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 | 54089395 | G | GAT | intron_variant | MODIFIER | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(16): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0002t0001others(3): Show | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(16): Show | 19 | 272 | 0.0699 | 2 | c.277 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54094532 | T | TTG | intron_variant | MODIFIER | HG02572.hp1 HG02622.hp2 HG03098.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002 | a0001c0001t0001g0215a0001c0002t0001g0099a0001c0002t0002g0034others(1): Show | 4 | 272 | 0.0147 | 2 | c.277 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54095953 | C | CAG | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp2 HG00438.hp1 others(55): Show |
a0001a0004 | a0001c0001a0001c0002a0004c0006 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(5): Show | a0001c0001t0001g0001a0001c0001t0001g0186a0001c0001t0001g0188others(55): Show | 58 | 272 | 0.2132 | 2 | c.277 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 4/6 | chr2 | TogoVar | ||||||
ACYP2_chr2_53966113_54310300 | 54095953 | C | CGG | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(190): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(11): Show | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0115others(190): Show | 193 | 272 | 0.7096 | 2 | c.277 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54095974 | C | CCT | 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 | 2 | c.277 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 4/6 | chr2 | TogoVar | ||||||
ACYP2_chr2_53966113_54310300 | 54096234 | G | GAT | intron_variant | MODIFIER | HG02559.hp1 HG02572.hp1 HG03098.hp1 others(1): Show |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0002 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(1): Show | 4 | 272 | 0.0147 | 2 | c.277 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 4/6 | chr2 | TogoVar | ||||||
ACYP2_chr2_53966113_54310300 | 54096269 | A | ATG | intron_variant | MODIFIER | HG02559.hp1 HG02572.hp1 HG03098.hp1 others(1): Show |
a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0002 | a0001c0002t0001g0098a0001c0002t0001g0099a0001c0002t0001g0100others(1): Show | 4 | 272 | 0.0147 | 2 | c.277 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 4/6 | chr2 | TogoVar | ||||||
ACYP2_chr2_53966113_54310300 | 54097886 | C | CCT | intron_variant | MODIFIER | HG00738.hp2 HG01070.hp1 HG01071.hp2 others(31): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(5): Show | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(31): Show | 34 | 272 | 0.1250 | 2 | c.278 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54102638 | C | CAA | intron_variant | MODIFIER | HG00544.hp2 HG00558.hp2 HG00597.hp1 others(20): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0136a0001c0001t0001g0137a0001c0001t0001g0148others(20): Show | 23 | 272 | 0.0846 | 2 | c.278 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54114813 | G | GAA | intron_variant | MODIFIER | HG00408.hp2 HG00423.hp1 HG00438.hp1 others(43): Show |
a0001a0004 | a0001c0001a0001c0002a0004c0006 | a0001c0001t0001a0001c0001t0004a0001c0001t0012others(2): Show | a0001c0001t0001g0001a0001c0001t0001g0186a0001c0001t0001g0188others(43): Show | 46 | 272 | 0.1691 | 2 | c.278 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54116502 | G | GTT | intron_variant | MODIFIER | HG01070.hp1 HG01071.hp2 HG01074.hp2 others(10): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(2): Show | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(10): Show | 13 | 272 | 0.0478 | 2 | c.278 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54119051 | C | CTT | intron_variant | MODIFIER | HG01516.hp1 HG02145.hp2 HG02572.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0125a0001c0001t0001g0136a0001c0001t0001g0162others(4): Show | 7 | 272 | 0.0257 | 2 | c.278 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54126597 | C | CAA | intron_variant | MODIFIER | HG00408.hp1 HG01978.hp2 HG02451.hp1 others(4): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0002t0002a0001c0002t0003others(1): Show | a0001c0001t0001g0180a0001c0002t0002g0036a0001c0002t0002g0045others(4): Show | 7 | 272 | 0.0257 | 2 | c.278 others(19): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54126954 | C | CAA | intron_variant | MODIFIER | HG00099.hp1 HG00423.hp2 HG00438.hp2 others(51): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0004a0001c0002t0001others(8): Show | a0001c0001t0001g0115a0001c0001t0001g0116a0001c0001t0001g0117others(51): Show | 54 | 272 | 0.1985 | 2 | c.278 others(19): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 4/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54140519 | T | TTC | intron_variant | MODIFIER | HG02559.hp1 HG03225.hp2 |
a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0098a0001c0002t0001g0100 | 2 | 272 | 0.0074 | 2 | c.404 others(19): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54140528 | T | TCA | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(93): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0002t0001others(3): Show | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0124others(93): Show | 96 | 272 | 0.3529 | 2 | c.404 others(19): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54141983 | T | TTG | intron_variant | MODIFIER | HG00438.hp2 HG02155.hp1 HG02559.hp1 others(10): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(2): Show | a0001c0001t0001g0174a0001c0001t0001g0183a0001c0001t0001g0192others(10): Show | 13 | 272 | 0.0478 | 2 | c.404 others(19): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54143757 | T | TTG | intron_variant | MODIFIER | HG01891.hp2 HG01978.hp1 HG02257.hp2 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(1): Show | a0001c0001t0001g0149a0001c0001t0001g0224a0001c0001t0001g0242others(4): Show | 7 | 272 | 0.0257 | 2 | c.404 others(19): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | chr2 | TogoVar | ||||||
ACYP2_chr2_53966113_54310300 | 54144673 | C | CAA | intron_variant | MODIFIER | HG01070.hp1 HG01071.hp2 HG01081.hp1 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(2): Show | a0001c0001t0001g0118a0001c0001t0001g0212a0001c0001t0004g0226others(3): Show | 6 | 272 | 0.0221 | 2 | c.404 others(19): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54148320 | A | ATG | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(101): Show |
a0001a0003a0004 | a0001c0001a0001c0002a0003c0004others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(12): Show | a0001c0001t0001g0001a0001c0001t0001g0105a0001c0001t0001g0115others(101): Show | 104 | 272 | 0.3824 | 2 | c.404 others(19): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54152115 | C | CTT | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00408.hp1 others(72): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(8): Show | a0001c0001t0001g0127a0001c0001t0001g0165a0001c0001t0001g0196others(72): Show | 75 | 272 | 0.2757 | 2 | c.404 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54153460 | G | GTT | intron_variant | MODIFIER | HG00423.hp2 HG01123.hp1 HG01168.hp2 others(33): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(3): Show | a0001c0001t0001g0196a0001c0002t0001g0098a0001c0002t0001g0100others(33): Show | 36 | 272 | 0.1324 | 2 | c.404 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54165529 | T | TCA | intron_variant | MODIFIER | HG00099.hp1 HG00558.hp1 HG01257.hp2 others(7): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(4): Show | a0001c0001t0001g0245a0001c0001t0004g0238a0001c0002t0002g0016others(7): Show | 10 | 272 | 0.0368 | 2 | c.404 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54165535 | T | TCA | intron_variant | MODIFIER | HG01255.hp2 HG01346.hp1 HG01516.hp1 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0124a0001c0001t0001g0125a0001c0001t0001g0137others(6): Show | 9 | 272 | 0.0331 | 2 | c.404 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54182047 | A | ATT | intron_variant | MODIFIER | HG00438.hp2 HG00738.hp2 HG01109.hp2 others(23): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0012others(6): Show | a0001c0001t0001g0105a0001c0001t0001g0117a0001c0001t0001g0129others(23): Show | 26 | 272 | 0.0956 | 2 | c.404 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54184861 | T | TTC | intron_variant | MODIFIER | HG00738.hp2 HG01891.hp1 HG01891.hp2 others(9): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0012a0001c0002t0001others(2): Show | a0001c0001t0001g0224a0001c0001t0001g0242a0001c0001t0012g0264others(9): Show | 12 | 272 | 0.0441 | 2 | c.404 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54195638 | C | CAA | intron_variant | MODIFIER | HG00423.hp1 HG01175.hp1 HG01928.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0002t0002 | a0001c0001t0001g0117a0001c0001t0001g0255a0001c0001t0004g0141others(5): Show | 8 | 272 | 0.0294 | 2 | c.404 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54200875 | A | AGT | 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 | 2 | c.404 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54201594 | C | CTT | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp2 HG00438.hp1 others(45): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(4): Show | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0118others(45): Show | 48 | 272 | 0.1765 | 2 | c.404 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54201612 | C | CTT | intron_variant | MODIFIER | HG00621.hp1 HG01928.hp1 HG02132.hp2 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(1): Show | a0001c0001t0001g0117a0001c0001t0001g0215a0001c0001t0001g0216others(7): Show | 10 | 272 | 0.0368 | 2 | c.404 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54201620 | C | CTT | intron_variant | MODIFIER | HG00408.hp2 HG00738.hp2 HG01175.hp1 others(14): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(2): Show | a0001c0001t0001g0115a0001c0001t0001g0119a0001c0001t0001g0160others(14): Show | 17 | 272 | 0.0625 | 2 | c.404 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54201622 | T | TTC | intron_variant | MODIFIER | HG01952.hp2 HG02165.hp2 NA18940.hp1 others(1): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0002t0002a0002c0003t0002others(1): Show | a0001c0001t0001g0245a0001c0002t0002g0056a0002c0003t0002g0093others(1): Show | 4 | 272 | 0.0147 | 2 | c.404 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54201626 | T | TTC | intron_variant | MODIFIER | HG00558.hp2 NA19070.hp1 NA19091.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0249a0001c0001t0001g0258a0001c0001t0001g0259 | 3 | 272 | 0.0110 | 2 | c.404 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54201628 | C | CTT | intron_variant | MODIFIER | HG00423.hp1 HG00438.hp1 HG00597.hp2 others(6): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0118a0001c0001t0001g0153a0001c0001t0001g0186others(6): Show | 9 | 272 | 0.0331 | 2 | c.404 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54201636 | C | CTT | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp2 HG00423.hp1 others(52): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(7): Show | a0001c0001t0001g0134a0001c0001t0001g0142a0001c0001t0001g0146others(52): Show | 55 | 272 | 0.2022 | 2 | c.404 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54201678 | C | CTG | intron_variant | MODIFIER | HG01934.hp2 HG01978.hp1 HG03471.hp1 others(1): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0004a0001c0002t0002a0001c0002t0015 | a0001c0001t0004g0158a0001c0001t0004g0238a0001c0002t0002g0108others(1): Show | 4 | 272 | 0.0147 | 2 | c.404 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54201682 | C | CTG | intron_variant | MODIFIER | HG00323.hp2 HG00408.hp1 HG00423.hp2 others(54): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0002t0002a0001c0002t0003others(5): Show | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(54): Show | 57 | 272 | 0.2096 | 2 | c.404 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54201682 | C | CTT | intron_variant | MODIFIER | HG00408.hp2 HG01346.hp1 HG02647.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004 | a0001c0001t0001g0134a0001c0001t0001g0187a0001c0001t0001g0199others(5): Show | 8 | 272 | 0.0294 | 2 | c.404 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54202706 | C | CTT | intron_variant | MODIFIER | HG00280.hp1 HG01123.hp2 HG01891.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002a0001c0002t0009 | a0001c0001t0001g0151a0001c0001t0001g0152a0001c0001t0001g0227others(2): Show | 5 | 272 | 0.0184 | 2 | c.404 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54204298 | A | ATT | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp2 HG00408.hp1 others(109): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(5): Show | a0001c0001t0001g0001a0001c0001t0001g0112a0001c0001t0001g0113others(109): Show | 112 | 272 | 0.4118 | 2 | c.404 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54207171 | A | ATG | intron_variant | MODIFIER | HG02809.hp1 HG02886.hp2 HG03098.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0011 | a0001c0001t0001g0175a0001c0001t0001g0219a0001c0001t0011g0126 | 3 | 272 | 0.0110 | 2 | c.404 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54207173 | A | ATG | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG01109.hp2 others(13): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0012a0001c0002t0001others(3): Show | a0001c0001t0001g0105a0001c0001t0001g0165a0001c0001t0001g0201others(13): Show | 16 | 272 | 0.0588 | 2 | c.404 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54208705 | C | CTT | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(60): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(3): Show | a0001c0001t0001g0001a0001c0001t0001g0115a0001c0001t0001g0117others(60): Show | 63 | 272 | 0.2316 | 2 | c.404 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54216535 | C | CAT | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00323.hp2 others(165): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(13): Show | a0001c0001t0001g0001a0001c0001t0001g0105a0001c0001t0001g0112others(165): Show | 168 | 272 | 0.6177 | 2 | c.404 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | chr2 | TogoVar | ||||||
ACYP2_chr2_53966113_54310300 | 54219857 | A | ATG | intron_variant | MODIFIER | HG01884.hp2 HG02109.hp1 HG02145.hp2 others(8): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0002t0003 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0164others(8): Show | 11 | 272 | 0.0404 | 2 | c.404 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54221520 | C | CTT | intron_variant | MODIFIER | HG00099.hp1 HG00544.hp1 HG00544.hp2 others(12): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0012others(4): Show | a0001c0001t0001g0165a0001c0001t0001g0206a0001c0001t0001g0242others(12): Show | 15 | 272 | 0.0552 | 2 | c.404 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54224719 | C | CCT | 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 | 2 | c.405 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | chr2 | TogoVar | ||||||
ACYP2_chr2_53966113_54310300 | 54230829 | C | CTT | intron_variant | MODIFIER | HG01175.hp2 HG02630.hp1 HG02717.hp1 others(10): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0002t0003a0001c0002t0005others(1): Show | a0001c0001t0001g0129a0001c0001t0001g0131a0001c0001t0001g0132others(10): Show | 13 | 272 | 0.0478 | 2 | c.405 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54233305 | C | CTT | intron_variant | MODIFIER | HG01074.hp1 HG01884.hp1 HG02970.hp1 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0012others(1): Show | a0001c0001t0001g0135a0001c0001t0001g0165a0001c0001t0004g0205others(2): Show | 5 | 272 | 0.0184 | 2 | c.405 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54235278 | G | GTT | intron_variant | MODIFIER | HG00738.hp2 HG01884.hp2 HG02109.hp1 others(9): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0011a0001c0002t0003 | a0001c0001t0001g0112a0001c0001t0001g0113a0001c0001t0001g0164others(9): Show | 12 | 272 | 0.0441 | 2 | c.405 others(21): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |