Variant #0001046317 (NC_000011.9:g.47470355C>T, NM_005055.4:c.162G>A (RAPSN))

Chromosome 11
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.47470355C>T
DNA change (hg38) -
Published as RAPSN(NM_005055.4):c.162G>A (p.(Ser54=)), RAPSN(NM_005055.5):c.162G>A (p.S54=)
ISCN -
DB-ID RAPSN_000087 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) 0.00347 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-07-08 13:22:38 +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     
RAPSN NM_005055.4 -?/. - c.162G>A r.(?) p.(Ser54=)


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