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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP23_chr17_38423464_38517385 | 38453422 | C | CGTGT | intron_variant | MODIFIER | HG01433.hp2 HG02145.hp2 HG02280.hp1 others(1): Show |
a0001a0003a0005 | a0001c0001a0001c0004a0003c0028others(1): Show | a0001c0001t0001a0001c0004t0001a0003c0028t0001others(1): Show | a0001c0001t0001g0285a0001c0004t0001g0131a0003c0028t0001g0015others(1): Show | 4 | 309 | 0.0129 | 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 | 38481905 | C | CAGAT | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(75): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(7): Show | a0001c0001t0001a0001c0001t0003a0001c0002t0002others(8): Show | a0001c0001t0001g0001a0001c0001t0001g0004a0001c0001t0001g0005others(74): Show | 78 | 309 | 0.2524 | 4 | c.263 others(21): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 14/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP23_chr17_38423464_38517385 | 38503049 | A | AAAAC | intron_variant | MODIFIER | HG02451.hp1 HG03041.hp1 HG03471.hp1 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0001 | a0001c0001t0001g0056a0001c0001t0001g0154a0001c0004t0001g0057 | 3 | 309 | 0.0097 | 4 | c.344 others(23): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP23_chr17_38423464_38517385 | 38504978 | C | CTTTT | intron_variant | MODIFIER | HG01070.hp1 HG01074.hp2 HG01099.hp2 others(4): Show |
a0001a0010 | a0001c0001a0001c0003a0001c0004others(3): Show | a0001c0001t0001a0001c0003t0001a0001c0004t0001others(3): Show | a0001c0001t0001g0122a0001c0001t0001g0248a0001c0003t0001g0193others(4): Show | 7 | 309 | 0.0227 | 4 | c.344 others(23): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP23_chr17_38423464_38517385 | 38514128 | C | CAATA | downstream_gene_variant | MODIFIER | HG01884.hp1 HG02257.hp2 HG02258.hp1 others(4): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0005t0001 | a0001c0001t0001g0056a0001c0001t0001g0077a0001c0005t0001g0048others(4): Show | 7 | 309 | 0.0227 | 4 | c.*31 others(15): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1744 | chr17 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85514817 | T | TAAAA | intron_variant | MODIFIER | HG00423.hp2 HG00639.hp2 HG00642.hp1 others(16): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0002t0002a0001c0002t0013others(5): Show | a0001c0001t0001g0001a0001c0001t0001g0016a0001c0001t0001g0021others(16): Show | 19 | 108 | 0.1759 | 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 | 85564924 | G | GTATA | intron_variant | MODIFIER | HG00639.hp2 HG02109.hp1 |
a0001a0003 | a0001c0007a0003c0014 | a0001c0007t0003a0003c0014t0001 | a0001c0007t0003g0072a0003c0014t0001g0017 | 2 | 108 | 0.0185 | 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 | 85570317 | C | CTCTT | intron_variant | MODIFIER | HG02055.hp2 HG02717.hp1 HG03130.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0062a0001c0001t0001g0065a0001c0001t0001g0069 | 3 | 108 | 0.0278 | 4 | c.-20 others(19): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85590161 | T | TCTGC | intron_variant | MODIFIER | HG02055.hp2 HG02257.hp2 HG02258.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0002a0001c0003t0011others(1): Show | a0001c0001t0001g0045a0001c0001t0001g0062a0001c0001t0001g0065others(4): Show | 7 | 108 | 0.0648 | 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 | 85612083 | T | TACAC | intron_variant | MODIFIER | HG00323.hp1 HG00735.hp2 HG02055.hp1 others(6): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0002others(5): Show | a0001c0001t0001g0022a0001c0001t0001g0032a0001c0001t0005g0036others(6): Show | 9 | 108 | 0.0833 | 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 | 85612792 | C | CTTTT | intron_variant | MODIFIER | HG02055.hp1 HG02109.hp1 HG02451.hp1 others(8): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(5): Show | a0001c0001t0001g0032a0001c0001t0001g0062a0001c0001t0001g0090others(8): Show | 11 | 108 | 0.1019 | 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 | 85623887 | C | CTGTT | intron_variant | MODIFIER | HG00323.hp1 HG00423.hp2 HG00735.hp2 others(33): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(8): Show | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0018others(33): Show | 36 | 108 | 0.3333 | 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 | 85649011 | A | ATGTG | intron_variant | MODIFIER | HG02109.hp1 HG02486.hp1 HG02630.hp1 others(2): Show |
