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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ADAM32_chr8_39102734_39289917 | 39285625 | GTT | G | downstream_gene_variant | MODIFIER | HG00621.hp2 HG00642.hp1 HG01433.hp1 others(10): Show |
a0001a0002a0005others(1): Show | a0001c0001a0001c0002a0002c0003others(3): Show | a0001c0001t0002a0001c0002t0001a0001c0002t0002others(4): Show | a0001c0001t0002g0015 a0001c0001t0002g0019 a0001c0002t0001g0188 others(10): Show |
13 | 45 | 0.2889 | -2 | c.*82 others(11): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 709 | chr8 | TogoVar | |||||||
ADAM33_chr20_3662975_3687010 | 3666741 | CTT | C | downstream_gene_variant | MODIFIER | HG00423.hp2 HG00609.hp1 HG01099.hp1 others(54): Show |
a0001a0002a0006others(5): Show | a0001c0001a0001c0012a0001c0033others(7): Show | a0001c0001t0005a0001c0001t0006a0001c0001t0011others(13): Show | a0001c0001t0005g0027 a0001c0001t0005g0045 a0001c0001t0005g0162 others(50): Show |
57 | 178 | 0.3202 | -2 | c.*22 others(13): Show |
ADAM33 | ENSG00000149451.19 | transcript | ENST00000356518.7 | protein_coding | 1233 | chr20 | TogoVar | |||||||
ADAM33_chr20_3662975_3687010 | 3683125 | CTT | C | upstream_gene_variant | MODIFIER | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(89): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0006a0001c0012others(17): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(32): Show | a0001c0001t0001g0030 a0001c0001t0001g0031 a0001c0001t0001g0192 others(79): Show |
92 | 363 | 0.2534 | -2 | c.-11 others(13): Show |
ADAM33 | ENSG00000149451.19 | transcript | ENST00000356518.7 | protein_coding | 1116 | chr20 | TogoVar | |||||||
ADAM33_chr20_3662975_3687010 | 3683702 | CTT | C | upstream_gene_variant | MODIFIER | HG02622.hp1 HG02965.hp1 HG03486.hp2 others(3): Show |
a0001a0003a0006 | a0001c0001a0001c0006a0001c0012others(2): Show | a0001c0001t0001a0001c0006t0006a0001c0012t0006others(2): Show | a0001c0001t0001g0251 a0001c0006t0006g0265 a0001c0012t0006g0264 others(3): Show |
6 | 346 | 0.0173 | -2 | c.-17 others(13): Show |
ADAM33 | ENSG00000149451.19 | transcript | ENST00000356518.7 | protein_coding | 1693 | chr20 | TogoVar | |||||||
ADAM7_chr8_24436026_24514565 | 24438273 | TTA | T | upstream_gene_variant | MODIFIER | HG01069.hp2 HG01071.hp2 HG01433.hp2 others(11): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0002c0002t0001 | a0001c0001t0001g0007 a0001c0001t0001g0024 a0001c0001t0001g0055 others(9): Show |
14 | 284 | 0.0493 | -2 | c.-28 others(13): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2752 | chr8 | TogoVar | |||||||
ADAM7_chr8_24436026_24514565 | 24438304 | TAG | T | upstream_gene_variant | MODIFIER | HG01993.hp1 HG02129.hp1 HG02572.hp1 others(9): Show |
a0001a0002a0003others(2): Show | a0001c0001a0002c0002a0003c0004others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(4): Show | a0001c0001t0001g0185 a0001c0001t0001g0204 a0001c0001t0002g0270 others(8): Show |
12 | 113 | 0.1062 | -2 | c.-28 others(13): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2721 | chr8 | TogoVar | |||||||
ADAM7_chr8_24436026_24514565 | 24447937 | AAC | A | intron_variant | MODIFIER | HG00099.hp2 HG00408.hp2 HG00438.hp2 others(55): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0003a0002c0002others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0003t0003others(8): Show | a0001c0001t0001g0028 a0001c0001t0001g0119 a0001c0001t0001g0191 others(49): Show |
58 | 120 | 0.4833 | -2 | c.233 others(17): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM7_chr8_24436026_24514565 | 24449275 | TAA | T | intron_variant | MODIFIER | HG01167.hp1 HG01169.hp2 HG02055.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0026 a0001c0001t0001g0202 |
3 | 358 | 0.0084 | -2 | c.233 others(19): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM7_chr8_24436026_24514565 | 24457861 | TGA | T | intron_variant | MODIFIER | HG01256.hp1 HG01981.hp2 HG01993.hp1 |
a0002 | a0002c0002 | a0002c0002t0001a0002c0002t0015 | a0002c0002t0001g0013 a0002c0002t0015g0139 |
3 | 358 | 0.0084 | -2 | c.234 others(19): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM7_chr8_24436026_24514565 | 24457863 | AGT | A | intron_variant | MODIFIER | HG01243.hp1 HG02055.hp2 HG02258.hp2 others(15): Show |
a0001a0005 | a0001c0001a0005c0006 | a0001c0001t0004a0005c0006t0001 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(13): Show |
18 | 140 | 0.1286 | -2 | c.234 others(19): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM7_chr8_24436026_24514565 | 24460648 | TAA | T | intron_variant | MODIFIER | HG00642.hp1 HG01106.hp1 HG01361.hp1 others(9): Show |
a0001a0016 | a0001c0001a0016c0021 | a0001c0001t0001a0001c0001t0002a0016c0021t0008 | a0001c0001t0001g0010 a0001c0001t0001g0051 a0001c0001t0001g0052 others(8): Show |
12 | 358 | 0.0335 | -2 | c.234 others(19): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM7_chr8_24436026_24514565 | 24460751 | ATG | A | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(127): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0003a0002c0002others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(13): Show | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(109): Show |
130 | 358 | 0.3631 | -2 | c.234 others(19): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM7_chr8_24436026_24514565 | 24484802 | CTT | C | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp1 HG00280.hp2 others(136): Show |
a0001a0002a0003others(5): Show | a0001c0001a0002c0002a0002c0007others(8): Show | a0001c0001t0001a0002c0002t0001a0002c0002t0012others(10): Show | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(114): Show |
139 | 278 | 0.5000 | -2 | c.876 others(17): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 9/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM7_chr8_24436026_24514565 | 24490774 | ATC | A | intron_variant | MODIFIER | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(4): Show |
8 | 358 | 0.0223 | -2 | c.126 others(17): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM7_chr8_24436026_24514565 | 24495722 | AAG | A | intron_variant | MODIFIER | HG03453.hp1 NA19043.hp1 NA21309.hp2 |
a0003 | a0003c0004 | a0003c0004t0005 | a0003c0004t0005g0023 a0003c0004t0005g0181 |
3 | 358 | 0.0084 | -2 | c.184 others(21): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 16/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM7_chr8_24436026_24514565 | 24499797 | TAC | T | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp1 HG00438.hp1 others(56): Show |
a0001a0003a0007others(2): Show | a0001c0001a0001c0003a0001c0011others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(6): Show | a0001c0001t0001g0006 a0001c0001t0001g0007 a0001c0001t0001g0034 others(49): Show |
59 | 193 | 0.3057 | -2 | c.192 others(19): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM7_chr8_24436026_24514565 | 24499836 | TCA | T | intron_variant | MODIFIER | HG02451.hp2 HG02809.hp1 HG02895.hp2 others(6): Show |
a0005a0016 | a0005c0006a0016c0021 | a0005c0006t0001a0016c0021t0008 | a0005c0006t0001g0009 a0005c0006t0001g0040 a0005c0006t0001g0041 others(5): Show |
9 | 356 | 0.0253 | -2 | c.192 others(19): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 17/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM7_chr8_24436026_24514565 | 24501612 | ATT | A | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(91): Show |
a0002a0003a0004others(3): Show | a0002c0002a0002c0007a0002c0014others(6): Show | a0002c0002t0001a0002c0002t0012a0002c0002t0015others(8): Show | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(80): Show |
94 | 337 | 0.2789 | -2 | c.220 others(17): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM7_chr8_24436026_24514565 | 24502028 | TAA | T | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(92): Show |
a0002a0003a0004others(3): Show | a0002c0002a0002c0007a0002c0014others(6): Show | a0002c0002t0001a0002c0002t0012a0002c0002t0015others(8): Show | a0002c0002t0001g0001 a0002c0002t0001g0013 a0002c0002t0001g0014 others(81): Show |
95 | 358 | 0.2654 | -2 | c.220 others(19): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM7_chr8_24436026_24514565 | 24502919 | GAA | G | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(229): Show |
a0001a0002a0003others(12): Show | a0001c0001a0001c0003a0001c0011others(17): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(26): Show | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(198): Show |
232 | 358 | 0.6480 | -2 | c.220 others(21): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM7_chr8_24436026_24514565 | 24506753 | GCA | G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(160): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0003a0002c0002others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0007others(17): Show | a0001c0001t0001g0005 a0001c0001t0001g0182 a0001c0001t0001g0183 others(137): Show |
163 | 256 | 0.6367 | -2 | c.220 others(19): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM7_chr8_24436026_24514565 | 24507644 | TCA | T | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00280.hp1 others(223): Show |
a0001a0002a0003others(12): Show | a0001c0001a0001c0003a0001c0011others(17): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0007others(25): Show | a0001c0001t0001g0003 a0001c0001t0001g0005 a0001c0001t0001g0006 others(192): Show |
226 | 358 | 0.6313 | -2 | c.226 others(19): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM7_chr8_24436026_24514565 | 24509199 | CAG | C | 3_prime_UTR_variant | MODIFIER | HG01243.hp1 HG02055.hp2 HG02486.hp2 others(7): Show |
a0001a0003a0011 | a0001c0001a0003c0004a0011c0009 | a0001c0001t0004a0003c0004t0004a0011c0009t0004 | a0001c0001t0004g0020 a0001c0001t0004g0155 a0001c0001t0004g0156 others(6): Show |
10 | 358 | 0.0279 | -2 | c.*65 others(11): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 22/22 | 657 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM8_chr10_133257423_133281868 | 133264058 | CTT | C | intron_variant | MODIFIER | HG01168.hp2 HG01192.hp1 HG01975.hp2 others(6): Show |
a0001a0005a0006 | a0001c0001a0005c0009a0006c0010 | a0001c0001t0001a0005c0009t0001a0006c0010t0001 | a0001c0001t0001g0009 a0001c0001t0001g0090 a0001c0001t0001g0091 others(3): Show |
9 | 95 | 0.0947 | -2 | c.232 others(19): Show |
ADAM8 | ENSG00000151651.16 | transcript | ENST00000445355.8 | protein_coding | 21/22 | chr10 | TogoVar | |||||||
ADAM9_chr8_38991973_39110261 | 38992303 | CAA | C | upstream_gene_variant | MODIFIER | HG01074.hp2 HG02257.hp1 HG02615.hp2 others(7): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0004a0002c0002t0002 | a0001c0001t0001g0282 a0001c0001t0004g0332 a0002c0002t0002g0130 others(7): Show |
10 | 94 | 0.1064 | -2 | c.-47 others(13): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 4669 | chr8 | TogoVar | |||||||
ADAM9_chr8_38991973_39110261 | 38994851 | ACT | A | upstream_gene_variant | MODIFIER | HG02055.hp2 HG02258.hp1 HG02280.hp1 others(18): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0010 | a0001c0001t0001a0001c0001t0003a0002c0002t0002others(1): Show | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(18): Show |
21 | 330 | 0.0636 | -2 | c.-22 others(13): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2121 | chr8 | TogoVar | |||||||
ADAM9_chr8_38991973_39110261 | 39009895 | TGG | T | intron_variant | MODIFIER | HG00280.hp1 HG02055.hp2 HG02257.hp1 others(31): Show |
a0001a0002a0003others(1): Show | a0001c0001a0001c0006a0002c0002others(3): Show | a0001c0001t0001a0001c0001t0003a0001c0006t0001others(4): Show | a0001c0001t0001g0005 a0001c0001t0001g0006 a0001c0001t0001g0007 others(31): Show |
34 | 139 | 0.2446 | -2 | c.196 others(19): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 2/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39022064 | TTG | T | intron_variant | MODIFIER | HG02055.hp1 HG02257.hp2 HG02559.hp2 others(8): Show |
a0001a0003 | a0001c0001a0003c0004 | a0001c0001t0001a0003c0004t0001 | a0001c0001t0001g0016 a0001c0001t0001g0017 a0001c0001t0001g0018 others(8): Show |
11 | 265 | 0.0415 | -2 | c.744 others(17): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 8/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39037050 | CTT | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(121): Show |
a0001a0003a0004 | a0001c0001a0001c0003a0001c0006others(3): Show | a0001c0001t0001a0001c0001t0003a0001c0003t0001others(4): Show | a0001c0001t0001g0017 a0001c0001t0001g0019 a0001c0001t0001g0020 others(121): Show |
124 | 225 | 0.5511 | -2 | c.113 others(21): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39037441 | AGT | A | intron_variant | MODIFIER | HG01109.hp2 HG02257.hp1 HG02258.hp2 others(12): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0010 | a0001c0001t0001a0002c0002t0002a0002c0010t0002 | a0001c0001t0001g0298 a0002c0002t0002g0130 a0002c0002t0002g0187 others(12): Show |
15 | 322 | 0.0466 | -2 | c.113 others(21): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 11/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39044952 | GTA | G | intron_variant | MODIFIER | HG00280.hp2 HG01256.hp2 HG01361.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0148 a0001c0001t0001g0149 a0001c0001t0001g0150 others(1): Show |
4 | 328 | 0.0122 | -2 | c.130 others(21): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39044956 | ATG | A | intron_variant | MODIFIER | HG01928.hp1 HG01952.hp2 HG03710.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0083 a0001c0001t0001g0257 a0001c0001t0001g0311 |
3 | 314 | 0.0096 | -2 | c.130 others(21): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39045028 | GCA | G | intron_variant | MODIFIER | HG01891.hp1 HG02622.hp2 HG02897.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0250 a0001c0001t0001g0251 a0001c0001t0001g0308 |
3 | 330 | 0.0091 | -2 | c.130 others(21): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | chr8 | TogoVar | |||||||
ADAM9_chr8_38991973_39110261 | 39045135 | CAT | C | intron_variant | MODIFIER | HG00639.hp2 HG00735.hp1 HG01255.hp1 others(8): Show |
a0001a0005 | a0001c0001a0005c0008 | a0001c0001t0001a0005c0008t0001 | a0001c0001t0001g0042 a0001c0001t0001g0072 a0001c0001t0001g0074 others(8): Show |
11 | 310 | 0.0355 | -2 | c.130 others(21): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39045163 | CAT | C | intron_variant | MODIFIER | HG01361.hp1 HG02135.hp1 HG03831.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0043 a0001c0001t0001g0045 a0001c0001t0001g0089 others(1): Show |
4 | 317 | 0.0126 | -2 | c.130 others(21): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39045172 | GTA | G | intron_variant | MODIFIER | NA18961.hp2 NA18965.hp2 NA18977.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0059 a0001c0001t0001g0064 a0001c0001t0001g0065 others(4): Show |
7 | 326 | 0.0215 | -2 | c.130 others(21): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39045191 | CAT | C | intron_variant | MODIFIER | HG00438.hp2 HG00738.hp2 HG01069.hp1 others(28): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0047 others(28): Show |
31 | 326 | 0.0951 | -2 | c.130 others(21): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39045200 | GTA | G | intron_variant | MODIFIER | HG00673.hp1 HG01109.hp1 HG01496.hp1 others(24): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0027 a0001c0001t0001g0028 a0001c0001t0001g0029 others(24): Show |
27 | 293 | 0.0922 | -2 | c.130 others(21): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39045278 | ATG | A | intron_variant | MODIFIER | HG00738.hp2 HG01069.hp1 HG01070.hp1 others(17): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0047 others(17): Show |
20 | 307 | 0.0651 | -2 | c.130 others(21): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39045280 | GTA | G | intron_variant | MODIFIER | HG01884.hp2 HG02622.hp1 HG02683.hp2 others(7): Show |
a0001a0005 | a0001c0001a0005c0008 | a0001c0001t0001a0005c0008t0001 | a0001c0001t0001g0082 a0001c0001t0001g0113 a0001c0001t0001g0114 others(7): Show |
10 | 312 | 0.0321 | -2 | c.130 others(21): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39045409 | TGC | T | intron_variant | MODIFIER | HG02572.hp1 NA18961.hp2 NA18987.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0060 a0001c0001t0001g0064 a0001c0001t0001g0100 others(1): Show |
4 | 330 | 0.0121 | -2 | c.130 others(21): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39045419 | TAC | T | intron_variant | MODIFIER | HG00639.hp2 HG01168.hp2 HG01169.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0014 a0001c0001t0001g0049 a0001c0001t0001g0050 others(1): Show |
4 | 330 | 0.0121 | -2 | c.130 others(21): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39045445 | TAC | T | intron_variant | MODIFIER | HG00639.hp2 HG00738.hp2 HG01069.hp1 others(15): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0044 a0001c0001t0001g0046 a0001c0001t0001g0047 others(15): Show |
18 | 330 | 0.0545 | -2 | c.130 others(21): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39045471 | TAC | T | intron_variant | MODIFIER | HG00438.hp2 HG00639.hp2 HG00738.hp2 others(28): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0043 a0001c0001t0001g0044 a0001c0001t0001g0045 others(28): Show |
31 | 330 | 0.0939 | -2 | c.130 others(21): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39045570 | GTA | G | intron_variant | MODIFIER | HG00438.hp2 HG00639.hp2 HG00673.hp1 others(85): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0025 a0001c0001t0001g0026 a0001c0001t0001g0027 others(85): Show |
88 | 277 | 0.3177 | -2 | c.130 others(21): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39048998 | GTT | G | intron_variant | MODIFIER | HG02257.hp1 HG02258.hp2 HG02451.hp1 others(12): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0010 | a0001c0001t0001a0002c0002t0002a0002c0010t0002 | a0001c0001t0001g0136 a0002c0002t0002g0130 a0002c0002t0002g0187 others(12): Show |
15 | 157 | 0.0955 | -2 | c.130 others(21): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39050830 | GTT | G | intron_variant | MODIFIER | HG01168.hp1 HG02040.hp1 HG02451.hp2 others(5): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0006 a0001c0001t0001g0029 a0001c0001t0001g0080 others(5): Show |
8 | 103 | 0.0777 | -2 | c.130 others(21): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39052530 | CTA | C | intron_variant | MODIFIER | HG02074.hp2 NA18944.hp1 NA18969.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0254 a0001c0001t0001g0262 a0001c0001t0001g0263 others(4): Show |
7 | 330 | 0.0212 | -2 | c.130 others(21): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 12/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39054602 | GAA | G | intron_variant | MODIFIER | HG01257.hp2 HG02257.hp1 HG02258.hp2 others(13): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0010 | a0001c0001t0001a0002c0002t0002a0002c0010t0002 | a0001c0001t0001g0072 a0001c0001t0001g0109 a0002c0002t0002g0130 others(13): Show |
16 | 150 | 0.1067 | -2 | c.139 others(17): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 13/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39057493 | TTG | T | 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 | 330 | 0.4061 | -2 | c.159 others(21): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar |