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 |
---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
ADAM22_chr7_87929251_88207889 | 88029866 | G | GT | intron_variant | MODIFIER | HG00140.hp2 HG00280.hp2 HG00544.hp1 others(28): Show |
a0001a0002a0011 | a0001c0001a0002c0002a0002c0011others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0012others(8): Show | a0001c0001t0001g0013a0001c0001t0001g0016a0001c0001t0001g0080others(28): Show | 31 | 230 | 0.1348 | 1 | c.324 others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88039460 | A | AT | intron_variant | MODIFIER | HG01192.hp1 HG03041.hp1 |
a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0011 | a0001c0001t0002g0095a0001c0001t0011g0230 | 2 | 230 | 0.0087 | 1 | c.324 others(20): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | TogoVar | ||||||
ADAM22_chr7_87929251_88207889 | 88039462 | A | AT | intron_variant | MODIFIER | HG00544.hp2 HG00597.hp2 HG00738.hp1 others(30): Show |
a0001a0002a0008others(3): Show | a0001c0001a0001c0019a0002c0002others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(12): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0026others(30): Show | 33 | 230 | 0.1435 | 1 | c.324 others(20): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | TogoVar | ||||||
ADAM22_chr7_87929251_88207889 | 88039464 | A | AT | intron_variant | MODIFIER | HG00099.hp2 HG01071.hp2 HG01074.hp1 others(9): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0008others(3): Show | a0001c0001t0001g0062a0001c0001t0001g0081a0001c0001t0001g0083others(9): Show | 12 | 230 | 0.0522 | 1 | c.324 others(20): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | chr7 | TogoVar | ||||||
ADAM22_chr7_87929251_88207889 | 88043484 | C | CA | intron_variant | MODIFIER | HG00099.hp2 HG00544.hp2 HG00597.hp2 others(62): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0018a0001c0019others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(23): Show | a0001c0001t0001g0003a0001c0001t0001g0004a0001c0001t0001g0022others(62): Show | 65 | 230 | 0.2826 | 1 | c.324 others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88050221 | T | TA | intron_variant | MODIFIER | HG00423.hp1 HG00544.hp1 HG00597.hp1 others(55): Show |
a0001a0002a0003others(5): Show | a0001c0001a0001c0018a0002c0002others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(22): Show | a0001c0001t0001g0003a0001c0001t0001g0018a0001c0001t0001g0022others(55): Show | 58 | 230 | 0.2522 | 1 | c.324 others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88050484 | C | CA | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(154): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0012a0001c0014others(14): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(47): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0013others(154): Show | 157 | 230 | 0.6826 | 1 | c.324 others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88052341 | C | CA | intron_variant | MODIFIER | HG00099.hp1 HG00323.hp1 HG02630.hp2 others(5): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0014others(1): Show | a0001c0001t0001g0035a0001c0001t0001g0062a0001c0001t0001g0079others(5): Show | 8 | 230 | 0.0348 | 1 | c.324 others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88055365 | C | CA | intron_variant | MODIFIER | HG00423.hp1 HG02723.hp2 NA18980.hp2 others(6): Show |
a0001a0004a0005others(1): Show | a0001c0001a0004c0004a0005c0005others(1): Show | a0001c0001t0001a0004c0004t0001a0004c0004t0002others(3): Show | a0001c0001t0001g0062a0004c0004t0001g0074a0004c0004t0002g0067others(6): Show | 9 | 230 | 0.0391 | 1 | c.324 others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88060766 | C | CA | intron_variant | MODIFIER | HG01884.hp2 HG02027.hp1 HG02145.hp2 others(12): Show |
a0001a0002a0003others(1): Show | a0001c0001a0002c0002a0003c0003others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(9): Show | a0001c0001t0001g0141a0001c0001t0002g0017a0001c0001t0003g0032others(12): Show | 15 | 230 | 0.0652 | 1 | c.324 others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88061839 | C | CT | intron_variant | MODIFIER | HG02683.hp2 HG03195.hp1 NA18970.hp2 others(2): Show |
a0002a0003a0006 | a0002c0002a0003c0003a0006c0006 | a0002c0002t0001a0002c0002t0002a0003c0003t0009others(1): Show | a0002c0002t0001g0215a0002c0002t0002g0213a0002c0002t0002g0227others(2): Show | 5 | 230 | 0.0217 | 1 | c.324 others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88071391 | A | AT | intron_variant | MODIFIER | HG00140.hp1 HG02257.hp2 HG02572.hp2 others(15): Show |
a0001a0002a0003 | a0001c0001a0001c0019a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(11): Show | a0001c0001t0001g0116a0001c0001t0001g0155a0001c0001t0001g0189others(15): Show | 18 | 230 | 0.0783 | 1 | c.324 others(9): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 3/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88088510 | G | GA | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00280.hp1 others(76): Show |
a0001a0002a0003others(6): Show | a0001c0001a0001c0012a0002c0002others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(27): Show | a0001c0001t0001g0012a0001c0001t0001g0035a0001c0001t0001g0039others(76): Show | 79 | 230 | 0.3435 | 1 | c.390 others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88092959 | T | TC | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(116): Show |
a0001a0002a0003others(9): Show | a0001c0001a0001c0014a0002c0002others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(34): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(116): Show | 119 | 230 | 0.5174 | 1 | c.391 others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88096474 | G | GT | intron_variant | MODIFIER | HG00099.hp2 HG00735.hp1 HG01074.hp2 others(8): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0002a0001c0001t0005a0001c0001t0007others(5): Show | a0001c0001t0002g0157a0001c0001t0002g0173a0001c0001t0005g0053others(8): Show | 11 | 230 | 0.0478 | 1 | c.391 others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88097151 | C | CT | intron_variant | MODIFIER | HG01515.hp1 HG02055.hp1 HG02071.hp2 others(4): Show |
a0001a0002a0005 | a0001c0001a0001c0014a0002c0002others(1): Show | a0001c0001t0001a0001c0001t0007a0001c0001t0026others(3): Show | a0001c0001t0001g0065a0001c0001t0001g0119a0001c0001t0007g0059others(4): Show | 7 | 230 | 0.0304 | 1 | c.391 others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88097620 | T | TA | intron_variant | MODIFIER | HG01517.hp2 HG02109.hp2 HG02145.hp2 others(10): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0002a0001c0001t0006a0002c0002t0001others(6): Show | a0001c0001t0002g0064a0001c0001t0006g0228a0002c0002t0001g0207others(10): Show | 13 | 230 | 0.0565 | 1 | c.391 others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88101217 | A | AG | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0014a0001c0018others(14): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(47): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(168): Show | 171 | 230 | 0.7435 | 1 | c.391 others(9): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88104798 | A | AT | intron_variant | MODIFIER | HG00140.hp1 HG00423.hp2 HG01192.hp2 others(22): Show |
a0002a0003a0009others(1): Show | a0002c0002a0003c0003a0009c0009others(1): Show | a0002c0002t0001a0003c0003t0001a0003c0003t0002others(7): Show | a0002c0002t0001g0190a0003c0003t0001g0007a0003c0003t0001g0009others(22): Show | 25 | 230 | 0.1087 | 1 | c.391 others(9): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88107198 | C | CT | intron_variant | MODIFIER | HG00597.hp1 HG00597.hp2 HG01433.hp1 others(18): Show |
a0001a0002a0003others(3): Show | a0001c0001a0002c0002a0003c0003others(3): Show | a0001c0001t0001a0001c0001t0002a0002c0002t0001others(9): Show | a0001c0001t0001g0018a0001c0001t0001g0035a0001c0001t0001g0149others(18): Show | 21 | 230 | 0.0913 | 1 | c.391 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88107368 | A | AT | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp1 HG00140.hp2 others(168): Show |
a0001a0002a0003others(10): Show | a0001c0001a0001c0014a0001c0018others(14): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(47): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(168): Show | 171 | 230 | 0.7435 | 1 | c.391 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88107758 | A | AT | intron_variant | MODIFIER | HG01081.hp1 HG02572.hp1 HG02809.hp2 others(3): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0017others(1): Show | a0001c0001t0001g0151a0001c0001t0002g0027a0001c0001t0002g0047others(3): Show | 6 | 230 | 0.0261 | 1 | c.391 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 4/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88109732 | G | GA | intron_variant | MODIFIER | HG00099.hp2 HG01074.hp2 HG02055.hp1 others(3): Show |
a0001a0002a0003 | a0001c0001a0002c0002a0003c0003 | a0001c0001t0001a0001c0001t0002a0002c0002t0001others(2): Show | a0001c0001t0001g0065a0001c0001t0001g0079a0001c0001t0002g0157others(3): Show | 6 | 230 | 0.0261 | 1 | c.473 others(9): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88110589 | C | CG | intron_variant | MODIFIER | HG02055.hp2 HG02257.hp1 HG02486.hp1 others(9): Show |
a0001 | a0001c0001a0001c0014 | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(6): Show | a0001c0001t0001g0147a0001c0001t0001g0149a0001c0001t0001g0152others(9): Show | 12 | 230 | 0.0522 | 1 | c.473 others(9): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88113119 | C | CT | intron_variant | MODIFIER | HG00423.hp2 HG02055.hp1 HG02109.hp2 others(8): Show |
a0001a0003a0007 | a0001c0001a0003c0003a0007c0007 | a0001c0001t0001a0001c0001t0003a0001c0001t0006others(5): Show | a0001c0001t0001g0065a0001c0001t0001g0136a0001c0001t0003g0133others(8): Show | 11 | 230 | 0.0478 | 1 | c.474 others(9): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 5/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88114719 | T | TA | intron_variant | MODIFIER | HG00140.hp1 HG00423.hp2 HG01884.hp1 others(22): Show |
a0001a0003a0009 | a0001c0001a0003c0003a0009c0009 | a0001c0001t0001a0003c0003t0001a0003c0003t0002others(6): Show | a0001c0001t0001g0055a0001c0001t0001g0166a0003c0003t0001g0007others(22): Show | 25 | 230 | 0.1087 | 1 | c.537 others(7): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 6/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88117693 | A | AT | intron_variant | MODIFIER | HG00741.hp2 HG02055.hp1 HG02145.hp1 others(6): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(3): Show | a0001c0001t0001g0039a0001c0001t0001g0062a0001c0001t0001g0065others(6): Show | 9 | 230 | 0.0391 | 1 | c.607 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88119773 | G | GC | intron_variant | MODIFIER | HG02717.hp2 HG02965.hp2 HG03209.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0014a0001c0001t0022 | a0001c0001t0001g0189a0001c0001t0014g0068a0001c0001t0022g0066 | 3 | 230 | 0.0130 | 1 | c.607 others(9): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 7/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88130273 | A | AT | intron_variant | MODIFIER | HG00099.hp2 HG00140.hp2 HG00280.hp2 others(111): Show |
a0001a0002a0004others(8): Show | a0001c0001a0001c0014a0002c0002others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(32): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(111): Show | 114 | 230 | 0.4957 | 1 | c.754 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 9/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88132136 | G | GT | intron_variant | MODIFIER | HG00639.hp1 HG00738.hp2 HG02257.hp2 others(7): Show |
a0001 | a0001c0001a0001c0018 | a0001c0001t0001a0001c0001t0003a0001c0001t0005others(2): Show | a0001c0001t0001g0060a0001c0001t0001g0113a0001c0001t0001g0115others(7): Show | 10 | 230 | 0.0435 | 1 | c.992 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 11/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88134259 | A | AT | intron_variant | MODIFIER | HG01243.hp2 HG02109.hp1 HG02723.hp1 others(1): Show |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0030 | a0001c0001t0001g0044a0001c0001t0001g0062a0001c0001t0001g0079others(1): Show | 4 | 230 | 0.0174 | 1 | c.107 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 12/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88148928 | A | AT | intron_variant | MODIFIER | HG02027.hp1 NA18988.hp2 NA19009.hp2 others(2): Show |
a0001a0002 | a0001c0001a0002c0002 | a0001c0001t0001a0001c0001t0002a0002c0002t0002 | a0001c0001t0001g0003a0001c0001t0001g0141a0001c0001t0002g0109others(2): Show | 5 | 230 | 0.0217 | 1 | c.148 others(8): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 17/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88157635 | G | GT | intron_variant | MODIFIER | HG00140.hp1 HG00280.hp2 HG00423.hp1 others(116): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0012a0001c0014others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(36): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(116): Show | 119 | 230 | 0.5174 | 1 | c.190 others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88161193 | G | GA | intron_variant | MODIFIER | HG00099.hp1 HG00140.hp1 HG00280.hp2 others(120): Show |
a0001a0002a0003others(8): Show | a0001c0001a0001c0012a0001c0014others(10): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(37): Show | a0001c0001t0001g0001a0001c0001t0001g0003a0001c0001t0001g0004others(120): Show | 123 | 230 | 0.5348 | 1 | c.190 others(10): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 22/31 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | |||||
ADAM22_chr7_87929251_88207889 | 88199312 | T | TC | 3_prime_UTR_variant | MODIFIER | HG00423.hp2 HG00738.hp1 HG01074.hp2 others(12): Show |
a0001a0002a0003others(4): Show | a0001c0001a0002c0002a0003c0003others(4): Show | a0001c0001t0004a0001c0001t0008a0001c0001t0011others(7): Show | a0001c0001t0004g0005a0001c0001t0004g0131a0001c0001t0008g0087others(12): Show | 15 | 230 | 0.0652 | 1 | c.*28 others(6): Show |
ADAM22 | ENSG00000008277.15 | transcript | ENST00000413139.2 | protein_coding | 32/32 | 2826 | INFO_REALIGN_3_PRIME | chr7 | TogoVar | ||||
ADAM23_chr2_206438532_206626127 | 206441595 | C | CA | upstream_gene_variant | MODIFIER | HG02486.hp2 HG02630.hp1 HG02647.hp2 others(5): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001 | a0001c0001t0001g0003a0001c0001t0001g0036a0001c0001t0001g0069others(5): Show | 8 | 358 | 0.0224 | 1 | c.-22 others(12): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 1936 | chr2 | TogoVar | ||||||
ADAM23_chr2_206438532_206626127 | 206442937 | A | AC | upstream_gene_variant | MODIFIER | HG00323.hp1 HG00544.hp1 HG00609.hp2 others(29): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0018a0001c0001t0021others(4): Show | a0001c0001t0001g0190a0001c0001t0001g0267a0001c0001t0001g0268others(29): Show | 32 | 358 | 0.0894 | 1 | c.-93 others(10): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 594 | chr2 | TogoVar | ||||||
ADAM23_chr2_206438532_206626127 | 206444998 | A | AC | intron_variant | MODIFIER | HG00099.hp2 HG00738.hp1 HG02559.hp1 others(12): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(4): Show | a0001c0001t0001g0324a0001c0001t0001g0331a0001c0001t0001g0334others(12): Show | 15 | 358 | 0.0419 | 1 | c.215 others(8): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 1/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206460105 | C | CT | intron_variant | MODIFIER | HG00673.hp2 HG01496.hp2 HG02083.hp1 others(23): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0006others(3): Show | a0001c0001t0001g0197a0001c0001t0001g0203a0001c0001t0001g0208others(23): Show | 26 | 358 | 0.0726 | 1 | c.432 others(10): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206461063 | C | CT | intron_variant | MODIFIER | HG00438.hp2 HG02486.hp2 HG02647.hp2 others(8): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0020others(4): Show | a0001c0001t0001g0118a0001c0001t0001g0119a0001c0001t0001g0260others(8): Show | 11 | 358 | 0.0307 | 1 | c.432 others(10): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206464572 | C | CA | intron_variant | MODIFIER | HG02145.hp1 HG02451.hp1 HG02683.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0002t0001a0001c0002t0002 | a0001c0001t0001g0070a0001c0002t0001g0092a0001c0002t0002g0007others(4): Show | 7 | 358 | 0.0196 | 1 | c.433 others(10): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206472615 | G | GA | intron_variant | MODIFIER | HG00099.hp1 HG00099.hp2 HG00140.hp2 others(250): Show |
a0001a0003a0004 | a0001c0001a0001c0002a0001c0005others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(36): Show | a0001c0001t0001g0002a0001c0001t0001g0003a0001c0001t0001g0004others(244): Show | 253 | 358 | 0.7067 | 1 | c.433 others(9): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206474011 | C | CA | intron_variant | MODIFIER | HG02258.hp1 HG03195.hp2 HG06807.hp1 others(4): Show |
a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0181a0001c0001t0001g0309a0001c0001t0001g0316others(4): Show | 7 | 358 | 0.0196 | 1 | c.433 others(9): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206474025 | C | CA | intron_variant | MODIFIER | HG01243.hp1 HG01952.hp2 HG02895.hp2 others(14): Show |
a0001a0003 | a0001c0001a0001c0002a0003c0004 | a0001c0001t0001a0001c0001t0002a0001c0001t0013others(5): Show | a0001c0001t0001g0036a0001c0001t0001g0069a0001c0001t0001g0085others(14): Show | 17 | 358 | 0.0475 | 1 | c.433 others(9): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206477880 | T | TA | intron_variant | MODIFIER | HG01257.hp2 HG01433.hp2 HG03942.hp2 others(3): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0002t0002others(1): Show | a0001c0001t0001g0217a0001c0001t0001g0232a0001c0001t0002g0233others(3): Show | 6 | 358 | 0.0168 | 1 | c.433 others(9): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206477897 | A | AT | intron_variant | MODIFIER | HG00738.hp2 HG01361.hp1 HG01517.hp1 others(7): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0020a0001c0002t0003others(1): Show | a0001c0001t0001g0286a0001c0001t0020g0329a0001c0002t0003g0093others(7): Show | 10 | 358 | 0.0279 | 1 | c.433 others(18): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 2/25 | chr2 | TogoVar | ||||||
ADAM23_chr2_206438532_206626127 | 206486340 | C | CT | intron_variant | MODIFIER | HG02630.hp1 HG02896.hp1 HG02897.hp1 others(4): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0026a0001c0002t0002others(1): Show | a0001c0001t0001g0264a0001c0001t0001g0265a0001c0001t0026g0299others(4): Show | 7 | 358 | 0.0196 | 1 | c.509 others(9): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206493394 | C | CG | intron_variant | MODIFIER | HG00642.hp1 HG01515.hp2 HG01517.hp2 |
a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0041 | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0041g0028 | 3 | 358 | 0.0084 | 1 | c.509 others(10): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206500993 | C | CT | intron_variant | MODIFIER | HG00558.hp1 HG01975.hp2 HG02055.hp2 others(21): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(5): Show | a0001c0001t0001g0006a0001c0001t0001g0170a0001c0001t0001g0185others(20): Show | 24 | 358 | 0.0670 | 1 | c.509 others(10): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar | |||||
ADAM23_chr2_206438532_206626127 | 206508655 | C | CA | intron_variant | MODIFIER | HG00609.hp1 HG00642.hp1 HG01069.hp2 others(39): Show |
a0001 | a0001c0001a0001c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0004others(7): Show | a0001c0001t0001g0027a0001c0001t0001g0029a0001c0001t0001g0248others(39): Show | 42 | 358 | 0.1173 | 1 | c.510 others(10): Show |
ADAM23 | ENSG00000114948.13 | transcript | ENST00000264377.8 | protein_coding | 3/25 | INFO_REALIGN_3_PRIME | chr2 | TogoVar |