regionname | pos | ref | alt | annotation | impact | samples | ahapids | achapids | acthapids | actghapids | 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 | 24502028 | TAA | T | intron_variant | MODIFIER | HG00099.hp2 HG00280.hp2 HG00323.hp1 others(93): Show |
a0002a0003a0004others(3): Show | a0002c0003a0002c0007a0002c0012others(9): Show | a0002c0003t0001a0002c0003t0012a0002c0003t0015others(11): Show | a0002c0003t0001g0001a0002c0003t0001g0012a0002c0003t0001g0013others(82): Show | 96 | 360 | 0.2667 | -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(230): Show |
a0001a0002a0003others(12): Show | a0001c0001a0001c0002a0001c0004others(29): Show | a0001c0001t0002a0001c0002t0001a0001c0002t0004others(34): Show | a0001c0001t0002g0046a0001c0001t0002g0047a0001c0001t0002g0048others(201): Show | 233 | 360 | 0.6472 | -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(161): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0002a0001c0004others(16): Show | a0001c0001t0002a0001c0001t0011a0001c0002t0001others(21): Show | a0001c0001t0002g0003a0001c0001t0002g0028a0001c0001t0002g0029others(138): Show | 164 | 360 | 0.4556 | -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(224): Show |
a0001a0002a0003others(12): Show | a0001c0002a0001c0004a0001c0008others(28): Show | a0001c0002t0001a0001c0002t0004a0001c0002t0013others(33): Show | a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0019others(195): Show | 227 | 360 | 0.6306 | -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 |
a0001a0003a0016 | a0001c0002a0003c0033a0016c0015 | a0001c0002t0004a0003c0033t0004a0016c0015t0004 | a0001c0002t0004g0155a0001c0002t0004g0156a0001c0002t0004g0157others(7): Show | 10 | 360 | 0.0278 | -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 |
a0001a0005a0007 | a0001c0001a0005c0009a0007c0010 | a0001c0001t0001a0005c0009t0001a0007c0010t0001 | a0001c0001t0001g0013a0001c0001t0001g0074a0001c0001t0001g0097others(4): Show | 9 | 386 | 0.0233 | -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 | a0001c0001t0001g0282a0001c0001t0004g0332a0002c0002t0002g0130others(7): Show | 10 | 332 | 0.0301 | -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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(18): Show | 21 | 332 | 0.0633 | -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 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(31): Show | 34 | 332 | 0.1024 | -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 | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(8): Show | 11 | 332 | 0.0331 | -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 |
a0001a0003a0006 | a0001c0001a0001c0003a0001c0006others(3): Show | a0001c0001t0001a0001c0001t0003a0001c0003t0001others(4): Show | a0001c0001t0001g0017a0001c0001t0001g0019a0001c0001t0001g0020others(121): Show | 124 | 332 | 0.3735 | -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 | a0001c0001t0001g0298a0002c0002t0002g0130a0002c0002t0002g0187others(12): Show | 15 | 332 | 0.0452 | -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 | a0001c0001t0001g0148a0001c0001t0001g0149a0001c0001t0001g0150others(1): Show | 4 | 332 | 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 | 39044956 | ATG | A | intron_variant | MODIFIER | HG01928.hp1 HG01952.hp2 HG03710.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0083a0001c0001t0001g0257a0001c0001t0001g0311 | 3 | 332 | 0.0090 | -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 | a0001c0001t0001g0250a0001c0001t0001g0251a0001c0001t0001g0308 | 3 | 332 | 0.0090 | -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 |
a0001a0004 | a0001c0001a0004c0008 | a0001c0001t0001a0004c0008t0001 | a0001c0001t0001g0042a0001c0001t0001g0072a0001c0001t0001g0074others(8): Show | 11 | 332 | 0.0331 | -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 | a0001c0001t0001g0043a0001c0001t0001g0045a0001c0001t0001g0089others(1): Show | 4 | 332 | 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 | 39045172 | GTA | G | intron_variant | MODIFIER | NA18961.hp2 NA18965.hp2 NA18977.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0058a0001c0001t0001g0063a0001c0001t0001g0065others(4): Show | 7 | 332 | 0.0211 | -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 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(28): Show | 31 | 332 | 0.0934 | -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 | a0001c0001t0001g0027a0001c0001t0001g0028a0001c0001t0001g0029others(24): Show | 27 | 332 | 0.0813 | -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 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(17): Show | 20 | 332 | 0.0602 | -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 |
a0001a0004 | a0001c0001a0004c0008 | a0001c0001t0001a0004c0008t0001 | a0001c0001t0001g0082a0001c0001t0001g0113a0001c0001t0001g0114others(7): Show | 10 | 332 | 0.0301 | -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 | a0001c0001t0001g0061a0001c0001t0001g0065a0001c0001t0001g0100others(1): Show | 4 | 332 | 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 | a0001c0001t0001g0015a0001c0001t0001g0049a0001c0001t0001g0050others(1): Show | 4 | 332 | 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 | a0001c0001t0001g0044a0001c0001t0001g0046a0001c0001t0001g0047others(15): Show | 18 | 332 | 0.0542 | -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 | a0001c0001t0001g0043a0001c0001t0001g0044a0001c0001t0001g0045others(28): Show | 31 | 332 | 0.0934 | -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 | a0001c0001t0001g0025a0001c0001t0001g0026a0001c0001t0001g0027others(85): Show | 88 | 332 | 0.2651 | -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 | a0001c0001t0001g0136a0002c0002t0002g0130a0002c0002t0002g0187others(12): Show | 15 | 332 | 0.0452 | -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 | a0001c0001t0001g0005a0001c0001t0001g0028a0001c0001t0001g0080others(5): Show | 8 | 332 | 0.0241 | -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 | a0001c0001t0001g0254a0001c0001t0001g0262a0001c0001t0001g0263others(4): Show | 7 | 332 | 0.0211 | -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 | a0001c0001t0001g0072a0001c0001t0001g0109a0002c0002t0002g0130others(13): Show | 16 | 332 | 0.0482 | -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 |
a0001a0003a0006 | a0001c0001a0001c0003a0001c0006others(3): Show | a0001c0001t0001a0001c0003t0001a0001c0006t0001others(3): Show | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(131): Show | 134 | 332 | 0.4036 | -2 | c.159 others(21): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM9_chr8_38991973_39110261 | 39065659 | CAA | C | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00280.hp1 others(127): Show |
a0001a0003a0006 | a0001c0001a0001c0003a0001c0006others(3): Show | a0001c0001t0001a0001c0003t0001a0001c0006t0001others(3): Show | a0001c0001t0001g0016a0001c0001t0001g0017a0001c0001t0001g0018others(127): Show | 130 | 332 | 0.3916 | -2 | c.159 others(21): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM9_chr8_38991973_39110261 | 39068675 | CAA | C | intron_variant | MODIFIER | HG00738.hp1 HG01074.hp2 HG01081.hp1 others(47): Show |
a0001a0005 | a0001c0001a0001c0003a0001c0006others(2): Show | a0001c0001t0001a0001c0003t0001a0001c0006t0001others(2): Show | a0001c0001t0001g0001a0001c0001t0001g0002a0001c0001t0001g0003others(47): Show | 50 | 332 | 0.1506 | -2 | c.159 others(21): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM9_chr8_38991973_39110261 | 39069979 | TAA | T | intron_variant | MODIFIER | HG00323.hp1 HG00438.hp2 HG00639.hp2 others(92): Show |
a0001a0002 | a0001c0001a0002c0002a0002c0010 | a0001c0001t0001a0002c0002t0002a0002c0010t0002 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0030others(92): Show | 95 | 332 | 0.2861 | -2 | c.159 others(21): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 14/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM9_chr8_38991973_39110261 | 39083787 | CAG | C | intron_variant | MODIFIER | HG00735.hp1 HG01255.hp1 HG01257.hp2 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0042a0001c0001t0001g0072a0001c0001t0001g0078others(1): Show | 4 | 332 | 0.0121 | -2 | c.206 others(19): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 18/21 | chr8 | TogoVar | ||||||
ADAM9_chr8_38991973_39110261 | 39092331 | TAC | T | intron_variant | MODIFIER | HG00621.hp1 HG00735.hp1 HG01255.hp1 others(30): Show |
a0001a0004 | a0001c0001a0004c0008 | a0001c0001t0001a0004c0008t0001 | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(30): Show | 33 | 332 | 0.0994 | -2 | c.229 others(21): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM9_chr8_38991973_39110261 | 39099875 | GTT | G | intron_variant | MODIFIER | HG01192.hp1 HG01884.hp2 HG02055.hp2 others(11): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0003a0001c0001t0004 | a0001c0001t0001g0020a0001c0001t0001g0024a0001c0001t0001g0030others(11): Show | 14 | 332 | 0.0422 | -2 | c.229 others(21): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 20/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAM9_chr8_38991973_39110261 | 39103406 | ATT | A | intron_variant | MODIFIER | HG02717.hp1 HG02895.hp1 HG02897.hp2 |
a0002 | a0002c0002 | a0002c0002t0002 | a0002c0002t0002g0194a0002c0002t0002g0195a0002c0002t0002g0196 | 3 | 332 | 0.0090 | -2 | c.236 others(19): Show |
ADAM9 | ENSG00000168615.13 | transcript | ENST00000487273.7 | protein_coding | 21/21 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAMDEC1_chr8_24379285_24411013 | 24383205 | TAG | T | upstream_gene_variant | MODIFIER | NA18975.hp2 NA19058.hp1 NA19077.hp1 |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0004a0001c0001t0001g0101 | 3 | 404 | 0.0074 | -2 | c.-12 others(13): Show |
ADAMDEC1 | ENSG00000134028.14 | transcript | ENST00000256412.8 | protein_coding | 1079 | chr8 | TogoVar | ||||||
ADAMDEC1_chr8_24379285_24411013 | 24391673 | CTT | C | intron_variant | MODIFIER | NA18945.hp1 NA18991.hp2 NA19009.hp1 |
a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0096a0001c0001t0004g0097a0001c0001t0004g0098 | 3 | 404 | 0.0074 | -2 | c.89- others(15): Show |
ADAMDEC1 | ENSG00000134028.14 | transcript | ENST00000256412.8 | protein_coding | 1/13 | chr8 | TogoVar | ||||||
ADAMDEC1_chr8_24379285_24411013 | 24400632 | CAT | C | intron_variant | MODIFIER | HG00408.hp1 HG00423.hp1 HG00639.hp1 others(93): Show |
a0001a0003a0004others(1): Show | a0001c0001a0003c0004a0004c0008others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(5): Show | a0001c0001t0001g0004a0001c0001t0001g0010a0001c0001t0001g0018others(40): Show | 96 | 404 | 0.2376 | -2 | c.114 others(19): Show |
ADAMDEC1 | ENSG00000134028.14 | transcript | ENST00000256412.8 | protein_coding | 11/13 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAMDEC1_chr8_24379285_24411013 | 24403390 | TTC | T | intron_variant | MODIFIER | HG02451.hp1 HG02809.hp2 HG02922.hp2 others(3): Show |
a0003 | a0003c0004 | a0003c0004t0005 | a0003c0004t0005g0016a0003c0004t0005g0166 | 6 | 404 | 0.0149 | -2 | c.132 others(19): Show |
ADAMDEC1 | ENSG00000134028.14 | transcript | ENST00000256412.8 | protein_coding | 12/13 | INFO_REALIGN_3_PRIME | chr8 | TogoVar | |||||
ADAMTS10_chr19_8575240_8615715 | 8579971 | AAT | A | downstream_gene_variant | MODIFIER | HG00609.hp1 HG00609.hp2 HG00621.hp1 others(39): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0003a0003c0004others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(6): Show | a0001c0001t0001g0005a0001c0001t0001g0046a0001c0001t0001g0048others(38): Show | 42 | 384 | 0.1094 | -2 | c.*92 others(11): Show |
ADAMTS10 | ENSG00000142303.14 | transcript | ENST00000597188.6 | protein_coding | 268 | chr19 | TogoVar | ||||||
ADAMTS10_chr19_8575240_8615715 | 8581130 | CTT | C | intron_variant | MODIFIER | HG00408.hp1 HG00423.hp1 HG00544.hp1 others(95): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0013others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0005a0001c0001t0001g0006a0001c0001t0001g0007others(91): Show | 98 | 384 | 0.2552 | -2 | c.320 others(19): Show |
ADAMTS10 | ENSG00000142303.14 | transcript | ENST00000597188.6 | protein_coding | 25/25 | chr19 | TogoVar | ||||||
ADAMTS10_chr19_8575240_8615715 | 8582668 | ATT | A | intron_variant | MODIFIER | HG00408.hp2 HG00621.hp2 HG02257.hp1 others(12): Show |
a0001a0004a0006others(1): Show | a0001c0001a0004c0006a0006c0008others(1): Show | a0001c0001t0001a0001c0001t0009a0004c0006t0004others(3): Show | a0001c0001t0001g0059a0001c0001t0009g0364a0004c0006t0004g0122others(12): Show | 15 | 384 | 0.0391 | -2 | c.320 others(21): Show |
ADAMTS10 | ENSG00000142303.14 | transcript | ENST00000597188.6 | protein_coding | 25/25 | chr19 | TogoVar | ||||||
ADAMTS10_chr19_8575240_8615715 | 8584154 | CAA | C | intron_variant | MODIFIER | HG00741.hp1 HG01070.hp2 HG01071.hp1 others(10): Show |
a0001a0002a0008 | a0001c0001a0001c0002a0002c0005others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0002t0001others(4): Show | a0001c0001t0001g0323a0001c0001t0001g0327a0001c0001t0001g0330others(10): Show | 13 | 384 | 0.0339 | -2 | c.320 others(19): Show |
ADAMTS10 | ENSG00000142303.14 | transcript | ENST00000597188.6 | protein_coding | 25/25 | chr19 | TogoVar | ||||||
ADAMTS10_chr19_8575240_8615715 | 8587930 | CAA | C | intron_variant | MODIFIER | HG00408.hp2 HG00621.hp2 HG02145.hp1 others(5): Show |
a0001a0006a0012others(1): Show | a0001c0001a0001c0010a0006c0008others(2): Show | a0001c0001t0002a0001c0010t0001a0006c0008t0006others(2): Show | a0001c0001t0002g0295a0001c0010t0001g0157a0006c0008t0006g0103others(5): Show | 8 | 384 | 0.0208 | -2 | c.215 others(21): Show |
ADAMTS10 | ENSG00000142303.14 | transcript | ENST00000597188.6 | protein_coding | 18/25 | chr19 | TogoVar | ||||||
ADAMTS10_chr19_8575240_8615715 | 8592242 | CAG | C | intron_variant | MODIFIER | HG00639.hp1 HG00673.hp1 HG00733.hp1 others(52): Show |
a0001a0002a0005others(1): Show | a0001c0001a0001c0002a0001c0009others(3): Show | a0001c0001t0002a0001c0002t0001a0001c0002t0002others(10): Show | a0001c0001t0002g0128a0001c0002t0001g0003a0001c0002t0001g0051others(51): Show | 55 | 384 | 0.1432 | -2 | c.158 others(19): Show |
ADAMTS10 | ENSG00000142303.14 | transcript | ENST00000597188.6 | protein_coding | 13/25 | chr19 | TogoVar | ||||||
ADAMTS10_chr19_8575240_8615715 | 8598565 | ATT | A | intron_variant | MODIFIER | HG00140.hp2 HG00741.hp1 HG01070.hp2 others(48): Show |
a0001a0002a0004others(4): Show | a0001c0001a0001c0002a0001c0011others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(17): Show | a0001c0001t0001g0134a0001c0001t0001g0304a0001c0001t0001g0317others(47): Show | 51 | 384 | 0.1328 | -2 | c.811 others(19): Show |
ADAMTS10 | ENSG00000142303.14 | transcript | ENST00000597188.6 | protein_coding | 6/25 | chr19 | TogoVar |