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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP25_chr2_68729811_68831833 | 68810728 | TCTC | T | intron_variant | MODIFIER | HG00408.hp1 HG01074.hp1 HG01167.hp1 others(18): Show |
a0002a0004a0006 | a0002c0002a0004c0009a0006c0011 | a0002c0002t0002a0002c0002t0003a0002c0002t0006others(7): Show | a0002c0002t0002g0020a0002c0002t0002g0070a0002c0002t0003g0164others(18): Show | 21 | 368 | 0.0571 | -3 | c.675 others(20): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | TogoVar | ||||||
ARHGAP25_chr2_68729811_68831833 | 68810731 | CTTT | C | intron_variant | MODIFIER | HG02280.hp1 HG02451.hp2 HG02572.hp2 others(3): Show |
a0002 | a0002c0005a0002c0020 | a0002c0005t0002a0002c0005t0012a0002c0020t0001 | a0002c0005t0002g0275a0002c0005t0012g0019a0002c0005t0012g0208others(3): Show | 6 | 368 | 0.0163 | -3 | c.675 others(20): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP25_chr2_68729811_68831833 | 68812253 | CTCT | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
a0001a0002a0003others(4): Show | a0001c0001a0002c0004a0002c0008others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(29): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(230): Show | 248 | 368 | 0.6739 | -3 | c.675 others(20): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
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 | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(108): Show | 123 | 368 | 0.3342 | -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 | a0002c0002t0001g0263a0002c0002t0003g0056a0002c0002t0003g0338 | 3 | 368 | 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 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0042a0001c0002t0002 | a0001c0001t0002g0043a0001c0001t0002g0045a0001c0001t0002g0046others(2): Show | 5 | 198 | 0.0253 | -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 | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0001g0141others(48): Show | 51 | 198 | 0.2576 | -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 | a0001c0001t0001g0153a0001c0001t0001g0158a0001c0001t0003g0176others(22): Show | 25 | 198 | 0.1263 | -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 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0196a0001c0001t0002g0128a0001c0001t0003g0165others(5): Show | 8 | 198 | 0.0404 | -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 | a0001c0001t0006a0001c0001t0020 | a0001c0001t0006g0084a0001c0001t0020g0049 | 2 | 198 | 0.0101 | -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 | a0001c0001t0001g0029a0001c0001t0001g0131a0001c0001t0001g0138others(38): Show | 41 | 198 | 0.2071 | -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 | a0001c0001a0001c0003 | a0001c0001t0002a0001c0001t0004a0001c0001t0007others(10): Show | a0001c0001t0002g0190a0001c0001t0002g0195a0001c0001t0004g0105others(17): Show | 20 | 198 | 0.1010 | -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 | a0001c0001a0001c0002 | a0001c0001t0043a0001c0002t0001a0001c0002t0049 | a0001c0001t0043g0052a0001c0002t0001g0149a0001c0002t0049g0089 | 3 | 198 | 0.0152 | -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 | a0001c0001t0002a0001c0001t0022a0001c0001t0036 | a0001c0001t0002g0023a0001c0001t0022g0081a0001c0001t0036g0160 | 3 | 198 | 0.0152 | -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 | a0001c0001t0001g0034a0001c0001t0002g0117a0001c0001t0003g0033others(2): Show | 5 | 198 | 0.0253 | -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(30): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(13): Show | a0001c0001t0001g0034a0001c0001t0002g0117a0001c0001t0003g0033others(30): Show | 33 | 198 | 0.1667 | -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 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(11): Show | a0001c0001t0001g0012a0001c0001t0002g0121a0001c0001t0002g0128others(14): Show | 17 | 198 | 0.0859 | -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 | a0001c0001a0001c0002a0002c0007 | a0001c0001t0004a0001c0001t0006a0001c0001t0009others(14): Show | a0001c0001t0004g0002a0001c0001t0004g0099a0001c0001t0006g0064others(22): Show | 25 | 198 | 0.1263 | -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 | a0001c0001t0004g0002a0001c0001t0004g0098a0001c0001t0004g0099others(18): Show | 21 | 198 | 0.1061 | -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 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0029a0001c0001t0054others(1): Show | a0001c0001t0002g0023a0001c0001t0029g0085a0001c0001t0054g0072others(1): Show | 4 | 198 | 0.0202 | -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 | a0001c0001a0001c0002 | a0001c0001t0006a0001c0001t0022a0001c0002t0004others(1): Show | a0001c0001t0006g0084a0001c0001t0022g0073a0001c0002t0004g0100others(1): Show | 4 | 198 | 0.0202 | -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 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0006a0001c0001t0029others(3): Show | a0001c0001t0002g0118a0001c0001t0006g0084a0001c0001t0029g0085others(3): Show | 6 | 198 | 0.0303 | -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 | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0020others(62): Show | 65 | 198 | 0.3283 | -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 | a0001c0001t0015a0001c0001t0025 | a0001c0001t0015g0037a0001c0001t0015g0123a0001c0001t0025g0103 | 3 | 198 | 0.0152 | -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 | a0001c0001a0001c0002 | a0001c0001t0004a0001c0002t0002 | a0001c0001t0004g0002a0001c0002t0002g0044 | 2 | 198 | 0.0101 | -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 | a0001c0001t0001g0018a0001c0001t0001g0116a0001c0001t0001g0153others(61): Show | 64 | 198 | 0.3232 | -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 | a0004c0004t0004a0004c0004t0026 | a0004c0004t0004g0001a0004c0004t0004g0304a0004c0004t0004g0305others(8): Show | 18 | 347 | 0.0519 | -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 | a0001c0001t0007g0116a0001c0001t0007g0117a0001c0001t0022g0067others(4): Show | 7 | 248 | 0.0282 | -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 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(9): Show | 12 | 248 | 0.0484 | -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 | a0001c0001t0001g0149a0001c0001t0001g0150a0001c0001t0001g0151others(9): Show | 12 | 248 | 0.0484 | -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 | a0001c0001t0001g0049a0001c0001t0001g0071a0001c0001t0001g0128others(38): Show | 41 | 248 | 0.1653 | -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 |
a0001a0002a0007 | a0001c0003a0002c0002a0007c0008 | a0001c0003t0003a0002c0002t0002a0007c0008t0002 | a0001c0003t0003g0084a0002c0002t0002g0148a0007c0008t0002g0146 | 3 | 248 | 0.0121 | -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 |
a0001a0007 | a0001c0001a0001c0019a0007c0008 | a0001c0001t0001a0001c0001t0006a0001c0019t0021others(1): Show | a0001c0001t0001g0003a0001c0001t0001g0072a0001c0001t0006g0155others(2): Show | 5 | 248 | 0.0202 | -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 | a0001c0001t0001g0003a0001c0001t0001g0100a0001c0001t0001g0107others(4): Show | 7 | 248 | 0.0282 | -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 | a0001c0001t0001g0124a0001c0001t0001g0149a0001c0001t0001g0150others(7): Show | 10 | 248 | 0.0403 | -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 | a0001c0003t0003g0094a0001c0003t0003g0095a0001c0003t0003g0123others(3): Show | 6 | 248 | 0.0242 | -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 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0070others(40): Show | 43 | 248 | 0.1734 | -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 |
a0001a0002a0007 | a0001c0001a0002c0002a0007c0008 | a0001c0001t0001a0001c0001t0006a0001c0001t0008others(2): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0072others(11): Show | 14 | 248 | 0.0565 | -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 | a0001c0001t0001g0044a0001c0001t0001g0049a0001c0001t0001g0070others(47): Show | 50 | 248 | 0.2016 | -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 | a0001c0018t0020g0007a0001c0019t0021g0073a0002c0017t0002g0086 | 3 | 248 | 0.0121 | -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(66): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0005a0003c0004others(2): Show | a0001c0001t0001a0001c0001t0017a0001c0001t0019others(4): Show | a0001c0001t0001g0018a0001c0001t0001g0019a0001c0001t0001g0026others(66): Show | 69 | 248 | 0.2782 | -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 | a0001c0001t0001g0003a0001c0001t0001g0106a0001c0001t0009g0245 | 3 | 248 | 0.0121 | -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 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(3): Show | 7 | 356 | 0.0197 | -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 | a0001c0001t0010g0029a0001c0001t0010g0288a0001c0001t0010g0289others(3): Show | 7 | 356 | 0.0197 | -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(60): Show |
a0001a0006 | a0001c0001a0001c0005a0001c0009others(1): Show | a0001c0001t0003a0001c0001t0012a0001c0001t0013others(7): Show | a0001c0001t0003g0006a0001c0001t0003g0020a0001c0001t0003g0021others(54): Show | 63 | 356 | 0.1770 | -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 | a0001c0001t0003g0021a0001c0001t0003g0176a0001c0001t0005g0046 | 4 | 356 | 0.0112 | -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 | a0001c0001t0010g0288a0001c0001t0010g0289a0001c0001t0010g0290others(2): Show | 5 | 356 | 0.0140 | -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 |
a0001a0006 | a0001c0001a0001c0005a0001c0009others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0226a0001c0001t0002g0175a0001c0001t0003g0020others(33): Show | 40 | 356 | 0.1124 | -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(260): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0002a0001c0007others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(41): Show | a0001c0001t0001g0001a0001c0001t0001g0007a0001c0001t0001g0013others(233): Show | 263 | 356 | 0.7388 | -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 |
a0002a0006a0010others(1): Show | a0002c0002a0002c0003a0002c0015others(3): Show | a0002c0002t0001a0002c0002t0004a0002c0003t0001others(6): Show | a0002c0002t0001g0001a0002c0002t0001g0005a0002c0002t0001g0006others(134): Show | 143 | 390 | 0.3667 | -3 | c.*40 others(14): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 3325 | chr1 | TogoVar |