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 | 54095998 | C | CG | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(251): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(14): Show | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0113others(251): Show | 254 | 272 | 0.9338 | 1 | c.277 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54097965 | C | CT | intron_variant | MODIFIER | HG02559.hp1 HG02572.hp1 HG02630.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002 | a0001c0001t0001g0174a0001c0001t0001g0192a0001c0001t0001g0193others(7): Show | 10 | 272 | 0.0368 | 1 | c.278 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54102638 | C | CA | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00323.hp2 others(17): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0142others(17): Show | 20 | 272 | 0.0735 | 1 | c.278 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54110256 | A | AC | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00323.hp1 others(125): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(16): Show | a0001c0001t0001g0105a0001c0001t0001g0115a0001c0001t0001g0116others(125): Show | 128 | 272 | 0.4706 | 1 | c.278 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54114380 | C | CA | intron_variant | MODIFIER | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(44): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(3): Show | a0001c0001t0001g0105a0001c0001t0001g0112a0001c0001t0001g0113others(44): Show | 47 | 272 | 0.1728 | 1 | c.278 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54116502 | G | GT | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(78): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(7): Show | a0001c0001t0001g0001a0001c0001t0001g0129a0001c0001t0001g0152others(78): Show | 81 | 272 | 0.2978 | 1 | c.278 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54119051 | C | CT | intron_variant | MODIFIER | HG00099.hp2 HG00544.hp2 HG01168.hp1 others(14): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0124a0001c0001t0001g0153a0001c0001t0001g0160others(14): Show | 17 | 272 | 0.0625 | 1 | c.278 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54125429 | G | GA | intron_variant | MODIFIER | HG02451.hp1 HG02630.hp1 HG02896.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0003 | a0001c0001t0001g0267a0001c0002t0003g0070a0001c0002t0003g0071others(4): Show | 7 | 272 | 0.0257 | 1 | c.278 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54126597 | C | CA | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(126): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(8): Show | a0001c0001t0001g0001a0001c0001t0001g0124a0001c0001t0001g0125others(126): Show | 129 | 272 | 0.4743 | 1 | c.278 others(9): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54126954 | C | CA | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(47): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(5): Show | a0001c0001t0001g0215a0001c0001t0001g0218a0001c0001t0004g0272others(47): Show | 50 | 272 | 0.1838 | 1 | c.278 others(9): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54127099 | C | CT | intron_variant | MODIFIER | HG01243.hp2 HG01934.hp1 HG02615.hp2 others(8): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0001c0001t0010a0001c0001t0011others(1): Show | a0001c0001t0001g0127a0001c0001t0001g0128a0001c0001t0001g0175others(8): Show | 11 | 272 | 0.0404 | 1 | c.278 others(9): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54129245 | A | AT | intron_variant | MODIFIER | HG00738.hp2 HG01891.hp1 HG02451.hp2 others(5): Show |
a0001 | a0001c0002 | a0001c0002t0003a0001c0002t0009 | a0001c0002t0003g0080a0001c0002t0003g0081a0001c0002t0003g0082others(5): Show | 8 | 272 | 0.0294 | 1 | c.278 others(9): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54132177 | C | CT | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(84): Show |
a0001a0003a0004 | a0001c0001a0001c0002a0003c0004others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0012others(8): Show | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0116others(84): Show | 87 | 272 | 0.3199 | 1 | c.278 others(18): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 4/6 | chr2 | TogoVar | ||||||
ACYP2_chr2_53966113_54310300 | 54132744 | A | AT | intron_variant | MODIFIER | HG02027.hp2 HG02615.hp1 HG02970.hp2 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002a0001c0002t0003 | a0001c0001t0001g0201a0001c0001t0001g0241a0001c0001t0001g0244others(5): Show | 8 | 272 | 0.0294 | 1 | c.278 others(9): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54136204 | A | AT | intron_variant | MODIFIER | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(41): Show |
a0001a0004 | a0001c0001a0001c0002a0004c0006 | a0001c0001t0001a0001c0001t0004a0001c0001t0012others(2): Show | a0001c0001t0001g0001a0001c0001t0001g0186a0001c0001t0001g0188others(41): Show | 44 | 272 | 0.1618 | 1 | c.294 others(16): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 5/6 | chr2 | TogoVar | ||||||
ACYP2_chr2_53966113_54310300 | 54141109 | C | CT | intron_variant | MODIFIER | HG02615.hp1 HG02970.hp2 NA19043.hp1 |
a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0109a0001c0002t0003g0110a0001c0002t0003g0111 | 3 | 272 | 0.0110 | 1 | c.404 others(9): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54142016 | T | TG | intron_variant | MODIFIER | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(8): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(2): Show | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(8): Show | 11 | 272 | 0.0404 | 1 | c.404 others(18): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | chr2 | TogoVar | ||||||
ACYP2_chr2_53966113_54310300 | 54142021 | T | TA | intron_variant | MODIFIER | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(8): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(2): Show | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(8): Show | 11 | 272 | 0.0404 | 1 | c.404 others(18): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | chr2 | TogoVar | ||||||
ACYP2_chr2_53966113_54310300 | 54143756 | T | TG | intron_variant | MODIFIER | HG01934.hp1 HG01934.hp2 HG02109.hp1 others(6): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(2): Show | a0001c0001t0001g0134a0001c0001t0001g0164a0001c0001t0001g0241others(6): Show | 9 | 272 | 0.0331 | 1 | c.404 others(18): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | chr2 | TogoVar | ||||||
ACYP2_chr2_53966113_54310300 | 54143757 | T | TG | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp2 HG00423.hp2 others(62): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0004a0001c0002t0001others(8): Show | a0001c0001t0001g0113a0001c0001t0001g0127a0001c0001t0001g0129others(62): Show | 65 | 272 | 0.2390 | 1 | c.404 others(9): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54144673 | C | CA | intron_variant | MODIFIER | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(48): Show |
a0001a0004 | a0001c0001a0001c0002a0004c0006 | a0001c0001t0001a0001c0001t0004a0001c0001t0012others(5): Show | a0001c0001t0001g0001a0001c0001t0001g0186a0001c0001t0001g0188others(48): Show | 51 | 272 | 0.1875 | 1 | c.404 others(9): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54146439 | A | AT | intron_variant | MODIFIER | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(44): Show |
a0001a0004 | a0001c0001a0001c0002a0004c0006 | a0001c0001t0001a0001c0001t0004a0001c0001t0012others(4): Show | a0001c0001t0001g0001a0001c0001t0001g0186a0001c0001t0001g0188others(44): Show | 47 | 272 | 0.1728 | 1 | c.404 others(9): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54150739 | C | CT | intron_variant | MODIFIER | HG00597.hp1 HG01109.hp2 HG01978.hp1 others(8): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0002t0003 | a0001c0001t0001g0105a0001c0001t0001g0149a0001c0001t0001g0174others(8): Show | 11 | 272 | 0.0404 | 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 | 54152115 | C | CT | intron_variant | MODIFIER | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(51): Show |
a0001a0004 | a0001c0001a0001c0002a0004c0006 | a0001c0001t0001a0001c0001t0004a0001c0001t0012others(5): Show | a0001c0001t0001g0001a0001c0001t0001g0105a0001c0001t0001g0115others(51): Show | 54 | 272 | 0.1985 | 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 | 54153460 | G | GT | intron_variant | MODIFIER | HG00597.hp1 HG01070.hp1 HG01071.hp2 others(22): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(3): Show | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(22): Show | 25 | 272 | 0.0919 | 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 | 54153593 | C | CT | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(74): Show |
a0001a0004 | a0001c0001a0001c0002a0004c0006 | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(9): Show | a0001c0001t0001g0001a0001c0001t0001g0105a0001c0001t0001g0115others(74): Show | 77 | 272 | 0.2831 | 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 | 54158197 | G | GT | intron_variant | MODIFIER | HG01891.hp2 HG02257.hp2 HG03453.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0136a0001c0001t0001g0149a0001c0001t0001g0188others(2): Show | 5 | 272 | 0.0184 | 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 | 54159372 | C | CT | intron_variant | MODIFIER | HG01243.hp2 HG02622.hp1 HG02886.hp2 others(9): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0010a0001c0002t0002others(1): Show | a0001c0001t0001g0112a0001c0001t0001g0175a0001c0001t0001g0208others(9): Show | 12 | 272 | 0.0441 | 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 | 54167003 | C | CT | intron_variant | MODIFIER | HG00099.hp1 HG00738.hp2 HG01243.hp2 others(37): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(8): Show | a0001c0001t0001g0165a0001c0001t0001g0175a0001c0001t0001g0208others(37): Show | 40 | 272 | 0.1471 | 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 | 54169457 | A | AT | intron_variant | MODIFIER | HG01243.hp2 HG02809.hp1 HG02886.hp2 others(6): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0010a0001c0001t0011others(2): Show | a0001c0001t0001g0175a0001c0001t0001g0208a0001c0001t0001g0210others(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 | 54182047 | A | AT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(72): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(8): Show | a0001c0001t0001g0115a0001c0001t0001g0118a0001c0001t0001g0119others(72): Show | 75 | 272 | 0.2757 | 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 | 54182583 | C | CT | intron_variant | MODIFIER | HG02647.hp2 HG02717.hp1 HG02818.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(2): Show | 5 | 272 | 0.0184 | 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 | 54184845 | A | AT | intron_variant | MODIFIER | HG00408.hp1 HG00597.hp1 HG02622.hp2 others(2): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(1): Show | a0001c0001t0001g0211a0001c0001t0001g0234a0001c0002t0001g0106others(2): Show | 5 | 272 | 0.0184 | 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 | 54184861 | T | TC | intron_variant | MODIFIER | HG00099.hp1 HG01978.hp1 HG02293.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0002t0003others(1): Show | a0001c0001t0001g0216a0001c0001t0004g0238a0001c0002t0003g0072others(3): Show | 6 | 272 | 0.0221 | 1 | c.404 others(20): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | chr2 | TogoVar | ||||||
ACYP2_chr2_53966113_54310300 | 54185535 | A | AT | intron_variant | MODIFIER | HG01074.hp1 HG01243.hp2 HG02630.hp1 others(13): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0010a0001c0001t0011others(3): Show | a0001c0001t0001g0135a0001c0001t0001g0175a0001c0001t0001g0208others(13): Show | 16 | 272 | 0.0588 | 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 | 54186918 | T | TA | intron_variant | MODIFIER | HG02572.hp2 HG02818.hp1 HG03098.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002 | a0001c0001t0001g0230a0001c0001t0001g0231a0001c0002t0001g0099others(2): Show | 5 | 272 | 0.0184 | 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 | 54195638 | C | CA | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(63): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0004a0001c0002t0001others(6): Show | a0001c0001t0001g0001a0001c0001t0001g0105a0001c0001t0001g0115others(63): Show | 66 | 272 | 0.2427 | 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 | 54195794 | G | GT | intron_variant | MODIFIER | HG00738.hp1 HG01109.hp1 HG01934.hp1 others(12): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(3): Show | a0001c0001t0001g0113a0001c0001t0001g0120a0001c0001t0001g0142others(12): Show | 15 | 272 | 0.0552 | 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 | 54198624 | T | TA | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(167): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(14): Show | a0001c0001t0001g0001a0001c0001t0001g0105a0001c0001t0001g0112others(167): Show | 170 | 272 | 0.6250 | 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 | 54201616 | C | CT | intron_variant | MODIFIER | HG02809.hp1 HG02886.hp2 HG03471.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0011a0001c0002t0002 | a0001c0001t0001g0219a0001c0001t0011g0126a0001c0002t0002g0108 | 3 | 272 | 0.0110 | 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 | 54201699 | T | TC | intron_variant | MODIFIER | HG00621.hp2 NA18940.hp1 NA18995.hp1 |
a0001a0004 | a0001c0001a0001c0002a0004c0006 | a0001c0001t0001a0001c0002t0002a0004c0006t0001 | a0001c0001t0001g0236a0001c0002t0002g0028a0004c0006t0001g0185 | 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 | 54202297 | C | CG | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(68): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(9): Show | a0001c0001t0001g0129a0001c0001t0001g0130a0001c0001t0001g0131others(68): Show | 71 | 272 | 0.2610 | 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 | 54202405 | C | CT | intron_variant | MODIFIER | HG02083.hp2 HG02293.hp2 HG03486.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0002t0002 | a0001c0001t0001g0001a0001c0001t0001g0160a0001c0001t0001g0216others(4): Show | 7 | 272 | 0.0257 | 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 | 54202706 | C | CT | intron_variant | MODIFIER | HG00621.hp1 HG00738.hp1 HG01070.hp2 others(13): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0002t0002 | a0001c0001t0001g0116a0001c0001t0001g0120a0001c0001t0001g0149others(13): Show | 16 | 272 | 0.0588 | 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 | 54203803 | C | CT | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(75): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0004a0001c0001t0012others(9): Show | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0129others(75): Show | 78 | 272 | 0.2868 | 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 | 54204298 | A | AT | intron_variant | MODIFIER | HG00099.hp1 HG01071.hp2 HG01074.hp1 others(22): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0012others(7): Show | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(22): Show | 25 | 272 | 0.0919 | 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 | 54210141 | C | CA | intron_variant | MODIFIER | HG00408.hp1 HG00423.hp2 HG00597.hp1 others(15): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0002t0002a0002c0003t0002 | a0001c0001t0001g0129a0001c0001t0001g0146a0001c0001t0001g0159others(15): Show | 18 | 272 | 0.0662 | 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 | 54210731 | C | CT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(166): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(13): Show | a0001c0001t0001g0001a0001c0001t0001g0105a0001c0001t0001g0112others(166): Show | 169 | 272 | 0.6213 | 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 | 54212922 | T | TA | intron_variant | MODIFIER | HG01255.hp1 HG01346.hp1 HG02615.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0003a0001c0002t0006 | a0001c0001t0001g0193a0001c0001t0001g0233a0001c0001t0001g0263others(4): Show | 7 | 272 | 0.0257 | 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 | 54213773 | C | CT | intron_variant | MODIFIER | HG00738.hp2 HG01109.hp2 HG01243.hp1 others(36): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0011a0001c0001t0012others(4): Show | a0001c0001t0001g0105a0001c0001t0001g0112a0001c0001t0001g0113others(36): Show | 39 | 272 | 0.1434 | 1 | c.404 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |