 188 | 0.0160 | -3 | c.487 others(20): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 5/22 | chr5 | TogoVar | |||||||
ARHGAP26_chr5_142765377_143234007 | 142973719 | TAAG | T | intron_variant | MODIFIER | HG00323.hp1 HG03486.hp2 NA19043.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0021a0001c0001t0037 | a0001c0001t0002g0023 a0001c0001t0021g0081 a0001c0001t0037g0160 |
3 | 196 | 0.0153 | -3 | c.110 others(24): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143006316 | CTTT | C | intron_variant | MODIFIER | HG02886.hp2 HG03490.hp2 HG03492.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0034 a0001c0001t0002g0117 a0001c0001t0003g0033 others(2): Show |
5 | 116 | 0.0431 | -3 | c.110 others(22): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143020632 | CTTT | C | intron_variant | MODIFIER | HG01069.hp1 HG01071.hp1 HG01167.hp2 others(29): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0034 a0001c0001t0002g0117 a0001c0001t0003g0033 others(29): Show |
32 | 104 | 0.3077 | -3 | c.114 others(22): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143029392 | GTTT | G | intron_variant | MODIFIER | HG00408.hp2 HG02056.hp1 HG02280.hp1 others(14): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(11): Show | a0001c0001t0001g0012 a0001c0001t0002g0121 a0001c0001t0002g0128 others(14): Show |
17 | 64 | 0.2656 | -3 | c.114 others(22): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143033787 | ACTT | A | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(22): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0007 | a0001c0001t0004a0001c0001t0006a0001c0001t0009others(14): Show | a0001c0001t0004g0002 a0001c0001t0004g0099 a0001c0001t0006g0064 others(22): Show |
25 | 196 | 0.1276 | -3 | c.114 others(22): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 12/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143041722 | GAAA | G | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(18): Show |
a0001a0002 | a0001c0001a0002c0007 | a0001c0001t0004a0001c0001t0006a0001c0001t0009others(11): Show | a0001c0001t0004g0002 a0001c0001t0004g0098 a0001c0001t0004g0099 others(18): Show |
21 | 65 | 0.3231 | -3 | c.121 others(18): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 13/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143080918 | AGTG | A | intron_variant | MODIFIER | HG01243.hp2 HG02257.hp2 HG03486.hp2 others(1): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0002a0001c0001t0028a0001c0001t0055others(1): Show | a0001c0001t0002g0023 a0001c0001t0028g0085 a0001c0001t0055g0072 others(1): Show |
4 | 196 | 0.0204 | -3 | c.153 others(24): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143115336 | AAAC | A | intron_variant | MODIFIER | HG02809.hp1 HG03139.hp2 HG03471.hp2 others(1): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0006a0001c0001t0021a0001c0003t0004others(1): Show | a0001c0001t0006g0084 a0001c0001t0021g0073 a0001c0003t0004g0100 others(1): Show |
4 | 196 | 0.0204 | -3 | c.153 others(22): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143167482 | CAAA | C | intron_variant | MODIFIER | HG01175.hp1 HG02257.hp2 HG02809.hp1 others(3): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0002a0001c0001t0006a0001c0001t0028others(3): Show | a0001c0001t0002g0118 a0001c0001t0006g0084 a0001c0001t0028g0085 others(3): Show |
6 | 38 | 0.1579 | -3 | c.198 others(24): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 143226485 | GAAA | G | 3_prime_UTR_variant | MODIFIER | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(62): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0006others(15): Show | a0001c0001t0001g0012 a0001c0001t0001g0017 a0001c0001t0001g0020 others(62): Show |
65 | 108 | 0.6019 | -3 | c.*40 others(14): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 23/23 | 4058 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143227524 | GACA | G | 3_prime_UTR_variant | MODIFIER | HG02109.hp1 HG02280.hp2 HG02723.hp1 |
a0001 | a0001c0001 | a0001c0001t0015a0001c0001t0024 | a0001c0001t0015g0037 a0001c0001t0015g0123 a0001c0001t0024g0103 |
3 | 196 | 0.0153 | -3 | c.*50 others(14): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 23/23 | 5082 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143231371 | ATGT | A | downstream_gene_variant | MODIFIER | HG02723.hp2 HG03098.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0004a0001c0003t0002 | a0001c0001t0004g0002 a0001c0003t0002g0044 |
2 | 196 | 0.0102 | -3 | c.*89 others(14): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 2365 | chr5 | TogoVar | |||||||
ARHGAP26_chr5_142765377_143234007 | 143233740 | CAAA | C | downstream_gene_variant | MODIFIER | HG00323.hp1 HG00408.hp1 HG00408.hp2 others(61): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(29): Show | a0001c0001t0001g0017 a0001c0001t0001g0116 a0001c0001t0001g0153 others(61): Show |
64 | 129 | 0.4961 | -3 | c.*11 others(16): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 4734 | chr5 | TogoVar | |||||||
ARHGAP27_chr17_45388908_45437870 | 45414902 | CAAA | C | intron_variant | MODIFIER | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(15): Show |
a0004 | a0004c0004 | a0004c0004t0004a0004c0004t0014 | a0004c0004t0004g0001 a0004c0004t0004g0158 a0004c0004t0004g0159 others(8): Show |
18 | 153 | 0.1176 | -3 | c.658 others(20): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | TogoVar | |||||||
ARHGAP28_chr18_6724716_6920716 | 6730501 | CATT | C | intron_variant | MODIFIER | HG01884.hp1 HG02630.hp1 HG02896.hp1 others(4): Show |
a0001a0004 | a0001c0001a0001c0003a0001c0019others(1): Show | a0001c0001t0007a0001c0001t0022a0001c0003t0003others(2): Show | a0001c0001t0007g0116 a0001c0001t0007g0117 a0001c0001t0022g0067 others(4): Show |
7 | 246 | 0.0285 | -3 | c.122 others(18): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6743760 | CAAG | C | intron_variant | MODIFIER | HG01243.hp2 HG01346.hp1 HG02280.hp2 others(9): Show |
a0001a0002a0006others(2): Show | a0001c0001a0001c0003a0002c0002others(3): Show | a0001c0001t0001a0001c0001t0008a0001c0003t0003others(6): Show | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(9): Show |
12 | 246 | 0.0488 | -3 | c.122 others(22): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6744941 | TTAA | T | intron_variant | MODIFIER | HG01243.hp2 HG01346.hp1 HG02280.hp2 others(9): Show |
a0001a0002a0006others(2): Show | a0001c0001a0001c0003a0002c0002others(3): Show | a0001c0001t0001a0001c0001t0008a0001c0003t0003others(6): Show | a0001c0001t0001g0149 a0001c0001t0001g0150 a0001c0001t0001g0151 others(9): Show |
12 | 246 | 0.0488 | -3 | c.122 others(22): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6776247 | GCCT | G | intron_variant | MODIFIER | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(38): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0002c0002others(4): Show | a0001c0001t0001a0001c0003t0001a0001c0003t0003others(6): Show | a0001c0001t0001g0049 a0001c0001t0001g0071 a0001c0001t0001g0128 others(38): Show |
41 | 246 | 0.1667 | -3 | c.122 others(22): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6800604 | CAAG | C | intron_variant | MODIFIER | HG01346.hp1 HG02922.hp2 HG02976.hp2 |
a0001a0002a0006 | a0001c0003a0002c0002a0006c0008 | a0001c0003t0003a0002c0002t0002a0006c0008t0002 | a0001c0003t0003g0084 a0002c0002t0002g0148 a0006c0008t0002g0146 |
3 | 246 | 0.0122 | -3 | c.123 others(22): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6807120 | ACTC | A | intron_variant | MODIFIER | HG02258.hp1 HG02886.hp1 HG03209.hp1 others(2): Show |
a0001a0006 | a0001c0001a0001c0019a0006c0008 | a0001c0001t0001a0001c0001t0006a0001c0019t0021others(1): Show | a0001c0001t0001g0003 a0001c0001t0001g0072 a0001c0001t0006g0155 others(2): Show |
5 | 246 | 0.0203 | -3 | c.123 others(22): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6831471 | GTTT | G | intron_variant | MODIFIER | HG01243.hp1 HG02451.hp1 HG02886.hp1 others(4): Show |
a0001a0003 | a0001c0001a0001c0003a0001c0019others(1): Show | a0001c0001t0001a0001c0001t0008a0001c0003t0003others(2): Show | a0001c0001t0001g0003 a0001c0001t0001g0100 a0001c0001t0001g0107 others(4): Show |
