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 | 39247778 | GT | G | intron_variant | MODIFIER | HG00639.hp2 HG00735.hp2 HG01175.hp1 others(16): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0001c0001t0002a0002c0003t0001 | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0182 others(16): Show |
19 | 257 | 0.0739 | -1 | c.190 others(10): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39247895 | CT | C | intron_variant | MODIFIER | HG02055.hp1 HG02257.hp2 HG02258.hp2 others(17): Show |
a0002a0003a0004others(4): Show | a0002c0003a0003c0004a0004c0007others(4): Show | a0002c0003t0001a0003c0004t0001a0003c0004t0002others(5): Show | a0002c0003t0001g0150 a0003c0004t0001g0133 a0003c0004t0001g0134 others(17): Show |
20 | 257 | 0.0778 | -1 | c.190 others(10): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39251378 | CA | C | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(98): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0002a0002c0003others(9): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(12): Show | a0001c0001t0001g0248 a0001c0002t0001g0145 a0001c0002t0001g0147 others(97): Show |
101 | 257 | 0.3930 | -1 | c.190 others(10): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39252405 | CA | C | intron_variant | MODIFIER | HG02723.hp1 HG03209.hp1 NA18522.hp1 |
a0005 | a0005c0006 | a0005c0006t0001 | a0005c0006t0001g0143 a0005c0006t0001g0215 a0005c0006t0001g0221 |
3 | 257 | 0.0117 | -1 | c.190 others(10): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39254225 | CT | C | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(85): Show |
a0001a0002a0005others(4): Show | a0001c0001a0001c0002a0002c0003others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(9): Show | a0001c0001t0001g0248 a0001c0001t0002g0028 a0001c0002t0001g0145 others(84): Show |
88 | 257 | 0.3424 | -1 | c.190 others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 17/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39257157 | GT | G | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(77): Show |
a0001a0002a0009others(1): Show | a0001c0001a0001c0002a0002c0003others(3): Show | a0001c0001t0001a0001c0002t0001a0001c0002t0002others(5): Show | a0001c0001t0001g0248 a0001c0002t0001g0145 a0001c0002t0001g0147 others(76): Show |
80 | 257 | 0.3113 | -1 | c.200 others(8): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 18/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39258395 | TA | T | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(119): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0002a0002c0003others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(15): Show | a0001c0001t0001g0148 a0001c0001t0001g0176 a0001c0001t0001g0209 others(118): Show |
122 | 257 | 0.4747 | -1 | c.216 others(10): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39262204 | GT | G | intron_variant | MODIFIER | HG02257.hp2 HG02258.hp2 HG02615.hp2 others(8): Show |
a0003a0011 | a0003c0004a0011c0012 | a0003c0004t0001a0003c0004t0002a0011c0012t0001 | a0003c0004t0001g0133 a0003c0004t0001g0134 a0003c0004t0001g0135 others(8): Show |
11 | 257 | 0.0428 | -1 | c.216 others(10): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 19/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39270991 | AT | A | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(74): Show |
a0001a0002a0009others(1): Show | a0001c0002a0002c0005a0009c0016others(1): Show | a0001c0002t0001a0001c0002t0002a0002c0005t0001others(3): Show | a0001c0002t0001g0145 a0001c0002t0001g0147 a0001c0002t0001g0161 others(73): Show |
77 | 257 | 0.2996 | -1 | c.220 others(8): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39271460 | CA | C | intron_variant | MODIFIER | HG00438.hp2 HG00735.hp1 HG00738.hp2 others(48): Show |
a0001a0002 | a0001c0001a0002c0003 | a0001c0001t0001a0001c0001t0002a0002c0003t0001others(1): Show | a0001c0001t0001g0002 a0001c0001t0001g0148 a0001c0001t0001g0149 others(47): Show |
51 | 257 | 0.1984 | -1 | c.220 others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39271539 | CA | C | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(89): Show |
a0001a0002a0009others(1): Show | a0001c0001a0001c0002a0002c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(6): Show | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0182 others(88): Show |
92 | 257 | 0.3580 | -1 | c.220 others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39272101 | GA | G | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(248): Show |
a0001a0002a0003others(11): Show | a0001c0001a0001c0002a0002c0003others(13): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(19): Show | a0001c0001t0001g0002 a0001c0001t0001g0003 a0001c0001t0001g0004 others(246): Show |
251 | 257 | 0.9767 | -1 | c.220 others(10): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39273803 | AT | A | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(73): Show |
a0001a0002a0009others(1): Show | a0001c0002a0002c0005a0009c0016others(1): Show | a0001c0002t0001a0001c0002t0002a0002c0005t0001others(3): Show | a0001c0002t0001g0145 a0001c0002t0001g0147 a0001c0002t0001g0161 others(72): Show |
76 | 257 | 0.2957 | -1 | c.220 others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39274018 | GT | G | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(115): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0002a0002c0003others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(15): Show | a0001c0001t0001g0148 a0001c0001t0001g0176 a0001c0001t0001g0209 others(114): Show |
118 | 257 | 0.4591 | -1 | c.220 others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 20/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39276297 | GA | G | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00408.hp1 others(76): Show |
a0001a0002a0009others(1): Show | a0001c0002a0002c0003a0002c0005others(2): Show | a0001c0002t0001a0001c0002t0002a0002c0003t0001others(4): Show | a0001c0002t0001g0145 a0001c0002t0001g0147 a0001c0002t0001g0161 others(75): Show |
79 | 257 | 0.3074 | -1 | c.227 others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39281013 | AC | A | intron_variant | MODIFIER | HG03225.hp1 HG03486.hp1 NA20300.hp2 |
a0002a0005 | a0002c0003a0005c0006 | a0002c0003t0001a0005c0006t0001 | a0002c0003t0001g0164 a0002c0003t0001g0165 a0005c0006t0001g0222 |
3 | 257 | 0.0117 | -1 | c.228 others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 22/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39283411 | TA | T | intron_variant | MODIFIER | HG00280.hp2 HG02895.hp2 NA19074.hp1 others(2): Show |
a0001a0002 | a0001c0001a0001c0002a0002c0003 | a0001c0001t0001a0001c0001t0002a0001c0002t0002others(1): Show | a0001c0001t0001g0157 a0001c0001t0002g0079 a0001c0001t0002g0080 others(2): Show |
5 | 257 | 0.0195 | -1 | c.231 others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 23/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39283771 | CT | C | intron_variant | MODIFIER | HG02895.hp2 HG02896.hp1 HG02897.hp2 others(5): Show |
a0001a0002a0003 | a0001c0002a0002c0003a0002c0005others(1): Show | a0001c0002t0002a0002c0003t0001a0002c0005t0002others(1): Show | a0001c0002t0002g0090 a0002c0003t0001g0150 a0002c0003t0001g0156 others(5): Show |
8 | 257 | 0.0311 | -1 | c.235 others(9): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 24/24 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM32_chr8_39102734_39289917 | 39285476 | AC | A | downstream_gene_variant | MODIFIER | HG02717.hp2 HG02886.hp2 HG03471.hp2 others(1): Show |
a0004 | a0004c0007 | a0004c0007t0001 | a0004c0007t0001g0153 a0004c0007t0001g0154 a0004c0007t0001g0155 others(1): Show |
4 | 257 | 0.0156 | -1 | c.*67 others(5): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 560 | chr8 | TogoVar | |||||||
ADAM32_chr8_39102734_39289917 | 39285625 | GT | G | downstream_gene_variant | MODIFIER | HG00099.hp1 HG00408.hp2 HG01169.hp2 others(12): Show |
a0001a0002a0005 | a0001c0001a0001c0002a0002c0003others(2): Show | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(3): Show | a0001c0001t0001g0170 a0001c0001t0001g0174 a0001c0001t0002g0020 others(12): Show |
15 | 257 | 0.0584 | -1 | c.*82 others(5): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 709 | chr8 | TogoVar | |||||||
ADAM32_chr8_39102734_39289917 | 39285660 | CG | C | downstream_gene_variant | MODIFIER | HG00639.hp1 HG00639.hp2 HG00642.hp1 others(26): Show |
a0001a0009 | a0001c0001a0001c0002a0009c0016 | a0001c0001t0001a0001c0001t0002a0001c0002t0001others(2): Show | a0001c0001t0001g0178 a0001c0001t0001g0179 a0001c0001t0001g0201 others(26): Show |
29 | 257 | 0.1128 | -1 | c.*86 others(5): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 744 | chr8 | TogoVar | |||||||
ADAM32_chr8_39102734_39289917 | 39286739 | CT | C | downstream_gene_variant | MODIFIER | HG00735.hp1 HG01943.hp1 HG02015.hp2 others(2): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0002t0001 | a0001c0001t0001g0252 a0001c0001t0002g0019 a0001c0001t0002g0022 others(2): Show |
5 | 257 | 0.0195 | -1 | c.*19 others(6): Show |
ADAM32 | ENSG00000197140.15 | transcript | ENST00000379907.9 | protein_coding | 1823 | chr8 | TogoVar | |||||||
ADAM33_chr20_3662975_3687010 | 3666741 | CT | C | downstream_gene_variant | MODIFIER | HG00140.hp2 HG00323.hp1 HG00673.hp1 others(32): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0006a0001c0037others(7): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0015others(11): Show | a0001c0001t0001g0273 a0001c0001t0003g0268 a0001c0001t0003g0326 others(30): Show |
35 | 462 | 0.0758 | -1 | c.*22 others(6): Show |
ADAM33 | ENSG00000149451.19 | transcript | ENST00000356518.7 | protein_coding | 1233 | chr20 | TogoVar | |||||||
ADAM33_chr20_3662975_3687010 | 3671098 | TG | T | frameshift_variant | HIGH | NA18956.hp1 | a0021 | a0021c0038 | a0021c0038t0001 | a0021c0038t0001g0061 | 1 | 462 | 0.0022 | -1 | c.214 others(5): Show |
p.Pro others(5): Show |
ADAM33 | ENSG00000149451.19 | transcript | ENST00000356518.7 | protein_coding | 19/22 | 2153/3436 | 2147/2442 | 716/813 | chr20 | TogoVar | |||
ADAM33_chr20_3662975_3687010 | 3671423 | TG | T | frameshift_variant | HIGH | NA19055.hp1 | a0028 | a0028c0027 | a0028c0027t0008 | a0028c0027t0008g0240 | 1 | 462 | 0.0022 | -1 | c.197 others(5): Show |
p.His others(5): Show |
ADAM33 | ENSG00000149451.19 | transcript | ENST00000356518.7 | protein_coding | 17/22 | 1984/3436 | 1978/2442 | 660/813 | chr20 | TogoVar | |||
ADAM33_chr20_3662975_3687010 | 3672276 | AG | A | frameshift_variant | HIGH | NA19054.hp1 | a0027 | a0027c0041 | a0027c0041t0003 | a0027c0041t0003g0175 | 1 | 462 | 0.0022 | -1 | c.145 others(5): Show |
p.Pro others(5): Show |
ADAM33 | ENSG00000149451.19 | transcript | ENST00000356518.7 | protein_coding | 14/22 | 1460/3436 | 1454/2442 | 485/813 | chr20 | TogoVar | |||
ADAM33_chr20_3662975_3687010 | 3673441 | TG | T | frameshift_variant | HIGH | NA19076.hp2 | a0032 | a0032c0052 | a0032c0052t0034 | a0032c0052t0034g0350 | 1 | 462 | 0.0022 | -1 | c.104 others(5): Show |
p.His others(5): Show |
ADAM33 | ENSG00000149451.19 | transcript | ENST00000356518.7 | protein_coding | 11/22 | 1051/3436 | 1045/2442 | 349/813 | chr20 | TogoVar | |||
ADAM33_chr20_3662975_3687010 | 3674548 | TC | T | frameshift_variant | HIGH | NA18968.hp1 | a0023 | a0023c0028 | a0023c0028t0001 | a0023c0028t0001g0327 | 1 | 462 | 0.0022 | -1 | c.555 others(4): Show |
p.Asn others(5): Show |
ADAM33 | ENSG00000149451.19 | transcript | ENST00000356518.7 | protein_coding | 6/22 | 561/3436 | 555/2442 | 185/813 | chr20 | TogoVar | |||
ADAM33_chr20_3662975_3687010 | 3674665 | TG | T | frameshift_variant | HIGH | NA19055.hp1 | a0028 | a0028c0027 | a0028c0027t0008 | a0028c0027t0008g0240 | 1 | 462 | 0.0022 | -1 | c.438 others(4): Show |
p.Ser others(5): Show |
ADAM33 | ENSG00000149451.19 | transcript | ENST00000356518.7 | protein_coding | 6/22 | 444/3436 | 438/2442 | 146/813 | chr20 | TogoVar | |||
ADAM33_chr20_3662975_3687010 | 3676418 | CT | C | intron_variant | MODIFIER | HG00140.hp2 HG00733.hp2 HG02257.hp2 others(7): Show |
a0001 | a0001c0001a0001c0012 | a0001c0001t0001a0001c0001t0003a0001c0001t0013others(1): Show | a0001c0001t0001g0014 a0001c0001t0001g0060 a0001c0001t0001g0194 others(6): Show |
10 | 462 | 0.0217 | -1 | c.254 others(8): Show |
ADAM33 | ENSG00000149451.19 | transcript | ENST00000356518.7 | protein_coding | 3/21 | chr20 | TogoVar | |||||||
ADAM33_chr20_3662975_3687010 | 3679136 | CT | C | intron_variant | MODIFIER | HG00597.hp1 HG01516.hp2 HG01517.hp1 others(14): Show |
a0001a0003a0004others(5): Show | a0001c0001a0001c0006a0001c0030others(7): Show | a0001c0001t0001a0001c0001t0003a0001c0006t0006others(9): Show | a0001c0001t0001g0068 a0001c0001t0001g0111 a0001c0001t0001g0368 others(14): Show |
17 | 462 | 0.0368 | -1 | c.177 others(8): Show |
ADAM33 | ENSG00000149451.19 | transcript | ENST00000356518.7 | protein_coding | 2/21 | chr20 | TogoVar | |||||||
ADAM33_chr20_3662975_3687010 | 3683125 | CT | C | upstream_gene_variant | MODIFIER | HG00140.hp1 HG00323.hp1 HG01069.hp1 others(48): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0006a0001c0015others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(18): Show | a0001c0001t0001g0001 a0001c0001t0001g0003 a0001c0001t0001g0006 others(42): Show |
51 | 462 | 0.1104 | -1 | c.-11 others(6): Show |
ADAM33 | ENSG00000149451.19 | transcript | ENST00000356518.7 | protein_coding | 1116 | chr20 | TogoVar | |||||||
ADAM33_chr20_3662975_3687010 | 3683702 | CT | C | upstream_gene_variant | MODIFIER | HG00323.hp2 HG00408.hp1 HG00558.hp1 others(87): Show |
a0001a0002a0003others(7): Show | a0001c0001a0001c0006a0001c0012others(19): Show | a0001c0001t0001a0001c0001t0003a0001c0001t0004others(33): Show | a0001c0001t0001g0029 a0001c0001t0001g0030 a0001c0001t0001g0053 others(77): Show |
90 | 462 | 0.1948 | -1 | c.-16 others(6): Show |
ADAM33 | ENSG00000149451.19 | transcript | ENST00000356518.7 | protein_coding | 1693 | chr20 | TogoVar | |||||||
ADAM33_chr20_3662975_3687010 | 3683956 | AG | A | upstream_gene_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(457): Show |
a0001a0002a0003others(30): Show | a0001c0001a0001c0006a0001c0012others(51): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(95): Show | a0001c0001t0001g0001 a0001c0001t0001g0002 a0001c0001t0001g0003 others(378): Show |
460 | 462 | 0.9957 | -1 | c.-19 others(6): Show |
ADAM33 | ENSG00000149451.19 | transcript | ENST00000356518.7 | protein_coding | 1947 | chr20 | TogoVar | |||||||
ADAM7_chr8_24436026_24514565 | 24440582 | AC | A | upstream_gene_variant | MODIFIER | HG01243.hp1 HG02055.hp2 HG02258.hp1 others(7): Show |
a0001a0009a0011 | a0001c0001a0009c0010a0011c0009 | a0001c0001t0004a0009c0010t0008a0011c0009t0004 | a0001c0001t0004g0155 a0001c0001t0004g0156 a0001c0001t0004g0157 others(7): Show |
10 | 360 | 0.0278 | -1 | c.-52 others(5): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 443 | chr8 | TogoVar | |||||||
ADAM7_chr8_24436026_24514565 | 24446727 | GA | G | intron_variant | MODIFIER | HG02572.hp1 HG02970.hp1 HG03139.hp2 |
a0003 | a0003c0004 | a0003c0004t0001 | a0003c0004t0001g0011 a0003c0004t0001g0074 |
3 | 360 | 0.0083 | -1 | c.157 others(8): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 2/21 | chr8 | TogoVar | |||||||
ADAM7_chr8_24436026_24514565 | 24453259 | TC | T | intron_variant | MODIFIER | HG02004.hp2 HG02818.hp2 HG02976.hp2 others(2): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0027 a0001c0001t0001g0206 a0001c0001t0001g0207 others(1): Show |
5 | 360 | 0.0139 | -1 | c.233 others(9): Show |
ADAM7 | ENSG00000069206.15 | transcript | ENST00000175238.10 | protein_coding | 3/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | ||||||
ADAM7_chr8_24436026_24514565 | 24456632 | AT | A | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp1 others(333): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0003a0002c0002others(14): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(25): Show | a0001c0001t0001g0004 a0001c0001t0001g0005 a0001c0001t0001g0006 others(293): Show |
336 | 360 | 0.9333 | -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 | 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 |