Variant #0000807400 (NC_000016.9:g.3860674C>T, NM_004380.2:c.905G>A (CREBBP))

Chromosome 16
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.3860674C>T
DNA change (hg38) -
Published as CREBBP(NM_001079846.1):c.905G>A (p.(Ser302Asn)), CREBBP(NM_004380.2):c.905G>A (p.S302N)
ISCN -
DB-ID CREBBP_000329 See all 2 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) 0.00015 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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CREBBP NM_004380.2 -?/. - c.905G>A r.(?) p.(Ser302Asn)


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