Variant #0000925232 (NC_000010.10:g.95353609_95353628del, NM_006744.3:c.524_543del (RBP4))

Chromosome 10
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.95353609_95353628del
DNA change (hg38) -
Published as RBP4(NM_006744.4):c.524_543delAGGAGCTGTGCCTGGCCAGG (p.E175Afs*27)
ISCN -
DB-ID RBP4_000020
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 2023-04-16 21:50:28 +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     
RBP4 NM_006744.3 +?/. - c.524_543del r.(?) p.(Glu175Alafs*27)
FFAR4 NM_181745.3 +?/. - c.*6243_*6262del r.(=) p.(=)


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