Variant #0000946999 (NC_000001.10:g.155657869G>A, NM_139118.2:c.171C>T (YY1AP1))

Chromosome 1
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.155657869G>A
DNA change (hg38) -
Published as YY1AP1(NM_001198903.1):c.387C>T (p.L129=)
ISCN -
DB-ID YY1AP1_000026
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) 1.0E-5 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-11-27 17:35:39 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
DAP3 NM_004632.3 -?/. - c.-1104G>A r.(?) p.(=)
YY1AP1 NM_139118.2 -?/. - c.171C>T r.(?) p.(=)


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