Variant #0001033461 (NC_000002.11:g.73308254_73308256dup, NC_000002.11(NM_015470.2):c.1569-4916_1569-4914dup (RAB11FIP5))

Chromosome 2
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.73308254_73308256dup
DNA change (hg38) -
Published as RAB11FIP5(NM_001371272.1):c.2134_2136dup (p.(Gly712dup))
ISCN -
DB-ID RAB11FIP5_000002
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 2025-05-05 21:14:00 +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     
RAB11FIP5 NM_015470.2 ?/. - c.1569-4916_1569-4914dup r.(=) p.(=)


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