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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP24_chr4_85470150_86007666 | 85495341 | ATTT | A | intron_variant | MODIFIER | HG01884.hp2 HG02630.hp2 HG03471.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0004others(2): Show | a0001c0001t0005a0001c0002t0008a0001c0004t0004others(2): Show | a0001c0001t0005g0075 a0001c0002t0008g0052 a0001c0002t0008g0053 others(3): Show |
6 | 48 | 0.1250 | -3 | c.-21 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85514817 | TAAA | T | intron_variant | MODIFIER | HG00323.hp2 HG00642.hp2 HG00735.hp2 others(3): Show |
a0001a0003 | a0001c0001a0001c0007a0001c0008others(2): Show | a0001c0001t0001a0001c0007t0004a0001c0008t0017others(2): Show | a0001c0001t0001g0079 a0001c0001t0001g0081 a0001c0007t0004g0057 others(3): Show |
6 | 34 | 0.1765 | -3 | c.-21 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85548069 | CTAT | C | intron_variant | MODIFIER | HG00323.hp1 HG00423.hp2 HG01070.hp1 others(20): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0002a0001c0003t0001others(1): Show | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(20): Show |
23 | 108 | 0.2130 | -3 | c.-20 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85554837 | ATTT | A | intron_variant | MODIFIER | HG00323.hp1 HG00423.hp2 HG00735.hp2 others(26): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0002t0002a0001c0003t0001others(6): Show | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(26): Show |
29 | 40 | 0.7250 | -3 | c.-20 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85554985 | TTTC | T | intron_variant | MODIFIER | HG00323.hp1 HG00423.hp2 HG01070.hp1 others(20): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0002a0001c0003t0001others(2): Show | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(20): Show |
23 | 108 | 0.2130 | -3 | c.-20 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 1/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85591031 | GTTT | G | intron_variant | MODIFIER | HG00642.hp1 HG01069.hp1 HG01433.hp1 others(11): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0002others(4): Show | a0001c0001t0001g0001 a0001c0001t0001g0032 a0001c0001t0001g0042 others(11): Show |
14 | 21 | 0.6667 | -3 | c.180 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85608551 | GTTT | G | intron_variant | MODIFIER | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(51): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(24): Show | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0021 others(51): Show |
54 | 61 | 0.8852 | -3 | c.180 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85610451 | CAAA | C | intron_variant | MODIFIER | HG00735.hp1 HG01069.hp1 HG01243.hp1 others(12): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0002others(8): Show | a0001c0001t0001g0042 a0001c0001t0001g0068 a0001c0001t0001g0094 others(12): Show |
15 | 28 | 0.5357 | -3 | c.180 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85636436 | GTCA | G | intron_variant | MODIFIER | HG02055.hp1 HG02109.hp1 HG02451.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(5): Show | a0001c0001t0001g0032 a0001c0001t0001g0094 a0001c0001t0005g0035 others(7): Show |
10 | 108 | 0.0926 | -3 | c.180 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85643210 | CTTT | C | intron_variant | MODIFIER | HG00323.hp1 HG00423.hp2 HG00735.hp2 others(30): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0002t0002a0001c0002t0008others(7): Show | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0016 others(30): Show |
33 | 108 | 0.3056 | -3 | c.180 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85647194 | AATT | A | intron_variant | MODIFIER | HG00423.hp1 HG00423.hp2 HG00642.hp1 others(24): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0002a0001c0002t0013others(3): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(24): Show |
27 | 96 | 0.2813 | -3 | c.181 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85647205 | TTAG | T | intron_variant | MODIFIER | HG02055.hp1 HG02109.hp1 HG02451.hp1 others(9): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(6): Show | a0001c0001t0001g0032 a0001c0001t0001g0094 a0001c0001t0005g0035 others(9): Show |
12 | 68 | 0.1765 | -3 | c.181 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85649721 | GTCT | G | intron_variant | MODIFIER | HG02055.hp1 HG02109.hp1 HG02451.hp1 others(9): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(6): Show | a0001c0001t0001g0032 a0001c0001t0001g0094 a0001c0001t0005g0035 others(9): Show |
12 | 108 | 0.1111 | -3 | c.181 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85669245 | AAAC | A | intron_variant | MODIFIER | HG00323.hp2 HG00639.hp2 HG00642.hp2 others(7): Show |
a0001a0003 | a0001c0001a0001c0011a0003c0014 | a0001c0001t0001a0001c0001t0005a0001c0001t0020others(2): Show | a0001c0001t0001g0010 a0001c0001t0001g0014 a0001c0001t0001g0021 others(7): Show |
10 | 108 | 0.0926 | -3 | c.181 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85672469 | ATCC | A | intron_variant | MODIFIER | HG01884.hp1 HG02055.hp2 HG02257.hp2 others(6): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0008a0001c0003t0011others(3): Show | a0001c0001t0001g0061 a0001c0001t0001g0063 a0001c0001t0001g0066 others(6): Show |
9 | 108 | 0.0833 | -3 | c.181 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85673988 | GTGT | G | intron_variant | MODIFIER | HG00642.hp1 HG02258.hp1 HG02809.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0001 a0001c0001t0001g0042 a0001c0001t0001g0045 others(4): Show |
7 | 108 | 0.0648 | -3 | c.181 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85683171 | GATA | G | intron_variant | MODIFIER | HG00639.hp2 HG01433.hp2 HG02738.hp1 others(6): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0014 | a0001c0001t0001a0001c0001t0005a0001c0002t0002others(2): Show | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0108 others(6): Show |
9 | 108 | 0.0833 | -3 | c.181 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85683176 | TAAC | T | intron_variant | MODIFIER | HG00323.hp1 HG00423.hp1 HG00423.hp2 others(29): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0015a0001c0001t0020others(11): Show | a0001c0001t0001g0003 a0001c0001t0001g0016 a0001c0001t0001g0023 others(29): Show |
32 | 108 | 0.2963 | -3 | c.181 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85720258 | TATA | T | intron_variant | MODIFIER | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(54): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(9): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(21): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0007 others(54): Show |
57 | 108 | 0.5278 | -3 | c.181 others(20): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85720812 | AAAG | A | intron_variant | MODIFIER | HG02258.hp2 HG02622.hp1 HG02622.hp2 others(2): Show |
a0001 | a0001c0001a0001c0003a0001c0008 | a0001c0001t0001a0001c0001t0015a0001c0003t0011others(1): Show | a0001c0001t0001g0042 a0001c0001t0001g0063 a0001c0001t0015g0049 others(2): Show |
5 | 108 | 0.0463 | -3 | c.181 others(20): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85728232 | CAAA | C | intron_variant | MODIFIER | HG02622.hp2 HG02717.hp1 HG02897.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0003 | a0001c0001t0001a0001c0001t0015a0001c0002t0002others(1): Show | a0001c0001t0001g0042 a0001c0001t0001g0063 a0001c0001t0015g0049 others(2): Show |
5 | 47 | 0.1064 | -3 | c.268 others(20): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85738367 | TTTA | T | intron_variant | MODIFIER | HG00323.hp2 HG01167.hp1 HG02109.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002a0001c0007 | a0001c0001t0001a0001c0002t0002a0001c0007t0003 | a0001c0001t0001g0026 a0001c0001t0001g0048 a0001c0001t0001g0063 others(4): Show |
7 | 47 | 0.1489 | -3 | c.268 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85744845 | TTTG | T | intron_variant | MODIFIER | HG02622.hp1 HG02622.hp2 |
a0001 | a0001c0001a0001c0008 | a0001c0001t0015a0001c0008t0014 | a0001c0001t0015g0049 a0001c0008t0014g0065 |
2 | 108 | 0.0185 | -3 | c.268 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85763467 | CCAA | C | intron_variant | MODIFIER | HG00323.hp1 HG00423.hp2 HG01069.hp2 others(56): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0002others(14): Show | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0011 others(56): Show |
59 | 108 | 0.5463 | -3 | c.268 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85775201 | ATCT | A | intron_variant | MODIFIER | HG00323.hp1 HG01109.hp1 HG01168.hp2 others(17): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0002t0002a0001c0002t0007others(7): Show | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0014 others(17): Show |
20 | 108 | 0.1852 | -3 | c.268 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85816465 | GACA | G | intron_variant | MODIFIER | HG01243.hp1 HG02145.hp2 HG02258.hp1 others(5): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0002others(3): Show | a0001c0001t0001g0094 a0001c0001t0005g0035 a0001c0001t0005g0074 others(5): Show |
8 | 108 | 0.0741 | -3 | c.268 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85822279 | TTGG | T | intron_variant | MODIFIER | HG00423.hp2 HG01346.hp1 HG02080.hp2 others(10): Show |
a0001a0004 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0020a0001c0002t0002others(7): Show | a0001c0001t0001g0016 a0001c0001t0001g0105 a0001c0001t0020g0002 others(10): Show |
13 | 108 | 0.1204 | -3 | c.268 others(24): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85839090 | CACA | C | intron_variant | MODIFIER | HG00639.hp1 HG02055.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0021 | a0001c0001t0001g0032 a0001c0001t0021g0054 |
2 | 108 | 0.0185 | -3 | c.269 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85874832 | AAAT | A | intron_variant | MODIFIER | HG01243.hp1 HG02145.hp2 HG02451.hp1 others(3): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0006 | a0001c0001t0001a0001c0001t0005a0001c0003t0001others(1): Show | a0001c0001t0001g0094 a0001c0001t0005g0035 a0001c0001t0005g0074 others(3): Show |
6 | 108 | 0.0556 | -3 | c.269 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85874935 | ATAT | A | intron_variant | MODIFIER | HG02258.hp1 HG02897.hp2 HG03471.hp1 others(2): Show |
a0001 | a0001c0002 | a0001c0002t0002a0001c0002t0008 | a0001c0002t0002g0004 a0001c0002t0002g0041 a0001c0002t0002g0069 others(2): Show |
5 | 108 | 0.0463 | -3 | c.269 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | chr4 | TogoVar | |||||||
ARHGAP24_chr4_85470150_86007666 | 85874998 | ATAT | A | intron_variant | MODIFIER | HG01167.hp2 HG02486.hp1 |
a0001 | a0001c0002a0001c0007 | a0001c0002t0007a0001c0007t0003 | a0001c0002t0007g0056 a0001c0007t0003g0043 |
2 | 108 | 0.0185 | -3 | c.269 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85875018 | TAAA | T | intron_variant | MODIFIER | HG01167.hp2 HG02486.hp1 |
a0001 | a0001c0002a0001c0007 | a0001c0002t0007a0001c0007t0003 | a0001c0002t0007g0056 a0001c0007t0003g0043 |
2 | 108 | 0.0185 | -3 | c.269 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85875072 | TATA | T | intron_variant | MODIFIER | HG00642.hp1 HG02615.hp2 |
a0001 | a0001c0001a0001c0004 | a0001c0001t0001a0001c0004t0003 | a0001c0001t0001g0001 a0001c0004t0003g0044 |
2 | 108 | 0.0185 | -3 | c.269 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | chr4 | TogoVar | |||||||
ARHGAP24_chr4_85470150_86007666 | 85875092 | TATC | T | intron_variant | MODIFIER | HG01167.hp2 HG02486.hp1 |
a0001 | a0001c0002a0001c0007 | a0001c0002t0007a0001c0007t0003 | a0001c0002t0007g0056 a0001c0007t0003g0043 |
2 | 108 | 0.0185 | -3 | c.269 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | chr4 | TogoVar | |||||||
ARHGAP24_chr4_85470150_86007666 | 85875104 | TATA | T | intron_variant | MODIFIER | HG01167.hp2 HG02486.hp1 |
a0001 | a0001c0002a0001c0007 | a0001c0002t0007a0001c0007t0003 | a0001c0002t0007g0056 a0001c0007t0003g0043 |
2 | 108 | 0.0185 | -3 | c.269 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | chr4 | TogoVar | |||||||
ARHGAP24_chr4_85470150_86007666 | 85875252 | TATC | T | intron_variant | MODIFIER | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(6): Show |
a0001a0002 | a0001c0002a0001c0003a0001c0004others(1): Show | a0001c0002t0002a0001c0003t0001a0001c0004t0003others(1): Show | a0001c0002t0002g0009 a0001c0002t0002g0080 a0001c0002t0002g0085 others(6): Show |
9 | 108 | 0.0833 | -3 | c.269 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | chr4 | TogoVar | |||||||
ARHGAP24_chr4_85470150_86007666 | 85875264 | TATA | T | intron_variant | MODIFIER | HG01070.hp1 HG01071.hp1 HG01074.hp1 others(6): Show |
a0001a0002 | a0001c0002a0001c0003a0001c0004others(1): Show | a0001c0002t0002a0001c0003t0001a0001c0004t0003others(1): Show | a0001c0002t0002g0009 a0001c0002t0002g0080 a0001c0002t0002g0085 others(6): Show |
9 | 108 | 0.0833 | -3 | c.269 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | chr4 | TogoVar | |||||||
ARHGAP24_chr4_85470150_86007666 | 85894960 | CAAA | C | intron_variant | MODIFIER | HG01346.hp1 HG02109.hp1 HG02738.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002a0001c0005others(1): Show | a0001c0001t0001a0001c0001t0020a0001c0002t0002others(2): Show | a0001c0001t0001g0016 a0001c0001t0001g0042 a0001c0001t0020g0002 others(3): Show |
6 | 52 | 0.1154 | -3 | c.269 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85894986 | AAAC | A | intron_variant | MODIFIER | HG00323.hp1 HG01071.hp2 HG01074.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0018 a0001c0001t0001g0023 a0001c0001t0001g0064 others(1): Show |
4 | 108 | 0.0370 | -3 | c.269 others(22): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 3/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85932435 | CTTT | C | intron_variant | MODIFIER | HG00735.hp2 HG01884.hp1 HG02109.hp1 others(12): Show |
a0001a0003 | a0001c0001a0001c0003a0001c0005others(3): Show | a0001c0001t0001a0001c0001t0015a0001c0003t0001others(8): Show | a0001c0001t0001g0048 a0001c0001t0015g0049 a0001c0003t0001g0050 others(12): Show |
15 | 18 | 0.8333 | -3 | c.391 others(20): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 4/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85974009 | ATTT | A | intron_variant | MODIFIER | HG00323.hp1 HG00423.hp1 HG00639.hp2 others(33): Show |
a0001a0003a0005 | a0001c0001a0001c0003a0003c0012others(2): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(6): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(33): Show |
36 | 75 | 0.4800 | -3 | c.733 others(18): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85976779 | CTTT | C | intron_variant | MODIFIER | HG01243.hp2 HG01884.hp2 HG01978.hp2 others(7): Show |
a0001 | a0001c0001a0001c0004a0001c0008 | a0001c0001t0001a0001c0004t0003a0001c0004t0004others(2): Show | a0001c0001t0001g0007 a0001c0004t0003g0044 a0001c0004t0003g0051 others(7): Show |
10 | 26 | 0.3846 | -3 | c.807 others(18): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 7/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85989795 | AGAT | A | intron_variant | MODIFIER | HG01243.hp2 HG02451.hp2 HG02615.hp2 others(4): Show |
a0001 | a0001c0004 | a0001c0004t0003a0001c0004t0004 | a0001c0004t0003g0044 a0001c0004t0003g0051 a0001c0004t0003g0062 others(4): Show |
7 | 108 | 0.0648 | -3 | c.929 others(20): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 8/9 | chr4 | TogoVar | |||||||
ARHGAP24_chr4_85470150_86007666 | 86003042 | TAAA | T | downstream_gene_variant | MODIFIER | HG02258.hp1 HG02897.hp2 HG03471.hp1 others(2): Show |
a0001 | a0001c0002 | a0001c0002t0002a0001c0002t0008 | a0001c0002t0002g0004 a0001c0002t0002g0041 a0001c0002t0002g0069 others(2): Show |
5 | 41 | 0.1220 | -3 | c.*23 others(14): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 377 | chr4 | TogoVar | |||||||
ARHGAP24_chr4_85470150_86007666 | 86004827 | TTTA | T | downstream_gene_variant | MODIFIER | HG00323.hp2 HG00423.hp2 HG00639.hp1 others(64): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0021others(24): Show | a0001c0001t0001g0010 a0001c0001t0001g0021 a0001c0001t0001g0024 others(64): Show |
67 | 108 | 0.6204 | -3 | c.*41 others(14): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2162 | chr4 | TogoVar | |||||||
ARHGAP25_chr2_68729811_68831833 | 68731047 | CCTT | C | upstream_gene_variant | MODIFIER | HG02615.hp2 HG02630.hp1 HG02647.hp2 others(11): Show |
a0001a0002a0009 | a0001c0001a0002c0002a0002c0005others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0017 a0001c0001t0002g0012 a0001c0001t0002g0015 others(10): Show |
14 | 366 | 0.0383 | -3 | c.-41 others(14): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 3763 | chr2 | TogoVar | |||||||
ARHGAP25_chr2_68729811_68831833 | 68780586 | TCTC | T | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp2 HG00323.hp1 others(89): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0002c0004others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(14): Show | a0001c0001t0001g0010 a0001c0001t0001g0013 a0001c0001t0001g0023 others(87): Show |
92 | 366 | 0.2514 | -3 | c.262 others(20): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 2/10 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP25_chr2_68729811_68831833 | 68810728 | TCTC | T | intron_variant | MODIFIER | HG00408.hp1 HG01074.hp1 HG01167.hp1 others(18): Show |
a0002a0004a0005 | a0002c0002a0004c0009a0005c0011 | a0002c0002t0002a0002c0002t0003a0002c0002t0006others(7): Show | a0002c0002t0002g0020 a0002c0002t0002g0071 a0002c0002t0003g0156 others(18): Show |
21 | 366 | 0.0574 | -3 | c.675 others(20): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | chr2 | TogoVar | |||||||
ARHGAP25_chr2_68729811_68831833 | 68810731 | CTTT | C | intron_variant | MODIFIER | HG02280.hp1 HG02451.hp2 HG02572.hp2 others(3): Show |
a0002 | a0002c0005a0002c0020 | a0002c0005t0002a0002c0005t0012a0002c0020t0001 | a0002c0005t0002g0274 a0002c0005t0012g0019 a0002c0005t0012g0185 others(3): Show |
6 | 289 | 0.0208 | -3 | c.675 others(20): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ARHGAP25_chr2_68729811_68831833 | 68812253 | CTCT | C | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00140.hp2 others(245): Show |
a0001a0002a0003others(4): Show | a0001c0001a0002c0004a0002c0008others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(29): Show | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0007 others(230): Show |
248 | 366 | 0.6776 | -3 | c.675 others(20): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 5/10 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |