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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP26_chr5_142765377_143234007 | 142820450 | A | AAAAC | intron_variant | MODIFIER | HG00438.hp1 HG00438.hp2 HG00544.hp2 others(80): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(33): Show | a0001c0001t0001g0018a0001c0001t0001g0020a0001c0001t0001g0116others(80): Show | 83 | 198 | 0.4192 | 4 | c.154 others(23): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142844051 | G | GTTTT | intron_variant | MODIFIER | HG00738.hp2 HG01167.hp1 HG02109.hp2 others(12): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(6): Show | a0001c0001t0002g0022a0001c0001t0002g0023a0001c0001t0004g0087others(12): Show | 15 | 198 | 0.0758 | 4 | c.155 others(23): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142857640 | C | CCCTA | intron_variant | MODIFIER | HG00438.hp2 HG00609.hp1 HG01192.hp2 others(20): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(14): Show | a0001c0001t0001g0020a0001c0001t0001g0141a0001c0001t0001g0153others(20): Show | 23 | 198 | 0.1162 | 4 | c.155 others(23): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142858061 | C | CTGTG | intron_variant | MODIFIER | HG00738.hp2 HG01167.hp1 HG01243.hp2 others(11): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0006others(10): Show | a0001c0001t0001g0029a0001c0001t0004g0087a0001c0001t0006g0088others(11): Show | 14 | 198 | 0.0707 | 4 | c.155 others(23): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142858114 | A | AGAGG | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp2 |
a0001 | a0001c0001 | a0001c0001t0019 | a0001c0001t0019g0010a0001c0001t0019g0011 | 2 | 198 | 0.0101 | 4 | c.155 others(23): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142867288 | G | GGTGT | intron_variant | MODIFIER | HG02109.hp2 HG02451.hp1 HG02615.hp1 others(4): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0007 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0034a0001c0001t0002g0008a0001c0001t0002g0027others(4): Show | 7 | 198 | 0.0354 | 4 | c.155 others(21): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142904525 | G | GAAAA | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp2 HG02258.hp1 others(11): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0002a0001c0001t0004a0001c0001t0006others(8): Show | a0001c0001t0002g0013a0001c0001t0004g0098a0001c0001t0006g0086others(11): Show | 14 | 198 | 0.0707 | 4 | c.832 others(19): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142936108 | A | AACAC | intron_variant | MODIFIER | HG01243.hp2 HG01934.hp1 HG02280.hp2 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0034a0001c0001t0002g0117a0001c0001t0003g0033others(5): Show | 8 | 198 | 0.0404 | 4 | c.110 others(23): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142947095 | T | TAAAA | intron_variant | MODIFIER | HG00544.hp2 HG00558.hp2 HG00597.hp2 others(35): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(17): Show | a0001c0001t0001g0029a0001c0001t0001g0034a0001c0001t0001g0131others(35): Show | 38 | 198 | 0.1919 | 4 | c.110 others(25): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142955095 | T | TACAC | intron_variant | MODIFIER | HG00609.hp1 HG02258.hp2 HG02572.hp2 others(10): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0002a0001c0001t0004a0001c0001t0009others(10): Show | a0001c0001t0002g0126a0001c0001t0004g0002a0001c0001t0009g0039others(10): Show | 13 | 198 | 0.0657 | 4 | c.110 others(25): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142963172 | G | GTATA | intron_variant | MODIFIER | HG01167.hp2 HG02723.hp2 HG03017.hp2 others(1): Show |
