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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ARHGAP21_chr10_24578614_24728887 | 24695566 | C | CAAA | intron_variant | MODIFIER | HG02559.hp1 HG02572.hp2 HG02717.hp1 others(4): Show |
a0001a0005 | a0001c0001a0005c0005 | a0001c0001t0001a0005c0005t0001 | a0001c0001t0001g0162a0001c0001t0001g0163a0001c0001t0001g0164others(4): Show | 7 | 352 | 0.0199 | 3 | c.64- others(20): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24702127 | C | CTTT | intron_variant | MODIFIER | HG00438.hp1 HG00621.hp2 HG01175.hp2 others(17): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0002a0003c0003others(3): Show | a0001c0001t0001a0001c0001t0005a0002c0002t0001others(4): Show | a0001c0001t0001g0176a0001c0001t0001g0178a0001c0001t0001g0191others(17): Show | 20 | 352 | 0.0568 | 3 | c.63+ others(20): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24720254 | C | CAAA | intron_variant | MODIFIER | HG00609.hp2 HG02280.hp1 HG02451.hp2 others(8): Show |
a0001a0002a0005 | a0001c0001a0002c0002a0005c0005 | a0001c0001t0001a0002c0002t0001a0005c0005t0003 | a0001c0001t0001g0141a0001c0001t0001g0142a0001c0001t0001g0143others(8): Show | 11 | 352 | 0.0313 | 3 | c.63+ others(18): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 2/25 | chr10 | TogoVar | ||||||
ARHGAP21_chr10_24578614_24728887 | 24723673 | C | CCCG | 5_prime_UTR_variant | MODIFIER | HG00280.hp1 HG03017.hp2 HG03688.hp1 |
a0002 | a0002c0002 | a0002c0002t0007 | a0002c0002t0007g0007a0002c0002t0007g0008a0002c0002t0007g0009 | 3 | 352 | 0.0085 | 3 | c.-49 others(12): Show |
ARHGAP21 | ENSG00000107863.20 | transcript | ENST00000396432.7 | protein_coding | 1/26 | 1775 | chr10 | TogoVar | |||||
ARHGAP22_chr10_48441036_48610073 | 48504103 | C | CCTG | intron_variant | MODIFIER | HG00735.hp1 HG01167.hp2 HG01175.hp1 others(16): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0002a0001c0002t0005a0001c0002t0014others(8): Show | a0001c0001t0002g0027a0001c0002t0005g0259a0001c0002t0014g0248others(16): Show | 19 | 270 | 0.0704 | 3 | c.323 others(22): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 3/9 | chr10 | TogoVar | ||||||
ARHGAP22_chr10_48441036_48610073 | 48539291 | A | ATTT | intron_variant | MODIFIER | HG02809.hp1 HG03098.hp1 HG03139.hp1 others(4): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0007a0001c0002t0003a0001c0003t0004others(2): Show | a0001c0001t0007g0015a0001c0002t0003g0253a0001c0003t0004g0006others(4): Show | 7 | 270 | 0.0259 | 3 | c.322 others(22): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 3/9 | chr10 | TogoVar | ||||||
ARHGAP22_chr10_48441036_48610073 | 48562225 | C | CAAA | intron_variant | MODIFIER | HG02055.hp2 HG02258.hp1 HG02559.hp1 others(5): Show |
a0001a0003 | a0001c0001a0001c0003a0001c0004others(2): Show | a0001c0001t0002a0001c0003t0004a0001c0004t0004others(2): Show | a0001c0001t0002g0177a0001c0003t0004g0166a0001c0003t0004g0167others(5): Show | 8 | 270 | 0.0296 | 3 | c.235 others(20): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 2/9 | chr10 | TogoVar | ||||||
ARHGAP22_chr10_48441036_48610073 | 48584993 | C | CAAA | intron_variant | MODIFIER | HG00642.hp1 HG01167.hp2 HG02040.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(4): Show | a0001c0001t0002g0120a0001c0001t0002g0177a0001c0001t0005g0228others(7): Show | 10 | 270 | 0.0370 | 3 | c.35- others(18): Show |
ARHGAP22 | ENSG00000128805.15 | transcript | ENST00000249601.9 | protein_coding | 1/9 | chr10 | TogoVar | ||||||
ARHGAP23_chr17_38423464_38517385 | 38447437 | G | GAAA | intron_variant | MODIFIER | HG00733.hp1 HG02055.hp2 HG02145.hp1 others(4): Show |
a0001a0006 | a0001c0001a0001c0005a0001c0012others(1): Show | a0001c0001t0003a0001c0005t0001a0001c0005t0006others(2): Show | a0001c0001t0003g0174a0001c0005t0001g0031a0001c0005t0001g0034others(4): Show | 7 | 309 | 0.0227 | 3 | c.64- others(20): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 1/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP23_chr17_38423464_38517385 | 38487731 | G | GCAC | intron_variant | MODIFIER | HG01361.hp2 HG03834.hp2 HG03942.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0118a0001c0001t0001g0132a0001c0001t0001g0133 | 3 | 309 | 0.0097 | 3 | c.298 others(22): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 17/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP23_chr17_38423464_38517385 | 38504978 | C | CTTT | intron_variant | MODIFIER | HG01074.hp1 HG01361.hp1 HG01361.hp2 others(4): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0006others(2): Show | a0001c0001t0001a0001c0003t0001a0001c0006t0002others(2): Show | a0001c0001t0001g0118a0001c0001t0001g0133a0001c0001t0001g0298others(4): Show | 7 | 309 | 0.0227 | 3 | c.344 others(22): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP23_chr17_38423464_38517385 | 38507276 | A | AAAT | intron_variant | MODIFIER | HG02293.hp1 HG02451.hp1 HG03041.hp1 |
a0001 | a0001c0001a0001c0003a0001c0004 | a0001c0001t0001a0001c0003t0001a0001c0004t0001 | a0001c0001t0001g0056a0001c0003t0001g0193a0001c0004t0001g0057 | 3 | 309 | 0.0097 | 3 | c.344 others(22): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 23/23 | INFO_REALIGN_3_PRIME | chr17 | TogoVar | |||||
ARHGAP23_chr17_38423464_38517385 | 38515547 | A | AAAC | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(236): Show |
a0001a0002a0004others(13): Show | a0001c0001a0001c0002a0001c0004others(40): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0008others(51): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(234): Show | 239 | 309 | 0.7735 | 3 | c.*45 others(14): Show |
ARHGAP23 | ENSG00000275832.5 | transcript | ENST00000622683.5 | protein_coding | 3163 | chr17 | TogoVar | ||||||
ARHGAP24_chr4_85470150_86007666 | 85495094 | C | CAAA | intron_variant | MODIFIER | HG00642.hp1 HG01884.hp1 HG02486.hp2 others(1): Show |
a0001 | a0001c0001a0001c0004a0001c0005 | a0001c0001t0001a0001c0001t0005a0001c0004t0004others(1): Show | a0001c0001t0001g0001a0001c0001t0005g0036a0001c0004t0004g0035others(1): Show | 4 | 108 | 0.0370 | 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 | T | TAAA | intron_variant | MODIFIER | HG00323.hp1 HG00423.hp1 HG00639.hp1 others(34): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0020a0001c0001t0021others(9): Show | a0001c0001t0001g0003a0001c0001t0001g0008a0001c0001t0001g0009others(34): Show | 37 | 108 | 0.3426 | 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 | 85515371 | C | CTTT | intron_variant | MODIFIER | HG00323.hp2 HG00642.hp2 HG00735.hp2 others(5): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0004others(4): Show | a0001c0001t0001a0001c0002t0002a0001c0004t0004others(4): Show | a0001c0001t0001g0079a0001c0001t0001g0082a0001c0002t0002g0078others(5): Show | 8 | 108 | 0.0741 | 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 | 85524791 | T | TTAC | intron_variant | MODIFIER | HG02055.hp1 HG02258.hp1 HG02615.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002a0001c0004 | a0001c0001t0001a0001c0002t0002a0001c0004t0003 | a0001c0001t0001g0032a0001c0001t0001g0043a0001c0001t0001g0102others(2): Show | 5 | 108 | 0.0463 | 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 | 85525257 | C | CTTT | intron_variant | MODIFIER | HG00642.hp1 HG02109.hp1 HG02145.hp1 others(7): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0016others(5): Show | a0001c0001t0001g0001a0001c0001t0001g0039a0001c0001t0005g0101others(7): Show | 10 | 108 | 0.0926 | 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 | 85576217 | C | CAGG | intron_variant | MODIFIER | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(100): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(30): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(100): Show | 103 | 108 | 0.9537 | 3 | c.180 others(20): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85578749 | T | TATC | intron_variant | MODIFIER | HG00323.hp1 HG00323.hp2 HG00423.hp1 others(98): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0002a0001c0003others(11): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(29): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0008others(98): Show | 101 | 108 | 0.9352 | 3 | c.180 others(20): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 2/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 85596582 | C | CTGT | intron_variant | MODIFIER | HG00323.hp2 HG00639.hp1 HG00639.hp2 others(42): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0001c0003others(8): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0020others(19): Show | a0001c0001t0001g0008a0001c0001t0001g0019a0001c0001t0001g0023others(42): Show | 45 | 108 | 0.4167 | 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 | C | CAAA | intron_variant | MODIFIER | HG00423.hp1 HG01884.hp2 HG03492.hp2 others(1): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0013a0001c0003t0001others(1): Show | a0001c0001t0001g0003a0001c0002t0013g0029a0001c0003t0001g0014others(1): Show | 4 | 108 | 0.0370 | 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 | A | AATT | intron_variant | MODIFIER | HG02055.hp1 HG02109.hp1 HG02451.hp1 others(9): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0015others(6): Show | a0001c0001t0001g0032a0001c0001t0001g0090a0001c0001t0005g0036others(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 | 85647205 | T | TTAG | intron_variant | MODIFIER | HG00423.hp1 HG00423.hp2 HG00642.hp1 others(24): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0002a0001c0002t0013others(3): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0012others(24): Show | 27 | 108 | 0.2500 | 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 | 85654720 | G | GGAA | 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 | 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 | 85657160 | C | CTTA | intron_variant | MODIFIER | HG00323.hp1 HG00423.hp2 HG00735.hp2 others(41): Show |
a0001a0003 | a0001c0001a0001c0002a0001c0003others(5): Show | a0001c0001t0001a0001c0001t0015a0001c0002t0002others(12): Show | a0001c0001t0001g0012a0001c0001t0001g0016a0001c0001t0001g0018others(41): Show | 44 | 108 | 0.4074 | 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 | 85660794 | C | CAAA | intron_variant | MODIFIER | HG00423.hp2 HG01070.hp1 HG01071.hp1 others(17): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0002t0002a0001c0003t0001others(1): Show | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0021others(17): Show | 20 | 108 | 0.1852 | 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 | 85704725 | G | GGAC | intron_variant | MODIFIER | HG01243.hp1 HG03130.hp2 |
a0001a0002 | a0001c0001a0002c0006 | a0001c0001t0005a0002c0006t0018 | a0001c0001t0005g0074a0002c0006t0018g0040 | 2 | 108 | 0.0185 | 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 | 85734636 | A | ATTT | intron_variant | MODIFIER | HG02486.hp1 HG02622.hp1 HG02622.hp2 others(8): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(3): Show | a0001c0001t0001a0001c0001t0015a0001c0002t0007others(5): Show | a0001c0001t0001g0018a0001c0001t0001g0039a0001c0001t0001g0043others(8): Show | 11 | 108 | 0.1019 | 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 | 85738367 | T | TTTA | intron_variant | MODIFIER | HG00639.hp1 HG00642.hp2 HG00735.hp1 others(17): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0001c0003others(6): Show | a0001c0001t0001a0001c0001t0020a0001c0001t0021others(10): Show | a0001c0001t0001g0024a0001c0001t0001g0032a0001c0001t0001g0043others(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 | 85742251 | C | CAGT | 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 | 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 | 85755626 | G | GTTT | intron_variant | MODIFIER | HG00323.hp1 HG01168.hp2 HG02080.hp2 others(6): Show |
a0001a0005 | a0001c0001a0001c0002a0001c0004others(1): Show | a0001c0001t0001a0001c0002t0002a0001c0002t0013others(2): Show | a0001c0001t0001g0022a0001c0001t0001g0026a0001c0001t0001g0066others(6): Show | 9 | 108 | 0.0833 | 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 | 85784924 | T | TATC | intron_variant | MODIFIER | HG01109.hp2 NA21309.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002 | a0001c0001t0001g0030a0001c0002t0002g0060 | 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 | 85872595 | C | CTTT | intron_variant | MODIFIER | HG01243.hp1 HG02055.hp2 HG02080.hp1 others(8): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0001t0005a0001c0002t0002others(3): Show | a0001c0001t0001g0012a0001c0001t0001g0066a0001c0001t0001g0069others(8): Show | 11 | 108 | 0.1019 | 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 | 85893290 | C | CTGA | intron_variant | MODIFIER | HG00735.hp2 HG01069.hp1 HG01516.hp2 others(1): Show |
a0001a0003 | a0001c0001a0003c0012 | a0001c0001t0001a0003c0012t0001 | a0001c0001t0001g0019a0001c0001t0001g0021a0001c0001t0001g0103others(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 | 85894099 | T | TAAA | intron_variant | MODIFIER | HG00423.hp2 HG01433.hp1 HG02109.hp2 others(8): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(2): Show | a0001c0001t0001a0001c0002t0016a0001c0003t0001others(4): Show | a0001c0001t0001g0097a0001c0002t0016g0055a0001c0003t0001g0004others(8): Show | 11 | 108 | 0.1019 | 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 | 85973839 | T | TTTG | intron_variant | MODIFIER | HG00642.hp2 HG00735.hp1 HG01070.hp1 others(21): Show |
a0001a0005 | a0001c0002a0001c0011a0005c0009 | a0001c0002t0002a0001c0002t0007a0001c0002t0008others(5): Show | a0001c0002t0002g0005a0001c0002t0002g0006a0001c0002t0002g0011others(21): Show | 24 | 108 | 0.2222 | 3 | c.733 others(20): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 6/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 86000080 | C | CTTT | intron_variant | MODIFIER | HG01243.hp2 HG01884.hp1 HG02257.hp2 others(10): Show |
a0001 | a0001c0004a0001c0005a0001c0007 | a0001c0004t0003a0001c0004t0004a0001c0005t0003others(3): Show | a0001c0004t0003g0042a0001c0004t0003g0050a0001c0004t0003g0061others(10): Show | 13 | 108 | 0.1204 | 3 | c.200 others(20): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP24_chr4_85470150_86007666 | 86000309 | T | TACA | intron_variant | MODIFIER | HG02145.hp1 HG03130.hp2 NA20300.hp2 |
a0002 | a0002c0006 | a0002c0006t0006a0002c0006t0018 | a0002c0006t0006g0031a0002c0006t0006g0095a0002c0006t0018g0040 | 3 | 108 | 0.0278 | 3 | c.200 others(20): Show |
ARHGAP24 | ENSG00000138639.18 | transcript | ENST00000395184.6 | protein_coding | 9/9 | INFO_REALIGN_3_PRIME | chr4 | TogoVar | |||||
ARHGAP25_chr2_68729811_68831833 | 68798517 | G | GAAA | intron_variant | MODIFIER | HG00735.hp2 HG01123.hp2 HG02257.hp2 others(8): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0002c0008others(1): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(5): Show | a0001c0001t0001g0023a0001c0001t0003g0341a0001c0001t0004g0336others(7): Show | 11 | 368 | 0.0299 | 3 | c.467 others(20): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 4/10 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP25_chr2_68729811_68831833 | 68815443 | C | CTTT | intron_variant | MODIFIER | HG00280.hp2 HG01109.hp1 HG01168.hp1 others(15): Show |
a0002a0003 | a0002c0002a0003c0003 | a0002c0002t0011a0003c0003t0001a0003c0003t0006others(1): Show | a0002c0002t0011g0149a0002c0002t0011g0161a0003c0003t0001g0103others(15): Show | 18 | 368 | 0.0489 | 3 | c.808 others(18): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 6/10 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP25_chr2_68729811_68831833 | 68821092 | C | CTTT | intron_variant | MODIFIER | HG00621.hp1 HG02647.hp2 HG02717.hp1 others(15): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(1): Show | a0001c0001t0001g0109a0001c0001t0001g0118a0001c0001t0001g0201others(14): Show | 18 | 368 | 0.0489 | 3 | c.120 others(22): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 9/10 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP25_chr2_68729811_68831833 | 68823298 | A | ACTT | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(139): Show |
a0001a0007a0009others(1): Show | a0001c0001a0007c0013a0009c0018others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0007others(127): Show | 142 | 368 | 0.3859 | 3 | c.173 others(20): Show |
ARHGAP25 | ENSG00000163219.12 | transcript | ENST00000409202.8 | protein_coding | 10/10 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142768900 | T | TTGG | upstream_gene_variant | MODIFIER | HG01069.hp2 HG01071.hp2 HG02109.hp2 others(22): Show |
a0001 | a0001c0001a0001c0002a0001c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0020others(22): Show | 25 | 198 | 0.1263 | 3 | c.-18 others(14): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1476 | chr5 | TogoVar | ||||||
ARHGAP26_chr5_142765377_143234007 | 142791082 | G | GTTT | intron_variant | MODIFIER | HG02451.hp2 HG02622.hp1 HG02622.hp2 others(16): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(11): Show | a0001c0001t0001g0034a0001c0001t0002g0008a0001c0001t0002g0043others(16): Show | 19 | 198 | 0.0960 | 3 | c.154 others(22): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142844051 | G | GTTT | intron_variant | MODIFIER | HG01175.hp2 HG02615.hp1 HG02615.hp2 others(4): Show |
a0001a0002 | a0001c0001a0002c0007 | a0001c0001t0002a0001c0001t0005a0001c0001t0013others(4): Show | a0001c0001t0002g0036a0001c0001t0005g0109a0001c0001t0013g0065others(4): Show | 7 | 198 | 0.0354 | 3 | c.155 others(22): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 1/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142904525 | G | GAAA | intron_variant | MODIFIER | HG00323.hp1 HG00323.hp2 HG00408.hp1 others(148): Show |
a0001a0002 | a0001c0001a0001c0002a0001c0003others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(58): Show | a0001c0001t0001g0012a0001c0001t0001g0018a0001c0001t0001g0020others(148): Show | 151 | 198 | 0.7626 | 3 | c.832 others(18): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 8/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142947095 | T | TAAA | intron_variant | MODIFIER | HG00438.hp1 HG00544.hp1 HG02698.hp1 others(10): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0141a0001c0001t0002g0005a0001c0001t0002g0006others(10): Show | 13 | 198 | 0.0657 | 3 | c.110 others(24): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142949198 | A | AGAG | intron_variant | MODIFIER | HG02280.hp2 HG03579.hp2 |
a0001 | a0001c0001 | a0001c0001t0006a0001c0001t0025 | a0001c0001t0006g0064a0001c0001t0025g0103 | 2 | 198 | 0.0101 | 3 | c.110 others(24): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar | |||||
ARHGAP26_chr5_142765377_143234007 | 142949200 | A | AGAG | intron_variant | MODIFIER | NA18961.hp1 NA19010.hp1 |
a0001 | a0001c0003 | a0001c0003t0001a0001c0003t0007 | a0001c0003t0001g0134a0001c0003t0007g0067 | 2 | 198 | 0.0101 | 3 | c.110 others(24): Show |
ARHGAP26 | ENSG00000145819.18 | transcript | ENST00000645722.2 | protein_coding | 11/22 | INFO_REALIGN_3_PRIME | chr5 | TogoVar |