SNP Links for Nucleotide (Select 223941843) - SNP

Links from Nucleotide

Items: 1 to 20 of 2546

<< First< Prev

Page of 128

Next >Last >>

Select item 14915715911.

rs1491571591 [Homo sapiens]

Variant type:: DEL
Alleles:: CT>- [Show Flanks]
Chromosome:: 17:49295007 (GRCh38)
17:47372369 (GRCh37)
Canonical SPDI:: NC_000017.11:49295006:CT:
Gene:: ZNF652 (Varview)
Functional Consequence:: 3_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.0002/1 (ALFA)
-=0.0002/1 (Estonian)
HGVS:: NC_000017.11:g.49295007_49295008del, NC_000017.10:g.47372369_47372370del, NM_001145365.3:c.*3405_*3406del, NM_001145365.2:c.*3405_*3406del, NM_001145365.1:c.*3405_*3406del, XM_024450655.2:c.*3405_*3406del, XM_024450655.1:c.*3405_*3406del, XM_024450653.2:c.*3405_*3406del, XM_024450653.1:c.*3405_*3406del, NM_014897.2:c.*3405_*3406del, XM_024450656.2:c.*3405_*3406del, XM_024450656.1:c.*3405_*3406del, XM_047435626.1:c.*3405_*3406del, XM_047435627.1:c.*3405_*3406del, XM_047435628.1:c.*3405_*3406del, XM_047435629.1:c.*3405_*3406del

Select item 14914906592.

rs1491490659 has merged into rs10609861 [Homo sapiens]

