Variant #0000623466 (NC_000016.9:g.3900915_3900916insTTTA, NM_004380.2:c.180_181insTAAA (CREBBP))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.3900915_3900916insTTTA
DNA change (hg38) g.3850914_3850915insTTTA
Published as CREBBP(NM_004380.3):c.180_181insTAAA (p.P61*)
ISCN -
DB-ID CREBBP_000318
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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-07-09 11:28:08 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CREBBP NM_004380.2 +/. - c.180_181insTAAA r.(?) p.(Pro61Ter)


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