Variant #0001002355 (NC_000016.9:g.3900713G>C, NM_004380.2:c.383C>G (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.3900713G>C
DNA change (hg38) -
Published as CREBBP(NM_004380.2):c.383C>G (p.S128C), CREBBP(NM_004380.3):c.383C>G (p.S128C)
ISCN -
DB-ID CREBBP_000229 See all 4 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) 0.00073 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2024-08-28 13:16:32 +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.383C>G r.(?) p.(Ser128Cys)


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