Variant #0000321047 (NC_000001.10:g.155629930C>T, NM_139118.2:c.1909G>A (YY1AP1))

Chromosome 1
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.155629930C>T
DNA change (hg38) g.155660139C>T
Published as YY1AP1(NM_001198899.1):c.1738G>A (p.(Ala580Thr)), YY1AP1(NM_001198903.1):c.2185G>A (p.A729T)
ISCN -
DB-ID YY1AP1_000002 See all 3 reported entries
Variant remarks VKGL data sharing initiative Nederland
Reference -
ClinVar ID -
dbSNP ID -
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.0002 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-05-09 15:24:52 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
YY1AP1 NM_139118.2 ?/. - c.1909G>A r.(?) p.(Ala637Thr)


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