7 | 96 | 0.0729 | -3 | c.326 others(20): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6831485 | TTTC | T | intron_variant | MODIFIER | HG01884.hp1 HG01884.hp2 HG02055.hp1 others(7): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0003a0001c0012others(4): Show | a0001c0001t0001a0001c0001t0006a0001c0003t0003others(5): Show | a0001c0001t0001g0124 a0001c0001t0001g0149 a0001c0001t0001g0150 others(7): Show |
10 | 246 | 0.0407 | -3 | c.326 others(20): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 2/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6849252 | CAAA | C | intron_variant | MODIFIER | HG02040.hp2 HG02523.hp1 HG02895.hp1 others(3): Show |
a0001a0002a0003 | a0001c0003a0002c0002a0003c0013 | a0001c0003t0003a0002c0002t0002a0003c0013t0011 | a0001c0003t0003g0094 a0001c0003t0003g0095 a0001c0003t0003g0123 others(3): Show |
6 | 49 | 0.1224 | -3 | c.544 others(20): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6849506 | ATCT | A | intron_variant | MODIFIER | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(40): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0012others(4): Show | a0001c0001t0001a0001c0001t0018a0001c0003t0001others(9): Show | a0001c0001t0001g0044 a0001c0001t0001g0049 a0001c0001t0001g0070 others(40): Show |
43 | 246 | 0.1748 | -3 | c.544 others(20): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6856619 | CCCT | C | intron_variant | MODIFIER | HG01346.hp1 HG01884.hp2 HG02258.hp1 others(11): Show |
a0001a0002a0006 | a0001c0001a0002c0002a0006c0008 | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(2): Show | a0001c0001t0001g0003 a0001c0001t0001g0004 a0001c0001t0001g0072 others(11): Show |
14 | 246 | 0.0569 | -3 | c.637 others(20): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6859077 | AAAC | A | intron_variant | MODIFIER | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(47): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0003a0002c0002others(3): Show | a0001c0001t0001a0001c0001t0007a0001c0003t0001others(9): Show | a0001c0001t0001g0044 a0001c0001t0001g0049 a0001c0001t0001g0070 others(47): Show |
50 | 246 | 0.2033 | -3 | c.637 others(18): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 4/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6877083 | CAAA | C | intron_variant | MODIFIER | HG02922.hp1 HG03139.hp2 NA20129.hp1 |
a0001a0002 | a0001c0018a0001c0019a0002c0017 | a0001c0018t0020a0001c0019t0021a0002c0017t0002 | a0001c0018t0020g0007 a0001c0019t0021g0073 a0002c0017t0002g0086 |
3 | 246 | 0.0122 | -3 | c.129 others(20): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 10/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6900696 | TATC | T | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00408.hp2 others(65): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0005a0003c0004others(2): Show | a0001c0001t0001a0001c0001t0017a0001c0001t0019others(4): Show | a0001c0001t0001g0019 a0001c0001t0001g0026 a0001c0001t0001g0029 others(65): Show |
68 | 246 | 0.2764 | -3 | c.203 others(22): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 16/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6918904 | AGTT | A | downstream_gene_variant | MODIFIER | HG02647.hp1 HG02886.hp1 HG02895.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0009 | a0001c0001t0001g0003 a0001c0001t0001g0106 a0001c0001t0009g0245 |
3 | 246 | 0.0122 | -3 | c.*67 others(14): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3189 | chr18 | TogoVar | |||||||
ARHGAP29_chr1_94163905_94242584 | 94169609 | TGAC | T | 3_prime_UTR_variant | MODIFIER | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(3): Show |
7 | 354 | 0.0198 | -3 | c.*42 others(14): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 4257 | chr1 | TogoVar | ||||||
ARHGAP29_chr1_94163905_94242584 | 94173832 | CACA | C | 3_prime_UTR_variant | MODIFIER | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0016 a0001c0001t0010g0136 a0001c0001t0010g0137 others(3): Show |
