Variant #0000301371 (NC_000002.11:g.109356978G>C, NM_006267.4:c.816G>C (RANBP2))

Chromosome 2
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.109356978G>C
DNA change (hg38) g.108740522G>C
Published as RANBP2(NM_006267.4):c.816G>C (p.L272F), RANBP2(NM_006267.5):c.816G>C (p.(Leu272Phe))
ISCN -
DB-ID RANBP2_000003 See all 2 reported entries
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) 0.02096 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-04-19 20:20:39 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RANBP2 NM_006267.4 -?/. - c.816G>C r.(?) p.(Leu272Phe)


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