view | regionname | pos | ref | alt | annotation | impact | samples | ahapids | chapids | thapids | thapids | ac | an | af | len | hgvs_c | hgvs_p | genename | geneid | featuretype | featureid | transcript_biotype | rank | cdna cdna pos length
|
cds cds pos length
|
aa aa pos length
|
distance | status | chr | external |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ACYP2_chr2_53966113_54310300 | 54205068 | TG | T | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(58): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(3): Show | a0001c0001t0001g0001 a0001c0001t0001g0115 a0001c0001t0001g0117 others(58): Show |
61 | 272 | 0.2243 | -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 | 54208392 | TC | T | intron_variant | MODIFIER | HG00099.hp1 HG01256.hp1 HG01934.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0004a0001c0002t0002a0001c0002t0003others(1): Show | a0001c0001t0004g0158 a0001c0001t0004g0238 a0001c0002t0002g0048 others(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 | 54208704 | AC | A | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(92): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0004a0001c0001t0012others(10): Show | a0001c0001t0001g0105 a0001c0001t0001g0112 a0001c0001t0001g0113 others(92): Show |
95 | 272 | 0.3493 | -1 | c.404 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | chr2 | TogoVar | |||||||
ACYP2_chr2_53966113_54310300 | 54209828 | AC | A | intron_variant | MODIFIER | HG00099.hp1 HG01256.hp1 HG01934.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0004a0001c0002t0002a0001c0002t0003others(1): Show | a0001c0001t0004g0158 a0001c0001t0004g0238 a0001c0002t0002g0048 others(2): Show |
5 | 272 | 0.0184 | -1 | c.404 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | chr2 | TogoVar | |||||||
ACYP2_chr2_53966113_54310300 | 54210141 | CA | C | intron_variant | MODIFIER | HG01099.hp1 HG01099.hp2 HG01109.hp2 others(17): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0005 | a0001c0001t0001a0001c0001t0010a0001c0002t0001others(4): Show | a0001c0001t0001g0105 a0001c0001t0001g0132 a0001c0001t0001g0144 others(17): Show |
20 | 272 | 0.0735 | -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 | 54212827 | TA | T | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(60): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(4): Show | a0001c0001t0001g0001 a0001c0001t0001g0115 a0001c0001t0001g0117 others(60): Show |
63 | 272 | 0.2316 | -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 | 54217542 | TG | T | intron_variant | MODIFIER | HG01192.hp1 HG01515.hp1 HG03239.hp2 others(1): Show |
a0001a0002 | a0001c0002a0002c0003 | a0001c0002t0002a0002c0003t0002a0002c0003t0005 | a0001c0002t0002g0058 a0002c0003t0002g0012 a0002c0003t0002g0021 others(1): Show |
4 | 272 | 0.0147 | -1 | c.404 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | chr2 | TogoVar | |||||||
ACYP2_chr2_53966113_54310300 | 54218637 | GT | G | intron_variant | MODIFIER | HG02886.hp1 HG02895.hp1 NA18906.hp1 |
a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0080 a0001c0002t0003g0081 a0001c0002t0003g0102 |
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 | 54219904 | TA | T | intron_variant | MODIFIER | HG01070.hp1 HG01257.hp1 HG01358.hp1 others(11): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(2): Show | a0001c0001t0001g0115 a0001c0001t0001g0117 a0001c0001t0001g0118 others(11): Show |
14 | 272 | 0.0515 | -1 | c.404 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | chr2 | TogoVar | |||||||
ACYP2_chr2_53966113_54310300 | 54219905 | AT | A | intron_variant | MODIFIER | HG01109.hp2 HG01255.hp1 HG01346.hp1 others(8): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0003a0001c0002t0006 | a0001c0001t0001g0105 a0001c0001t0001g0147 a0001c0001t0001g0193 others(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 | 54222549 | CA | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00408.hp1 others(191): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(14): Show | a0001c0001t0001g0001 a0001c0001t0001g0115 a0001c0001t0001g0117 others(191): Show |
194 | 272 | 0.7132 | -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 | CT | C | intron_variant | MODIFIER | HG00738.hp2 HG01070.hp2 HG01243.hp1 others(26): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0001t0012others(4): Show | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0157 others(26): Show |
29 | 272 | 0.1066 | -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 | 54234071 | CT | C | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(63): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0004 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(5): Show | a0001c0001t0001g0001 a0001c0001t0001g0115 a0001c0001t0001g0117 others(63): Show |
66 | 272 | 0.2427 | -1 | c.405 others(10): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 6/6 | chr2 | TogoVar | |||||||
ACYP2_chr2_53966113_54310300 | 54235278 | GT | G | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(58): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(7): Show | a0001c0001t0001g0129 a0001c0001t0001g0131 a0001c0001t0001g0132 others(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 | 54245710 | AT | A | intron_variant | MODIFIER | HG01884.hp2 HG02109.hp1 HG02451.hp2 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002a0001c0002t0003 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0164 others(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 | 54249940 | CA | C | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp2 HG00423.hp1 others(45): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(6): Show | a0001c0001t0001g0001 a0001c0001t0001g0115 a0001c0001t0001g0118 others(45): Show |
48 | 272 | 0.1765 | -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 | 54251588 | TA | T | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00408.hp1 others(139): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(14): Show | a0001c0001t0001g0001 a0001c0001t0001g0105 a0001c0001t0001g0112 others(139): Show |
142 | 272 | 0.5221 | -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 | 54263623 | GA | G | intron_variant | MODIFIER | HG00408.hp2 HG00423.hp1 HG00558.hp1 others(30): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0004 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(4): Show | a0001c0001t0001g0001 a0001c0001t0001g0115 a0001c0001t0001g0117 others(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 | 54266590 | CT | C | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00738.hp1 others(15): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0004a0001c0002t0002others(1): Show | a0001c0001t0001g0147 a0001c0001t0001g0149 a0001c0001t0001g0152 others(15): Show |
18 | 272 | 0.0662 | -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 | CA | C | intron_variant | MODIFIER | HG01884.hp2 HG02109.hp1 HG02451.hp2 others(8): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002a0001c0002t0003 | a0001c0001t0001g0112 a0001c0001t0001g0113 a0001c0001t0001g0164 others(8): Show |
11 | 272 | 0.0404 | -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 | 54272466 | TA | T | intron_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00280.hp2 others(168): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(13): Show | a0001c0001t0001g0001 a0001c0001t0001g0105 a0001c0001t0001g0112 others(168): Show |
171 | 272 | 0.6287 | -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 | CA | C | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp2 HG00423.hp1 others(93): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(8): Show | a0001c0001t0001g0001 a0001c0001t0001g0115 a0001c0001t0001g0116 others(93): Show |
96 | 272 | 0.3529 | -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 | 54275074 | GA | G | intron_variant | MODIFIER | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(75): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0001t0010a0001c0001t0011others(9): Show | a0001c0001t0001g0116 a0001c0001t0001g0120 a0001c0001t0001g0124 others(75): Show |
78 | 272 | 0.2868 | -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 | 54276241 | AT | A | intron_variant | MODIFIER | HG00558.hp2 HG00597.hp1 HG00621.hp2 others(74): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0001t0010a0001c0001t0011others(8): Show | a0001c0001t0001g0001 a0001c0001t0001g0116 a0001c0001t0001g0120 others(74): Show |
77 | 272 | 0.2831 | -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 | 54276661 | AC | A | intron_variant | MODIFIER | HG01255.hp1 HG01346.hp1 HG02559.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0003others(1): Show | a0001c0001t0001g0233 a0001c0001t0001g0263 a0001c0002t0001g0098 others(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 | 54277677 | TA | T | intron_variant | MODIFIER | HG02630.hp1 HG02896.hp2 HG03130.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0002a0001c0002t0003 | a0001c0001t0001g0267 a0001c0002t0002g0061 a0001c0002t0002g0108 others(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 | 54297115 | GT | G | intron_variant | MODIFIER | HG00423.hp2 HG00438.hp2 HG02040.hp2 others(10): Show |
a0001a0002a0004 | a0001c0001a0001c0002a0002c0003others(1): Show | a0001c0001t0001a0001c0002t0002a0002c0003t0002others(1): Show | a0001c0001t0001g0187 a0001c0001t0001g0234 a0001c0001t0001g0236 others(10): Show |
13 | 272 | 0.0478 | -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 | 54299591 | CA | C | intron_variant | MODIFIER | HG00438.hp2 HG00738.hp2 HG01192.hp1 others(47): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0001t0010a0001c0002t0001others(6): Show | a0001c0001t0001g0124 a0001c0001t0001g0125 a0001c0001t0001g0130 others(47): Show |
50 | 272 | 0.1838 | -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 | 54305266 | TA | T | 3_prime_UTR_variant | MODIFIER | HG00558.hp1 HG00597.hp2 HG01071.hp2 others(23): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0004a0001c0002t0005a0001c0002t0015others(1): Show | a0001c0001t0004g0114 a0001c0001t0004g0121 a0001c0001t0004g0140 others(23): Show |
26 | 272 | 0.0956 | -1 | c.*46 others(5): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 7/7 | 466 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ACYP2_chr2_53966113_54310300 | 54307828 | CT | C | downstream_gene_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00323.hp2 others(98): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0011others(10): Show | a0001c0001t0001g0001 a0001c0001t0001g0117 a0001c0001t0001g0132 others(98): Show |
101 | 272 | 0.3713 | -1 | c.*30 others(6): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 2529 | chr2 | TogoVar | |||||||
ACYP2_chr2_53966113_54310300 | 54308689 | TA | T | downstream_gene_variant | MODIFIER | HG01255.hp1 HG01346.hp1 HG02615.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0003others(1): Show | a0001c0001t0001g0233 a0001c0001t0001g0263 a0001c0002t0001g0100 others(5): Show |
8 | 272 | 0.0294 | -1 | c.*38 others(6): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 3390 | chr2 | TogoVar | |||||||
ACYP2_chr2_53966113_54310300 | 54309095 | TA | T | downstream_gene_variant | MODIFIER | HG00738.hp2 HG01109.hp1 HG01243.hp1 others(21): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0004 | a0001c0001t0001a0001c0002t0002a0001c0002t0003others(2): Show | a0001c0001t0001g0116 a0001c0001t0001g0120 a0001c0001t0001g0124 others(21): Show |
24 | 272 | 0.0882 | -1 | c.*42 others(6): Show |
ACYP2 | ENSG00000170634.13 | transcript | ENST00000607452.6 | protein_coding | 3796 | chr2 | TogoVar | |||||||
ADA2_chr22_17173790_17224435 | 17174835 | CA | C | downstream_gene_variant | MODIFIER | HG01175.hp1 HG01256.hp2 HG01361.hp2 others(28): Show |
a0001a0002a0004 | a0001c0001a0001c0003a0001c0004others(7): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(20): Show | a0001c0001t0001g0043 a0001c0001t0001g0155 a0001c0001t0004g0338 others(28): Show |
31 | 408 | 0.0760 | -1 | c.*66 others(6): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 3954 | chr22 | TogoVar | |||||||
ADA2_chr22_17173790_17224435 | 17175308 | CA | C | downstream_gene_variant | MODIFIER | HG00280.hp1 HG00408.hp1 HG00408.hp2 others(115): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0003a0001c0004others(14): Show | a0001c0001t0005a0001c0001t0009a0001c0001t0013others(40): Show | a0001c0001t0005g0062 a0001c0001t0005g0101 a0001c0001t0005g0102 others(115): Show |
118 | 408 | 0.2892 | -1 | c.*61 others(6): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 3481 | chr22 | TogoVar | |||||||
ADA2_chr22_17173790_17224435 | 17175704 | GA | G | downstream_gene_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(110): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0001c0004others(7): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(44): Show | a0001c0001t0001g0043 a0001c0001t0001g0135 a0001c0001t0003g0172 others(110): Show |
113 | 408 | 0.2770 | -1 | c.*57 others(6): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 3085 | chr22 | TogoVar | |||||||
ADA2_chr22_17173790_17224435 | 17177170 | CA | C | downstream_gene_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00408.hp2 others(107): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0001c0004others(9): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(37): Show | a0001c0001t0001g0059 a0001c0001t0001g0155 a0001c0001t0001g0269 others(107): Show |
110 | 408 | 0.2696 | -1 | c.*43 others(6): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 1619 | chr22 | TogoVar | |||||||
ADA2_chr22_17173790_17224435 | 17177189 | AT | A | downstream_gene_variant | MODIFIER | HG02258.hp1 HG02615.hp1 HG02630.hp2 others(12): Show |
a0001a0002 | a0001c0001a0001c0003a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0010others(4): Show | a0001c0001t0001g0043 a0001c0001t0004g0338 a0001c0001t0010g0052 others(12): Show |
15 | 408 | 0.0368 | -1 | c.*42 others(6): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 1600 | chr22 | TogoVar | |||||||
ADA2_chr22_17173790_17224435 | 17178435 | CA | C | downstream_gene_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(77): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0001c0004others(6): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(31): Show | a0001c0001t0001g0059 a0001c0001t0001g0162 a0001c0001t0003g0172 others(77): Show |
80 | 408 | 0.1961 | -1 | c.*30 others(6): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 354 | chr22 | TogoVar | |||||||
ADA2_chr22_17173790_17224435 | 17178735 | CA | C | downstream_gene_variant | MODIFIER | HG00673.hp2 HG01243.hp2 HG01891.hp1 others(21): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(3): Show | a0001c0001t0001a0001c0001t0007a0001c0003t0004others(14): Show | a0001c0001t0001g0061 a0001c0001t0001g0154 a0001c0001t0007g0152 others(21): Show |
24 | 408 | 0.0588 | -1 | c.*27 others(6): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 54 | chr22 | TogoVar | |||||||
ADA2_chr22_17173790_17224435 | 17179858 | CG | C | 3_prime_UTR_variant | MODIFIER | HG00408.hp2 HG00544.hp2 HG01928.hp2 others(42): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0001c0004others(4): Show | a0001c0001t0005a0001c0001t0013a0001c0001t0015others(16): Show | a0001c0001t0005g0062 a0001c0001t0005g0101 a0001c0001t0005g0102 others(42): Show |
45 | 408 | 0.1103 | -1 | c.*16 others(6): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 10/10 | 1624 | chr22 | TogoVar | ||||||
ADA2_chr22_17173790_17224435 | 17181514 | TC | T | frameshift_variant | HIGH | NA18968.hp2 | a0008 | a0008c0015 | a0008c0015t0005 | a0008c0015t0005g0222 | 1 | 408 | 0.0025 | -1 | c.150 others(5): Show |
p.Asp others(5): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 10/10 | 1630/4355 | 1504/1536 | 502/511 | chr22 | TogoVar | |||
ADA2_chr22_17173790_17224435 | 17181879 | GC | G | frameshift_variant | HIGH | NA19072.hp1 | a0009 | a0009c0017 | a0009c0017t0016 | a0009c0017t0016g0382 | 1 | 408 | 0.0025 | -1 | c.138 others(5): Show |
p.Gly others(5): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 9/10 | 1508/4355 | 1382/1536 | 461/511 | chr22 | TogoVar | |||
ADA2_chr22_17173790_17224435 | 17182733 | GT | G | frameshift_variant | HIGH | NA19072.hp1 | a0009 | a0009c0017 | a0009c0017t0016 | a0009c0017t0016g0382 | 1 | 408 | 0.0025 | -1 | c.110 others(5): Show |
p.Asn others(5): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 8/10 | 1235/4355 | 1109/1536 | 370/511 | chr22 | TogoVar | |||
ADA2_chr22_17173790_17224435 | 17183456 | CT | C | intron_variant | MODIFIER | HG01167.hp2 HG01256.hp2 HG01993.hp2 others(11): Show |
a0001a0002a0009others(1): Show | a0001c0001a0001c0003a0001c0004others(7): Show | a0001c0001t0001a0001c0003t0004a0001c0004t0036others(9): Show | a0001c0001t0001g0043 a0001c0001t0001g0154 a0001c0001t0001g0162 others(11): Show |
14 | 408 | 0.0343 | -1 | c.108 others(9): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 7/9 | chr22 | TogoVar | |||||||
ADA2_chr22_17173790_17224435 | 17186389 | TG | T | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(404): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0003a0001c0004others(22): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(111): Show | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0055 others(400): Show |
407 | 408 | 0.9976 | -1 | c.108 others(10): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 7/9 | chr22 | TogoVar | |||||||
ADA2_chr22_17173790_17224435 | 17187665 | TA | T | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(30): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(9): Show | a0001c0001t0001a0001c0001t0005a0001c0001t0011others(17): Show | a0001c0001t0001g0117 a0001c0001t0001g0119 a0001c0001t0001g0120 others(30): Show |
33 | 408 | 0.0809 | -1 | c.108 others(9): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 7/9 | chr22 | TogoVar | |||||||
ADA2_chr22_17173790_17224435 | 17188092 | AG | A | intron_variant | MODIFIER | HG02523.hp1 HG03486.hp1 NA18966.hp1 |
a0001a0002 | a0001c0001a0001c0005a0002c0002 | a0001c0001t0013a0001c0005t0002a0002c0002t0001 | a0001c0001t0013g0065 a0001c0005t0002g0103 a0002c0002t0001g0031 |
3 | 408 | 0.0074 | -1 | c.108 others(9): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 7/9 | chr22 | TogoVar | |||||||
ADA2_chr22_17173790_17224435 | 17189019 | CT | C | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(110): Show |
a0001a0002a0004others(2): Show | a0001c0001a0001c0003a0001c0004others(10): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(49): Show | a0001c0001t0001g0117 a0001c0001t0001g0164 a0001c0001t0001g0175 others(110): Show |
113 | 408 | 0.2770 | -1 | c.973 others(8): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 6/9 | chr22 | TogoVar | |||||||
ADA2_chr22_17173790_17224435 | 17192829 | GA | G | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(224): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0001c0004others(12): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(70): Show | a0001c0001t0001g0016 a0001c0001t0001g0043 a0001c0001t0001g0055 others(221): Show |
227 | 408 | 0.5564 | -1 | c.754 others(9): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 4/9 | chr22 | TogoVar | |||||||
ADA2_chr22_17173790_17224435 | 17193357 | GC | G | intron_variant | MODIFIER | HG00639.hp2 HG00741.hp1 HG01433.hp1 others(6): Show |
a0001a0002 | a0001c0001a0001c0003a0001c0004others(4): Show | a0001c0001t0008a0001c0003t0003a0001c0004t0001others(5): Show | a0001c0001t0008g0376 a0001c0003t0003g0111 a0001c0004t0001g0224 others(6): Show |
9 | 408 | 0.0221 | -1 | c.754 others(9): Show |
ADA2 | ENSG00000093072.19 | transcript | ENST00000399837.8 | protein_coding | 4/9 | chr22 | TogoVar |