a0001 | a0001c0002a0001c0003a0001c0007 | a0001c0002t0002a0001c0003t0001a0001c0003t0010others(1): Show | a0001c0002t0002g0060a0001c0003t0001g0086a0001c0003t0010g0083others(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 | 85653478 | A | AATTT | intron_variant | MODIFIER | HG00323.hp1 HG00423.hp2 HG00735.hp2 others(42): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(13): Show | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0018others(42): Show | 45 | 108 | 0.4167 | 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 | 85655766 | C | CATAT | intron_variant | MODIFIER | HG02109.hp1 HG03130.hp1 HG03471.hp1 |
a0001 | a0001c0001a0001c0002a0001c0007 | a0001c0001t0001a0001c0002t0008a0001c0007t0003 | a0001c0001t0001g0065a0001c0002t0008g0052a0001c0007t0003g0072 | 3 | 108 | 0.0278 | 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 | 85655782 | T | TAGAG | intron_variant | MODIFIER | HG01884.hp2 NA18906.hp1 |
a0001 | a0001c0004a0001c0008 | a0001c0004t0003a0001c0008t0017 | a0001c0004t0003g0089a0001c0008t0017g0057 | 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 | 85655810 | G | GAGAA | intron_variant | MODIFIER | NA19240.hp1 NA20300.hp2 |
a0001a0002 | a0001c0001a0002c0006 | a0001c0001t0001a0002c0006t0006 | a0001c0001t0001g0008a0002c0006t0006g0095 | 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 | 85656415 | T | TAGAC | intron_variant | MODIFIER | HG00323.hp1 HG00423.hp2 HG00642.hp1 others(53): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(14): Show | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0016others(53): Show | 56 | 108 | 0.5185 | 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 | 85668406 | A | AAAAC | intron_variant | MODIFIER | HG00642.hp1 HG02258.hp1 HG02615.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0001a0001c0002t0002a0001c0004t0003 | a0001c0001t0001g0001a0001c0001t0001g0043a0001c0001t0001g0045others(4): Show | 7 | 108 | 0.0648 | 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 | 85683107 | T | TGGGG | intron_variant | MODIFIER | HG00423.hp2 HG01074.hp1 HG01168.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0002a0001c0003t0001others(1): Show | a0001c0001t0001g0018a0001c0002t0002g0092a0001c0002t0002g0093others(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 | 85730986 | G | GCACA | intron_variant | MODIFIER | HG00735.hp2 HG02257.hp2 HG03471.hp1 others(3): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0001a0001c0002t0002a0001c0002t0008others(2): Show | a0001c0001t0001g0008a0001c0002t0002g0068a0001c0002t0008g0052others(3): Show | 6 | 108 | 0.0556 | 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 | 85734636 | A | ATTTT | intron_variant | MODIFIER | HG00423.hp2 HG01070.hp1 HG01070.hp2 others(19): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0020a0001c0002t0002others(8): Show | a0001c0001t0001g0024a0001c0001t0001g0048a0001c0001t0001g0065others(19): Show | 22 | 108 | 0.2037 | 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 | 85745897 | T | TGCTA | intron_variant | MODIFIER | HG02486.hp1 HG02630.hp2 NA19240.hp1 others(1): Show |
a0001 | a0001c0001a0001c0003a0001c0007 | a0001c0001t0001a0001c0003t0010a0001c0007t0003others(1): Show | a0001c0001t0001g0008a0001c0003t0010g0083a0001c0007t0003g0044others(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 | 85747708 | A | AAAAC | intron_variant | MODIFIER | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(38): Show |
a0001a0003a0004 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0021others(11): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(38): Show | 41 | 108 | 0.3796 | 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 | 85747723 | A | ACAAG | intron_variant | MODIFIER | HG02258.hp2 HG02622.hp1 HG02622.hp2 others(2): Show |
a0001 | a0001c0001a0001c0003a0001c0008 | a0001c0001t0001a0001c0001t0015a0001c0003t0011others(1): Show | a0001c0001t0001g0043a0001c0001t0001g0062a0001c0001t0015g0049others(2): Show | 5 | 108 | 0.0463 | 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 | 85755626 | G | GTTTT | intron_variant | MODIFIER | HG01109.hp1 HG01516.hp1 HG01978.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0002t0002a0001c0003t0001 | a0001c0001t0001g0016a0001c0001t0001g0081a0001c0002t0002g0006others(2): Show | 5 | 108 | 0.0463 | 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 | 85755633 | T | TTTTG | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp2 HG01243.hp1 others(11): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0002others(4): Show | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0046others(11): Show | 14 | 108 | 0.1296 | 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 | 85755643 | T | TTTTG | intron_variant | MODIFIER | HG00423.hp2 HG01070.hp1 HG01071.hp1 others(19): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0002t0002a0001c0003t0001others(5): Show | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0048others(19): Show | 22 | 108 | 0.2037 | 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 | G | GTGAA | intron_variant | MODIFIER | HG00323.hp2 HG00423.hp1 HG00423.hp2 others(66): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(10): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0020others(20): Show | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(66): Show | 69 | 108 | 0.6389 | 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 | 85796203 | T | TACAC | intron_variant | MODIFIER | HG02055.hp2 NA20300.hp2 |
a0001a0002 | a0001c0001a0002c0006 | a0001c0001t0001a0002c0006t0006 | a0001c0001t0001g0069a0002c0006t0006g0095 | 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 | T | TTATA | intron_variant | MODIFIER | HG00323.hp2 HG01070.hp2 HG01074.hp2 others(7): Show |
a0001 | a0001c0001a0001c0007 | a0001c0001t0001a0001c0001t0005a0001c0007t0004 | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0025others(7): Show | 10 | 108 | 0.0926 | 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 | C | CGTGT | intron_variant | MODIFIER | HG01070.hp1 HG01070.hp2 HG01071.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0026a0001c0001t0001g0079a0001c0001t0001g0099others(2): Show | 5 | 108 | 0.0463 | 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 | T | TACAC | intron_variant | MODIFIER | HG00735.hp1 HG01167.hp2 HG02486.hp1 others(2): Show |
a0001 | a0001c0002a0001c0007 | a0001c0002t0002a0001c0002t0007a0001c0002t0012others(1): Show | a0001c0002t0002g0077a0001c0002t0007g0056a0001c0002t0007g0100others(2): Show | 5 | 108 | 0.0463 | 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 | G | GCACA | intron_variant | MODIFIER | HG00735.hp1 HG02630.hp1 HG03486.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0002a0001c0002t0012others(3): Show | a0001c0001t0001g0008a0001c0001t0001g0039a0001c0001t0001g0073others(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 | 85861000 | G | GCGCA | intron_variant | MODIFIER | HG02109.hp1 HG02622.hp1 HG06807.hp2 |
a0001 | a0001c0001a0001c0007a0001c0008 | a0001c0001t0001a0001c0007t0003a0001c0008t0014 | a0001c0001t0001g0048a0001c0007t0003g0072a0001c0008t0014g0063 | 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 | 85867898 | C | CATAT | intron_variant | MODIFIER | HG00323.hp2 HG00642.hp2 HG00735.hp1 others(22): Show |
a0001a0003a0004 | a0001c0001a0001c0002a0001c0005others(4): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0002others(7): Show | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0016others(22): Show | 25 | 108 | 0.2315 | 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 | 85894099 | T | TAAAA | intron_variant | MODIFIER | HG00323.hp2 HG00642.hp2 HG01168.hp2 others(12): Show |
a0001 | a0001c0001a0001c0002a0001c0011 | a0001c0001t0001a0001c0001t0005a0001c0002t0002others(2): Show | a0001c0001t0001g0016a0001c0001t0001g0023a0001c0001t0001g0024others(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 | 85928213 | T | TTTCC | intron_variant | MODIFIER | HG00323.hp1 HG00423.hp1 HG00642.hp1 others(30): Show |
a0001a0003a0004 | a0001c0001a0001c0005a0001c0007others(2): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(6): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(30): Show | 33 | 108 | 0.3056 | 4 | c.391 others(21): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85965597 | C | CCTTT | intron_variant | MODIFIER | HG00642.hp2 HG00735.hp1 HG01070.hp1 others(22): Show |
a0001a0005 | a0001c0002a0001c0007a0001c0011others(1): Show | a0001c0002t0002a0001c0002t0007a0001c0002t0008others(6): Show | a0001c0002t0002g0005a0001c0002t0002g0006a0001c0002t0002g0011others(22): Show | 25 | 108 | 0.2315 | 4 | c.600 others(21): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85965598 | C | CTTTA | intron_variant | MODIFIER | HG01884.hp1 HG02109.hp1 HG02257.hp2 others(5): Show |
a0001 | a0001c0005a0001c0007 | a0001c0005t0003a0001c0005t0004a0001c0005t0019others(1): Show | a0001c0005t0003g0085a0001c0005t0003g0094a0001c0005t0004g0034others(5): Show | 8 | 108 | 0.0741 | 4 | c.600 others(21): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85973833 | G | GTTTT | intron_variant | MODIFIER | HG01168.hp2 HG01884.hp1 HG01884.hp2 others(6): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0005others(2): Show | a0001c0001t0001a0001c0003t0001a0001c0005t0003others(4): Show | a0001c0001t0001g0026a0001c0001t0001g0107a0001c0003t0001g0015others(6): Show | 9 | 108 | 0.0833 | 4 | c.733 others(21): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85997326 | T | TGATA | intron_variant | MODIFIER | HG00642.hp2 HG00735.hp1 HG01070.hp1 others(42): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0001c0004others(6): Show | a0001c0001t0005a0001c0002t0002a0001c0002t0007others(17): Show | a0001c0001t0005g0075a0001c0002t0002g0005a0001c0002t0002g0006others(42): Show | 45 | 108 | 0.4167 | 4 | c.200 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 86002832 | T | TAACA | downstream_gene_variant | MODIFIER | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(15): Show |
a0001 | a0001c0001a0001c0003a0001c0013 | a0001c0001t0001a0001c0001t0005a0001c0001t0021others(4): Show | a0001c0001t0001g0023a0001c0001t0001g0024a0001c0001t0001g0025others(15): Show | 18 | 108 | 0.1667 | 4 | c.*21 others(15): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 167 | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 86003091 | T | TTTTC | downstream_gene_variant | MODIFIER | HG01167.hp2 HG01243.hp2 HG01884.hp1 others(21): Show |
a0001a0002 | a0001c0002a0001c0003a0001c0004others(4): Show | a0001c0002t0002a0001c0002t0007a0001c0003t0005others(10): Show | a0001c0002t0002g0028a0001c0002t0002g0060a0001c0002t0007g0056others(21): Show | 24 | 108 | 0.2222 | 4 | c.*23 others(15): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 426 | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 86004392 | A | AACAC | downstream_gene_variant | MODIFIER | HG01884.hp2 HG02055.hp2 HG02145.hp1 others(5): Show |
a0001a0002 | a0001c0001a0001c0008a0002c0006 | a0001c0001t0001a0001c0008t0014a0001c0008t0017others(2): Show | a0001c0001t0001g0008a0001c0001t0001g0065a0001c0001t0001g0069others(5): Show | 8 | 108 | 0.0741 | 4 | c.*36 others(15): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1727 | chr4 | TogoVar | ||||||
ARHGAP25_chr2_68729811_68831833 | 68734776 | A | AACAC | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00408.hp1 others(17): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0005a0002c0002t0010a0002c0002t0014others(5): Show | a0001c0001t0005g0029a0001c0001t0005g0039a0001c0001t0005g0040others(16): Show | 20 | 368 | 0.0544 | 4 | c.-42 others(13): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 34 | chr2 | TogoVar | ||||||
ARHGAP25_chr2_68729811_68831833 | 68766714 | T | TTCTC | intron_variant | MODIFIER | HG01243.hp2 HG02486.hp2 HG02647.hp1 others(1): Show |
a0001a0002a0003 | a0001c0001a0002c0004a0003c0003 | a0001c0001t0001a0002c0004t0001a0003c0003t0001 | a0001c0001t0001g0013a0001c0001t0001g0023a0002c0004t0001g0348others(1): Show | 4 | 368 | 0.0109 | 4 | c.62- others(19): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 1/10 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP25_chr2_68729811_68831833 | 68815443 | C | CTTTT | intron_variant | MODIFIER | HG00408.hp1 HG01074.hp1 HG01261.hp1 others(5): Show |
a0002a0003 | a0002c0002a0003c0003 | a0002c0002t0006a0002c0002t0011a0002c0002t0014others(1): Show | a0002c0002t0006g0256a0002c0002t0006g0291a0002c0002t0006g0321others(5): Show | 8 | 368 | 0.0217 | 4 | c.808 others(19): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142791082 | G | GTTTT | intron_variant | MODIFIER | HG00558.hp2 HG00597.hp1 HG03486.hp1 others(3): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0002a0001c0001t0013a0001c0001t0047others(2): Show | a0001c0001t0002g0001a0001c0001t0002g0128a0001c0001t0013g0004others(3): Show | 6 | 198 | 0.0303 | 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 | 142796054 | C | CTGTG | intron_variant | MODIFIER | HG00597.hp2 HG01175.hp2 HG01192.hp1 others(29): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(20): Show | a0001c0001t0001g0131a0001c0001t0001g0138a0001c0001t0002g0036others(29): Show | 32 | 198 | 0.1616 | 4 | c.154 others(23): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar |