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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(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 | a0001c0003t0011g0087a0002c0006t0006g0095a0003c0012t0001g0027 | 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 |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(16): Show | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0030others(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 | a0001c0001t0001g0003a0001c0001t0001g0009a0001c0001t0001g0010others(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 | a0001c0001t0001g0046a0001c0001t0001g0065a0001c0001t0001g0069others(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 | a0001c0001t0001g0001a0001c0001t0001g0026a0001c0001t0001g0030others(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 | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0018others(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 | a0001c0001t0001g0026a0001c0001t0001g0032a0001c0001t0001g0062others(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 | a0001c0001t0001g0018a0001c0001t0001g0045 | 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 | a0001c0001t0015g0049a0001c0002t0002g0068a0001c0004t0003g0061others(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 | a0001c0001t0001g0030a0001c0001t0001g0103a0001c0001t0020g0002others(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 | a0001c0001t0001g0030a0001c0002t0002g0060 | 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 | a0001c0001t0001g0001a0001c0001t0001g0008a0001c0001t0001g0032others(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 |
a0001a0002a0005 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0020a0001c0002t0002others(6): Show | a0001c0001t0001g0016a0001c0001t0001g0022a0001c0001t0001g0026others(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 | a0001c0001t0001g0018a0001c0002t0002g0011a0001c0003t0001g0007others(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 | a0001c0004t0004g0033a0001c0004t0004g0035 | 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 | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(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 | a0001c0001t0001g0019a0001c0002t0007g0100a0001c0003t0005g0059others(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 | a0001c0001t0001g0030a0001c0003t0010g0083 | 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 | a0001c0001t0001g0016a0001c0001t0001g0026a0001c0001t0001g0081others(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 | a0001c0001t0001g0009a0001c0001t0001g0010a0001c0001t0001g0046others(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 | a0001c0001t0001g0048a0001c0007t0003g0072 | 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 | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0009others(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 | a0001c0001t0001g0030a0001c0002t0002g0060 | 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 | a0001c0001t0001g0069a0001c0003t0001g0086a0001c0004t0003g0061others(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 | a0001c0001t0001g0008a0001c0001t0001g0030a0001c0002t0002g0060others(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 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0090others(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 | a0001c0001t0001g0008a0001c0007t0003g0044a0001c0008t0017g0057 | 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 | a0001c0003t0001g0086a0001c0004t0003g0061 | 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 | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0022others(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 | a0001c0001t0001g0046a0001c0001t0001g0062a0001c0001t0001g0069others(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 | a0001c0003t0001g0086a0001c0004t0003g0061 | 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 | a0001c0001t0001g0032a0001c0001t0021g0054a0001c0002t0002g0005others(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 | 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 | 85861000 | GCACA | G | intron_variant | MODIFIER | HG02055.hp2 HG02451.hp2 NA18906.hp1 others(1): Show |
a0001a0002 | a0001c0001a0001c0004a0002c0006 | a0001c0001t0001a0001c0004t0003a0002c0006t0006 | a0001c0001t0001g0069a0001c0004t0003g0050a0001c0004t0003g0089others(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 | 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 | 85875359 | TTATA | T | intron_variant | MODIFIER | HG00639.hp1 HG01070.hp1 HG01071.hp1 others(36): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0021others(14): Show | a0001c0001t0001g0032a0001c0001t0001g0045a0001c0001t0001g0065others(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 | |||||
ARHGAP24_chr4_85470150_86007666 | 85875391 | TTATA | T | intron_variant | MODIFIER | HG00642.hp1 HG02080.hp2 HG02615.hp2 |
a0001a0005 | a0001c0001a0001c0004a0005c0009 | a0001c0001t0001a0001c0004t0003a0005c0009t0002 | a0001c0001t0001g0001a0001c0004t0003g0042a0005c0009t0002g0064 | 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 | 85875423 | TTATA | T | intron_variant | MODIFIER | HG02258.hp1 HG02897.hp2 HG03471.hp1 others(2): Show |
a0001 | a0001c0002 | a0001c0002t0002a0001c0002t0008 | a0001c0002t0002g0005a0001c0002t0002g0041a0001c0002t0002g0068others(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 | 85875478 | TCTTA | T | intron_variant | MODIFIER | HG01884.hp1 HG02257.hp2 HG02615.hp1 others(7): Show |
a0001 | a0001c0001a0001c0005 | a0001c0001t0001a0001c0005t0003a0001c0005t0004others(1): Show | a0001c0001t0001g0045a0001c0001t0001g0065a0001c0001t0001g0067others(7): Show | 10 | 108 | 0.0926 | -4 | c.269 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85880519 | TTGTG | T | intron_variant | MODIFIER | HG01069.hp2 HG01071.hp2 HG01109.hp2 others(19): Show |
a0001 | a0001c0001a0001c0003a0001c0004others(3): Show | a0001c0001t0001a0001c0003t0001a0001c0004t0003others(5): Show | a0001c0001t0001g0008a0001c0001t0001g0009a0001c0001t0001g0010others(19): Show | 22 | 108 | 0.2037 | -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 | 85898033 | GTATA | G | intron_variant | MODIFIER | HG00423.hp1 HG01071.hp2 HG02155.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0003a0001c0001t0001g0010a0001c0001t0001g0039others(4): Show | 7 | 108 | 0.0648 | -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 | TTTCC | T | intron_variant | MODIFIER | HG02145.hp1 HG03130.hp2 NA21309.hp2 |
a0001a0002 | a0001c0003a0002c0006 | a0001c0003t0010a0002c0006t0006a0002c0006t0018 | a0001c0003t0010g0083a0002c0006t0006g0031a0002c0006t0018g0040 | 3 | 108 | 0.0278 | -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 | 85932435 | CTTTT | C | intron_variant | MODIFIER | HG01884.hp2 HG02258.hp1 HG02897.hp2 others(3): Show |
a0001 | a0001c0002a0001c0008 | a0001c0002t0002a0001c0002t0008a0001c0008t0017 | a0001c0002t0002g0005a0001c0002t0002g0041a0001c0002t0002g0068others(3): Show | 6 | 108 | 0.0556 | -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 | 85957152 | TAGTC | T | intron_variant | MODIFIER | HG00642.hp2 HG00735.hp1 HG01070.hp1 others(21): Show |
a0001a0005 | a0001c0002a0001c0011a0005c0009 | a0001c0002t0002a0001c0002t0007a0001c0002t0008others(5): Show | a0001c0002t0002g0005a0001c0002t0002g0006a0001c0002t0002g0011others(21): Show | 24 | 108 | 0.2222 | -4 | c.600 others(23): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 5/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85997326 | TGATA | T | intron_variant | MODIFIER | HG02055.hp2 HG03130.hp1 HG03516.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0008a0001c0001t0001g0039a0001c0001t0001g0065others(1): Show | 4 | 108 | 0.0370 | -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 | 85997371 | TATAG | T | intron_variant | MODIFIER | HG00323.hp1 HG00642.hp1 HG01243.hp1 others(11): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0002c0006others(1): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0002others(3): Show | a0001c0001t0001g0001a0001c0001t0001g0012a0001c0001t0001g0022others(11): Show | 14 | 108 | 0.1296 | -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 | 86002863 | AAAAT | A | downstream_gene_variant | MODIFIER | HG01243.hp2 HG01884.hp1 HG02109.hp1 others(11): Show |
a0001 | a0001c0004a0001c0005a0001c0007 | a0001c0004t0003a0001c0004t0004a0001c0005t0003others(4): Show | a0001c0004t0003g0042a0001c0004t0003g0050a0001c0004t0003g0061others(11): Show | 14 | 108 | 0.1296 | -4 | c.*21 others(15): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 198 | chr4 | TogoVar | ||||||
ARHGAP25_chr2_68729811_68831833 | 68815443 | CTTTT | C | intron_variant | MODIFIER | HG01167.hp2 HG01169.hp2 HG02055.hp2 others(11): Show |
a0001a0002a0005others(1): Show | a0001c0001a0002c0007a0005c0010others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(4): Show | a0001c0001t0001g0013a0001c0001t0001g0023a0001c0001t0001g0143others(10): Show | 14 | 368 | 0.0380 | -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 | 142770466 | GCACT | G | 5_prime_UTR_variant | MODIFIER | HG00438.hp1 HG01243.hp1 HG02080.hp1 others(10): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0010a0001c0001t0021a0001c0001t0022others(7): Show | a0001c0001t0010g0076a0001c0001t0010g0080a0001c0001t0021g0079others(10): Show | 13 | 198 | 0.0657 | -4 | c.-29 others(13): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/23 | 291 | INFO_REALIGN_3_PRIME | chr5 | TogoVar |