a0001 | a0001c0002 | a0001c0002t0002a0001c0002t0003a0001c0002t0017 | a0001c0002t0002g0044a0001c0002t0002g0183a0001c0002t0003g0050others(1): Show | 4 | 198 | 0.0202 | 4 | c.110 others(25): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143011303 | C | CTTTT | intron_variant | MODIFIER | HG00323.hp1 HG00408.hp2 HG01243.hp1 others(13): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0158others(13): Show | 16 | 198 | 0.0808 | 4 | c.110 others(23): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143012537 | T | TTATA | intron_variant | MODIFIER | HG01175.hp2 HG01192.hp1 NA18972.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0005 | a0001c0001t0001g0158a0001c0001t0005g0108a0001c0001t0005g0109 | 3 | 198 | 0.0152 | 4 | c.110 others(23): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143087636 | C | CTTTT | intron_variant | MODIFIER | HG00323.hp1 HG00438.hp2 HG00597.hp1 others(47): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | a0001c0001t0001g0018a0001c0001t0001g0034a0001c0001t0001g0116others(47): Show | 50 | 198 | 0.2525 | 4 | c.153 others(25): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143090452 | C | CTCGG | intron_variant | MODIFIER | HG00408.hp2 HG00558.hp1 HG00597.hp2 others(36): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(13): Show | a0001c0001t0001g0020a0001c0001t0001g0131a0001c0001t0001g0158others(36): Show | 39 | 198 | 0.1970 | 4 | c.153 others(25): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143105378 | A | AAAAT | intron_variant | MODIFIER | HG00408.hp2 HG00438.hp1 HG00438.hp2 others(112): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(44): Show | a0001c0001t0001g0018a0001c0001t0001g0116a0001c0001t0001g0131others(112): Show | 115 | 198 | 0.5808 | 4 | c.153 others(25): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 17/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143123964 | A | AACAC | intron_variant | MODIFIER | HG00408.hp1 HG00408.hp2 HG00544.hp1 others(26): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(15): Show | a0001c0001t0001g0034a0001c0001t0001g0131a0001c0001t0001g0196others(26): Show | 29 | 198 | 0.1465 | 4 | c.169 others(23): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143142134 | C | CTTTT | intron_variant | MODIFIER | HG00558.hp2 HG01069.hp2 HG01071.hp2 others(33): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(19): Show | a0001c0001t0001g0196a0001c0001t0002g0043a0001c0001t0002g0046others(33): Show | 36 | 198 | 0.1818 | 4 | c.183 others(23): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143154160 | T | TAAAA | intron_variant | MODIFIER | HG03017.hp1 NA18939.hp1 NA18952.hp2 others(5): Show |
a0001 | a0001c0001a0001c0003a0001c0004 | a0001c0001t0002a0001c0001t0007a0001c0003t0001others(1): Show | a0001c0001t0002g0007a0001c0001t0002g0016a0001c0001t0002g0121others(5): Show | 8 | 198 | 0.0404 | 4 | c.198 others(23): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143162284 | T | TACAC | intron_variant | MODIFIER | HG00558.hp1 HG00597.hp1 HG00738.hp2 others(23): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0002a0001c0001t0003a0001c0001t0004others(13): Show | a0001c0001t0002g0008a0001c0001t0002g0022a0001c0001t0002g0023others(23): Show | 26 | 198 | 0.1313 | 4 | c.198 others(25): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143163432 | G | GGTTT | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp2 HG01175.hp2 others(24): Show |
a0001 | a0001c0001a0001c0002a0001c0008 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(13): Show | a0001c0001t0001g0012a0001c0001t0001g0034a0001c0001t0002g0022others(24): Show | 27 | 198 | 0.1364 | 4 | c.198 others(25): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143174405 | T | TCACA | intron_variant | MODIFIER | HG03098.hp1 HG03130.hp1 HG03516.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0014a0001c0001t0023a0001c0002t0049 | a0001c0001t0014g0038a0001c0001t0014g0041a0001c0001t0023g0055others(1): Show | 4 | 198 | 0.0202 | 4 | c.198 others(25): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 20/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 143221923 | T | TGGAA | intron_variant | MODIFIER | HG02109.hp1 HG02280.hp2 HG02572.hp1 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0008 | a0001c0001t0006a0001c0001t0013a0001c0001t0014others(7): Show | a0001c0001t0006g0096a0001c0001t0013g0004a0001c0001t0013g0065others(10): Show | 13 | 198 | 0.0657 | 4 | c.219 others(21): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 22/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP27_chr17_45388908_45437870 | 45407516 | T | TTTTC | intron_variant | MODIFIER | HG00140.hp2 HG01074.hp2 HG01099.hp2 others(16): Show |
a0004 | a0004c0004 | a0004c0004t0004a0004c0004t0026 | a0004c0004t0004g0001a0004c0004t0004g0017a0004c0004t0004g0304others(8): Show | 19 | 347 | 0.0548 | 4 | c.658 others(21): Show |
ARHGAP27 | ENSG00000159314.13 | transcript | ENST00000685559.1 | protein_coding | 4/19 | chr17 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6730221 | G | GTATA | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(66): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0001c0012others(5): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(8): Show | a0001c0001t0001g0179a0001c0001t0001g0181a0001c0001t0001g0182others(66): Show | 69 | 248 | 0.2782 | 4 | c.122 others(19): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6739645 | T | TTCTC | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(87): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0001c0010others(6): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(13): Show | a0001c0001t0001g0080a0001c0001t0001g0179a0001c0001t0001g0181others(87): Show | 90 | 248 | 0.3629 | 4 | c.122 others(21): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6763081 | G | GTTGT | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp1 HG00735.hp1 others(20): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0001c0010others(3): Show | a0001c0001t0001a0001c0001t0008a0001c0001t0018others(6): Show | a0001c0001t0001g0004a0001c0001t0001g0012a0001c0001t0001g0019others(20): Show | 23 | 248 | 0.0927 | 4 | c.122 others(23): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6777754 | A | ATGAG | intron_variant | MODIFIER | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(39): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0002c0002others(4): Show | a0001c0001t0001a0001c0003t0001a0001c0003t0003others(6): Show | a0001c0001t0001g0035a0001c0001t0001g0049a0001c0001t0001g0071others(39): Show | 42 | 248 | 0.1694 | 4 | c.123 others(23): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6782592 | A | ATTTT | intron_variant | MODIFIER | HG01993.hp1 HG02055.hp2 HG02145.hp1 others(15): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0006a0001c0003t0003others(3): Show | a0001c0001t0001g0018a0001c0001t0001g0070a0001c0001t0001g0082others(15): Show | 18 | 248 | 0.0726 | 4 | c.123 others(23): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6796821 | T | TACAC | intron_variant | MODIFIER | HG01346.hp1 HG02922.hp2 HG02976.hp2 |
a0001a0002a0007 | a0001c0003a0002c0002a0007c0008 | a0001c0003t0003a0002c0002t0002a0007c0008t0002 | a0001c0003t0003g0084a0002c0002t0002g0148a0007c0008t0002g0146 | 3 | 248 | 0.0121 | 4 | c.123 others(23): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 1/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6841159 | C | CACTG | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00408.hp1 others(14): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0017a0001c0003t0003others(3): Show | a0001c0001t0001g0052a0001c0001t0001g0071a0001c0001t0001g0072others(14): Show | 17 | 248 | 0.0686 | 4 | c.543 others(21): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | chr18 | TogoVar | ||||||
ARHGAP28_chr18_6724716_6920716 | 6847628 | G | GGTGT | intron_variant | MODIFIER | HG00140.hp2 HG00408.hp1 HG00597.hp2 others(47): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0003a0001c0020others(5): Show | a0001c0001t0001a0001c0001t0007a0001c0003t0001others(11): Show | a0001c0001t0001g0049a0001c0001t0001g0070a0001c0001t0001g0124others(47): Show | 50 | 248 | 0.2016 | 4 | c.544 others(21): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6847630 | G | GGTGT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(52): Show |
a0001a0002a0005others(2): Show | a0001c0001a0001c0003a0001c0015others(5): Show | a0001c0001t0001a0001c0001t0016a0001c0001t0017others(9): Show | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0034others(52): Show | 55 | 248 | 0.2218 | 4 | c.544 others(21): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 3/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP28_chr18_6724716_6920716 | 6892159 | T | TTTGA | intron_variant | MODIFIER | HG03041.hp1 HG03490.hp1 HG03492.hp1 |
a0003 | a0003c0013a0003c0023 | a0003c0013t0011a0003c0023t0001 | a0003c0013t0011g0062a0003c0013t0011g0063a0003c0023t0001g0120 | 3 | 248 | 0.0121 | 4 | c.184 others(23): Show |
ARHGAP28 | ENSG00000088756.13 | transcript | ENST00000383472.9 | protein_coding | 14/17 | INFO_REALIGN_3_PRIME | chr18 | TogoVar | |||||
ARHGAP29_chr1_94163905_94242584 | 94166813 | G | GCACA | downstream_gene_variant | MODIFIER | HG00280.hp1 HG00438.hp1 HG00544.hp1 others(63): Show |
a0001a0006 | a0001c0001a0001c0005a0001c0009others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(10): Show | a0001c0001t0001g0151a0001c0001t0003g0006a0001c0001t0003g0020others(57): Show | 66 | 356 | 0.1854 | 4 | c.*70 others(15): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 2091 | chr1 | TogoVar | ||||||
ARHGAP29_chr1_94163905_94242584 | 94172612 | G | GATAT | 3_prime_UTR_variant | MODIFIER | HG00323.hp2 HG00558.hp2 HG00639.hp2 others(73): Show |
a0001 | a0001c0001a0001c0002a0001c0011others(1): Show | a0001c0001t0004a0001c0001t0007a0001c0001t0009others(9): Show | a0001c0001t0004g0002a0001c0001t0004g0017a0001c0001t0004g0018others(65): Show | 76 | 356 | 0.2135 | 4 | c.*12 others(15): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 23/23 | 1256 | chr1 | TogoVar | |||||
ARHGAP29_chr1_94163905_94242584 | 94207001 | T | TTTTA | intron_variant | MODIFIER | HG02145.hp1 HG02148.hp2 HG02280.hp2 others(14): Show |
a0001a0005 | a0001c0001a0005c0014 | a0001c0001t0004a0001c0001t0011a0001c0001t0032others(2): Show | a0001c0001t0004g0017a0001c0001t0004g0033a0001c0001t0004g0044others(13): Show | 17 | 356 | 0.0478 | 4 | c.511 others(21): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 5/22 | chr1 | TogoVar | ||||||
ARHGAP29_chr1_94163905_94242584 | 94211287 | C | CAAAA | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00323.hp1 others(80): Show |
a0001 | a0001c0001a0001c0002a0001c0011 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(17): Show | a0001c0001t0001g0151a0001c0001t0002g0003a0001c0001t0002g0026others(70): Show | 83 | 356 | 0.2332 | 4 | c.341 others(21): Show |
ARHGAP29 | ENSG00000137962.13 | transcript | ENST00000260526.11 | protein_coding | 3/22 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161053462 | T | TTCTC | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp1 HG00738.hp2 others(17): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0003 | a0001c0001t0001a0001c0001t0003a0002c0002t0001others(1): Show | a0001c0001t0001g0048a0001c0001t0001g0064a0001c0001t0001g0084others(16): Show | 20 | 390 | 0.0513 | 4 | c.537 others(17): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 5/11 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161055866 | A | AAAAT | intron_variant | MODIFIER | HG00741.hp2 HG01081.hp1 HG02717.hp2 others(8): Show |
a0001a0005 | a0001c0001a0005c0006 | a0001c0001t0001a0005c0006t0001 | a0001c0001t0001g0027a0001c0001t0001g0081a0001c0001t0001g0084others(8): Show | 11 | 390 | 0.0282 | 4 | c.345 others(19): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 3/11 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161055911 | A | AAAAT | intron_variant | MODIFIER | HG01884.hp1 HG02109.hp2 HG02135.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0131a0001c0001t0001g0132a0001c0001t0001g0158others(6): Show | 9 | 390 | 0.0231 | 4 | c.345 others(19): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 3/11 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161064777 | G | GAGAA | intron_variant | MODIFIER | HG02735.hp1 HG03490.hp1 HG03492.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0144a0001c0001t0001g0153a0001c0001t0001g0154others(1): Show | 4 | 390 | 0.0103 | 4 | c.97+ others(19): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161064779 | A | AAAAG | intron_variant | MODIFIER | HG00408.hp1 HG00558.hp2 HG00738.hp2 others(16): Show |
a0001a0002 | a0001c0001a0001c0007a0002c0002 | a0001c0001t0001a0001c0001t0007a0001c0007t0001others(1): Show | a0001c0001t0001g0028a0001c0001t0001g0039a0001c0001t0001g0040others(16): Show | 19 | 390 | 0.0487 | 4 | c.97+ others(19): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161065868 | C | CTTAT | intron_variant | MODIFIER | HG00597.hp2 HG00639.hp1 HG00735.hp1 others(41): Show |
a0001a0002a0005others(3): Show | a0001c0001a0002c0002a0002c0003others(4): Show | a0001c0001t0001a0002c0002t0001a0002c0003t0001others(5): Show | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(41): Show | 44 | 390 | 0.1128 | 4 | c.97+ others(19): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161066644 | C | CAAAA | intron_variant | MODIFIER | HG00597.hp2 HG00609.hp2 HG00642.hp2 others(35): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(35): Show | 38 | 390 | 0.0974 | 4 | c.97+ others(19): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | ||||||
ARHGAP30_chr1_161041946_161074891 | 161067570 | A | AAAAG | intron_variant | MODIFIER | HG00639.hp1 HG01169.hp2 HG02976.hp1 others(3): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0003 | a0001c0001t0001a0002c0002t0001a0002c0003t0001 | a0001c0001t0001g0141a0002c0002t0001g0370a0002c0003t0001g0139others(3): Show | 6 | 390 | 0.0154 | 4 | c.97+ others(19): Show |
ARHGAP30 | ENSG00000186517.14 | transcript | ENST00000368013.8 | protein_coding | 1/11 | chr1 | TogoVar | ||||||
ARHGAP31_chr3_119289383_119425714 | 119297909 | A | AACAC | intron_variant | MODIFIER | HG00280.hp2 HG00735.hp1 HG01071.hp1 others(37): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0004others(5): Show | a0001c0001t0007a0001c0001t0008a0001c0001t0011others(18): Show | a0001c0001t0007g0202a0001c0001t0008g0192a0001c0001t0008g0199others(36): Show | 40 | 310 | 0.1290 | 4 | c.100 others(21): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP31_chr3_119289383_119425714 | 119300842 | A | AAAAG | intron_variant | MODIFIER | HG00280.hp2 HG00738.hp1 HG00741.hp1 others(12): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0006a0001c0001t0007a0001c0001t0008others(7): Show | a0001c0001t0006g0092a0001c0001t0007g0296a0001c0001t0008g0192others(12): Show | 15 | 310 | 0.0484 | 4 | c.100 others(21): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP31_chr3_119289383_119425714 | 119332635 | T | TCACA | intron_variant | MODIFIER | HG00280.hp2 HG00738.hp1 HG00741.hp1 others(24): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0001c0004others(3): Show | a0001c0001t0005a0001c0001t0006a0001c0001t0007others(14): Show | a0001c0001t0005g0096a0001c0001t0005g0111a0001c0001t0006g0027others(24): Show | 27 | 310 | 0.0871 | 4 | c.101 others(23): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar | |||||
ARHGAP31_chr3_119289383_119425714 | 119332635 | T | TCTCA | intron_variant | MODIFIER | HG01243.hp1 HG03669.hp2 NA18522.hp1 |
a0001 | a0001c0001a0001c0004a0001c0005 | a0001c0001t0006a0001c0004t0010a0001c0005t0001 | a0001c0001t0006g0102a0001c0004t0010g0176a0001c0005t0001g0190 | 3 | 310 | 0.0097 | 4 | c.101 others(23): Show |
ARHGAP31 | ENSG00000031081.11 | transcript | ENST00000264245.9 | protein_coding | 1/11 | INFO_REALIGN_3_PRIME | chr3 | TogoVar |