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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ADAM7_chr8_24436026_24514565 | 24460083 | AT | A | intron_variant | MODIFIER | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(19): Show |
a0001a0005a0016 | a0001c0001a0005c0006a0016c0021 | a0001c0001t0001a0001c0001t0002a0005c0006t0001others(1): Show | a0001c0001t0001g0009 a0001c0001t0001g0050 a0001c0001t0001g0051 others(17): Show |
22 | 360 | 0.0611 | -1 | c.234 others(9): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM7_chr8_24436026_24514565 | 24464316 | AC | A | intron_variant | MODIFIER | HG00280.hp1 HG00741.hp2 HG01069.hp2 others(28): Show |
a0001a0003 | a0001c0001a0003c0020 | a0001c0001t0001a0003c0020t0001 | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(21): Show |
31 | 360 | 0.0861 | -1 | c.312 others(8): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4/21 | chr8 | TogoVar | |||||||
ADAM7_chr8_24436026_24514565 | 24468290 | GA | G | intron_variant | MODIFIER | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002 | a0001c0001t0001g0009 a0001c0001t0001g0050 a0001c0001t0001g0051 others(10): Show |
14 | 360 | 0.0389 | -1 | c.580 others(8): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 6/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM7_chr8_24436026_24514565 | 24472122 | CA | C | intron_variant | MODIFIER | HG00408.hp1 HG00438.hp1 HG00558.hp2 others(26): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0002c0002t0015others(3): Show | a0001c0001t0001g0117 a0001c0001t0001g0300 a0001c0001t0002g0046 others(25): Show |
29 | 360 | 0.0806 | -1 | c.633 others(9): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM7_chr8_24436026_24514565 | 24477560 | AC | A | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(88): Show |
a0002a0003a0004others(3): Show | a0002c0002a0002c0007a0002c0014others(5): Show | a0002c0002t0001a0002c0002t0012a0002c0002t0015others(7): Show | a0002c0002t0001g0001 a0002c0002t0001g0012 a0002c0002t0001g0013 others(78): Show |
91 | 360 | 0.2528 | -1 | c.705 others(9): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM7_chr8_24436026_24514565 | 24482383 | GA | G | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(224): Show |
a0001a0002a0003others(12): Show | a0001c0001a0001c0003a0001c0011others(17): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(26): Show | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(196): Show |
227 | 360 | 0.6306 | -1 | c.875 others(7): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM7_chr8_24436026_24514565 | 24484802 | CT | C | intron_variant | MODIFIER | HG00323.hp2 HG00639.hp1 HG00642.hp1 others(46): Show |
a0001a0002a0003others(5): Show | a0001c0001a0002c0002a0003c0004others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(8): Show | a0001c0001t0001g0021 a0001c0001t0001g0027 a0001c0001t0001g0053 others(43): Show |
49 | 360 | 0.1361 | -1 | c.876 others(8): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM7_chr8_24436026_24514565 | 24494712 | GA | G | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(108): Show |
a0001a0003a0008others(4): Show | a0001c0001a0001c0003a0001c0011others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(10): Show | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(95): Show |
111 | 360 | 0.3083 | -1 | c.184 others(10): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM7_chr8_24436026_24514565 | 24502227 | GA | G | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(93): Show |
a0002a0003a0004others(3): Show | a0002c0002a0002c0007a0002c0014others(6): Show | a0002c0002t0001a0002c0002t0012a0002c0002t0015others(8): Show | a0002c0002t0001g0001 a0002c0002t0001g0012 a0002c0002t0001g0013 others(82): Show |
96 | 360 | 0.2667 | -1 | c.220 others(9): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM7_chr8_24436026_24514565 | 24504443 | TA | T | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00323.hp2 others(119): Show |
a0001a0003a0005others(2): Show | a0001c0001a0001c0003a0001c0011others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(8): Show | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(104): Show |
122 | 360 | 0.3389 | -1 | c.220 others(10): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM7_chr8_24436026_24514565 | 24504755 | AC | A | intron_variant | MODIFIER | HG00733.hp1 HG00738.hp2 HG02145.hp1 others(8): Show |
a0003a0006a0009others(1): Show | a0003c0004a0006c0008a0009c0010others(1): Show | a0003c0004t0005a0006c0008t0005a0009c0010t0008others(1): Show | a0003c0004t0005g0020 a0003c0004t0005g0034 a0003c0004t0005g0165 others(5): Show |
11 | 360 | 0.0306 | -1 | c.220 others(10): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM7_chr8_24436026_24514565 | 24507668 | AT | A | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(191): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0003a0001c0011others(13): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(19): Show | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0009 others(168): Show |
194 | 360 | 0.5389 | -1 | c.226 others(9): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM7_chr8_24436026_24514565 | 24513860 | CA | C | downstream_gene_variant | MODIFIER | HG02572.hp1 HG02886.hp1 HG02970.hp1 others(1): Show |
a0003 | a0003c0004 | a0003c0004t0001 | a0003c0004t0001g0011 a0003c0004t0001g0074 a0003c0004t0001g0143 |
4 | 360 | 0.0111 | -1 | c.*53 others(6): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 4296 | chr8 | TogoVar | |||||||
ADAM8_chr10_133257423_133281868 | 133262018 | CG | C | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00323.hp1 HG00323.hp2 others(283): Show |
a0001a0002a0003others(20): Show | a0001c0001a0001c0002a0001c0013others(26): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(28): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(122): Show |
286 | 386 | 0.7409 | -1 | c.*11 others(6): Show |
ADAM8 | ENSG00000151651.16 | transcript | ENST00000445355.8 | protein_coding | 404 | chr10 | TogoVar | |||||||
ADAM8_chr10_133257423_133281868 | 133264058 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(243): Show |
a0001a0002a0003others(17): Show | a0001c0001a0001c0013a0001c0028others(21): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(24): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(92): Show |
246 | 386 | 0.6373 | -1 | c.232 others(9): Show |
ADAM8 | ENSG00000151651.16 | transcript | ENST00000445355.8 | protein_coding | 21/22 | chr10 | TogoVar | |||||||
ADAM8_chr10_133257423_133281868 | 133265063 | GC | G | intron_variant | MODIFIER | HG02109.hp2 HG03195.hp1 NA18975.hp2 others(1): Show |
a0001a0004 | a0001c0001a0004c0005 | a0001c0001t0001a0004c0005t0002 | a0001c0001t0001g0026 a0004c0005t0002g0037 |
4 | 386 | 0.0104 | -1 | c.232 others(10): Show |
ADAM8 | ENSG00000151651.16 | transcript | ENST00000445355.8 | protein_coding | 21/22 | chr10 | TogoVar | |||||||
ADAM8_chr10_133257423_133281868 | 133278777 | CA | C | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp2 others(338): Show |
a0001a0003a0004others(23): Show | a0001c0001a0001c0002a0001c0007others(33): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0005others(38): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0004 others(154): Show |
341 | 386 | 0.8834 | -1 | c.-19 others(6): Show |
ADAM8 | ENSG00000151651.16 | transcript | ENST00000445355.8 | protein_coding | 1910 | chr10 | TogoVar | |||||||
ADAM8_chr10_133257423_133281868 | 133278819 | TC | T | upstream_gene_variant | MODIFIER | HG01516.hp1 HG01517.hp2 NA20752.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0001 | 3 | 386 | 0.0078 | -1 | c.-20 others(6): Show |
ADAM8 | ENSG00000151651.16 | transcript | ENST00000445355.8 | protein_coding | 1952 | chr10 | TogoVar | |||||||
ADAM9_chr8_38991973_39110261 | 38992303 | CA | C | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00639.hp1 HG00639.hp2 others(86): Show |
a0001a0002a0003 | a0001c0001a0001c0003a0001c0006others(3): Show | a0001c0001t0001a0001c0003t0001a0001c0006t0001others(3): Show | a0001c0001t0001g0017 a0001c0001t0001g0018 a0001c0001t0001g0019 others(86): Show |
89 | 332 | 0.2681 | -1 | c.-47 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 4669 | chr8 | TogoVar | |||||||
ADAM9_chr8_38991973_39110261 | 38992486 | CA | C | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00280.hp1 HG00438.hp1 others(132): Show |
a0001a0003a0004 | a0001c0001a0001c0003a0001c0006others(3): Show | a0001c0001t0001a0001c0003t0001a0001c0006t0001others(3): Show | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(132): Show |
135 | 332 | 0.4066 | -1 | c.-45 others(6): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 4486 | chr8 | TogoVar | |||||||
ADAM9_chr8_38991973_39110261 | 38998396 | AT | A | intron_variant | MODIFIER | HG00099.hp2 HG00323.hp1 HG00621.hp1 others(103): Show |
a0001a0005 | a0001c0001a0005c0008 | a0001c0001t0001a0005c0008t0001 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(103): Show |
106 | 332 | 0.3193 | -1 | c.97+ others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 38999328 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(245): Show |
a0001a0003a0004 | a0001c0001a0001c0003a0001c0006others(3): Show | a0001c0001t0001a0001c0001t0004a0001c0003t0001others(4): Show | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(245): Show |
248 | 332 | 0.7470 | -1 | c.97+ others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39002033 | TA | T | intron_variant | MODIFIER | HG00323.hp2 HG01255.hp2 HG01978.hp1 others(14): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0105 a0001c0001t0001g0106 a0001c0001t0001g0107 others(14): Show |
17 | 332 | 0.0512 | -1 | c.97+ others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39002312 | CT | C | intron_variant | MODIFIER | HG02055.hp2 HG03130.hp1 NA18948.hp2 others(7): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003 | a0001c0001t0001g0033 a0001c0001t0001g0034 a0001c0001t0001g0036 others(7): Show |
10 | 332 | 0.0301 | -1 | c.97+ others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39003225 | TG | T | intron_variant | MODIFIER | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
a0002 | a0002c0002a0002c0010 | a0002c0002t0002a0002c0010t0002 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(11): Show |
14 | 332 | 0.0422 | -1 | c.98- others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 1/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39009895 | TG | T | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00323.hp1 others(132): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0001c0007others(4): Show | a0001c0001t0001a0001c0003t0001a0001c0007t0001others(4): Show | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0019 others(132): Show |
135 | 332 | 0.4066 | -1 | c.196 others(9): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39013505 | CT | C | intron_variant | MODIFIER | HG00323.hp1 HG00639.hp1 HG00735.hp2 others(12): Show |
a0001 | a0001c0001a0001c0003 | a0001c0001t0001a0001c0003t0001 | a0001c0001t0001g0048 a0001c0001t0001g0112 a0001c0001t0001g0126 others(12): Show |
15 | 332 | 0.0452 | -1 | c.255 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39020892 | TA | T | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(274): Show |
a0001a0002a0003others(2): Show | a0001c0001a0001c0003a0001c0006others(6): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(8): Show | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(274): Show |
277 | 332 | 0.8343 | -1 | c.673 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 7/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39028365 | TA | T | intron_variant | MODIFIER | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
a0001a0005 | a0001c0001a0005c0008 | a0001c0001t0001a0005c0008t0001 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(30): Show |
33 | 332 | 0.0994 | -1 | c.113 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39030679 | CT | C | intron_variant | MODIFIER | HG00733.hp2 HG00738.hp2 HG01069.hp1 others(14): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0047 others(14): Show |
17 | 332 | 0.0512 | -1 | c.113 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39036373 | TC | T | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(165): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0003a0001c0006others(4): Show | a0001c0001t0001a0001c0003t0001a0001c0006t0001others(4): Show | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(165): Show |
168 | 332 | 0.5060 | -1 | c.113 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39037050 | CT | C | intron_variant | MODIFIER | HG00438.hp1 HG00639.hp2 HG00673.hp1 others(74): Show |
a0001a0003a0005 | a0001c0001a0003c0004a0005c0008 | a0001c0001t0001a0003c0004t0001a0005c0008t0001 | a0001c0001t0001g0016 a0001c0001t0001g0018 a0001c0001t0001g0025 others(74): Show |
77 | 332 | 0.2319 | -1 | c.113 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39037082 | AG | A | intron_variant | MODIFIER | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(86): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(86): Show |
89 | 332 | 0.2681 | -1 | c.113 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | chr8 | TogoVar | |||||||
ADAM9_chr8_38991973_39110261 | 39041495 | TC | T | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(132): Show |
a0001a0003a0004 | a0001c0001a0001c0003a0001c0006others(3): Show | a0001c0001t0001a0001c0003t0001a0001c0006t0001others(3): Show | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(132): Show |
135 | 332 | 0.4066 | -1 | c.113 others(9): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39046775 | AT | A | intron_variant | MODIFIER | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(11): Show |
a0002 | a0002c0002a0002c0010 | a0002c0002t0002a0002c0010t0002 | a0002c0002t0002g0130 a0002c0002t0002g0187 a0002c0002t0002g0188 others(11): Show |
14 | 332 | 0.0422 | -1 | c.130 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39048998 | GT | G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(163): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0003a0001c0006others(4): Show | a0001c0001t0001a0001c0001t0004a0001c0003t0001others(5): Show | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(163): Show |
166 | 332 | 0.5000 | -1 | c.130 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39050452 | CT | C | intron_variant | MODIFIER | HG00639.hp2 HG03704.hp1 NA18948.hp2 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0034 a0001c0001t0001g0038 a0001c0001t0001g0039 others(4): Show |
7 | 332 | 0.0211 | -1 | c.130 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39050830 | GT | G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(213): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0001c0006others(5): Show | a0001c0001t0001a0001c0001t0003a0001c0003t0001others(6): Show | a0001c0001t0001g0003 a0001c0001t0001g0006 a0001c0001t0001g0007 others(213): Show |
216 | 332 | 0.6506 | -1 | c.130 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39054602 | GA | G | intron_variant | MODIFIER | HG00621.hp1 HG01255.hp1 HG01258.hp1 others(33): Show |
a0001a0005 | a0001c0001a0005c0008 | a0001c0001t0001a0005c0008t0001 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(33): Show |
36 | 332 | 0.1084 | -1 | c.139 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39056380 | GT | G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(131): Show |
a0001a0003a0004 | a0001c0001a0001c0003a0001c0006others(3): Show | a0001c0001t0001a0001c0003t0001a0001c0006t0001others(3): Show | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(131): Show |
134 | 332 | 0.4036 | -1 | c.159 others(9): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39065659 | CA | C | intron_variant | MODIFIER | HG00438.hp1 HG00438.hp2 HG00639.hp2 others(117): Show |
a0001a0005 | a0001c0001a0005c0008 | a0001c0001t0001a0005c0008t0001 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0008 others(117): Show |
120 | 332 | 0.3615 | -1 | c.159 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39068675 | CA | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(56): Show |
a0001a0004 | a0001c0001a0001c0003a0004c0005 | a0001c0001t0001a0001c0003t0001a0004c0005t0001 | a0001c0001t0001g0017 a0001c0001t0001g0023 a0001c0001t0001g0032 others(56): Show |
59 | 332 | 0.1777 | -1 | c.159 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39069979 | TA | T | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(170): Show |
a0001a0003a0004others(1): Show | a0001c0001a0001c0003a0001c0006others(4): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(6): Show | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(170): Show |
173 | 332 | 0.5211 | -1 | c.159 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39070152 | CA | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(250): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0003a0001c0006others(5): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(7): Show | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(250): Show |
253 | 332 | 0.7621 | -1 | c.159 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39071465 | CT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(129): Show |
a0001a0003a0004 | a0001c0001a0001c0003a0001c0006others(3): Show | a0001c0001t0001a0001c0003t0001a0001c0006t0001others(3): Show | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(129): Show |
132 | 332 | 0.3976 | -1 | c.169 others(8): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39074903 | CT | C | intron_variant | MODIFIER | HG00639.hp2 HG02055.hp2 HG02647.hp2 others(3): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0004 | a0001c0001t0001g0009 a0001c0001t0001g0143 a0001c0001t0001g0240 others(3): Show |
6 | 332 | 0.0181 | -1 | c.169 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 15/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39078362 | CA | C | intron_variant | MODIFIER | HG00323.hp2 HG01070.hp1 HG01074.hp1 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0030 a0001c0001t0001g0040 a0001c0001t0001g0046 others(5): Show |
8 | 332 | 0.0241 | -1 | c.188 others(9): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39085597 | CA | C | intron_variant | MODIFIER | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
a0001a0005 | a0001c0001a0005c0008 | a0001c0001t0001a0005c0008t0001 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(30): Show |
33 | 332 | 0.0994 | -1 | c.206 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39086163 | TG | T | intron_variant | MODIFIER | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
a0001a0005 | a0001c0001a0005c0008 | a0001c0001t0001a0005c0008t0001 | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(30): Show |
33 | 332 | 0.0994 | -1 | c.206 others(10): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | TogoVar | |||||||
ADAM9_chr8_38991973_39110261 | 39091514 | GC | G | intron_variant | MODIFIER | HG00673.hp1 HG01109.hp1 HG01256.hp1 others(37): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(37): Show |
40 | 332 | 0.1205 | -1 | c.229 others(9): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar |