Variant #0000541654 (NC_000010.10:g.95353668G>A, NM_006744.3:c.480C>T (RBP4))

Chromosome 10
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.95353668G>A
DNA change (hg38) g.93593911G>A
Published as RBP4(NM_006744.4):c.480C>T (p.N160=)
ISCN -
DB-ID RBP4_000009
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) 9.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RBP4 NM_006744.3 -/. - c.480C>T r.(?) p.(Asn160=)
FFAR4 NM_181745.3 -/. - c.*6302G>A r.(=) p.(=)


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