view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | ac | an | af | len | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length
|
cds cds pos length
|
aa aa pos length
|
distance | status | chr | external |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP22_chr10_48441036_48610073 | 48578524 | ATGTG | A | intron_variant | MODIFIER | HG00735.hp1 HG02055.hp2 HG02258.hp1 others(10): Show |
a0001a0004a0008 | a0001c0002a0001c0003a0001c0004others(3): Show | a0001c0002t0002a0001c0003t0004a0001c0004t0004others(5): Show | a0001c0002t0002g0099 a0001c0003t0004g0166 a0001c0003t0004g0167 others(10): Show |
13 | 270 | 0.0482 | -4 | c.234 others(21): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 2/9 | chr10 | TogoVar | |||||||
ARHGAP23_chr17_38423464_38517385 | 38445303 | TAAAA | T | intron_variant | MODIFIER | HG00323.hp2 HG00733.hp1 HG00735.hp2 others(38): Show |
a0001a0002a0003others(4): Show | a0001c0003a0001c0005a0001c0009others(14): Show | a0001c0003t0001a0001c0005t0001a0001c0005t0006others(15): Show | a0001c0003t0001g0057 a0001c0003t0001g0069 a0001c0003t0001g0170 others(38): Show |
41 | 309 | 0.1327 | -4 | c.64- others(21): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38446181 | ATTTT | A | intron_variant | MODIFIER | HG00609.hp1 HG01891.hp1 HG02040.hp2 others(14): Show |
a0001a0005 | a0001c0001a0001c0003a0001c0006others(5): Show | a0001c0001t0001a0001c0003t0001a0001c0006t0002others(5): Show | a0001c0001t0001g0001 a0001c0001t0001g0211 a0001c0001t0001g0288 others(13): Show |
17 | 309 | 0.0550 | -4 | c.64- others(21): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38453382 | TTCTC | T | intron_variant | MODIFIER | HG00323.hp2 HG00735.hp2 HG01070.hp1 others(25): Show |
a0001a0003a0005others(2): Show | a0001c0003a0001c0009a0001c0010others(10): Show | a0001c0003t0001a0001c0003t0006a0001c0009t0003others(12): Show | a0001c0003t0001g0052 a0001c0003t0001g0053 a0001c0003t0001g0054 others(25): Show |
28 | 309 | 0.0906 | -4 | c.64- others(19): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38453415 | ATGCG | A | intron_variant | MODIFIER | HG00735.hp2 HG02622.hp2 HG02809.hp2 |
a0001 | a0001c0009a0001c0041 | a0001c0009t0003a0001c0041t0002 | a0001c0009t0003g0172 a0001c0009t0003g0173 a0001c0041t0002g0135 |
3 | 309 | 0.0097 | -4 | c.64- others(19): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38453422 | CGTGT | C | intron_variant | MODIFIER | HG00609.hp2 HG00642.hp2 HG00733.hp2 others(24): Show |
a0001a0002a0008others(1): Show | a0001c0001a0001c0002a0001c0004others(5): Show | a0001c0001t0001a0001c0001t0014a0001c0002t0002others(6): Show | a0001c0001t0001g0056 a0001c0001t0001g0079 a0001c0001t0001g0093 others(24): Show |
27 | 309 | 0.0874 | -4 | c.64- others(19): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38453458 | TGTGC | T | intron_variant | MODIFIER | HG00280.hp1 HG00323.hp1 HG00733.hp1 others(21): Show |
a0001a0002a0020 | a0001c0001a0001c0005a0001c0012others(3): Show | a0001c0001t0001a0001c0005t0001a0001c0005t0006others(4): Show | a0001c0001t0001g0006 a0001c0001t0001g0148 a0001c0001t0001g0203 others(21): Show |
24 | 309 | 0.0777 | -4 | c.64- others(19): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38462247 | CTTTT | C | intron_variant | MODIFIER | HG01891.hp1 HG02647.hp2 HG03225.hp2 others(4): Show |
a0001a0005 | a0001c0003a0001c0009a0001c0010others(1): Show | a0001c0003t0001a0001c0009t0003a0001c0010t0001others(1): Show | a0001c0003t0001g0052 a0001c0003t0001g0053 a0001c0003t0001g0054 others(4): Show |
7 | 309 | 0.0227 | -4 | c.254 others(19): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38516498 | GAGGA | G | downstream_gene_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(137): Show |
a0001a0002a0006others(14): Show | a0001c0001a0001c0002a0001c0003others(33): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0009others(38): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0006 others(136): Show |
140 | 309 | 0.4531 | -4 | c.*55 others(15): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 4114 | chr17 | TogoVar | |||||||
ARHGAP24_chr4_85470150_86007666 | 85475768 | CCTGT | C | intron_variant | MODIFIER | HG01109.hp2 HG02055.hp1 HG02145.hp1 |
a0001a0002 | a0001c0001a0002c0006 | a0001c0001t0001a0002c0006t0006 | a0001c0001t0001g0030 a0001c0001t0001g0032 a0002c0006t0006g0031 |
