SNP Links for Gene (Select 414764) - SNP

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Select item 14892259701.

rs1489225970 has merged into rs56342952 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAA>-,AAAAAAA,AAAAAAAAA,AAAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 6:32392535 (GRCh38)
6:32360312 (GRCh37)
Canonical SPDI:: NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAAAAAAAAAAAA,NC_000006.12:32392532:AAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAA
Gene:: HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAA=0./0 (ALFA)
HGVS:: NC_000006.12:g.32392535_32392549del, NC_000006.12:g.32392542_32392549del, NC_000006.12:g.32392544_32392549del, NC_000006.12:g.32392546_32392549del, NC_000006.12:g.32392547_32392549del, NC_000006.12:g.32392548_32392549del, NC_000006.12:g.32392549del, NC_000006.12:g.32392549dup, NC_000006.12:g.32392548_32392549dup, NC_000006.12:g.32392547_32392549dup, NC_000006.12:g.32392546_32392549dup, NC_000006.12:g.32392545_32392549dup, NC_000006.12:g.32392544_32392549dup, NC_000006.12:g.32392543_32392549dup, NC_000006.12:g.32392542_32392549dup, NC_000006.12:g.32392541_32392549dup, NC_000006.12:g.32392540_32392549dup, NC_000006.12:g.32392539_32392549dup, NC_000006.12:g.32392536_32392549dup, NC_000006.12:g.32392535_32392549dup, NC_000006.12:g.32392534_32392549dup, NC_000006.12:g.32392549_32392550insAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.32392549_32392550insAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.32392549_32392550insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.32392549_32392550insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.32392549_32392550insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.32392549_32392550insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.32392549_32392550insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.32392549_32392550insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.32392549_32392550insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.32392549_32392550insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.32392549_32392550insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.32392549_32392550insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.12:g.32392533_32392549A[33]GAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.12:g.32392533_32392549A[33]TAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.12:g.32392533_32392549A[28]GAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.12:g.32392533_32392549A[26]TAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.11:g.32360312_32360326del, NC_000006.11:g.32360319_32360326del, NC_000006.11:g.32360321_32360326del, NC_000006.11:g.32360323_32360326del, NC_000006.11:g.32360324_32360326del, NC_000006.11:g.32360325_32360326del, NC_000006.11:g.32360326del, NC_000006.11:g.32360326dup, NC_000006.11:g.32360325_32360326dup, NC_000006.11:g.32360324_32360326dup, NC_000006.11:g.32360323_32360326dup, NC_000006.11:g.32360322_32360326dup, NC_000006.11:g.32360321_32360326dup, NC_000006.11:g.32360320_32360326dup, NC_000006.11:g.32360319_32360326dup, NC_000006.11:g.32360318_32360326dup, NC_000006.11:g.32360317_32360326dup, NC_000006.11:g.32360316_32360326dup, NC_000006.11:g.32360313_32360326dup, NC_000006.11:g.32360312_32360326dup, NC_000006.11:g.32360311_32360326dup, NC_000006.11:g.32360326_32360327insAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.32360326_32360327insAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.32360326_32360327insAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.32360326_32360327insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.32360326_32360327insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.32360326_32360327insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.32360326_32360327insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.32360326_32360327insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.32360326_32360327insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.32360326_32360327insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.32360326_32360327insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.32360326_32360327insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NC_000006.11:g.32360310_32360326A[33]GAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.11:g.32360310_32360326A[33]TAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.11:g.32360310_32360326A[28]GAAAAAAAAAAAAAAAAAAAAAA[1], NC_000006.11:g.32360310_32360326A[26]TAAAAAAAAAAAAAAAAAAAAA[1], NG_054759.1:g.21333_21347del, NG_054759.1:g.21340_21347del, NG_054759.1:g.21342_21347del, NG_054759.1:g.21344_21347del, NG_054759.1:g.21345_21347del, NG_054759.1:g.21346_21347del, NG_054759.1:g.21347del, NG_054759.1:g.21347dup, NG_054759.1:g.21346_21347dup, NG_054759.1:g.21345_21347dup, NG_054759.1:g.21344_21347dup, NG_054759.1:g.21343_21347dup, NG_054759.1:g.21342_21347dup, NG_054759.1:g.21341_21347dup, NG_054759.1:g.21340_21347dup, NG_054759.1:g.21339_21347dup, NG_054759.1:g.21338_21347dup, NG_054759.1:g.21337_21347dup, NG_054759.1:g.21334_21347dup, NG_054759.1:g.21333_21347dup, NG_054759.1:g.21332_21347dup, NG_054759.1:g.21347_21348insTTTTTTTTTTTTTTTTTTT, NG_054759.1:g.21347_21348insTTTTTTTTTTTTTTTTTTTTT, NG_054759.1:g.21347_21348insTTTTTTTTTTTTTTTTTTTTTTTT, NG_054759.1:g.21347_21348insTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_054759.1:g.21347_21348insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_054759.1:g.21347_21348insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_054759.1:g.21347_21348insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_054759.1:g.21347_21348insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_054759.1:g.21347_21348insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_054759.1:g.21347_21348insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_054759.1:g.21347_21348insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_054759.1:g.21347_21348insTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NG_054759.1:g.21331_21347T[22]CTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_054759.1:g.21331_21347T[22]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_054759.1:g.21331_21347T[22]CTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NG_054759.1:g.21331_21347T[21]ATTTTTTTTTTTTTTTTTTTTTTTTTT[1], NT_113891.3:g.3830640_3830641dup, NT_113891.3:g.3830629_3830641del, NT_113891.3:g.3830636_3830641del, NT_113891.3:g.3830638_3830641del, NT_113891.3:g.3830640_3830641del, NT_113891.3:g.3830641del, NT_113891.3:g.3830641dup, NT_113891.3:g.3830639_3830641dup, NT_113891.3:g.3830638_3830641dup, NT_113891.3:g.3830637_3830641dup, NT_113891.3:g.3830636_3830641dup, NT_113891.3:g.3830635_3830641dup, NT_113891.3:g.3830634_3830641dup, NT_113891.3:g.3830633_3830641dup, NT_113891.3:g.3830632_3830641dup, NT_113891.3:g.3830631_3830641dup, NT_113891.3:g.3830630_3830641dup, NT_113891.3:g.3830629_3830641dup, NT_113891.3:g.3830641_3830642insAAAAAAAAAAAAAAAA, NT_113891.3:g.3830641_3830642insAAAAAAAAAAAAAAAAA, NT_113891.3:g.3830641_3830642insAAAAAAAAAAAAAAAAAA, NT_113891.3:g.3830641_3830642insAAAAAAAAAAAAAAAAAAAAA, NT_113891.3:g.3830641_3830642insAAAAAAAAAAAAAAAAAAAAAAA, NT_113891.3:g.3830641_3830642insAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_113891.3:g.3830641_3830642insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_113891.3:g.3830641_3830642insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_113891.3:g.3830641_3830642insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_113891.3:g.3830641_3830642insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_113891.3:g.3830641_3830642insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_113891.3:g.3830641_3830642insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_113891.3:g.3830641_3830642insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_113891.3:g.3830641_3830642insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_113891.3:g.3830641_3830642insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_113891.3:g.3830627_3830641A[33]GAAAAAAAAAAAAAAAAAAAAAA[1], NT_113891.3:g.3830627_3830641A[33]TAAAAAAAAAAAAAAAAAAAAAA[1], NT_113891.3:g.3830627_3830641A[28]GAAAAAAAAAAAAAAAAAAAAAA[1], NT_113891.3:g.3830627_3830641A[26]TAAAAAAAAAAAAAAAAAAAAA[1], NT_167244.2:g.3724766_3724780del, NT_167244.2:g.3724773_3724780del, NT_167244.2:g.3724775_3724780del, NT_167244.2:g.3724777_3724780del, NT_167244.2:g.3724778_3724780del, NT_167244.2:g.3724779_3724780del, NT_167244.2:g.3724780del, NT_167244.2:g.3724780dup, NT_167244.2:g.3724779_3724780dup, NT_167244.2:g.3724778_3724780dup, NT_167244.2:g.3724777_3724780dup, NT_167244.2:g.3724776_3724780dup, NT_167244.2:g.3724775_3724780dup, NT_167244.2:g.3724774_3724780dup, NT_167244.2:g.3724773_3724780dup, NT_167244.2:g.3724772_3724780dup, NT_167244.2:g.3724771_3724780dup, NT_167244.2:g.3724770_3724780dup, NT_167244.2:g.3724767_3724780dup, NT_167244.2:g.3724766_3724780dup, NT_167244.2:g.3724765_3724780dup, NT_167244.2:g.3724780_3724781insAAAAAAAAAAAAAAAAAAA, NT_167244.2:g.3724780_3724781insAAAAAAAAAAAAAAAAAAAAA, NT_167244.2:g.3724780_3724781insAAAAAAAAAAAAAAAAAAAAAAAA, NT_167244.2:g.3724780_3724781insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167244.2:g.3724780_3724781insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167244.2:g.3724780_3724781insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167244.2:g.3724780_3724781insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167244.2:g.3724780_3724781insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167244.2:g.3724780_3724781insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167244.2:g.3724780_3724781insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167244.2:g.3724780_3724781insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167244.2:g.3724780_3724781insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167244.2:g.3724764_3724780A[33]GAAAAAAAAAAAAAAAAAAAAAA[1], NT_167244.2:g.3724764_3724780A[33]TAAAAAAAAAAAAAAAAAAAAAA[1], NT_167244.2:g.3724764_3724780A[28]GAAAAAAAAAAAAAAAAAAAAAA[1], NT_167244.2:g.3724764_3724780A[26]TAAAAAAAAAAAAAAAAAAAAA[1], NT_167244.1:g.3674682_3674696del, NT_167244.1:g.3674689_3674696del, NT_167244.1:g.3674691_3674696del, NT_167244.1:g.3674693_3674696del, NT_167244.1:g.3674694_3674696del, NT_167244.1:g.3674695_3674696del, NT_167244.1:g.3674696del, NT_167244.1:g.3674696dup, NT_167244.1:g.3674695_3674696dup, NT_167244.1:g.3674694_3674696dup, NT_167244.1:g.3674693_3674696dup, NT_167244.1:g.3674692_3674696dup, NT_167244.1:g.3674691_3674696dup, NT_167244.1:g.3674690_3674696dup, NT_167244.1:g.3674689_3674696dup, NT_167244.1:g.3674688_3674696dup, NT_167244.1:g.3674687_3674696dup, NT_167244.1:g.3674686_3674696dup, NT_167244.1:g.3674683_3674696dup, NT_167244.1:g.3674682_3674696dup, NT_167244.1:g.3674681_3674696dup, NT_167244.1:g.3674696_3674697insAAAAAAAAAAAAAAAAAAA, NT_167244.1:g.3674696_3674697insAAAAAAAAAAAAAAAAAAAAA, NT_167244.1:g.3674696_3674697insAAAAAAAAAAAAAAAAAAAAAAAA, NT_167244.1:g.3674696_3674697insAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167244.1:g.3674696_3674697insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167244.1:g.3674696_3674697insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167244.1:g.3674696_3674697insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167244.1:g.3674696_3674697insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167244.1:g.3674696_3674697insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167244.1:g.3674696_3674697insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167244.1:g.3674696_3674697insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167244.1:g.3674696_3674697insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167244.1:g.3674680_3674696A[33]GAAAAAAAAAAAAAAAAAAAAAA[1], NT_167244.1:g.3674680_3674696A[33]TAAAAAAAAAAAAAAAAAAAAAA[1], NT_167244.1:g.3674680_3674696A[28]GAAAAAAAAAAAAAAAAAAAAAA[1], NT_167244.1:g.3674680_3674696A[26]TAAAAAAAAAAAAAAAAAAAAA[1], NT_167248.2:g.3615588dup, NT_167248.2:g.3615575_3615588del, NT_167248.2:g.3615582_3615588del, NT_167248.2:g.3615584_3615588del, NT_167248.2:g.3615586_3615588del, NT_167248.2:g.3615587_3615588del, NT_167248.2:g.3615588del, NT_167248.2:g.3615587_3615588dup, NT_167248.2:g.3615586_3615588dup, NT_167248.2:g.3615585_3615588dup, NT_167248.2:g.3615584_3615588dup, NT_167248.2:g.3615583_3615588dup, NT_167248.2:g.3615582_3615588dup, NT_167248.2:g.3615581_3615588dup, NT_167248.2:g.3615580_3615588dup, NT_167248.2:g.3615579_3615588dup, NT_167248.2:g.3615578_3615588dup, NT_167248.2:g.3615577_3615588dup, NT_167248.2:g.3615574_3615588dup, NT_167248.2:g.3615573_3615588dup, NT_167248.2:g.3615588_3615589insAAAAAAAAAAAAAAAAA, NT_167248.2:g.3615588_3615589insAAAAAAAAAAAAAAAAAAAA, NT_167248.2:g.3615588_3615589insAAAAAAAAAAAAAAAAAAAAAA, NT_167248.2:g.3615588_3615589insAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.2:g.3615588_3615589insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.2:g.3615588_3615589insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.2:g.3615588_3615589insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.2:g.3615588_3615589insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.2:g.3615588_3615589insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.2:g.3615588_3615589insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.2:g.3615588_3615589insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.2:g.3615588_3615589insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.2:g.3615588_3615589insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.2:g.3615573_3615588A[33]GAAAAAAAAAAAAAAAAAAAAAA[1], NT_167248.2:g.3615573_3615588A[33]TAAAAAAAAAAAAAAAAAAAAAA[1], NT_167248.2:g.3615573_3615588A[28]GAAAAAAAAAAAAAAAAAAAAAA[1], NT_167248.2:g.3615573_3615588A[26]TAAAAAAAAAAAAAAAAAAAAA[1], NT_167246.2:g.3697532delinsAA, NT_167246.2:g.3697529_3697542del, NT_167246.2:g.3697532_3697538del, NT_167246.2:g.3697532_3697536del, NT_167246.2:g.3697532_3697534del, NT_167246.2:g.3697532_3697533del, NT_167246.2:g.3697532del, NT_167246.2:g.3697532G>A, NT_167246.2:g.3697532delinsAAA, NT_167246.2:g.3697532delinsAAAA, NT_167246.2:g.3697532delinsAAAAA, NT_167246.2:g.3697532delinsAAAAAA, NT_167246.2:g.3697532delinsAAAAAAA, NT_167246.2:g.3697532delinsAAAAAAAA, NT_167246.2:g.3697532delinsAAAAAAAAA, NT_167246.2:g.3697532delinsAAAAAAAAAA, NT_167246.2:g.3697532delinsAAAAAAAAAAA, NT_167246.2:g.3697532delinsAAAAAAAAAAAA, NT_167246.2:g.3697532delinsAAAAAAAAAAAAA, NT_167246.2:g.3697532delinsAAAAAAAAAAAAAAAA, NT_167246.2:g.3697532delinsAAAAAAAAAAAAAAAAA, NT_167246.2:g.3697532delinsAAAAAAAAAAAAAAAAAA, NT_167246.2:g.3697532delinsAAAAAAAAAAAAAAAAAAAAA, NT_167246.2:g.3697532delinsAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.2:g.3697532delinsAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.2:g.3697532delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.2:g.3697532delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.2:g.3697532delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.2:g.3697532delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.2:g.3697532delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.2:g.3697532delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.2:g.3697532delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.2:g.3697532delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.2:g.3697532delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.2:g.3697532delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAA, NT_167246.2:g.3697532delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAA, NT_167246.2:g.3697532delinsAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAA, NT_167246.2:g.3697532delinsAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAA, NT_167249.2:g.3708461delinsAA, NT_167249.2:g.3708458_3708471del, NT_167249.2:g.3708461_3708467del, NT_167249.2:g.3708461_3708465del, NT_167249.2:g.3708461_3708463del, NT_167249.2:g.3708461_3708462del, NT_167249.2:g.3708461del, NT_167249.2:g.3708461G>A, NT_167249.2:g.3708461delinsAAA, NT_167249.2:g.3708461delinsAAAA, NT_167249.2:g.3708461delinsAAAAA, NT_167249.2:g.3708461delinsAAAAAA, NT_167249.2:g.3708461delinsAAAAAAA, NT_167249.2:g.3708461delinsAAAAAAAA, NT_167249.2:g.3708461delinsAAAAAAAAA, NT_167249.2:g.3708461delinsAAAAAAAAAA, NT_167249.2:g.3708461delinsAAAAAAAAAAA, NT_167249.2:g.3708461delinsAAAAAAAAAAAA, NT_167249.2:g.3708461delinsAAAAAAAAAAAAA, NT_167249.2:g.3708461delinsAAAAAAAAAAAAAAAA, NT_167249.2:g.3708461delinsAAAAAAAAAAAAAAAAA, NT_167249.2:g.3708461delinsAAAAAAAAAAAAAAAAAA, NT_167249.2:g.3708461delinsAAAAAAAAAAAAAAAAAAAAA, NT_167249.2:g.3708461delinsAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.2:g.3708461delinsAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.2:g.3708461delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.2:g.3708461delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.2:g.3708461delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.2:g.3708461delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.2:g.3708461delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.2:g.3708461delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.2:g.3708461delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.2:g.3708461delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.2:g.3708461delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.2:g.3708461delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAA, NT_167249.2:g.3708461delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAA, NT_167249.2:g.3708461delinsAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAA, NT_167249.2:g.3708461delinsAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAA, NT_167247.2:g.3734289delinsAA, NT_167247.2:g.3734286_3734299del, NT_167247.2:g.3734289_3734295del, NT_167247.2:g.3734289_3734293del, NT_167247.2:g.3734289_3734291del, NT_167247.2:g.3734289_3734290del, NT_167247.2:g.3734289del, NT_167247.2:g.3734289G>A, NT_167247.2:g.3734289delinsAAA, NT_167247.2:g.3734289delinsAAAA, NT_167247.2:g.3734289delinsAAAAA, NT_167247.2:g.3734289delinsAAAAAA, NT_167247.2:g.3734289delinsAAAAAAA, NT_167247.2:g.3734289delinsAAAAAAAA, NT_167247.2:g.3734289delinsAAAAAAAAA, NT_167247.2:g.3734289delinsAAAAAAAAAA, NT_167247.2:g.3734289delinsAAAAAAAAAAA, NT_167247.2:g.3734289delinsAAAAAAAAAAAA, NT_167247.2:g.3734289delinsAAAAAAAAAAAAA, NT_167247.2:g.3734289delinsAAAAAAAAAAAAAAAA, NT_167247.2:g.3734289delinsAAAAAAAAAAAAAAAAA, NT_167247.2:g.3734289delinsAAAAAAAAAAAAAAAAAA, NT_167247.2:g.3734289delinsAAAAAAAAAAAAAAAAAAAAA, NT_167247.2:g.3734289delinsAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.2:g.3734289delinsAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.2:g.3734289delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.2:g.3734289delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.2:g.3734289delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.2:g.3734289delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.2:g.3734289delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.2:g.3734289delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.2:g.3734289delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.2:g.3734289delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.2:g.3734289delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.2:g.3734289delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAA, NT_167247.2:g.3734289delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAA, NT_167247.2:g.3734289delinsAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAA, NT_167247.2:g.3734289delinsAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAA, NT_167245.2:g.3633640dup, NT_167245.2:g.3633627_3633640del, NT_167245.2:g.3633634_3633640del, NT_167245.2:g.3633636_3633640del, NT_167245.2:g.3633638_3633640del, NT_167245.2:g.3633639_3633640del, NT_167245.2:g.3633640del, NT_167245.2:g.3633639_3633640dup, NT_167245.2:g.3633638_3633640dup, NT_167245.2:g.3633637_3633640dup, NT_167245.2:g.3633636_3633640dup, NT_167245.2:g.3633635_3633640dup, NT_167245.2:g.3633634_3633640dup, NT_167245.2:g.3633633_3633640dup, NT_167245.2:g.3633632_3633640dup, NT_167245.2:g.3633631_3633640dup, NT_167245.2:g.3633630_3633640dup, NT_167245.2:g.3633629_3633640dup, NT_167245.2:g.3633626_3633640dup, NT_167245.2:g.3633625_3633640dup, NT_167245.2:g.3633640_3633641insAAAAAAAAAAAAAAAAA, NT_167245.2:g.3633640_3633641insAAAAAAAAAAAAAAAAAAAA, NT_167245.2:g.3633640_3633641insAAAAAAAAAAAAAAAAAAAAAA, NT_167245.2:g.3633640_3633641insAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.2:g.3633640_3633641insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.2:g.3633640_3633641insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.2:g.3633640_3633641insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.2:g.3633640_3633641insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.2:g.3633640_3633641insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.2:g.3633640_3633641insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.2:g.3633640_3633641insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.2:g.3633640_3633641insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.2:g.3633640_3633641insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.2:g.3633625_3633640A[33]GAAAAAAAAAAAAAAAAAAAAAA[1], NT_167245.2:g.3633625_3633640A[33]TAAAAAAAAAAAAAAAAAAAAAA[1], NT_167245.2:g.3633625_3633640A[28]GAAAAAAAAAAAAAAAAAAAAAA[1], NT_167245.2:g.3633625_3633640A[26]TAAAAAAAAAAAAAAAAAAAAA[1], NT_187692.1:g.61438delinsTTTTT, NT_187692.1:g.61433_61443del, NT_187692.1:g.61438_61441del, NT_187692.1:g.61438_61439del, NT_187692.1:g.61438C>T, NT_187692.1:g.61438delinsTT, NT_187692.1:g.61438delinsTTT, NT_187692.1:g.61438delinsTTTT, NT_187692.1:g.61438delinsTTTTTT, NT_187692.1:g.61438delinsTTTTTTT, NT_187692.1:g.61438delinsTTTTTTTT, NT_187692.1:g.61438delinsTTTTTTTTT, NT_187692.1:g.61438delinsTTTTTTTTTT, NT_187692.1:g.61438delinsTTTTTTTTTTT, NT_187692.1:g.61438delinsTTTTTTTTTTTT, NT_187692.1:g.61438delinsTTTTTTTTTTTTT, NT_187692.1:g.61438delinsTTTTTTTTTTTTTT, NT_187692.1:g.61438delinsTTTTTTTTTTTTTTT, NT_187692.1:g.61438delinsTTTTTTTTTTTTTTTT, NT_187692.1:g.61438delinsTTTTTTTTTTTTTTTTTTT, NT_187692.1:g.61438delinsTTTTTTTTTTTTTTTTTTTT, NT_187692.1:g.61438delinsTTTTTTTTTTTTTTTTTTTTT, NT_187692.1:g.61438delinsTTTTTTTTTTTTTTTTTTTTTTTT, NT_187692.1:g.61438delinsTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187692.1:g.61438delinsTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187692.1:g.61438delinsTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187692.1:g.61438delinsTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187692.1:g.61438delinsTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187692.1:g.61438delinsTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187692.1:g.61438delinsTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187692.1:g.61438delinsTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187692.1:g.61438delinsTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187692.1:g.61438delinsTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187692.1:g.61438delinsTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187692.1:g.61438delinsTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187692.1:g.61438delinsTTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTTTTTTTTT, NT_187692.1:g.61438delinsTTTTTTTTTTTTTTTCTTTTTTTTTTTTTTTTTTTTTTT, NT_187692.1:g.61438delinsTTTTTTTTTTTTTTATTTTTTTTTTTTTTTTTTTTT, NT_113891.2:g.3830746_3830747dup, NT_113891.2:g.3830735_3830747del, NT_113891.2:g.3830742_3830747del, NT_113891.2:g.3830744_3830747del, NT_113891.2:g.3830746_3830747del, NT_113891.2:g.3830747del, NT_113891.2:g.3830747dup, NT_113891.2:g.3830745_3830747dup, NT_113891.2:g.3830744_3830747dup, NT_113891.2:g.3830743_3830747dup, NT_113891.2:g.3830742_3830747dup, NT_113891.2:g.3830741_3830747dup, NT_113891.2:g.3830740_3830747dup, NT_113891.2:g.3830739_3830747dup, NT_113891.2:g.3830738_3830747dup, NT_113891.2:g.3830737_3830747dup, NT_113891.2:g.3830736_3830747dup, NT_113891.2:g.3830735_3830747dup, NT_113891.2:g.3830747_3830748insAAAAAAAAAAAAAAAA, NT_113891.2:g.3830747_3830748insAAAAAAAAAAAAAAAAA, NT_113891.2:g.3830747_3830748insAAAAAAAAAAAAAAAAAA, NT_113891.2:g.3830747_3830748insAAAAAAAAAAAAAAAAAAAAA, NT_113891.2:g.3830747_3830748insAAAAAAAAAAAAAAAAAAAAAAA, NT_113891.2:g.3830747_3830748insAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_113891.2:g.3830747_3830748insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_113891.2:g.3830747_3830748insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_113891.2:g.3830747_3830748insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_113891.2:g.3830747_3830748insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_113891.2:g.3830747_3830748insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_113891.2:g.3830747_3830748insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_113891.2:g.3830747_3830748insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_113891.2:g.3830747_3830748insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_113891.2:g.3830747_3830748insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_113891.2:g.3830733_3830747A[33]GAAAAAAAAAAAAAAAAAAAAAA[1], NT_113891.2:g.3830733_3830747A[33]TAAAAAAAAAAAAAAAAAAAAAA[1], NT_113891.2:g.3830733_3830747A[28]GAAAAAAAAAAAAAAAAAAAAAA[1], NT_113891.2:g.3830733_3830747A[26]TAAAAAAAAAAAAAAAAAAAAA[1], NT_167248.1:g.3621184dup, NT_167248.1:g.3621171_3621184del, NT_167248.1:g.3621178_3621184del, NT_167248.1:g.3621180_3621184del, NT_167248.1:g.3621182_3621184del, NT_167248.1:g.3621183_3621184del, NT_167248.1:g.3621184del, NT_167248.1:g.3621183_3621184dup, NT_167248.1:g.3621182_3621184dup, NT_167248.1:g.3621181_3621184dup, NT_167248.1:g.3621180_3621184dup, NT_167248.1:g.3621179_3621184dup, NT_167248.1:g.3621178_3621184dup, NT_167248.1:g.3621177_3621184dup, NT_167248.1:g.3621176_3621184dup, NT_167248.1:g.3621175_3621184dup, NT_167248.1:g.3621174_3621184dup, NT_167248.1:g.3621173_3621184dup, NT_167248.1:g.3621170_3621184dup, NT_167248.1:g.3621169_3621184dup, NT_167248.1:g.3621184_3621185insAAAAAAAAAAAAAAAAA, NT_167248.1:g.3621184_3621185insAAAAAAAAAAAAAAAAAAAA, NT_167248.1:g.3621184_3621185insAAAAAAAAAAAAAAAAAAAAAA, NT_167248.1:g.3621184_3621185insAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.1:g.3621184_3621185insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.1:g.3621184_3621185insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.1:g.3621184_3621185insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.1:g.3621184_3621185insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.1:g.3621184_3621185insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.1:g.3621184_3621185insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.1:g.3621184_3621185insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.1:g.3621184_3621185insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.1:g.3621184_3621185insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167248.1:g.3621169_3621184A[33]GAAAAAAAAAAAAAAAAAAAAAA[1], NT_167248.1:g.3621169_3621184A[33]TAAAAAAAAAAAAAAAAAAAAAA[1], NT_167248.1:g.3621169_3621184A[28]GAAAAAAAAAAAAAAAAAAAAAA[1], NT_167248.1:g.3621169_3621184A[26]TAAAAAAAAAAAAAAAAAAAAA[1], NT_167245.1:g.3639225dup, NT_167245.1:g.3639212_3639225del, NT_167245.1:g.3639219_3639225del, NT_167245.1:g.3639221_3639225del, NT_167245.1:g.3639223_3639225del, NT_167245.1:g.3639224_3639225del, NT_167245.1:g.3639225del, NT_167245.1:g.3639224_3639225dup, NT_167245.1:g.3639223_3639225dup, NT_167245.1:g.3639222_3639225dup, NT_167245.1:g.3639221_3639225dup, NT_167245.1:g.3639220_3639225dup, NT_167245.1:g.3639219_3639225dup, NT_167245.1:g.3639218_3639225dup, NT_167245.1:g.3639217_3639225dup, NT_167245.1:g.3639216_3639225dup, NT_167245.1:g.3639215_3639225dup, NT_167245.1:g.3639214_3639225dup, NT_167245.1:g.3639211_3639225dup, NT_167245.1:g.3639210_3639225dup, NT_167245.1:g.3639225_3639226insAAAAAAAAAAAAAAAAA, NT_167245.1:g.3639225_3639226insAAAAAAAAAAAAAAAAAAAA, NT_167245.1:g.3639225_3639226insAAAAAAAAAAAAAAAAAAAAAA, NT_167245.1:g.3639225_3639226insAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.1:g.3639225_3639226insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.1:g.3639225_3639226insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.1:g.3639225_3639226insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.1:g.3639225_3639226insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.1:g.3639225_3639226insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.1:g.3639225_3639226insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.1:g.3639225_3639226insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.1:g.3639225_3639226insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.1:g.3639225_3639226insAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167245.1:g.3639210_3639225A[33]GAAAAAAAAAAAAAAAAAAAAAA[1], NT_167245.1:g.3639210_3639225A[33]TAAAAAAAAAAAAAAAAAAAAAA[1], NT_167245.1:g.3639210_3639225A[28]GAAAAAAAAAAAAAAAAAAAAAA[1], NT_167245.1:g.3639210_3639225A[26]TAAAAAAAAAAAAAAAAAAAAA[1], NT_167249.1:g.3707759delinsAA, NT_167249.1:g.3707756_3707769del, NT_167249.1:g.3707759_3707765del, NT_167249.1:g.3707759_3707763del, NT_167249.1:g.3707759_3707761del, NT_167249.1:g.3707759_3707760del, NT_167249.1:g.3707759del, NT_167249.1:g.3707759G>A, NT_167249.1:g.3707759delinsAAA, NT_167249.1:g.3707759delinsAAAA, NT_167249.1:g.3707759delinsAAAAA, NT_167249.1:g.3707759delinsAAAAAA, NT_167249.1:g.3707759delinsAAAAAAA, NT_167249.1:g.3707759delinsAAAAAAAA, NT_167249.1:g.3707759delinsAAAAAAAAA, NT_167249.1:g.3707759delinsAAAAAAAAAA, NT_167249.1:g.3707759delinsAAAAAAAAAAA, NT_167249.1:g.3707759delinsAAAAAAAAAAAA, NT_167249.1:g.3707759delinsAAAAAAAAAAAAA, NT_167249.1:g.3707759delinsAAAAAAAAAAAAAAAA, NT_167249.1:g.3707759delinsAAAAAAAAAAAAAAAAA, NT_167249.1:g.3707759delinsAAAAAAAAAAAAAAAAAA, NT_167249.1:g.3707759delinsAAAAAAAAAAAAAAAAAAAAA, NT_167249.1:g.3707759delinsAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.1:g.3707759delinsAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.1:g.3707759delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.1:g.3707759delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.1:g.3707759delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.1:g.3707759delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.1:g.3707759delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.1:g.3707759delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.1:g.3707759delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.1:g.3707759delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.1:g.3707759delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167249.1:g.3707759delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAA, NT_167249.1:g.3707759delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAA, NT_167249.1:g.3707759delinsAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAA, NT_167249.1:g.3707759delinsAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAA, NT_167246.1:g.3703152delinsAA, NT_167246.1:g.3703149_3703162del, NT_167246.1:g.3703152_3703158del, NT_167246.1:g.3703152_3703156del, NT_167246.1:g.3703152_3703154del, NT_167246.1:g.3703152_3703153del, NT_167246.1:g.3703152del, NT_167246.1:g.3703152G>A, NT_167246.1:g.3703152delinsAAA, NT_167246.1:g.3703152delinsAAAA, NT_167246.1:g.3703152delinsAAAAA, NT_167246.1:g.3703152delinsAAAAAA, NT_167246.1:g.3703152delinsAAAAAAA, NT_167246.1:g.3703152delinsAAAAAAAA, NT_167246.1:g.3703152delinsAAAAAAAAA, NT_167246.1:g.3703152delinsAAAAAAAAAA, NT_167246.1:g.3703152delinsAAAAAAAAAAA, NT_167246.1:g.3703152delinsAAAAAAAAAAAA, NT_167246.1:g.3703152delinsAAAAAAAAAAAAA, NT_167246.1:g.3703152delinsAAAAAAAAAAAAAAAA, NT_167246.1:g.3703152delinsAAAAAAAAAAAAAAAAA, NT_167246.1:g.3703152delinsAAAAAAAAAAAAAAAAAA, NT_167246.1:g.3703152delinsAAAAAAAAAAAAAAAAAAAAA, NT_167246.1:g.3703152delinsAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.1:g.3703152delinsAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.1:g.3703152delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.1:g.3703152delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.1:g.3703152delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.1:g.3703152delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.1:g.3703152delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.1:g.3703152delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.1:g.3703152delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.1:g.3703152delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.1:g.3703152delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167246.1:g.3703152delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAA, NT_167246.1:g.3703152delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAA, NT_167246.1:g.3703152delinsAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAA, NT_167246.1:g.3703152delinsAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAA, NT_167247.1:g.3739874delinsAA, NT_167247.1:g.3739871_3739884del, NT_167247.1:g.3739874_3739880del, NT_167247.1:g.3739874_3739878del, NT_167247.1:g.3739874_3739876del, NT_167247.1:g.3739874_3739875del, NT_167247.1:g.3739874del, NT_167247.1:g.3739874G>A, NT_167247.1:g.3739874delinsAAA, NT_167247.1:g.3739874delinsAAAA, NT_167247.1:g.3739874delinsAAAAA, NT_167247.1:g.3739874delinsAAAAAA, NT_167247.1:g.3739874delinsAAAAAAA, NT_167247.1:g.3739874delinsAAAAAAAA, NT_167247.1:g.3739874delinsAAAAAAAAA, NT_167247.1:g.3739874delinsAAAAAAAAAA, NT_167247.1:g.3739874delinsAAAAAAAAAAA, NT_167247.1:g.3739874delinsAAAAAAAAAAAA, NT_167247.1:g.3739874delinsAAAAAAAAAAAAA, NT_167247.1:g.3739874delinsAAAAAAAAAAAAAAAA, NT_167247.1:g.3739874delinsAAAAAAAAAAAAAAAAA, NT_167247.1:g.3739874delinsAAAAAAAAAAAAAAAAAA, NT_167247.1:g.3739874delinsAAAAAAAAAAAAAAAAAAAAA, NT_167247.1:g.3739874delinsAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.1:g.3739874delinsAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.1:g.3739874delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.1:g.3739874delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.1:g.3739874delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.1:g.3739874delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.1:g.3739874delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.1:g.3739874delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.1:g.3739874delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.1:g.3739874delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.1:g.3739874delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA, NT_167247.1:g.3739874delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAA, NT_167247.1:g.3739874delinsAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAA, NT_167247.1:g.3739874delinsAAAAAAAAAAAAAAAAAAAAAAAGAAAAAAAAAAAA, NT_167247.1:g.3739874delinsAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAA

Select item 14890527632.

rs1489052763 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:32388934 (GRCh38)
6:32356711 (GRCh37)
Canonical SPDI:: NC_000006.12:32388933:T:C
Gene:: HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000014/2 (GnomAD)
C=0.000015/4 (TOPMED)
HGVS:: NC_000006.12:g.32388934T>C, NC_000006.11:g.32356711T>C, NT_113891.3:g.3827034T>C, NT_113891.2:g.3827140T>C, NT_167248.2:g.3611974T>C, NT_167248.1:g.3617570T>C, NT_167245.2:g.3630025T>C, NT_167245.1:g.3635610T>C, NT_167249.2:g.3704855T>C, NT_167249.1:g.3704153T>C, NT_167246.2:g.3693926T>C, NT_167246.1:g.3699546T>C, NT_167247.2:g.3730683T>C, NT_167247.1:g.3736268T>C, NT_167244.2:g.3721165T>C, NT_167244.1:g.3671081T>C, NT_187692.1:g.65032A>G

Select item 14890315683.

rs1489031568 [Homo sapiens]

Variant type:: SNV
Alleles:: G>C [Show Flanks]
Chromosome:: 6:32390282 (GRCh38)
6:32358059 (GRCh37)
Canonical SPDI:: NC_000006.12:32390281:G:C
Gene:: HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0./0 (ALFA)
C=0.000004/1 (TOPMED)
C=0.000014/2 (GnomAD)
HGVS:: NC_000006.12:g.32390282G>C, NC_000006.11:g.32358059G>C, NT_113891.3:g.3828382G>C, NT_113891.2:g.3828488G>C, NT_167248.2:g.3613322G>C, NT_167248.1:g.3618918G>C, NT_167245.2:g.3631373G>C, NT_167245.1:g.3636958G>C, NT_167249.2:g.3706203G>C, NT_167249.1:g.3705501G>C, NT_167246.2:g.3695274G>C, NT_167246.1:g.3700894G>C, NT_167247.2:g.3732031G>C, NT_167247.1:g.3737616G>C, NT_167244.2:g.3722513G>C, NT_167244.1:g.3672429G>C, NT_187692.1:g.63684C>G

Select item 14889010954.

rs1488901095 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:32393068 (GRCh38)
6:32360845 (GRCh37)
Canonical SPDI:: NC_000006.12:32393067:A:G
Gene:: BTNL2 (Varview), HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: downstream_transcript_variant,intron_variant,genic_downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.000071/1 (ALFA)
G=0.000014/2 (GnomAD)
G=0.000015/4 (TOPMED)
HGVS:: NC_000006.12:g.32393068A>G, NC_000006.11:g.32360845A>G, NG_054759.1:g.20812T>C, NT_113891.3:g.3831160A>G, NT_113891.2:g.3831266A>G, NT_167244.2:g.3725299A>G, NT_167244.1:g.3675215A>G, NT_167248.2:g.3616107A>G, NT_167248.1:g.3621703A>G, NT_167246.2:g.3698061A>G, NT_167246.1:g.3703681A>G, NT_167249.2:g.3708990A>G, NT_167249.1:g.3708288A>G, NT_167247.2:g.3734818A>G, NT_167247.1:g.3740403A>G, NT_167245.2:g.3634159A>G, NT_167245.1:g.3639744A>G, NT_187692.1:g.60913T>C

Select item 14883667905.

rs1488366790 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 6:32393952 (GRCh38)
6:32361729 (GRCh37)
Canonical SPDI:: NC_000006.12:32393951:C:G
Gene:: BTNL2 (Varview), HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: downstream_transcript_variant,genic_downstream_transcript_variant,500B_downstream_variant,intron_variant
Validated:: by frequency
MAF:: G=0.000007/1 (GnomAD_exomes)
HGVS:: NC_000006.12:g.32393952C>G, NC_000006.11:g.32361729C>G, NG_054759.1:g.19928G>C, NT_113891.3:g.3832044C>G, NT_113891.2:g.3832150C>G, NT_167244.2:g.3726183C>G, NT_167244.1:g.3676099C>G, NT_167248.2:g.3616991C>G, NT_167248.1:g.3622587C>G, NT_167246.2:g.3698945C>G, NT_167246.1:g.3704565C>G, NT_167249.2:g.3709874C>G, NT_167249.1:g.3709172C>G, NT_167247.2:g.3735702C>G, NT_167247.1:g.3741287C>G, NT_167245.2:g.3635043C>G, NT_167245.1:g.3640628C>G, NT_187692.1:g.60032G>C

Select item 14882478696.

rs1488247869 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:32392200 (GRCh38)
6:32359977 (GRCh37)
Canonical SPDI:: NC_000006.12:32392199:C:T
Gene:: HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000004/1 (TOPMED)
T=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.32392200C>T, NC_000006.11:g.32359977C>T, NG_054759.1:g.21680G>A, NT_113891.3:g.3830300C>T, NT_113891.2:g.3830406C>T, NT_167244.2:g.3724431C>T, NT_167244.1:g.3674347C>T, NT_167248.2:g.3615240C>T, NT_167248.1:g.3620836C>T, NT_167246.2:g.3697193C>T, NT_167246.1:g.3702813C>T, NT_167249.2:g.3708122C>T, NT_167249.1:g.3707420C>T, NT_167247.2:g.3733950C>T, NT_167247.1:g.3739535C>T, NT_167245.2:g.3633291C>T, NT_167245.1:g.3638876C>T, NT_187692.1:g.61766G>A

Select item 14875439457.

rs1487543945 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 6:32392900 (GRCh38)
6:32360677 (GRCh37)
Canonical SPDI:: NC_000006.12:32392899:G:T
Gene:: BTNL2 (Varview), HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: downstream_transcript_variant,intron_variant,genic_downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa
MAF:: T=0.000224/1 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000223/1 (Estonian)
HGVS:: NC_000006.12:g.32392900G>T, NC_000006.11:g.32360677G>T, NG_054759.1:g.20980C>A, NT_113891.3:g.3830992G>T, NT_113891.2:g.3831098G>T, NT_167244.2:g.3725131G>T, NT_167244.1:g.3675047G>T, NT_167248.2:g.3615939G>T, NT_167248.1:g.3621535G>T, NT_167246.2:g.3697893G>T, NT_167246.1:g.3703513G>T, NT_167249.2:g.3708822G>T, NT_167249.1:g.3708120G>T, NT_167247.2:g.3734650G>T, NT_167247.1:g.3740235G>T, NT_167245.2:g.3633991G>T, NT_167245.1:g.3639576G>T, NT_187692.1:g.61081C>A

Select item 14868338558.

rs1486833855 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:32391632 (GRCh38)
6:32359409 (GRCh37)
Canonical SPDI:: NC_000006.12:32391631:A:G
Gene:: HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000023/6 (TOPMED)
HGVS:: NC_000006.12:g.32391632A>G, NC_000006.11:g.32359409A>G, NG_054759.1:g.22248T>C, NT_113891.3:g.3829732A>G, NT_113891.2:g.3829838A>G, NT_167244.2:g.3723863A>G, NT_167244.1:g.3673779A>G, NT_167248.2:g.3614672A>G, NT_167248.1:g.3620268A>G, NT_167246.2:g.3696625A>G, NT_167246.1:g.3702245A>G, NT_167249.2:g.3707554A>G, NT_167249.1:g.3706852A>G, NT_167247.2:g.3733382A>G, NT_167247.1:g.3738967A>G, NT_167245.2:g.3632723A>G, NT_167245.1:g.3638308A>G, NT_187692.1:g.62329T>C, NR_044996.1:n.264A>G

Select item 14863110669.

rs1486311066 [Homo sapiens]

Variant type:: SNV
Alleles:: T>G [Show Flanks]
Chromosome:: 6:32391099 (GRCh38)
6:32358876 (GRCh37)
Canonical SPDI:: NC_000006.12:32391098:T:G
Gene:: HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000011/3 (TOPMED)
G=0.000021/3 (GnomAD)
HGVS:: NC_000006.12:g.32391099T>G, NC_000006.11:g.32358876T>G, NT_113891.3:g.3829199T>G, NT_113891.2:g.3829305T>G, NT_167248.2:g.3614139T>G, NT_167248.1:g.3619735T>G, NT_167245.2:g.3632190T>G, NT_167245.1:g.3637775T>G, NT_167249.2:g.3707021T>G, NT_167249.1:g.3706319T>G, NT_167246.2:g.3696092T>G, NT_167246.1:g.3701712T>G, NT_167247.2:g.3732849T>G, NT_167247.1:g.3738434T>G, NT_167244.2:g.3723330T>G, NT_167244.1:g.3673246T>G, NT_187692.1:g.62867A>C

Select item 148598000710.

rs1485980007 [Homo sapiens]

Variant type:: SNV
Alleles:: C>T [Show Flanks]
Chromosome:: 6:32390530 (GRCh38)
6:32358307 (GRCh37)
Canonical SPDI:: NC_000006.12:32390529:C:T
Gene:: HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: T=0./0 (ALFA)
HGVS:: NC_000006.12:g.32390530C>T, NC_000006.11:g.32358307C>T, NT_113891.3:g.3828630C>T, NT_113891.2:g.3828736C>T, NT_167248.2:g.3613570C>T, NT_167248.1:g.3619166C>T, NT_167245.2:g.3631621C>T, NT_167245.1:g.3637206C>T, NT_167249.2:g.3706451C>T, NT_167249.1:g.3705749C>T, NT_167246.2:g.3695522C>T, NT_167246.1:g.3701142C>T, NT_167247.2:g.3732279C>T, NT_167247.1:g.3737864C>T, NT_167244.2:g.3722761C>T, NT_167244.1:g.3672677C>T, NT_187692.1:g.63437G>A, NR_044996.1:n.21C>T

Select item 148594842811.

rs1485948428 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 6:32391735 (GRCh38)
6:32359512 (GRCh37)
Canonical SPDI:: NC_000006.12:32391734:T:C
Gene:: HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.32391735T>C, NC_000006.11:g.32359512T>C, NG_054759.1:g.22145A>G, NT_113891.3:g.3829835T>C, NT_113891.2:g.3829941T>C, NT_167244.2:g.3723966T>C, NT_167244.1:g.3673882T>C, NT_167248.2:g.3614775T>C, NT_167248.1:g.3620371T>C, NT_167246.2:g.3696728T>C, NT_167246.1:g.3702348T>C, NT_167249.2:g.3707657T>C, NT_167249.1:g.3706955T>C, NT_167247.2:g.3733485T>C, NT_167247.1:g.3739070T>C, NT_167245.2:g.3632826T>C, NT_167245.1:g.3638411T>C, NT_187692.1:g.62225A>G, NR_044996.1:n.367T>C

Select item 148577558512.

rs1485775585 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:32392877 (GRCh38)
6:32360654 (GRCh37)
Canonical SPDI:: NC_000006.12:32392876:G:A
Gene:: BTNL2 (Varview), HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: downstream_transcript_variant,intron_variant,genic_downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
HGVS:: NC_000006.12:g.32392877G>A, NC_000006.11:g.32360654G>A, NG_054759.1:g.21003C>T, NT_113891.3:g.3830969G>A, NT_113891.2:g.3831075G>A, NT_167244.2:g.3725108G>A, NT_167244.1:g.3675024G>A, NT_167248.2:g.3615916G>A, NT_167248.1:g.3621512G>A, NT_167246.2:g.3697870G>A, NT_167246.1:g.3703490G>A, NT_167249.2:g.3708799G>A, NT_167249.1:g.3708097G>A, NT_167247.2:g.3734627G>A, NT_167247.1:g.3740212G>A, NT_167245.2:g.3633968G>A, NT_167245.1:g.3639553G>A, NT_187692.1:g.61104C>T

Select item 148575483113.

rs1485754831 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 6:32393195 (GRCh38)
6:32360972 (GRCh37)
Canonical SPDI:: NC_000006.12:32393194:G:A
Gene:: BTNL2 (Varview), HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: downstream_transcript_variant,intron_variant,genic_downstream_transcript_variant,500B_downstream_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
A=0.000008/2 (TOPMED)
HGVS:: NC_000006.12:g.32393195G>A, NC_000006.11:g.32360972G>A, NG_054759.1:g.20685C>T, NT_113891.3:g.3831287G>A, NT_113891.2:g.3831393G>A, NT_167244.2:g.3725426G>A, NT_167244.1:g.3675342G>A, NT_167248.2:g.3616234G>A, NT_167248.1:g.3621830G>A, NT_167246.2:g.3698188G>A, NT_167246.1:g.3703808G>A, NT_167249.2:g.3709117G>A, NT_167249.1:g.3708415G>A, NT_167247.2:g.3734945G>A, NT_167247.1:g.3740530G>A, NT_167245.2:g.3634286G>A, NT_167245.1:g.3639871G>A, NT_187692.1:g.60786C>T

Select item 148569689314.

rs1485696893 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 6:32388654 (GRCh38)
6:32356431 (GRCh37)
Canonical SPDI:: NC_000006.12:32388653:C:G
Gene:: HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.32388654C>G, NC_000006.11:g.32356431C>G, NT_113891.3:g.3826754C>G, NT_113891.2:g.3826860C>G, NT_167248.2:g.3611694C>G, NT_167248.1:g.3617290C>G, NT_167245.2:g.3629745C>G, NT_167245.1:g.3635330C>G, NT_167249.2:g.3704575C>G, NT_167249.1:g.3703873C>G, NT_167246.2:g.3693646C>G, NT_167246.1:g.3699266C>G, NT_167247.2:g.3730403C>G, NT_167247.1:g.3735988C>G, NT_167244.2:g.3720885C>G, NT_167244.1:g.3670801C>G, NT_187692.1:g.65312G>C

Select item 148563356715.

rs1485633567 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A [Show Flanks]
Chromosome:: 6:32389935 (GRCh38)
6:32357712 (GRCh37)
Canonical SPDI:: NC_000006.12:32389934:C:A
Gene:: HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0.000071/1 (ALFA)
A=0.000144/38 (TOPMED)
A=0.000185/26 (GnomAD)
HGVS:: NC_000006.12:g.32389935C>A, NC_000006.11:g.32357712C>A, NT_113891.3:g.3828035C>A, NT_113891.2:g.3828141C>A, NT_167248.2:g.3612975C>A, NT_167248.1:g.3618571C>A, NT_167245.2:g.3631026C>A, NT_167245.1:g.3636611C>A, NT_167249.2:g.3705856C>A, NT_167249.1:g.3705154C>A, NT_167246.2:g.3694927C>A, NT_167246.1:g.3700547C>A, NT_167247.2:g.3731684C>A, NT_167247.1:g.3737269C>A, NT_167244.2:g.3722166C>A, NT_167244.1:g.3672082C>A, NT_187692.1:g.64031G>T

Select item 148529799216.

rs1485297992 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:32390678 (GRCh38)
6:32358455 (GRCh37)
Canonical SPDI:: NC_000006.12:32390677:A:G
Gene:: HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant,non_coding_transcript_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.32390678A>G, NC_000006.11:g.32358455A>G, NT_113891.3:g.3828778A>G, NT_113891.2:g.3828884A>G, NT_167248.2:g.3613718A>G, NT_167248.1:g.3619314A>G, NT_167245.2:g.3631769A>G, NT_167245.1:g.3637354A>G, NT_167249.2:g.3706600A>G, NT_167249.1:g.3705898A>G, NT_167246.2:g.3695671A>G, NT_167246.1:g.3701291A>G, NT_167247.2:g.3732428A>G, NT_167247.1:g.3738013A>G, NT_167244.2:g.3722909A>G, NT_167244.1:g.3672825A>G, NT_187692.1:g.63288T>C, NR_044996.1:n.169A>G

Select item 148474445717.

rs1484744457 [Homo sapiens]

Variant type:: SNV
Alleles:: C>A,G [Show Flanks]
Chromosome:: 6:32390099 (GRCh38)
6:32357876 (GRCh37)
Canonical SPDI:: NC_000006.12:32390098:C:A,NC_000006.12:32390098:C:G
Gene:: HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.32390099C>A, NC_000006.12:g.32390099C>G, NC_000006.11:g.32357876C>A, NC_000006.11:g.32357876C>G, NT_113891.3:g.3828199C>A, NT_113891.3:g.3828199C>G, NT_113891.2:g.3828305C>A, NT_113891.2:g.3828305C>G, NT_167248.2:g.3613139C>A, NT_167248.2:g.3613139C>G, NT_167248.1:g.3618735C>A, NT_167248.1:g.3618735C>G, NT_167245.2:g.3631190C>A, NT_167245.2:g.3631190C>G, NT_167245.1:g.3636775C>A, NT_167245.1:g.3636775C>G, NT_167249.2:g.3706020C>A, NT_167249.2:g.3706020C>G, NT_167249.1:g.3705318C>A, NT_167249.1:g.3705318C>G, NT_167246.2:g.3695091C>A, NT_167246.2:g.3695091C>G, NT_167246.1:g.3700711C>A, NT_167246.1:g.3700711C>G, NT_167247.2:g.3731848C>A, NT_167247.2:g.3731848C>G, NT_167247.1:g.3737433C>A, NT_167247.1:g.3737433C>G, NT_167244.2:g.3722330C>A, NT_167244.2:g.3722330C>G, NT_167244.1:g.3672246C>A, NT_167244.1:g.3672246C>G, NT_187692.1:g.63867G>T, NT_187692.1:g.63867G>C

Select item 148406189618.

rs1484061896 [Homo sapiens]

Variant type:: SNV
Alleles:: C>G [Show Flanks]
Chromosome:: 6:32388924 (GRCh38)
6:32356701 (GRCh37)
Canonical SPDI:: NC_000006.12:32388923:C:G
Gene:: HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,2KB_upstream_variant,upstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000014/2 (GnomAD)
HGVS:: NC_000006.12:g.32388924C>G, NC_000006.11:g.32356701C>G, NT_113891.3:g.3827024C>G, NT_113891.2:g.3827130C>G, NT_167248.2:g.3611964C>G, NT_167248.1:g.3617560C>G, NT_167245.2:g.3630015C>G, NT_167245.1:g.3635600C>G, NT_167249.2:g.3704845C>G, NT_167249.1:g.3704143C>G, NT_167246.2:g.3693916C>G, NT_167246.1:g.3699536C>G, NT_167247.2:g.3730673C>G, NT_167247.1:g.3736258C>G, NT_167244.2:g.3721155C>G, NT_167244.1:g.3671071C>G, NT_187692.1:g.65042G>C

Select item 148386839919.

rs1483868399 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:32392529 (GRCh38)
6:32360306 (GRCh37)
Canonical SPDI:: NC_000006.12:32392528:A:G
Gene:: HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0.00008/1 (ALFA)
G=0.01114/742 (GnomAD)
HGVS:: NC_000006.12:g.32392529A>G, NC_000006.11:g.32360306A>G, NG_054759.1:g.21351T>C, NT_113891.3:g.3830623A>G, NT_113891.2:g.3830729A>G, NT_167244.2:g.3724760A>G, NT_167244.1:g.3674676A>G, NT_167248.2:g.3615569A>G, NT_167248.1:g.3621165A>G, NT_167246.2:g.3697523A>G, NT_167246.1:g.3703143A>G, NT_167249.2:g.3708452A>G, NT_167249.1:g.3707750A>G, NT_167247.2:g.3734280A>G, NT_167247.1:g.3739865A>G, NT_167245.2:g.3633621A>G, NT_167245.1:g.3639206A>G, NT_187692.1:g.61447T>C

Select item 148322776620.

rs1483227766 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 6:32390980 (GRCh38)
6:32358757 (GRCh37)
Canonical SPDI:: NC_000006.12:32390979:A:G
Gene:: HCG23 (Varview), TSBP1-AS1 (Varview)
Functional Consequence:: genic_downstream_transcript_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
G=0.000007/1 (GnomAD)
HGVS:: NC_000006.12:g.32390980A>G, NC_000006.11:g.32358757A>G, NT_113891.3:g.3829080A>G, NT_113891.2:g.3829186A>G, NT_167248.2:g.3614020A>G, NT_167248.1:g.3619616A>G, NT_167245.2:g.3632071A>G, NT_167245.1:g.3637656A>G, NT_167249.2:g.3706902A>G, NT_167249.1:g.3706200A>G, NT_167246.2:g.3695973A>G, NT_167246.1:g.3701593A>G, NT_167247.2:g.3732730A>G, NT_167247.1:g.3738315A>G, NT_167244.2:g.3723211A>G, NT_167244.1:g.3673127A>G, NT_187692.1:g.62986T>C

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