Variant type:: DELINS
Alleles:: AAAAAAAAAAAAAAAAA>-,A,AA,AAA,AAAA,AAAAA,AAAAAA,AAAAAAA,AAAAAAAA,AAAAAAAAA,AAAAAAAAAA,AAAAAAAAAAAA,AAAAAAAAAAAAA,AAAAAAAAAAAAAA,AAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,AAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA [Show Flanks]
Chromosome:: 17:49293669 (GRCh38)
17:47371031 (GRCh37)
Canonical SPDI:: NC_000017.11:49293655:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAA,NC_000017.11:49293655:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAA,NC_000017.11:49293655:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAA,NC_000017.11:49293655:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAA,NC_000017.11:49293655:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAA,NC_000017.11:49293655:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAA,NC_000017.11:49293655:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAA,NC_000017.11:49293655:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAA,NC_000017.11:49293655:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAA,NC_000017.11:49293655:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:49293655:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:49293655:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:49293655:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:49293655:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:49293655:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:49293655:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:49293655:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:49293655:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:49293655:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:49293655:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:49293655:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:49293655:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:49293655:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:49293655:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA,NC_000017.11:49293655:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAA:AAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAATAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA
Gene:: ZNF652 (Varview)
Functional Consequence:: intron_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: AAAAAAAAAAAAA=0./0 (ALFA)
AAAAAAAAAAAAAA=0./0 (GENOME_DK)
HGVS:: NC_000017.11:g.49293669_49293685del, NC_000017.11:g.49293670_49293685del, NC_000017.11:g.49293671_49293685del, NC_000017.11:g.49293672_49293685del, NC_000017.11:g.49293673_49293685del, NC_000017.11:g.49293674_49293685del, NC_000017.11:g.49293675_49293685del, NC_000017.11:g.49293676_49293685del, NC_000017.11:g.49293677_49293685del, NC_000017.11:g.49293678_49293685del, NC_000017.11:g.49293679_49293685del, NC_000017.11:g.49293681_49293685del, NC_000017.11:g.49293682_49293685del, NC_000017.11:g.49293683_49293685del, NC_000017.11:g.49293684_49293685del, NC_000017.11:g.49293685del, NC_000017.11:g.49293685dup, NC_000017.11:g.49293684_49293685dup, NC_000017.11:g.49293683_49293685dup, NC_000017.11:g.49293682_49293685dup, NC_000017.11:g.49293681_49293685dup, NC_000017.11:g.49293680_49293685dup, NC_000017.11:g.49293667_49293685dup, NC_000017.11:g.49293663_49293685dup, NC_000017.11:g.49293656_49293685A[33]TAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NC_000017.10:g.47371031_47371047del, NC_000017.10:g.47371032_47371047del, NC_000017.10:g.47371033_47371047del, NC_000017.10:g.47371034_47371047del, NC_000017.10:g.47371035_47371047del, NC_000017.10:g.47371036_47371047del, NC_000017.10:g.47371037_47371047del, NC_000017.10:g.47371038_47371047del, NC_000017.10:g.47371039_47371047del, NC_000017.10:g.47371040_47371047del, NC_000017.10:g.47371041_47371047del, NC_000017.10:g.47371043_47371047del, NC_000017.10:g.47371044_47371047del, NC_000017.10:g.47371045_47371047del, NC_000017.10:g.47371046_47371047del, NC_000017.10:g.47371047del, NC_000017.10:g.47371047dup, NC_000017.10:g.47371046_47371047dup, NC_000017.10:g.47371045_47371047dup, NC_000017.10:g.47371044_47371047dup, NC_000017.10:g.47371043_47371047dup, NC_000017.10:g.47371042_47371047dup, NC_000017.10:g.47371029_47371047dup, NC_000017.10:g.47371025_47371047dup, NC_000017.10:g.47371018_47371047A[33]TAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAAA[1], NM_001145365.3:c.*4741_*4757del, NM_001145365.3:c.*4742_*4757del, NM_001145365.3:c.*4743_*4757del, NM_001145365.3:c.*4744_*4757del, NM_001145365.3:c.*4745_*4757del, NM_001145365.3:c.*4746_*4757del, NM_001145365.3:c.*4747_*4757del, NM_001145365.3:c.*4748_*4757del, NM_001145365.3:c.*4749_*4757del, NM_001145365.3:c.*4750_*4757del, NM_001145365.3:c.*4751_*4757del, NM_001145365.3:c.*4753_*4757del, NM_001145365.3:c.*4754_*4757del, NM_001145365.3:c.*4755_*4757del, NM_001145365.3:c.*4756_*4757del, NM_001145365.3:c.*4757del, NM_001145365.3:c.*4757dup, NM_001145365.3:c.*4756_*4757dup, NM_001145365.3:c.*4755_*4757dup, NM_001145365.3:c.*4754_*4757dup, NM_001145365.3:c.*4753_*4757dup, NM_001145365.3:c.*4752_*4757dup, NM_001145365.3:c.*4739_*4757dup, NM_001145365.3:c.*4735_*4757dup, NM_001145365.3:c.*4728_*4757T[46]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NM_001145365.2:c.*4741_*4757del, NM_001145365.2:c.*4742_*4757del, NM_001145365.2:c.*4743_*4757del, NM_001145365.2:c.*4744_*4757del, NM_001145365.2:c.*4745_*4757del, NM_001145365.2:c.*4746_*4757del, NM_001145365.2:c.*4747_*4757del, NM_001145365.2:c.*4748_*4757del, NM_001145365.2:c.*4749_*4757del, NM_001145365.2:c.*4750_*4757del, NM_001145365.2:c.*4751_*4757del, NM_001145365.2:c.*4753_*4757del, NM_001145365.2:c.*4754_*4757del, NM_001145365.2:c.*4755_*4757del, NM_001145365.2:c.*4756_*4757del, NM_001145365.2:c.*4757del, NM_001145365.2:c.*4757dup, NM_001145365.2:c.*4756_*4757dup, NM_001145365.2:c.*4755_*4757dup, NM_001145365.2:c.*4754_*4757dup, NM_001145365.2:c.*4753_*4757dup, NM_001145365.2:c.*4752_*4757dup, NM_001145365.2:c.*4739_*4757dup, NM_001145365.2:c.*4735_*4757dup, NM_001145365.2:c.*4728_*4757T[46]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NM_001145365.1:c.*4741_*4757del, NM_001145365.1:c.*4742_*4757del, NM_001145365.1:c.*4743_*4757del, NM_001145365.1:c.*4744_*4757del, NM_001145365.1:c.*4745_*4757del, NM_001145365.1:c.*4746_*4757del, NM_001145365.1:c.*4747_*4757del, NM_001145365.1:c.*4748_*4757del, NM_001145365.1:c.*4749_*4757del, NM_001145365.1:c.*4750_*4757del, NM_001145365.1:c.*4751_*4757del, NM_001145365.1:c.*4753_*4757del, NM_001145365.1:c.*4754_*4757del, NM_001145365.1:c.*4755_*4757del, NM_001145365.1:c.*4756_*4757del, NM_001145365.1:c.*4757del, NM_001145365.1:c.*4757dup, NM_001145365.1:c.*4756_*4757dup, NM_001145365.1:c.*4755_*4757dup, NM_001145365.1:c.*4754_*4757dup, NM_001145365.1:c.*4753_*4757dup, NM_001145365.1:c.*4752_*4757dup, NM_001145365.1:c.*4739_*4757dup, NM_001145365.1:c.*4735_*4757dup, NM_001145365.1:c.*4728_*4757T[46]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_024450655.2:c.*4741_*4757del, XM_024450655.2:c.*4742_*4757del, XM_024450655.2:c.*4743_*4757del, XM_024450655.2:c.*4744_*4757del, XM_024450655.2:c.*4745_*4757del, XM_024450655.2:c.*4746_*4757del, XM_024450655.2:c.*4747_*4757del, XM_024450655.2:c.*4748_*4757del, XM_024450655.2:c.*4749_*4757del, XM_024450655.2:c.*4750_*4757del, XM_024450655.2:c.*4751_*4757del, XM_024450655.2:c.*4753_*4757del, XM_024450655.2:c.*4754_*4757del, XM_024450655.2:c.*4755_*4757del, XM_024450655.2:c.*4756_*4757del, XM_024450655.2:c.*4757del, XM_024450655.2:c.*4757dup, XM_024450655.2:c.*4756_*4757dup, XM_024450655.2:c.*4755_*4757dup, XM_024450655.2:c.*4754_*4757dup, XM_024450655.2:c.*4753_*4757dup, XM_024450655.2:c.*4752_*4757dup, XM_024450655.2:c.*4739_*4757dup, XM_024450655.2:c.*4735_*4757dup, XM_024450655.2:c.*4728_*4757T[46]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_024450655.1:c.*4741_*4757del, XM_024450655.1:c.*4742_*4757del, XM_024450655.1:c.*4743_*4757del, XM_024450655.1:c.*4744_*4757del, XM_024450655.1:c.*4745_*4757del, XM_024450655.1:c.*4746_*4757del, XM_024450655.1:c.*4747_*4757del, XM_024450655.1:c.*4748_*4757del, XM_024450655.1:c.*4749_*4757del, XM_024450655.1:c.*4750_*4757del, XM_024450655.1:c.*4751_*4757del, XM_024450655.1:c.*4753_*4757del, XM_024450655.1:c.*4754_*4757del, XM_024450655.1:c.*4755_*4757del, XM_024450655.1:c.*4756_*4757del, XM_024450655.1:c.*4757del, XM_024450655.1:c.*4757dup, XM_024450655.1:c.*4756_*4757dup, XM_024450655.1:c.*4755_*4757dup, XM_024450655.1:c.*4754_*4757dup, XM_024450655.1:c.*4753_*4757dup, XM_024450655.1:c.*4752_*4757dup, XM_024450655.1:c.*4739_*4757dup, XM_024450655.1:c.*4735_*4757dup, XM_024450655.1:c.*4728_*4757T[46]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_024450653.2:c.*4741_*4757del, XM_024450653.2:c.*4742_*4757del, XM_024450653.2:c.*4743_*4757del, XM_024450653.2:c.*4744_*4757del, XM_024450653.2:c.*4745_*4757del, XM_024450653.2:c.*4746_*4757del, XM_024450653.2:c.*4747_*4757del, XM_024450653.2:c.*4748_*4757del, XM_024450653.2:c.*4749_*4757del, XM_024450653.2:c.*4750_*4757del, XM_024450653.2:c.*4751_*4757del, XM_024450653.2:c.*4753_*4757del, XM_024450653.2:c.*4754_*4757del, XM_024450653.2:c.*4755_*4757del, XM_024450653.2:c.*4756_*4757del, XM_024450653.2:c.*4757del, XM_024450653.2:c.*4757dup, XM_024450653.2:c.*4756_*4757dup, XM_024450653.2:c.*4755_*4757dup, XM_024450653.2:c.*4754_*4757dup, XM_024450653.2:c.*4753_*4757dup, XM_024450653.2:c.*4752_*4757dup, XM_024450653.2:c.*4739_*4757dup, XM_024450653.2:c.*4735_*4757dup, XM_024450653.2:c.*4728_*4757T[46]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_024450653.1:c.*4741_*4757del, XM_024450653.1:c.*4742_*4757del, XM_024450653.1:c.*4743_*4757del, XM_024450653.1:c.*4744_*4757del, XM_024450653.1:c.*4745_*4757del, XM_024450653.1:c.*4746_*4757del, XM_024450653.1:c.*4747_*4757del, XM_024450653.1:c.*4748_*4757del, XM_024450653.1:c.*4749_*4757del, XM_024450653.1:c.*4750_*4757del, XM_024450653.1:c.*4751_*4757del, XM_024450653.1:c.*4753_*4757del, XM_024450653.1:c.*4754_*4757del, XM_024450653.1:c.*4755_*4757del, XM_024450653.1:c.*4756_*4757del, XM_024450653.1:c.*4757del, XM_024450653.1:c.*4757dup, XM_024450653.1:c.*4756_*4757dup, XM_024450653.1:c.*4755_*4757dup, XM_024450653.1:c.*4754_*4757dup, XM_024450653.1:c.*4753_*4757dup, XM_024450653.1:c.*4752_*4757dup, XM_024450653.1:c.*4739_*4757dup, XM_024450653.1:c.*4735_*4757dup, XM_024450653.1:c.*4728_*4757T[46]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], NM_014897.2:c.*4741_*4757del, NM_014897.2:c.*4742_*4757del, NM_014897.2:c.*4743_*4757del, NM_014897.2:c.*4744_*4757del, NM_014897.2:c.*4745_*4757del, NM_014897.2:c.*4746_*4757del, NM_014897.2:c.*4747_*4757del, NM_014897.2:c.*4748_*4757del, NM_014897.2:c.*4749_*4757del, NM_014897.2:c.*4750_*4757del, NM_014897.2:c.*4751_*4757del, NM_014897.2:c.*4753_*4757del, NM_014897.2:c.*4754_*4757del, NM_014897.2:c.*4755_*4757del, NM_014897.2:c.*4756_*4757del, NM_014897.2:c.*4757del, NM_014897.2:c.*4757dup, NM_014897.2:c.*4756_*4757dup, NM_014897.2:c.*4755_*4757dup, NM_014897.2:c.*4754_*4757dup, NM_014897.2:c.*4753_*4757dup, NM_014897.2:c.*4752_*4757dup, NM_014897.2:c.*4739_*4757dup, NM_014897.2:c.*4735_*4757dup, NM_014897.2:c.*4728_*4757T[46]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_024450656.2:c.*4741_*4757del, XM_024450656.2:c.*4742_*4757del, XM_024450656.2:c.*4743_*4757del, XM_024450656.2:c.*4744_*4757del, XM_024450656.2:c.*4745_*4757del, XM_024450656.2:c.*4746_*4757del, XM_024450656.2:c.*4747_*4757del, XM_024450656.2:c.*4748_*4757del, XM_024450656.2:c.*4749_*4757del, XM_024450656.2:c.*4750_*4757del, XM_024450656.2:c.*4751_*4757del, XM_024450656.2:c.*4753_*4757del, XM_024450656.2:c.*4754_*4757del, XM_024450656.2:c.*4755_*4757del, XM_024450656.2:c.*4756_*4757del, XM_024450656.2:c.*4757del, XM_024450656.2:c.*4757dup, XM_024450656.2:c.*4756_*4757dup, XM_024450656.2:c.*4755_*4757dup, XM_024450656.2:c.*4754_*4757dup, XM_024450656.2:c.*4753_*4757dup, XM_024450656.2:c.*4752_*4757dup, XM_024450656.2:c.*4739_*4757dup, XM_024450656.2:c.*4735_*4757dup, XM_024450656.2:c.*4728_*4757T[46]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_024450656.1:c.*4741_*4757del, XM_024450656.1:c.*4742_*4757del, XM_024450656.1:c.*4743_*4757del, XM_024450656.1:c.*4744_*4757del, XM_024450656.1:c.*4745_*4757del, XM_024450656.1:c.*4746_*4757del, XM_024450656.1:c.*4747_*4757del, XM_024450656.1:c.*4748_*4757del, XM_024450656.1:c.*4749_*4757del, XM_024450656.1:c.*4750_*4757del, XM_024450656.1:c.*4751_*4757del, XM_024450656.1:c.*4753_*4757del, XM_024450656.1:c.*4754_*4757del, XM_024450656.1:c.*4755_*4757del, XM_024450656.1:c.*4756_*4757del, XM_024450656.1:c.*4757del, XM_024450656.1:c.*4757dup, XM_024450656.1:c.*4756_*4757dup, XM_024450656.1:c.*4755_*4757dup, XM_024450656.1:c.*4754_*4757dup, XM_024450656.1:c.*4753_*4757dup, XM_024450656.1:c.*4752_*4757dup, XM_024450656.1:c.*4739_*4757dup, XM_024450656.1:c.*4735_*4757dup, XM_024450656.1:c.*4728_*4757T[46]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_047435626.1:c.*4741_*4757del, XM_047435626.1:c.*4742_*4757del, XM_047435626.1:c.*4743_*4757del, XM_047435626.1:c.*4744_*4757del, XM_047435626.1:c.*4745_*4757del, XM_047435626.1:c.*4746_*4757del, XM_047435626.1:c.*4747_*4757del, XM_047435626.1:c.*4748_*4757del, XM_047435626.1:c.*4749_*4757del, XM_047435626.1:c.*4750_*4757del, XM_047435626.1:c.*4751_*4757del, XM_047435626.1:c.*4753_*4757del, XM_047435626.1:c.*4754_*4757del, XM_047435626.1:c.*4755_*4757del, XM_047435626.1:c.*4756_*4757del, XM_047435626.1:c.*4757del, XM_047435626.1:c.*4757dup, XM_047435626.1:c.*4756_*4757dup, XM_047435626.1:c.*4755_*4757dup, XM_047435626.1:c.*4754_*4757dup, XM_047435626.1:c.*4753_*4757dup, XM_047435626.1:c.*4752_*4757dup, XM_047435626.1:c.*4739_*4757dup, XM_047435626.1:c.*4735_*4757dup, XM_047435626.1:c.*4728_*4757T[46]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_047435627.1:c.*4741_*4757del, XM_047435627.1:c.*4742_*4757del, XM_047435627.1:c.*4743_*4757del, XM_047435627.1:c.*4744_*4757del, XM_047435627.1:c.*4745_*4757del, XM_047435627.1:c.*4746_*4757del, XM_047435627.1:c.*4747_*4757del, XM_047435627.1:c.*4748_*4757del, XM_047435627.1:c.*4749_*4757del, XM_047435627.1:c.*4750_*4757del, XM_047435627.1:c.*4751_*4757del, XM_047435627.1:c.*4753_*4757del, XM_047435627.1:c.*4754_*4757del, XM_047435627.1:c.*4755_*4757del, XM_047435627.1:c.*4756_*4757del, XM_047435627.1:c.*4757del, XM_047435627.1:c.*4757dup, XM_047435627.1:c.*4756_*4757dup, XM_047435627.1:c.*4755_*4757dup, XM_047435627.1:c.*4754_*4757dup, XM_047435627.1:c.*4753_*4757dup, XM_047435627.1:c.*4752_*4757dup, XM_047435627.1:c.*4739_*4757dup, XM_047435627.1:c.*4735_*4757dup, XM_047435627.1:c.*4728_*4757T[46]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_047435628.1:c.*4741_*4757del, XM_047435628.1:c.*4742_*4757del, XM_047435628.1:c.*4743_*4757del, XM_047435628.1:c.*4744_*4757del, XM_047435628.1:c.*4745_*4757del, XM_047435628.1:c.*4746_*4757del, XM_047435628.1:c.*4747_*4757del, XM_047435628.1:c.*4748_*4757del, XM_047435628.1:c.*4749_*4757del, XM_047435628.1:c.*4750_*4757del, XM_047435628.1:c.*4751_*4757del, XM_047435628.1:c.*4753_*4757del, XM_047435628.1:c.*4754_*4757del, XM_047435628.1:c.*4755_*4757del, XM_047435628.1:c.*4756_*4757del, XM_047435628.1:c.*4757del, XM_047435628.1:c.*4757dup, XM_047435628.1:c.*4756_*4757dup, XM_047435628.1:c.*4755_*4757dup, XM_047435628.1:c.*4754_*4757dup, XM_047435628.1:c.*4753_*4757dup, XM_047435628.1:c.*4752_*4757dup, XM_047435628.1:c.*4739_*4757dup, XM_047435628.1:c.*4735_*4757dup, XM_047435628.1:c.*4728_*4757T[46]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1], XM_047435629.1:c.*4741_*4757del, XM_047435629.1:c.*4742_*4757del, XM_047435629.1:c.*4743_*4757del, XM_047435629.1:c.*4744_*4757del, XM_047435629.1:c.*4745_*4757del, XM_047435629.1:c.*4746_*4757del, XM_047435629.1:c.*4747_*4757del, XM_047435629.1:c.*4748_*4757del, XM_047435629.1:c.*4749_*4757del, XM_047435629.1:c.*4750_*4757del, XM_047435629.1:c.*4751_*4757del, XM_047435629.1:c.*4753_*4757del, XM_047435629.1:c.*4754_*4757del, XM_047435629.1:c.*4755_*4757del, XM_047435629.1:c.*4756_*4757del, XM_047435629.1:c.*4757del, XM_047435629.1:c.*4757dup, XM_047435629.1:c.*4756_*4757dup, XM_047435629.1:c.*4755_*4757dup, XM_047435629.1:c.*4754_*4757dup, XM_047435629.1:c.*4753_*4757dup, XM_047435629.1:c.*4752_*4757dup, XM_047435629.1:c.*4739_*4757dup, XM_047435629.1:c.*4735_*4757dup, XM_047435629.1:c.*4728_*4757T[46]ATTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT[1]

Select item 14914839953.

rs1491483995 [Homo sapiens]

Variant type:: DEL
Alleles:: TA>- [Show Flanks]
Chromosome:: 17:49293655 (GRCh38)
17:47371017 (GRCh37)
Canonical SPDI:: NC_000017.11:49293654:TA:
Gene:: ZNF652 (Varview)
Functional Consequence:: 3_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0./0 (ALFA)
HGVS:: NC_000017.11:g.49293655_49293656del, NC_000017.10:g.47371017_47371018del, NM_001145365.3:c.*4757_*4758del, NM_001145365.2:c.*4757_*4758del, NM_001145365.1:c.*4757_*4758del, XM_024450655.2:c.*4757_*4758del, XM_024450655.1:c.*4757_*4758del, XM_024450653.2:c.*4757_*4758del, XM_024450653.1:c.*4757_*4758del, NM_014897.2:c.*4757_*4758del, XM_024450656.2:c.*4757_*4758del, XM_024450656.1:c.*4757_*4758del, XM_047435626.1:c.*4757_*4758del, XM_047435627.1:c.*4757_*4758del, XM_047435628.1:c.*4757_*4758del, XM_047435629.1:c.*4757_*4758del

Select item 14912786274.

rs1491278627 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 17:49295007 (GRCh38)
17:47372370 (GRCh37)
Canonical SPDI:: NC_000017.11:49295007:T:TT
Gene:: ZNF652 (Varview)
Functional Consequence:: 3_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: TT=0./0 (ALFA)
T=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.49295008dup, NC_000017.10:g.47372370dup, NM_001145365.3:c.*3405dup, NM_001145365.2:c.*3405dup, NM_001145365.1:c.*3405dup, XM_024450655.2:c.*3405dup, XM_024450655.1:c.*3405dup, XM_024450653.2:c.*3405dup, XM_024450653.1:c.*3405dup, NM_014897.2:c.*3405dup, XM_024450656.2:c.*3405dup, XM_024450656.1:c.*3405dup, XM_047435626.1:c.*3405dup, XM_047435627.1:c.*3405dup, XM_047435628.1:c.*3405dup, XM_047435629.1:c.*3405dup

Select item 14909511165.

rs1490951116 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C,G [Show Flanks]
Chromosome:: 17:49293270 (GRCh38)
17:47370632 (GRCh37)
Canonical SPDI:: NC_000017.11:49293269:T:C,NC_000017.11:49293269:T:G
Gene:: ZNF652 (Varview)
Functional Consequence:: 3_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: C=0.000066/1 (ALFA)
G=0.000008/2 (TOPMED)
C=0.000223/1 (Estonian)
HGVS:: NC_000017.11:g.49293270T>C, NC_000017.11:g.49293270T>G, NC_000017.10:g.47370632T>C, NC_000017.10:g.47370632T>G, NM_001145365.3:c.*5143A>G, NM_001145365.3:c.*5143A>C, NM_001145365.2:c.*5143A>G, NM_001145365.2:c.*5143A>C, NM_001145365.1:c.*5143A>G, NM_001145365.1:c.*5143A>C, XM_024450655.2:c.*5143A>G, XM_024450655.2:c.*5143A>C, XM_024450655.1:c.*5143A>G, XM_024450655.1:c.*5143A>C, XM_024450653.2:c.*5143A>G, XM_024450653.2:c.*5143A>C, XM_024450653.1:c.*5143A>G, XM_024450653.1:c.*5143A>C, NM_014897.2:c.*5143A>G, NM_014897.2:c.*5143A>C, XM_024450656.2:c.*5143A>G, XM_024450656.2:c.*5143A>C, XM_024450656.1:c.*5143A>G, XM_024450656.1:c.*5143A>C, XM_047435626.1:c.*5143A>G, XM_047435626.1:c.*5143A>C, XM_047435627.1:c.*5143A>G, XM_047435627.1:c.*5143A>C, XM_047435628.1:c.*5143A>G, XM_047435628.1:c.*5143A>C, XM_047435629.1:c.*5143A>G, XM_047435629.1:c.*5143A>C

Select item 14909155856.

rs1490915585 [Homo sapiens]

Variant type:: DELINS
Alleles:: ->T [Show Flanks]
Chromosome:: 17:49295140 (GRCh38)
17:47372503 (GRCh37)
Canonical SPDI:: NC_000017.11:49295140:T:TT
Gene:: ZNF652 (Varview)
Functional Consequence:: 3_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: TT=0./0 (ALFA)
T=0.000007/1 (GnomAD)
T=0.000008/2 (TOPMED)
HGVS:: NC_000017.11:g.49295141dup, NC_000017.10:g.47372503dup, NM_001145365.3:c.*3272dup, NM_001145365.2:c.*3272dup, NM_001145365.1:c.*3272dup, XM_024450655.2:c.*3272dup, XM_024450655.1:c.*3272dup, XM_024450653.2:c.*3272dup, XM_024450653.1:c.*3272dup, NM_014897.2:c.*3272dup, XM_024450656.2:c.*3272dup, XM_024450656.1:c.*3272dup, XM_047435626.1:c.*3272dup, XM_047435627.1:c.*3272dup, XM_047435628.1:c.*3272dup, XM_047435629.1:c.*3272dup

Select item 14904989057.

rs1490498905 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:49297498 (GRCh38)
17:47374860 (GRCh37)
Canonical SPDI:: NC_000017.11:49297497:G:A
Gene:: ZNF652 (Varview)
Functional Consequence:: 3_prime_UTR_variant,intron_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_000017.11:g.49297498G>A, NC_000017.10:g.47374860G>A, NM_001145365.3:c.*915C>T, NM_001145365.2:c.*915C>T, NM_001145365.1:c.*915C>T, XM_024450655.2:c.*915C>T, XM_024450655.1:c.*915C>T, XM_024450653.2:c.*915C>T, XM_024450653.1:c.*915C>T, NM_014897.2:c.*915C>T, XM_024450656.2:c.*915C>T, XM_024450656.1:c.*915C>T, XM_047435626.1:c.*915C>T, XM_047435627.1:c.*915C>T, XM_047435628.1:c.*915C>T, XM_047435629.1:c.*915C>T

Select item 14904027488.

rs1490402748 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:49294332 (GRCh38)
17:47371694 (GRCh37)
Canonical SPDI:: NC_000017.11:49294331:G:A
Gene:: ZNF652 (Varview)
Functional Consequence:: 3_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000007/1 (GnomAD)
HGVS:: NC_000017.11:g.49294332G>A, NC_000017.10:g.47371694G>A, NM_001145365.3:c.*4081C>T, NM_001145365.2:c.*4081C>T, NM_001145365.1:c.*4081C>T, XM_024450655.2:c.*4081C>T, XM_024450655.1:c.*4081C>T, XM_024450653.2:c.*4081C>T, XM_024450653.1:c.*4081C>T, NM_014897.2:c.*4081C>T, XM_024450656.2:c.*4081C>T, XM_024450656.1:c.*4081C>T, XM_047435626.1:c.*4081C>T, XM_047435627.1:c.*4081C>T, XM_047435628.1:c.*4081C>T, XM_047435629.1:c.*4081C>T

Select item 14899111999.

rs1489911199 [Homo sapiens]

Variant type:: SNV:
Alleles:: A>T
Chromosome:: no mapping
Canonical SPDI:

Select item 148923175010.

rs1489231750 [Homo sapiens]

Variant type:: SNV
Alleles:: G>T [Show Flanks]
Chromosome:: 17:49298269 (GRCh38)
17:47375631 (GRCh37)
Canonical SPDI:: NC_000017.11:49298268:G:T
Gene:: ZNF652 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: T=0./0 (ALFA)
T=0.000008/2 (TOPMED)
T=0.000014/2 (GnomAD)
HGVS:: NC_000017.11:g.49298269G>T, NC_000017.10:g.47375631G>T, NM_001145365.3:c.*144C>A, NM_001145365.2:c.*144C>A, NM_001145365.1:c.*144C>A, XR_934423.3:n.2347C>A, XR_934423.2:n.2377C>A, XR_934423.1:n.2176C>A, XM_024450655.2:c.*144C>A, XM_024450655.1:c.*144C>A, XM_024450653.2:c.*144C>A, XM_024450653.1:c.*144C>A, NM_014897.2:c.*144C>A, XM_024450656.2:c.*144C>A, XM_024450656.1:c.*144C>A, NR_135579.2:n.2149C>A, NR_135579.1:n.2013C>A, XM_047435626.1:c.*144C>A, XM_047435627.1:c.*144C>A, XM_047435628.1:c.*144C>A, XM_047435629.1:c.*144C>A

Select item 148904841611.

rs1489048416 [Homo sapiens]

Variant type:: DEL
Alleles:: CC>- [Show Flanks]
Chromosome:: 17:49295981 (GRCh38)
17:47373343 (GRCh37)
Canonical SPDI:: NC_000017.11:49295980:CC:
Gene:: ZNF652 (Varview)
Functional Consequence:: 3_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa,by cluster
MAF:: -=0.00224/10 (ALFA)
-=0.00018/5 (TOMMO)
-=0.00246/11 (Estonian)
HGVS:: NC_000017.11:g.49295981_49295982del, NC_000017.10:g.47373343_47373344del, NM_001145365.3:c.*2431_*2432del, NM_001145365.2:c.*2431_*2432del, NM_001145365.1:c.*2431_*2432del, XM_024450655.2:c.*2431_*2432del, XM_024450655.1:c.*2431_*2432del, XM_024450653.2:c.*2431_*2432del, XM_024450653.1:c.*2431_*2432del, NM_014897.2:c.*2431_*2432del, XM_024450656.2:c.*2431_*2432del, XM_024450656.1:c.*2431_*2432del, XM_047435626.1:c.*2431_*2432del, XM_047435627.1:c.*2431_*2432del, XM_047435628.1:c.*2431_*2432del, XM_047435629.1:c.*2431_*2432del

Select item 148892792012.

rs1488927920 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 17:49317078 (GRCh38)
17:47394440 (GRCh37)
Canonical SPDI:: NC_000017.11:49317077:A:G
Gene:: ZNF652 (Varview)
Functional Consequence:: synonymous_variant,non_coding_transcript_variant,coding_sequence_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: G=0./0 (ALFA)
G=0.000014/2 (GnomAD)
HGVS:: NC_000017.11:g.49317078A>G, NC_000017.10:g.47394440A>G, NM_001145365.3:c.648T>C, NM_001145365.2:c.648T>C, NM_001145365.1:c.648T>C, XR_934423.3:n.1030T>C, XR_934423.2:n.1060T>C, XR_934423.1:n.859T>C, XM_024450655.2:c.648T>C, XM_024450655.1:c.648T>C, XM_024450653.2:c.648T>C, XM_024450653.1:c.648T>C, NM_014897.2:c.648T>C, XM_047435626.1:c.648T>C, XM_047435627.1:c.648T>C

Select item 148883346913.

rs1488833469 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 17:49290580 (GRCh38)
17:47367942 (GRCh37)
Canonical SPDI:: NC_000017.11:49290579:A:G
Gene:: ZNF652 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: G=0./0 (ALFA)
G=0.000004/1 (TOPMED)
HGVS:: NC_000017.11:g.49290580A>G, NC_000017.10:g.47367942A>G, NM_001145365.3:c.*7833T>C, NM_001145365.2:c.*7833T>C, NM_001145365.1:c.*7833T>C, XR_934423.3:n.3626T>C, XR_934423.2:n.3656T>C, XR_934423.1:n.3455T>C, XM_024450655.2:c.*7833T>C, XM_024450655.1:c.*7833T>C, XM_024450653.2:c.*7833T>C, XM_024450653.1:c.*7833T>C, NM_014897.2:c.*7833T>C, XM_024450656.2:c.*7833T>C, XM_024450656.1:c.*7833T>C, NR_135579.2:n.3428T>C, NR_135579.1:n.3292T>C, XM_047435626.1:c.*7833T>C, XM_047435627.1:c.*7833T>C, XM_047435628.1:c.*7833T>C, XM_047435629.1:c.*7833T>C

Select item 148876918214.

rs1488769182 [Homo sapiens]

Variant type:: DEL
Alleles:: TT>- [Show Flanks]
Chromosome:: 17:49295985 (GRCh38)
17:47373347 (GRCh37)
Canonical SPDI:: NC_000017.11:49295984:TT:
Gene:: ZNF652 (Varview)
Functional Consequence:: 3_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: -=0.0004/2 (ALFA)
-=0.0004/2 (Estonian)
HGVS:: NC_000017.11:g.49295985_49295986del, NC_000017.10:g.47373347_47373348del, NM_001145365.3:c.*2427_*2428del, NM_001145365.2:c.*2427_*2428del, NM_001145365.1:c.*2427_*2428del, XM_024450655.2:c.*2427_*2428del, XM_024450655.1:c.*2427_*2428del, XM_024450653.2:c.*2427_*2428del, XM_024450653.1:c.*2427_*2428del, NM_014897.2:c.*2427_*2428del, XM_024450656.2:c.*2427_*2428del, XM_024450656.1:c.*2427_*2428del, XM_047435626.1:c.*2427_*2428del, XM_047435627.1:c.*2427_*2428del, XM_047435628.1:c.*2427_*2428del, XM_047435629.1:c.*2427_*2428del

Select item 148868104715.

rs1488681047 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:49311381 (GRCh38)
17:47388743 (GRCh37)
Canonical SPDI:: NC_000017.11:49311380:T:C
Gene:: ZNF652 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,missense_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.49311381T>C, NC_000017.10:g.47388743T>C, NM_001145365.3:c.1240A>G, NM_001145365.2:c.1240A>G, NM_001145365.1:c.1240A>G, XR_934423.3:n.1622A>G, XR_934423.2:n.1652A>G, XR_934423.1:n.1451A>G, XM_024450655.2:c.1240A>G, XM_024450655.1:c.1240A>G, XM_024450653.2:c.1240A>G, XM_024450653.1:c.1240A>G, NM_014897.2:c.1240A>G, XM_024450656.2:c.700A>G, XM_024450656.1:c.700A>G, NR_135579.2:n.1424A>G, NR_135579.1:n.1288A>G, XM_047435626.1:c.1240A>G, XM_047435627.1:c.1240A>G, XM_047435628.1:c.700A>G, XM_047435629.1:c.700A>G, NP_001138837.1:p.Met414Val, XP_024306423.1:p.Met414Val, XP_024306421.1:p.Met414Val, NP_055712.1:p.Met414Val, XP_024306424.1:p.Met234Val, XP_047291582.1:p.Met414Val, XP_047291583.1:p.Met414Val, XP_047291584.1:p.Met234Val, XP_047291585.1:p.Met234Val

Select item 148865071616.

rs1488650716 [Homo sapiens]

Variant type:: SNV
Alleles:: A>G [Show Flanks]
Chromosome:: 17:49317137 (GRCh38)
17:47394499 (GRCh37)
Canonical SPDI:: NC_000017.11:49317136:A:G
Gene:: ZNF652 (Varview)
Functional Consequence:: non_coding_transcript_variant,coding_sequence_variant,missense_variant,intron_variant
Validated:: by frequency
MAF:: G=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.49317137A>G, NC_000017.10:g.47394499A>G, NM_001145365.3:c.589T>C, NM_001145365.2:c.589T>C, NM_001145365.1:c.589T>C, XR_934423.3:n.971T>C, XR_934423.2:n.1001T>C, XR_934423.1:n.800T>C, XM_024450655.2:c.589T>C, XM_024450655.1:c.589T>C, XM_024450653.2:c.589T>C, XM_024450653.1:c.589T>C, NM_014897.2:c.589T>C, XM_047435626.1:c.589T>C, XM_047435627.1:c.589T>C, NP_001138837.1:p.Ser197Pro, XP_024306423.1:p.Ser197Pro, XP_024306421.1:p.Ser197Pro, NP_055712.1:p.Ser197Pro, XP_047291582.1:p.Ser197Pro, XP_047291583.1:p.Ser197Pro

Select item 148861112317.

rs1488611123 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:49316835 (GRCh38)
17:47394197 (GRCh37)
Canonical SPDI:: NC_000017.11:49316834:T:C
Gene:: ZNF652 (Varview)
Functional Consequence:: synonymous_variant,non_coding_transcript_variant,coding_sequence_variant,intron_variant
Validated:: by frequency
MAF:: C=0.000004/1 (GnomAD_exomes)
HGVS:: NC_000017.11:g.49316835T>C, NC_000017.10:g.47394197T>C, NM_001145365.3:c.891A>G, NM_001145365.2:c.891A>G, NM_001145365.1:c.891A>G, XR_934423.3:n.1273A>G, XR_934423.2:n.1303A>G, XR_934423.1:n.1102A>G, XM_024450655.2:c.891A>G, XM_024450655.1:c.891A>G, XM_024450653.2:c.891A>G, XM_024450653.1:c.891A>G, NM_014897.2:c.891A>G, XM_047435626.1:c.891A>G, XM_047435627.1:c.891A>G

Select item 148807541018.

rs1488075410 [Homo sapiens]

Variant type:: SNV
Alleles:: G>A [Show Flanks]
Chromosome:: 17:49296860 (GRCh38)
17:47374222 (GRCh37)
Canonical SPDI:: NC_000017.11:49296859:G:A
Gene:: ZNF652 (Varview)
Functional Consequence:: 3_prime_UTR_variant,intron_variant
Validated:: by frequency,by alfa
MAF:: A=0./0 (ALFA)
A=0.000014/2 (GnomAD)
HGVS:: NC_000017.11:g.49296860G>A, NC_000017.10:g.47374222G>A, NM_001145365.3:c.*1553C>T, NM_001145365.2:c.*1553C>T, NM_001145365.1:c.*1553C>T, XM_024450655.2:c.*1553C>T, XM_024450655.1:c.*1553C>T, XM_024450653.2:c.*1553C>T, XM_024450653.1:c.*1553C>T, NM_014897.2:c.*1553C>T, XM_024450656.2:c.*1553C>T, XM_024450656.1:c.*1553C>T, XM_047435626.1:c.*1553C>T, XM_047435627.1:c.*1553C>T, XM_047435628.1:c.*1553C>T, XM_047435629.1:c.*1553C>T

Select item 148741721419.

rs1487417214 [Homo sapiens]

Variant type:: SNV
Alleles:: T>C [Show Flanks]
Chromosome:: 17:49291083 (GRCh38)
17:47368445 (GRCh37)
Canonical SPDI:: NC_000017.11:49291082:T:C
Gene:: ZNF652 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa
MAF:: C=0./0 (ALFA)
C=0.000011/3 (TOPMED)
HGVS:: NC_000017.11:g.49291083T>C, NC_000017.10:g.47368445T>C, NM_001145365.3:c.*7330A>G, NM_001145365.2:c.*7330A>G, NM_001145365.1:c.*7330A>G, XR_934423.3:n.3123A>G, XR_934423.2:n.3153A>G, XR_934423.1:n.2952A>G, XM_024450655.2:c.*7330A>G, XM_024450655.1:c.*7330A>G, XM_024450653.2:c.*7330A>G, XM_024450653.1:c.*7330A>G, NM_014897.2:c.*7330A>G, XM_024450656.2:c.*7330A>G, XM_024450656.1:c.*7330A>G, NR_135579.2:n.2925A>G, NR_135579.1:n.2789A>G, XM_047435626.1:c.*7330A>G, XM_047435627.1:c.*7330A>G, XM_047435628.1:c.*7330A>G, XM_047435629.1:c.*7330A>G

Select item 148701294820.

rs1487012948 [Homo sapiens]

Variant type:: SNV
Alleles:: T>A [Show Flanks]
Chromosome:: 17:49291206 (GRCh38)
17:47368568 (GRCh37)
Canonical SPDI:: NC_000017.11:49291205:T:A
Gene:: ZNF652 (Varview)
Functional Consequence:: non_coding_transcript_variant,3_prime_UTR_variant
Validated:: by frequency,by alfa,by cluster
MAF:: A=0./0 (ALFA)
A=0.000004/1 (TOPMED)
A=0.000007/1 (GnomAD)
HGVS:: NC_000017.11:g.49291206T>A, NC_000017.10:g.47368568T>A, NM_001145365.3:c.*7207A>T, NM_001145365.2:c.*7207A>T, NM_001145365.1:c.*7207A>T, XR_934423.3:n.3000A>T, XR_934423.2:n.3030A>T, XR_934423.1:n.2829A>T, XM_024450655.2:c.*7207A>T, XM_024450655.1:c.*7207A>T, XM_024450653.2:c.*7207A>T, XM_024450653.1:c.*7207A>T, NM_014897.2:c.*7207A>T, XM_024450656.2:c.*7207A>T, XM_024450656.1:c.*7207A>T, NR_135579.2:n.2802A>T, NR_135579.1:n.2666A>T, XM_047435626.1:c.*7207A>T, XM_047435627.1:c.*7207A>T, XM_047435628.1:c.*7207A>T, XM_047435629.1:c.*7207A>T

<< First< Prev

Page of 128

Next >Last >>

dbSNP

Result Filters

Validation Status

Publication

Function Class

Variation Class

Annotation

Global MAF

Custom range

Additional filters

Display Settings:

Send to:

Links from Nucleotide

Items: 1 to 20 of 2546

Display Settings:

Send to:

Supplemental Content

Find related data

Recent activity