3 | 108 | 0.0278 | -4 | c.-21 others(19): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85485376 | AATAT | A | intron_variant | MODIFIER | HG00639.hp2 HG01168.hp2 HG01978.hp2 others(4): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0001a0001c0002t0002a0001c0004t0003others(1): Show | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0026 others(4): Show |
7 | 108 | 0.0648 | -4 | c.-21 others(21): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85487271 | ATATT | A | intron_variant | MODIFIER | HG00639.hp1 HG03471.hp1 HG03471.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0021a0001c0002t0008a0001c0005t0004 | a0001c0001t0021g0054 a0001c0002t0008g0052 a0001c0002t0008g0053 others(1): Show |
4 | 108 | 0.0370 | -4 | c.-21 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85490645 | ATTTG | A | intron_variant | MODIFIER | HG02723.hp2 HG03516.hp1 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0005 | a0001c0001t0001g0039 a0001c0003t0005g0059 |
2 | 108 | 0.0185 | -4 | c.-21 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85510832 | GCTCT | G | intron_variant | MODIFIER | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(100): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(29): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0008 others(100): Show |
103 | 108 | 0.9537 | -4 | c.-21 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85530560 | ACACT | A | intron_variant | MODIFIER | HG00735.hp2 HG02258.hp2 NA20300.hp2 |
a0001a0002a0003 | a0001c0003a0002c0006a0003c0012 | a0001c0003t0011a0002c0006t0006a0003c0012t0001 | a0001c0003t0011g0087 a0002c0006t0006g0095 a0003c0012t0001g0027 |
3 | 108 | 0.0278 | -4 | c.-20 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85542699 | ATAAT | A | intron_variant | MODIFIER | HG00639.hp1 HG00642.hp1 HG00735.hp1 others(28): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(16): Show | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0030 others(28): Show |
31 | 108 | 0.2870 | -4 | c.-20 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85554837 | ATTTT | A | intron_variant | MODIFIER | HG00323.hp2 HG00423.hp1 HG00639.hp2 others(41): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0020others(15): Show | a0001c0001t0001g0003 a0001c0001t0001g0009 a0001c0001t0001g0010 others(41): Show |
44 | 108 | 0.4074 | -4 | c.-20 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85564924 | GTATA | G | intron_variant | MODIFIER | HG00642.hp2 HG00735.hp1 HG00735.hp2 others(17): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0004others(6): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0002others(10): Show | a0001c0001t0001g0046 a0001c0001t0001g0065 a0001c0001t0001g0069 others(17): Show |
20 | 108 | 0.1852 | -4 | c.-20 others(21): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85590192 | GCCTT | G | intron_variant | MODIFIER | HG00639.hp2 HG00642.hp1 HG01069.hp1 others(20): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0020others(8): Show | a0001c0001t0001g0001 a0001c0001t0001g0026 a0001c0001t0001g0030 others(20): Show |
23 | 108 | 0.2130 | -4 | c.180 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85591031 | GTTTT | G | intron_variant | MODIFIER | HG00323.hp1 HG00423.hp2 HG00735.hp2 others(25): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0015a0001c0002t0002others(5): Show | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0018 others(25): Show |
28 | 108 | 0.2593 | -4 | c.180 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85608551 | GTTTT | G | intron_variant | MODIFIER | HG01168.hp2 HG02055.hp1 HG02055.hp2 others(11): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0002others(4): Show | a0001c0001t0001g0026 a0001c0001t0001g0032 a0001c0001t0001g0062 others(11): Show |
14 | 108 | 0.1296 | -4 | c.180 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85655814 | GAGAA | G | intron_variant | MODIFIER | HG02809.hp2 HG04204.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0018 a0001c0001t0001g0045 |
2 | 108 | 0.0185 | -4 | c.181 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85660794 | CAAAA | C | intron_variant | MODIFIER | HG02109.hp1 HG02486.hp1 HG02622.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0015a0001c0002t0002a0001c0004t0003others(1): Show | a0001c0001t0015g0049 a0001c0002t0002g0068 a0001c0004t0003g0061 others(2): Show |
5 | 108 | 0.0463 | -4 | c.181 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85669644 | AATAT | A | intron_variant | MODIFIER | HG00639.hp1 HG01069.hp1 HG01109.hp2 others(2): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0001t0020a0001c0001t0021others(1): Show | a0001c0001t0001g0030 a0001c0001t0001g0103 a0001c0001t0020g0002 others(2): Show |
5 | 108 | 0.0463 | -4 | c.181 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85687114 | TGATG | T | intron_variant | MODIFIER | HG01109.hp2 NA21309.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0030 a0001c0002t0002g0060 |
2 | 108 | 0.0185 | -4 | c.181 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85704281 | CTTCT | C | intron_variant | MODIFIER | HG00639.hp1 HG00642.hp1 HG01884.hp2 others(3): Show |
a0001 | a0001c0001a0001c0007a0001c0008 | a0001c0001t0001a0001c0001t0021a0001c0007t0004others(1): Show | a0001c0001t0001g0001 a0001c0001t0001g0008 a0001c0001t0001g0032 others(3): Show |
6 | 108 | 0.0556 | -4 | c.181 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85713628 | TCTGA | T | intron_variant | MODIFIER | HG00323.hp1 HG01109.hp1 HG01168.hp2 others(16): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0020a0001c0002t0002others(6): Show | a0001c0001t0001g0016 a0001c0001t0001g0022 a0001c0001t0001g0026 others(16): Show |
19 | 108 | 0.1759 | -4 | c.181 others(21): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85724489 | GTGTA | G | intron_variant | MODIFIER | HG02155.hp1 HG02738.hp2 HG03492.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0002a0001c0003t0001 | a0001c0001t0001g0018 a0001c0002t0002g0011 a0001c0003t0001g0007 others(1): Show |
4 | 108 | 0.0370 | -4 | c.268 others(21): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85724491 | GTATA | G | intron_variant | MODIFIER | HG03579.hp1 NA18522.hp2 |
a0001 | a0001c0004 | a0001c0004t0004 | a0001c0004t0004g0033 a0001c0004t0004g0035 |
2 | 108 | 0.0185 | -4 | c.268 others(21): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85730434 | TCTCA | T | intron_variant | MODIFIER | HG00423.hp2 HG01069.hp2 HG01070.hp1 others(36): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0002others(9): Show | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0010 others(36): Show |
39 | 108 | 0.3611 | -4 | c.268 others(21): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85730986 | GCACA | G | intron_variant | MODIFIER | HG01516.hp2 HG02723.hp2 HG02809.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0007a0001c0003t0005others(1): Show | a0001c0001t0001g0019 a0001c0002t0007g0100 a0001c0003t0005g0059 others(1): Show |
4 | 108 | 0.0370 | -4 | c.268 others(21): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85731025 | CACAG | C | intron_variant | MODIFIER | HG01109.hp2 NA21309.hp2 |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0010 | a0001c0001t0001g0030 a0001c0003t0010g0083 |
2 | 108 | 0.0185 | -4 | c.268 others(21): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85737118 | TTTTG | T | intron_variant | MODIFIER | HG01168.hp2 HG01516.hp1 HG01978.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0016 a0001c0001t0001g0026 a0001c0001t0001g0081 others(1): Show |
4 | 108 | 0.0370 | -4 | c.268 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85744693 | CCTGA | C | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(10): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0002others(3): Show | a0001c0001t0001g0009 a0001c0001t0001g0010 a0001c0001t0001g0046 others(10): Show |
13 | 108 | 0.1204 | -4 | c.268 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85747708 | AAAAC | A | intron_variant | MODIFIER | HG02109.hp1 HG06807.hp2 |
a0001 | a0001c0001a0001c0007 | a0001c0001t0001a0001c0007t0003 | a0001c0001t0001g0048 a0001c0007t0003g0072 |
2 | 108 | 0.0185 | -4 | c.268 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85756208 | TAATA | T | intron_variant | MODIFIER | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(81): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0020others(22): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0009 others(81): Show |
84 | 108 | 0.7778 | -4 | c.268 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85777779 | GTGAA | G | intron_variant | MODIFIER | HG01109.hp2 NA21309.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0030 a0001c0002t0002g0060 |
2 | 108 | 0.0185 | -4 | c.268 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85782059 | AAAAG | A | intron_variant | MODIFIER | HG02055.hp2 HG02630.hp1 HG03486.hp1 others(1): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(1): Show | a0001c0001t0001a0001c0003t0001a0001c0004t0003others(1): Show | a0001c0001t0001g0069 a0001c0003t0001g0086 a0001c0004t0003g0061 others(1): Show |
4 | 108 | 0.0370 | -4 | c.268 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85782883 | ATGAC | A | intron_variant | MODIFIER | HG01109.hp2 HG01884.hp2 HG02155.hp1 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0002a0001c0002t0013others(3): Show | a0001c0001t0001g0008 a0001c0001t0001g0030 a0001c0002t0002g0060 others(6): Show |
9 | 108 | 0.0833 | -4 | c.268 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85784905 | CTCTA | C | intron_variant | MODIFIER | HG00642.hp2 HG01243.hp1 HG01243.hp2 others(15): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(7): Show | a0001c0001t0001g0019 a0001c0001t0001g0021 a0001c0001t0001g0090 others(15): Show |
18 | 108 | 0.1667 | -4 | c.268 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85789387 | AAGAG | A | intron_variant | MODIFIER | HG01884.hp2 HG02486.hp1 NA19240.hp1 |
a0001 | a0001c0001a0001c0007a0001c0008 | a0001c0001t0001a0001c0007t0003a0001c0008t0017 | a0001c0001t0001g0008 a0001c0007t0003g0044 a0001c0008t0017g0057 |
3 | 108 | 0.0278 | -4 | c.268 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85795493 | ATTAT | A | intron_variant | MODIFIER | HG02630.hp1 HG03486.hp1 |
a0001 | a0001c0003a0001c0004 | a0001c0003t0001a0001c0004t0003 | a0001c0003t0001g0086 a0001c0004t0003g0061 |
2 | 108 | 0.0185 | -4 | c.268 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85813818 | TTATA | T | intron_variant | MODIFIER | HG00323.hp1 HG00423.hp1 HG00735.hp1 others(15): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0012a0001c0002t0013others(5): Show | a0001c0001t0001g0003 a0001c0001t0001g0008 a0001c0001t0001g0022 others(15): Show |
18 | 108 | 0.1667 | -4 | c.268 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85827461 | CGTGT | C | intron_variant | MODIFIER | HG01168.hp1 HG02055.hp2 HG02615.hp2 others(5): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0001a0001c0002t0002a0001c0002t0013others(3): Show | a0001c0001t0001g0046 a0001c0001t0001g0062 a0001c0001t0001g0069 others(5): Show |
8 | 108 | 0.0741 | -4 | c.269 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85835681 | TTTTG | T | intron_variant | MODIFIER | HG02630.hp1 HG03486.hp1 |
a0001 | a0001c0003a0001c0004 | a0001c0003t0001a0001c0004t0003 | a0001c0003t0001g0086 a0001c0004t0003g0061 |
2 | 108 | 0.0185 | -4 | c.269 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85851207 | GCTTT | G | intron_variant | MODIFIER | HG00639.hp1 HG01243.hp2 HG01433.hp1 others(17): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0021a0001c0002t0002others(9): Show | a0001c0001t0001g0032 a0001c0001t0021g0054 a0001c0002t0002g0005 others(17): Show |
20 | 108 | 0.1852 | -4 | c.269 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85859212 | TACAC | T | intron_variant | MODIFIER | HG02109.hp1 HG02622.hp1 HG06807.hp2 |
a0001 | a0001c0001a0001c0007a0001c0008 | a0001c0001t0001a0001c0007t0003a0001c0008t0014 | a0001c0001t0001g0048 a0001c0007t0003g0072 a0001c0008t0014g0063 |
3 | 108 | 0.0278 | -4 | c.269 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85861000 | GCACA | G | intron_variant | MODIFIER | HG02055.hp2 HG02451.hp2 NA18906.hp1 others(1): Show |
a0001a0002 | a0001c0001a0001c0004a0002c0006 | a0001c0001t0001a0001c0004t0003a0002c0006t0006 | a0001c0001t0001g0069 a0001c0004t0003g0050 a0001c0004t0003g0089 others(1): Show |
4 | 108 | 0.0370 | -4 | c.269 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85875295 | TTATA | T | intron_variant | MODIFIER | HG00323.hp2 HG00642.hp2 HG00735.hp1 others(12): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0011others(1): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0002others(3): Show | a0001c0001t0001g0016 a0001c0001t0001g0023 a0001c0001t0001g0024 others(12): Show |
15 | 108 | 0.1389 | -4 | c.269 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85875359 | TTATA | T | intron_variant | MODIFIER | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(36): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0021others(14): Show | a0001c0001t0001g0032 a0001c0001t0001g0045 a0001c0001t0001g0065 others(36): Show |
39 | 108 | 0.3611 | -4 | c.269 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar |