Variant #0000541655 (NC_000010.10:g.95353677C>T, NM_006744.3:c.471G>A (RBP4))

Chromosome 10
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.95353677C>T
DNA change (hg38) g.93593920C>T
Published as RBP4(NM_006744.3):c.471G>A (p.R157=)
ISCN -
DB-ID RBP4_000010
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) 3.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-06-29 09:16:40 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RBP4 NM_006744.3 -?/. - c.471G>A r.(?) p.(Arg157=)
FFAR4 NM_181745.3 -?/. - c.*6311C>T r.(=) p.(=)


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