Variant #0000717431 (NC_000001.10:g.33134914A>T, NM_005610.2:c.844A>T (RBBP4))

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.33134914A>T
DNA change (hg38) -
Published as RBBP4(NM_005610.3):c.844A>T (p.N282Y)
ISCN -
DB-ID RBBP4_000001
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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RBBP4 NM_005610.2 ?/. - c.844A>T r.(?) p.(Asn282Tyr)
SYNC NM_030786.2 ?/. - c.*12537T>A r.(=) p.(=)


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