Variant #0001051870 (NC_000004.11:g.160277030_160277032dup, NM_014247.2:c.4194_4196dup (RAPGEF2))

Chromosome 4
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.160277030_160277032dup
DNA change (hg38) -
Published as RAPGEF2(NM_001351724.3):c.4752_4754dup (p.(Pro1587dup))
ISCN -
DB-ID RAPGEF2_000012
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

Haplotype     

RNA change     

Protein     
RAPGEF2 NM_014247.2 ?/. - c.4194_4196dup - r.(?) p.(Pro1401dup)


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