7 | 354 | 0.0198 | -3 | c.*34 others(10): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 34 | chr1 | TogoVar | ||||||
ARHGAP29_chr1_94163905_94242584 | 94178498 | CATT | C | intron_variant | MODIFIER | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(59): Show |
a0001a0004 | a0001c0001a0001c0005a0001c0009others(1): Show | a0001c0001t0003a0001c0001t0012a0001c0001t0013others(7): Show | a0001c0001t0003g0006 a0001c0001t0003g0009 a0001c0001t0003g0025 others(53): Show |
62 | 354 | 0.1751 | -3 | c.248 others(20): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 20/22 | chr1 | TogoVar | |||||||
ARHGAP29_chr1_94163905_94242584 | 94181744 | AAAC | A | intron_variant | MODIFIER | HG00280.hp1 HG02738.hp1 HG04184.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0005 | a0001c0001t0003g0026 a0001c0001t0003g0261 a0001c0001t0005g0117 |
4 | 354 | 0.0113 | -3 | c.224 others(22): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 19/22 | chr1 | TogoVar | |||||||
ARHGAP29_chr1_94163905_94242584 | 94199668 | ATGC | A | intron_variant | MODIFIER | HG01891.hp2 HG02257.hp2 HG02723.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0010 | a0001c0001t0010g0136 a0001c0001t0010g0137 a0001c0001t0010g0138 others(2): Show |
5 | 354 | 0.0141 | -3 | c.128 others(22): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 12/22 | chr1 | TogoVar | |||||||
ARHGAP29_chr1_94163905_94242584 | 94211287 | CAAA | C | intron_variant | MODIFIER | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(37): Show |
a0001a0004 | a0001c0001a0001c0005a0001c0009others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0054 a0001c0001t0002g0260 a0001c0001t0003g0009 others(33): Show |
40 | 100 | 0.4000 | -3 | c.341 others(20): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | TogoVar | |||||||
ARHGAP29_chr1_94163905_94242584 | 94241722 | TATA | T | upstream_gene_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00280.hp2 others(259): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0001c0007others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(41): Show | a0001c0001t0001g0002 a0001c0001t0001g0007 a0001c0001t0001g0018 others(232): Show |
262 | 354 | 0.7401 | -3 | c.-43 others(14): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 4139 | chr1 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161043620 | CTTT | C | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(140): Show |
a0002a0006a0009others(1): Show | a0002c0002a0002c0003a0002c0015others(3): Show | a0002c0002t0001a0002c0002t0004a0002c0003t0001others(6): Show | a0002c0002t0001g0001 a0002c0002t0001g0002 a0002c0002t0001g0003 others(113): Show |
143 | 358 | 0.3994 | -3 | c.*40 others(14): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 3325 | chr1 | TogoVar | |||||||
ARHGAP30_chr1_161041946_161074891 | 161055801 | AAAT | A | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(148): Show |
a0001a0002a0006others(2): Show | a0001c0001a0002c0002a0002c0003others(4): Show | a0001c0001t0001a0002c0002t0001a0002c0002t0004others(7): Show | a0001c0001t0001g0245 a0001c0001t0001g0250 a0001c0001t0001g0339 others(119): Show |
151 | 388 | 0.3892 | -3 | c.345 others(18): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 3/11 | chr1 | TogoVar | |||||||
ARHGAP31_chr3_119289383_119425714 | 119354678 | ATTT | A | intron_variant | MODIFIER | HG00408.hp2 HG00609.hp2 HG02056.hp1 others(15): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0007a0001c0001t0008a0001c0002t0004others(2): Show | a0001c0001t0007g0233 a0001c0001t0007g0248 a0001c0001t0007g0249 others(15): Show |
18 | 237 | 0.0759 | -3 | c.101 others(22): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119357614 | AAAT | A | intron_variant | MODIFIER | HG00609.hp1 HG01943.hp2 HG02083.hp1 others(9): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0005a0001c0001t0006a0001c0001t0021others(6): Show | a0001c0001t0005g0169 a0001c0001t0005g0170 a0001c0001t0005g0173 others(9): Show |
12 | 308 | 0.0390 | -3 | c.101 others(20): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar |