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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ADAM20_chr14_70517358_70540004 | 70534082 | CAAAA | C | intron_variant | MODIFIER | HG01069.hp2 HG01243.hp2 HG01433.hp2 others(26): Show |
a0001a0002a0005others(1): Show | a0001c0001a0002c0003a0005c0009others(1): Show | a0001c0001t0001a0001c0001t0002a0002c0003t0001others(2): Show | a0001c0001t0001g0007 a0001c0001t0001g0010 a0001c0001t0001g0024 others(6): Show |
29 | 220 | 0.1318 | -4 | c.-17 others(21): Show |
ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | TogoVar | |||||||
ADAM20_chr14_70517358_70540004 | 70534105 | AAAAC | A | intron_variant | MODIFIER | HG00621.hp1 HG02615.hp2 HG03098.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0003 | a0001c0001t0001g0054 a0001c0001t0001g0088 a0001c0002t0003g0004 |
7 | 398 | 0.0176 | -4 | c.-17 others(21): Show |
ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1/1 | chr14 | TogoVar | |||||||
ADAM20_chr14_70517358_70540004 | 70536465 | CAAAA | C | upstream_gene_variant | MODIFIER | HG01081.hp2 HG01243.hp1 HG02109.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0008 a0001c0001t0001g0027 a0001c0001t0001g0060 others(2): Show |
7 | 42 | 0.1667 | -4 | c.-18 others(15): Show |
ADAM20 | ENSG00000134007.5 | transcript | ENST00000256389.5 | protein_coding | 1462 | chr14 | TogoVar | |||||||
ADAM22_chr7_87929251_88207889 | 87955340 | TTTCC | T | intron_variant | MODIFIER | HG02145.hp2 HG02615.hp2 HG02809.hp1 others(5): Show |
a0003 | a0003c0003 | a0003c0003t0001a0003c0003t0002a0003c0003t0005others(2): Show | a0003c0003t0001g0046 a0003c0003t0001g0051 a0003c0003t0001g0142 others(5): Show |
8 | 228 | 0.0351 | -4 | c.246 others(23): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 2/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
ADAM22_chr7_87929251_88207889 | 87982044 | CATAT | C | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp1 HG01071.hp2 others(23): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0012 a0001c0001t0001g0085 a0001c0001t0001g0160 others(23): Show |
26 | 197 | 0.1320 | -4 | c.323 others(21): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
ADAM22_chr7_87929251_88207889 | 87982066 | TATAC | T | intron_variant | MODIFIER | HG01243.hp2 HG03195.hp1 NA18906.hp1 others(1): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0030a0002c0002t0013a0003c0003t0002others(1): Show | a0001c0001t0030g0168 a0002c0002t0013g0172 a0003c0003t0002g0050 others(1): Show |
4 | 160 | 0.0250 | -4 | c.323 others(21): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
ADAM22_chr7_87929251_88207889 | 87982106 | CACAT | C | intron_variant | MODIFIER | HG00544.hp2 HG01952.hp1 HG01975.hp2 others(4): Show |
a0001a0002a0014 | a0001c0001a0002c0002a0014c0013 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(3): Show | a0001c0001t0001g0130 a0001c0001t0002g0127 a0001c0001t0002g0129 others(4): Show |
7 | 228 | 0.0307 | -4 | c.323 others(21): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | TogoVar | |||||||
ADAM22_chr7_87929251_88207889 | 88011714 | TTCTC | T | intron_variant | MODIFIER | HG00099.hp2 HG00423.hp1 HG01071.hp2 others(20): Show |
a0001a0002a0004others(2): Show | a0001c0001a0002c0002a0004c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(11): Show | a0001c0001t0001g0081 a0001c0001t0001g0083 a0001c0001t0001g0085 others(20): Show |
23 | 228 | 0.1009 | -4 | c.323 others(23): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
ADAM22_chr7_87929251_88207889 | 88017478 | ATACT | A | intron_variant | MODIFIER | HG00639.hp2 HG03453.hp1 HG03579.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0017others(1): Show | a0001c0001t0001g0029 a0001c0001t0002g0202 a0001c0001t0017g0036 others(1): Show |
4 | 228 | 0.0175 | -4 | c.323 others(23): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
ADAM22_chr7_87929251_88207889 | 88019857 | ATGTG | A | intron_variant | MODIFIER | HG00323.hp1 HG00423.hp2 HG00544.hp1 others(29): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0002a0003c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(16): Show | a0001c0001t0001g0001 a0001c0001t0001g0039 a0001c0001t0001g0055 others(29): Show |
32 | 86 | 0.3721 | -4 | c.323 others(23): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
ADAM22_chr7_87929251_88207889 | 88031117 | AAAAC | A | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00323.hp2 others(85): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0014a0001c0018others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | a0001c0001t0001g0001 a0001c0001t0001g0013 a0001c0001t0001g0016 others(85): Show |
88 | 228 | 0.3860 | -4 | c.324 others(23): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
ADAM22_chr7_87929251_88207889 | 88036815 | AAGAG | A | intron_variant | MODIFIER | HG02717.hp1 HG02896.hp2 HG02897.hp1 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(2): Show | a0001c0001t0002g0173 a0001c0001t0005g0053 a0001c0001t0007g0059 others(2): Show |
5 | 228 | 0.0219 | -4 | c.324 others(23): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
ADAM22_chr7_87929251_88207889 | 88045888 | TTGTG | T | intron_variant | MODIFIER | HG00099.hp2 HG00609.hp1 HG00673.hp2 others(17): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0019others(7): Show | a0001c0001t0001g0063 a0001c0001t0001g0097 a0001c0001t0001g0100 others(17): Show |
20 | 41 | 0.4878 | -4 | c.324 others(23): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
ADAM22_chr7_87929251_88207889 | 88053572 | GAGGA | G | intron_variant | MODIFIER | HG00423.hp1 HG00738.hp1 HG02015.hp1 others(14): Show |
a0001a0002a0004others(5): Show | a0001c0001a0002c0002a0004c0004others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(8): Show | a0001c0001t0001g0013 a0001c0001t0001g0039 a0001c0001t0001g0081 others(14): Show |
17 | 228 | 0.0746 | -4 | c.324 others(23): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
ADAM22_chr7_87929251_88207889 | 88053591 | GGAAA | G | intron_variant | MODIFIER | HG00140.hp1 HG00639.hp2 HG00673.hp2 others(22): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(7): Show | a0001c0001t0001g0029 a0001c0001t0001g0063 a0001c0001t0001g0097 others(22): Show |
25 | 133 | 0.1880 | -4 | c.324 others(23): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
ADAM22_chr7_87929251_88207889 | 88054588 | CTGTG | C | intron_variant | MODIFIER | HG00323.hp2 HG00609.hp2 HG01192.hp1 others(36): Show |
a0001a0002a0003others(5): Show | a0001c0001a0002c0002a0003c0003others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(14): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(36): Show |
39 | 83 | 0.4699 | -4 | c.324 others(23): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
ADAM22_chr7_87929251_88207889 | 88083587 | TTGTG | T | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(89): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0012a0001c0014others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(27): Show | a0001c0001t0001g0020 a0001c0001t0001g0021 a0001c0001t0001g0024 others(89): Show |
92 | 107 | 0.8598 | -4 | c.390 others(21): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
ADAM22_chr7_87929251_88207889 | 88108737 | TAAAG | T | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(138): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0014a0002c0002others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(41): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(138): Show |
141 | 227 | 0.6211 | -4 | c.473 others(19): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
ADAM22_chr7_87929251_88207889 | 88113687 | TATAA | T | intron_variant | MODIFIER | NA18990.hp1 NA18992.hp1 NA18994.hp2 others(1): Show |
a0004a0005 | a0004c0004a0005c0005 | a0004c0004t0001a0004c0004t0002a0005c0005t0004 | a0004c0004t0001g0074 a0004c0004t0002g0067 a0004c0004t0002g0070 others(1): Show |
4 | 212 | 0.0189 | -4 | c.474 others(19): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
ADAM22_chr7_87929251_88207889 | 88113703 | AATAT | A | intron_variant | MODIFIER | HG01106.hp2 HG02145.hp2 HG02723.hp2 |
a0001a0003 | a0001c0001a0003c0003 | a0001c0001t0001a0001c0001t0008a0003c0003t0001 | a0001c0001t0001g0062 a0001c0001t0008g0087 a0003c0003t0001g0051 |
3 | 55 | 0.0545 | -4 | c.474 others(19): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
ADAM22_chr7_87929251_88207889 | 88118199 | TTAGA | T | intron_variant | MODIFIER | HG01243.hp2 HG02109.hp1 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0030 | a0001c0001t0001g0044 a0001c0001t0030g0168 |
2 | 228 | 0.0088 | -4 | c.607 others(21): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
ADAM22_chr7_87929251_88207889 | 88133362 | CTAAA | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(103): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0012a0001c0014others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(32): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(103): Show |
106 | 194 | 0.5464 | -4 | c.107 others(21): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 12/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
ADAM22_chr7_87929251_88207889 | 88139418 | CTAAA | C | intron_variant | MODIFIER | HG00280.hp2 HG00609.hp2 HG00673.hp1 others(37): Show |
a0001a0002a0003others(4): Show | a0001c0001a0001c0012a0002c0002others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0001 a0001c0001t0001g0004 a0001c0001t0001g0018 others(37): Show |
40 | 196 | 0.2041 | -4 | c.122 others(23): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 14/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
ADAM22_chr7_87929251_88207889 | 88149352 | CAAAT | C | intron_variant | MODIFIER | HG00609.hp1 HG00673.hp2 HG01952.hp2 others(9): Show |
a0001a0002a0006 | a0001c0001a0002c0002a0006c0006 | a0001c0001t0001a0001c0001t0002a0001c0001t0021others(3): Show | a0001c0001t0001g0100 a0001c0001t0001g0134 a0001c0001t0001g0216 others(9): Show |
12 | 228 | 0.0526 | -4 | c.156 others(21): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 18/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
ADAM22_chr7_87929251_88207889 | 88162097 | TACAC | T | intron_variant | MODIFIER | HG01106.hp1 HG03516.hp2 NA18973.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0020 a0001c0001t0001g0097 a0001c0001t0001g0147 others(1): Show |
4 | 32 | 0.1250 | -4 | c.190 others(21): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
ADAM22_chr7_87929251_88207889 | 88174691 | TTGTC | T | intron_variant | MODIFIER | HG00609.hp2 HG03453.hp2 NA19091.hp2 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 a0001c0001t0001g0024 a0001c0001t0001g0055 |
3 | 228 | 0.0132 | -4 | c.230 others(23): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 26/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||||
ADAM22_chr7_87929251_88207889 | 88207507 | TTTTG | T | downstream_gene_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00738.hp2 others(58): Show |
a0001a0002a0003others(3): Show | a0001c0001a0001c0012a0001c0018others(6): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0007others(16): Show | a0001c0001t0001g0012 a0001c0001t0001g0018 a0001c0001t0001g0019 others(58): Show |
61 | 228 | 0.2675 | -4 | c.*11 others(17): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4619 | chr7 | TogoVar | |||||||
ADAM23_chr2_206438532_206626127 | 206439642 | TATAG | T | upstream_gene_variant | MODIFIER | HG00323.hp2 HG01361.hp2 HG02717.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0005a0001c0001t0012others(2): Show | a0001c0001t0001g0129 a0001c0001t0001g0180 a0001c0001t0001g0287 others(5): Show |
8 | 334 | 0.0240 | -4 | c.-42 others(15): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3889 | chr2 | TogoVar | |||||||
ADAM23_chr2_206438532_206626127 | 206439644 | TAGAG | T | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00609.hp1 HG01433.hp1 others(23): Show |
a0001a0004 | a0001c0001a0001c0002a0004c0003 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(5): Show | a0001c0001t0001g0064 a0001c0001t0001g0127 a0001c0001t0001g0128 others(23): Show |
26 | 299 | 0.0870 | -4 | c.-42 others(15): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3887 | chr2 | TogoVar | |||||||
ADAM23_chr2_206438532_206626127 | 206448497 | ATGAG | A | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00544.hp2 others(89): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0002a0001c0007others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(15): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0012 others(86): Show |
92 | 356 | 0.2584 | -4 | c.432 others(21): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ADAM23_chr2_206438532_206626127 | 206526141 | TACAC | T | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp2 HG00438.hp1 others(79): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0018a0001c0001t0021others(7): Show | a0001c0001t0001g0004 a0001c0001t0001g0036 a0001c0001t0001g0088 others(78): Show |
82 | 180 | 0.4556 | -4 | c.510 others(21): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ADAM23_chr2_206438532_206626127 | 206526177 | CACAG | C | intron_variant | MODIFIER | HG00323.hp1 HG03453.hp1 NA20805.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0028 | a0001c0001t0001g0190 a0001c0001t0001g0290 a0001c0001t0028g0297 |
3 | 356 | 0.0084 | -4 | c.510 others(21): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ADAM23_chr2_206438532_206626127 | 206540216 | TACAC | T | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00558.hp1 others(33): Show |
a0001 | a0001c0001a0001c0002a0001c0007 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(10): Show | a0001c0001t0001g0012 a0001c0001t0001g0016 a0001c0001t0001g0027 others(33): Show |
36 | 95 | 0.3789 | -4 | c.574 others(21): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ADAM23_chr2_206438532_206626127 | 206556203 | AATTT | A | intron_variant | MODIFIER | HG02055.hp2 HG02630.hp1 HG03516.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0185 a0001c0001t0001g0264 a0001c0001t0001g0265 |
3 | 356 | 0.0084 | -4 | c.934 others(21): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 9/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ADAM23_chr2_206438532_206626127 | 206558919 | GTTTT | G | intron_variant | MODIFIER | HG00280.hp2 HG01255.hp1 HG01361.hp2 others(32): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0008a0001c0001t0012others(2): Show | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0045 others(32): Show |
35 | 355 | 0.0986 | -4 | c.100 others(23): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ADAM23_chr2_206438532_206626127 | 206558921 | TTTTG | T | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(10): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(1): Show | a0001c0001t0001g0005 a0001c0001t0001g0012 a0001c0001t0001g0154 others(9): Show |
13 | 244 | 0.0533 | -4 | c.100 others(22): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 10/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ADAM23_chr2_206438532_206626127 | 206566479 | TTAAC | T | intron_variant | MODIFIER | HG00280.hp1 HG00558.hp1 HG00733.hp2 others(70): Show |
a0001 | a0001c0001a0001c0002a0001c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(13): Show | a0001c0001t0001g0006 a0001c0001t0001g0170 a0001c0001t0001g0180 others(69): Show |
73 | 356 | 0.2051 | -4 | c.139 others(21): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 14/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ADAM23_chr2_206438532_206626127 | 206576271 | TAAAA | T | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(209): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0002a0001c0007others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(25): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(204): Show |
212 | 356 | 0.5955 | -4 | c.173 others(23): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ADAM23_chr2_206438532_206626127 | 206578173 | TTTTA | T | intron_variant | MODIFIER | HG00280.hp2 HG00323.hp1 HG00544.hp1 others(142): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0002a0001c0007others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(19): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0013 others(140): Show |
145 | 356 | 0.4073 | -4 | c.173 others(23): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 18/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ADAM23_chr2_206438532_206626127 | 206596899 | CTTTT | C | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00733.hp2 others(50): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(6): Show | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(48): Show |
53 | 130 | 0.4077 | -4 | c.235 others(21): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 24/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ADAM23_chr2_206438532_206626127 | 206611435 | TTTTC | T | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG01070.hp1 others(13): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0020 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0012 others(11): Show |
16 | 356 | 0.0449 | -4 | c.245 others(23): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 25/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | ||||||
ADAM23_chr2_206438532_206626127 | 206625800 | TTTTA | T | downstream_gene_variant | MODIFIER | HG00558.hp1 HG00673.hp2 HG00738.hp1 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(1): Show | a0001c0001t0001g0070 a0001c0001t0002g0193 a0001c0001t0002g0194 others(5): Show |
8 | 55 | 0.1455 | -4 | c.*81 others(15): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 4674 | chr2 | TogoVar | |||||||
ADAM28_chr8_24289069_24364014 | 24308193 | TCTTA | T | intron_variant | MODIFIER | HG02055.hp2 HG02258.hp2 HG02572.hp1 others(4): Show |
a0003 | a0003c0006 | a0003c0006t0001a0003c0006t0002a0003c0006t0013 | a0003c0006t0001g0279 a0003c0006t0002g0275 a0003c0006t0002g0276 others(4): Show |
7 | 346 | 0.0202 | -4 | c.151 others(21): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 2/22 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM28_chr8_24289069_24364014 | 24316060 | CCATT | C | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(44): Show |
a0001a0017a0020 | a0001c0002a0001c0034a0017c0029others(1): Show | a0001c0002t0001a0001c0002t0002a0001c0002t0003others(8): Show | a0001c0002t0001g0003 a0001c0002t0001g0038 a0001c0002t0001g0280 others(38): Show |
47 | 345 | 0.1362 | -4 | c.576 others(21): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 6/22 | chr8 | TogoVar | |||||||
ADAM28_chr8_24289069_24364014 | 24329884 | TGTGA | T | intron_variant | MODIFIER | HG02074.hp2 HG02083.hp2 HG02698.hp1 others(3): Show |
a0001a0008a0012 | a0001c0001a0008c0011a0012c0021 | a0001c0001t0002a0001c0001t0005a0001c0001t0021others(3): Show | a0001c0001t0002g0154 a0001c0001t0005g0098 a0001c0001t0021g0150 others(3): Show |
6 | 317 | 0.0189 | -4 | c.973 others(17): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 10/22 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM28_chr8_24289069_24364014 | 24338227 | ATTAG | A | intron_variant | MODIFIER | HG00099.hp1 HG00408.hp1 HG00423.hp2 others(95): Show |
a0001a0002a0005others(5): Show | a0001c0001a0001c0002a0001c0034others(13): Show | a0001c0001t0001a0001c0001t0004a0001c0002t0001others(33): Show | a0001c0001t0001g0090 a0001c0001t0001g0181 a0001c0001t0004g0149 others(81): Show |
98 | 346 | 0.2832 | -4 | c.156 others(23): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 14/22 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM28_chr8_24289069_24364014 | 24345028 | CAAAA | C | intron_variant | MODIFIER | HG00621.hp2 HG01167.hp1 HG01169.hp1 others(41): Show |
a0002a0005a0008others(1): Show | a0002c0003a0002c0007a0002c0019others(7): Show | a0002c0003t0001a0002c0003t0002a0002c0003t0003others(18): Show | a0002c0003t0001g0002 a0002c0003t0001g0249 a0002c0003t0001g0256 others(34): Show |
44 | 281 | 0.1566 | -4 | c.199 others(23): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 18/22 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM28_chr8_24289069_24364014 | 24350864 | GTTTT | G | intron_variant | MODIFIER | HG00140.hp2 HG00597.hp1 HG01891.hp2 others(23): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0025others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(10): Show | a0001c0001t0001g0101 a0001c0001t0001g0202 a0001c0001t0002g0129 others(21): Show |
26 | 32 | 0.8125 | -4 | c.210 others(21): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 19/22 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM28_chr8_24289069_24364014 | 24354480 | ACTAT | A | 3_prime_UTR_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(335): Show |
a0001a0002a0003others(16): Show | a0001c0001a0001c0002a0001c0013others(30): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(84): Show | a0001c0001t0001g0008 a0001c0001t0001g0009 a0001c0001t0001g0011 others(308): Show |
338 | 346 | 0.9769 | -4 | c.*83 others(11): Show |
ADAM28 | ENSG00000042980.14 | transcript | ENST00000265769.9 | protein_coding | 23/23 | 83 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM29_chr4_174913358_174983180 | 174923525 | GTATA | G | intron_variant | MODIFIER | HG01256.hp2 HG01361.hp2 HG04184.hp2 others(1): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0003a0001c0001t0004a0002c0002t0003others(1): Show | a0001c0001t0003g0071 a0001c0001t0004g0015 a0002c0002t0003g0075 others(1): Show |
4 | 90 | 0.0444 | -4 | c.-45 others(23): Show |
ADAM29 | ENSG00000168594.15 | transcript | ENST00000359240.7 | protein_coding | 2/4 | INFO_REALIGN_3_PRIME | chr4 | TogoVar |