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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ACYP2_chr2_53966113_54310300 | 54216542 | A | AT | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(73): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(5): Show | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0113others(73): Show | 76 | 272 | 0.2794 | 1 | c.404 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54219906 | T | TA | intron_variant | MODIFIER | HG01243.hp1 HG02109.hp2 NA18962.hp1 |
a0001a0003 | a0001c0001a0001c0002a0003c0004 | a0001c0001t0001a0001c0002t0002a0003c0004t0007 | a0001c0001t0001g0243a0001c0002t0002g0033a0003c0004t0007g0003 | 3 | 272 | 0.0110 | 1 | c.404 others(20): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | chr2 | TogoVar | ||||||
ACYP2_chr2_53966113_54310300 | 54221520 | C | CT | intron_variant | MODIFIER | HG01515.hp2 HG02027.hp1 HG02109.hp2 others(6): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0004 | a0001c0001t0001a0001c0002t0006a0003c0004t0007 | a0001c0001t0001g0130a0001c0001t0001g0200a0001c0001t0001g0214others(6): Show | 9 | 272 | 0.0331 | 1 | c.404 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54222549 | C | CA | intron_variant | MODIFIER | HG01255.hp1 HG01346.hp1 HG02559.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0003others(1): Show | a0001c0001t0001g0193a0001c0001t0001g0233a0001c0001t0001g0263others(5): Show | 8 | 272 | 0.0294 | 1 | c.405 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54225788 | A | AT | intron_variant | MODIFIER | HG00323.hp2 HG00544.hp1 HG01081.hp2 others(25): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002a0001c0002t0005others(1): Show | a0001c0001t0001g0143a0001c0001t0001g0144a0001c0001t0001g0145others(25): Show | 28 | 272 | 0.1029 | 1 | c.405 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54226466 | G | GA | intron_variant | MODIFIER | HG00738.hp2 HG01074.hp1 HG01109.hp2 others(30): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0011a0001c0002t0001others(3): Show | a0001c0001t0001g0105a0001c0001t0001g0112a0001c0001t0001g0113others(30): Show | 33 | 272 | 0.1213 | 1 | c.405 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54227622 | C | CA | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(61): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0012others(4): Show | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0117others(61): Show | 64 | 272 | 0.2353 | 1 | c.405 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54230829 | C | CT | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(68): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(8): Show | a0001c0001t0001g0115a0001c0001t0001g0117a0001c0001t0001g0118others(68): Show | 71 | 272 | 0.2610 | 1 | c.405 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54233305 | C | CT | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(91): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0004 | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(8): Show | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0113others(91): Show | 94 | 272 | 0.3456 | 1 | c.405 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54241554 | G | GT | intron_variant | MODIFIER | HG00099.hp1 HG00544.hp2 HG01256.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(2): Show | a0001c0001t0001g0206a0001c0001t0004g0158a0001c0001t0004g0238others(4): Show | 7 | 272 | 0.0257 | 1 | c.405 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54242742 | C | CA | intron_variant | MODIFIER | HG01884.hp2 HG02109.hp1 HG02451.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0003 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0164others(4): Show | 7 | 272 | 0.0257 | 1 | c.405 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54243746 | C | CT | intron_variant | MODIFIER | HG00099.hp1 HG00544.hp2 HG01256.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(2): Show | a0001c0001t0001g0206a0001c0001t0004g0158a0001c0001t0004g0238others(4): Show | 7 | 272 | 0.0257 | 1 | c.405 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54245093 | C | CT | intron_variant | MODIFIER | HG01884.hp2 HG02109.hp1 HG02451.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0003 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0164others(4): Show | 7 | 272 | 0.0257 | 1 | c.405 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54245710 | A | AT | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(58): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(7): Show | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(58): Show | 61 | 272 | 0.2243 | 1 | c.405 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54249434 | C | CA | intron_variant | MODIFIER | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(59): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0012a0001c0002t0001others(8): Show | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(59): Show | 62 | 272 | 0.2279 | 1 | c.405 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54249940 | C | CA | intron_variant | MODIFIER | HG00323.hp2 HG00438.hp1 HG00438.hp2 others(32): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0004a0001c0002t0001others(3): Show | a0001c0001t0001g0139a0001c0001t0001g0143a0001c0001t0001g0144others(32): Show | 35 | 272 | 0.1287 | 1 | c.405 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54250477 | T | TG | intron_variant | MODIFIER | HG00408.hp1 HG00408.hp2 HG00423.hp1 others(48): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(5): Show | a0001c0001t0001g0001a0001c0001t0001g0105a0001c0001t0001g0115others(48): Show | 51 | 272 | 0.1875 | 1 | c.405 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54251359 | G | GT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(66): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(8): Show | a0001c0001t0001g0105a0001c0001t0001g0129a0001c0001t0001g0130others(66): Show | 69 | 272 | 0.2537 | 1 | c.405 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54252903 | C | CA | intron_variant | MODIFIER | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(38): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0004 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(5): Show | a0001c0001t0001g0115a0001c0001t0001g0117a0001c0001t0001g0118others(38): Show | 41 | 272 | 0.1507 | 1 | c.405 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54256816 | G | GT | intron_variant | MODIFIER | HG00738.hp2 HG02615.hp2 HG02809.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0011a0001c0002t0003 | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0175others(3): Show | 6 | 272 | 0.0221 | 1 | c.405 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54260881 | T | TA | intron_variant | MODIFIER | HG00099.hp1 HG00544.hp2 HG01256.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(2): Show | a0001c0001t0001g0206a0001c0001t0004g0158a0001c0001t0004g0238others(4): Show | 7 | 272 | 0.0257 | 1 | c.405 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54268639 | C | CA | intron_variant | MODIFIER | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(51): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(6): Show | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0119others(51): Show | 54 | 272 | 0.1985 | 1 | c.405 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54270189 | G | GT | intron_variant | MODIFIER | HG00099.hp1 HG01256.hp1 HG01934.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0004a0001c0002t0002a0001c0002t0003others(1): Show | a0001c0001t0004g0158a0001c0001t0004g0238a0001c0002t0002g0048others(4): Show | 7 | 272 | 0.0257 | 1 | c.405 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54270420 | G | GT | intron_variant | MODIFIER | HG01074.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0003 | a0001c0001t0001g0135a0001c0001t0001g0267a0001c0002t0003g0070others(4): Show | 7 | 272 | 0.0257 | 1 | c.405 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54271481 | G | GC | intron_variant | MODIFIER | HG01884.hp2 HG02109.hp1 HG02257.hp1 others(9): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002a0001c0002t0003 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0164others(9): Show | 12 | 272 | 0.0441 | 1 | c.405 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54274625 | C | CA | intron_variant | MODIFIER | HG00280.hp1 HG00280.hp2 HG00323.hp1 others(48): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0002t0001others(5): Show | a0001c0001t0001g0127a0001c0001t0001g0129a0001c0001t0001g0139others(48): Show | 51 | 272 | 0.1875 | 1 | c.405 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54279684 | T | TC | intron_variant | MODIFIER | HG02559.hp2 HG03130.hp1 HG03540.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002a0001c0002t0003 | a0001c0001t0001g0132a0001c0002t0002g0061a0001c0002t0003g0082 | 3 | 272 | 0.0110 | 1 | c.405 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54294917 | T | TA | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp1 HG00423.hp2 others(142): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0002c0003others(3): Show | a0001c0001t0001a0001c0001t0010a0001c0002t0001others(8): Show | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0116others(142): Show | 145 | 272 | 0.5331 | 1 | c.405 others(9): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54297102 | G | GA | intron_variant | MODIFIER | HG00280.hp1 HG00408.hp1 HG00438.hp1 others(112): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0010a0001c0002t0001others(6): Show | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0116others(112): Show | 115 | 272 | 0.4228 | 1 | c.405 others(9): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54307828 | C | CT | downstream_gene_variant | MODIFIER | HG01358.hp2 HG02027.hp1 HG02818.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0002t0002 | a0001c0001t0001g0229a0001c0001t0004g0114a0001c0002t0002g0013others(2): Show | 5 | 272 | 0.0184 | 1 | c.*30 others(12): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 2529 | chr2 | TogoVar | ||||||
ACYP2_chr2_53966113_54310300 | 54309095 | T | TA | downstream_gene_variant | MODIFIER | HG02109.hp1 HG02145.hp1 HG02559.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(2): Show | a0001c0001t0001g0127a0001c0001t0001g0130a0001c0001t0001g0164others(7): Show | 10 | 272 | 0.0368 | 1 | c.*42 others(12): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 3796 | chr2 | TogoVar | ||||||
ADA2_chr22_17173790_17224435 | 17174209 | G | GA | downstream_gene_variant | MODIFIER | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(114): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(10): Show | a0001c0001t0005a0001c0001t0009a0001c0001t0013others(35): Show | a0001c0001t0005g0062a0001c0001t0005g0101a0001c0001t0005g0102others(114): Show | 117 | 408 | 0.2868 | 1 | c.*72 others(12): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 4580 | chr22 | TogoVar | ||||||
ADA2_chr22_17173790_17224435 | 17174735 | G | GT | downstream_gene_variant | MODIFIER | HG00280.hp1 HG00408.hp2 HG00544.hp2 others(114): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(10): Show | a0001c0001t0005a0001c0001t0009a0001c0001t0013others(35): Show | a0001c0001t0005g0062a0001c0001t0005g0101a0001c0001t0005g0102others(114): Show | 117 | 408 | 0.2868 | 1 | c.*67 others(12): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 4054 | chr22 | TogoVar | ||||||
ADA2_chr22_17173790_17224435 | 17174835 | C | CA | downstream_gene_variant | MODIFIER | HG02145.hp2 HG02572.hp1 HG02630.hp1 others(9): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0015others(5): Show | a0001c0001t0001g0195a0001c0001t0004g0373a0001c0001t0015g0030others(9): Show | 12 | 408 | 0.0294 | 1 | c.*66 others(12): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 3954 | chr22 | TogoVar | ||||||
ADA2_chr22_17173790_17224435 | 17175308 | C | CA | downstream_gene_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(69): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0001c0004others(5): Show | a0001c0001t0003a0001c0001t0007a0001c0001t0008others(23): Show | a0001c0001t0003g0172a0001c0001t0003g0187a0001c0001t0003g0287others(69): Show | 72 | 408 | 0.1765 | 1 | c.*61 others(12): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 3481 | chr22 | TogoVar | ||||||
ADA2_chr22_17173790_17224435 | 17175884 | G | GT | downstream_gene_variant | MODIFIER | HG00280.hp1 HG00642.hp2 HG00735.hp1 others(61): Show |
a0001a0002 | a0001c0005a0001c0008a0001c0010others(6): Show | a0001c0005t0002a0001c0005t0006a0001c0005t0014others(17): Show | a0001c0005t0002g0024a0001c0005t0002g0028a0001c0005t0002g0033others(61): Show | 64 | 408 | 0.1569 | 1 | c.*55 others(12): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 2905 | chr22 | TogoVar | ||||||
ADA2_chr22_17173790_17224435 | 17177170 | C | CA | downstream_gene_variant | MODIFIER | HG00639.hp2 HG00738.hp2 HG01891.hp2 others(20): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(5): Show | a0001c0001t0001a0001c0001t0015a0001c0003t0012others(10): Show | a0001c0001t0001g0055a0001c0001t0001g0281a0001c0001t0001g0283others(20): Show | 23 | 408 | 0.0564 | 1 | c.*43 others(12): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 1619 | chr22 | TogoVar | ||||||
ADA2_chr22_17173790_17224435 | 17177709 | A | AG | downstream_gene_variant | MODIFIER | HG00280.hp1 HG00642.hp2 HG00735.hp1 others(77): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0005others(8): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(24): Show | a0001c0001t0001g0043a0001c0001t0004g0338a0001c0001t0010g0052others(77): Show | 80 | 408 | 0.1961 | 1 | c.*37 others(12): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 1080 | chr22 | TogoVar | ||||||
ADA2_chr22_17173790_17224435 | 17178435 | C | CA | downstream_gene_variant | MODIFIER | HG00741.hp2 HG01175.hp2 HG01496.hp2 others(14): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(2): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(8): Show | a0001c0001t0001g0117a0001c0001t0001g0267a0001c0001t0004g0373others(14): Show | 17 | 408 | 0.0417 | 1 | c.*30 others(12): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 354 | chr22 | TogoVar | ||||||
ADA2_chr22_17173790_17224435 | 17178735 | C | CA | downstream_gene_variant | MODIFIER | HG01175.hp2 HG01255.hp2 HG01358.hp1 others(20): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(3): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(10): Show | a0001c0001t0001g0112a0001c0001t0001g0162a0001c0001t0001g0192others(20): Show | 23 | 408 | 0.0564 | 1 | c.*27 others(12): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 54 | chr22 | TogoVar | ||||||
ADA2_chr22_17173790_17224435 | 17181324 | C | CT | 3_prime_UTR_variant | MODIFIER | HG00408.hp2 HG00544.hp2 HG01928.hp2 others(35): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(1): Show | a0001c0001t0005a0001c0001t0013a0001c0001t0016others(10): Show | a0001c0001t0005g0062a0001c0001t0005g0101a0001c0001t0005g0102others(35): Show | 38 | 408 | 0.0931 | 1 | c.*15 others(10): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 10/10 | 158 | chr22 | TogoVar | |||||
ADA2_chr22_17173790_17224435 | 17183456 | C | CT | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(100): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0004others(9): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(40): Show | a0001c0001t0001g0061a0001c0001t0001g0081a0001c0001t0001g0112others(100): Show | 103 | 408 | 0.2525 | 1 | c.108 others(9): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 7/9 | chr22 | TogoVar | ||||||
ADA2_chr22_17173790_17224435 | 17183955 | C | CT | intron_variant | MODIFIER | HG01993.hp2 HG02486.hp2 HG02896.hp2 others(15): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(3): Show | a0001c0001t0001a0001c0003t0001a0001c0003t0012others(9): Show | a0001c0001t0001g0112a0001c0001t0001g0154a0001c0001t0001g0281others(15): Show | 18 | 408 | 0.0441 | 1 | c.108 others(10): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 7/9 | chr22 | TogoVar | ||||||
ADA2_chr22_17173790_17224435 | 17184126 | A | AT | intron_variant | MODIFIER | HG00099.hp2 HG01099.hp1 HG01243.hp2 others(25): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0004others(6): Show | a0001c0001t0007a0001c0001t0008a0001c0003t0004others(15): Show | a0001c0001t0007g0152a0001c0001t0008g0376a0001c0003t0004g0339others(25): Show | 28 | 408 | 0.0686 | 1 | c.108 others(10): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 7/9 | chr22 | TogoVar | ||||||
ADA2_chr22_17173790_17224435 | 17187166 | C | CA | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(304): Show |
a0001a0002a0004others(1): Show | a0001c0001a0001c0003a0001c0004others(14): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(80): Show | a0001c0001t0001g0016a0001c0001t0001g0043a0001c0001t0001g0055others(300): Show | 307 | 408 | 0.7525 | 1 | c.108 others(10): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 7/9 | chr22 | TogoVar | ||||||
ADA2_chr22_17173790_17224435 | 17187665 | T | TA | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(61): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(4): Show | a0001c0001t0003a0001c0001t0008a0001c0001t0009others(23): Show | a0001c0001t0003g0172a0001c0001t0003g0187a0001c0001t0003g0287others(61): Show | 64 | 408 | 0.1569 | 1 | c.108 others(9): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 7/9 | chr22 | TogoVar | ||||||
ADA2_chr22_17173790_17224435 | 17187977 | G | GC | intron_variant | MODIFIER | HG00738.hp1 HG00741.hp1 HG01167.hp2 others(25): Show |
a0001a0002a0003 | a0001c0001a0001c0004a0001c0013others(4): Show | a0001c0001t0007a0001c0004t0007a0001c0013t0028others(13): Show | a0001c0001t0007g0152a0001c0004t0007g0263a0001c0013t0028g0036others(25): Show | 28 | 408 | 0.0686 | 1 | c.108 others(9): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 7/9 | chr22 | TogoVar | ||||||
ADA2_chr22_17173790_17224435 | 17189019 | C | CT | intron_variant | MODIFIER | HG01106.hp1 HG01106.hp2 HG03704.hp2 others(3): Show |
a0001 | a0001c0001a0001c0005a0001c0008 | a0001c0001t0011a0001c0005t0002a0001c0005t0039others(1): Show | a0001c0001t0011g0157a0001c0001t0011g0292a0001c0005t0002g0310others(3): Show | 6 | 408 | 0.0147 | 1 | c.973 others(8): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 6/9 | chr22 | TogoVar | ||||||
ADA2_chr22_17173790_17224435 | 17190594 | G | GC | intron_variant | MODIFIER | HG02055.hp1 HG02145.hp1 HG02896.hp1 others(1): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0006 | a0001c0001t0001a0002c0002t0009a0002c0002t0010others(1): Show | a0001c0001t0001g0043a0002c0002t0009g0027a0002c0002t0010g0066others(1): Show | 4 | 408 | 0.0098 | 1 | c.882 others(8): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 5/9 | chr22 | TogoVar | ||||||
ADA2_chr22_17173790_17224435 | 17191861 | A | AC | intron_variant | MODIFIER | HG01109.hp2 HG01175.hp2 HG01928.hp1 others(21): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(6): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0009others(15): Show | a0001c0001t0001g0081a0001c0001t0001g0162a0001c0001t0004g0381others(21): Show | 24 | 408 | 0.0588 | 1 | c.754 others(7): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 4/9 | chr22 | TogoVar |