Variant #0001054681 (NC_000013.10:g.77574839A>G, NM_006493.2:c.959A>G (CLN5))

Chromosome 13
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.77574839A>G
DNA change (hg38) -
Published as CLN5(NM_006493.4):c.812A>G (p.(Asn271Ser))
ISCN -
DB-ID CLN5_000063
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) 9.0E-5 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 2025-11-01 13:22:20 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLN5 NM_006493.2 ?/. - c.959A>G r.(?) p.(Asn320Ser)
FBXL3 NM_012158.2 ?/. - c.*6441T>C r.(=) p.(=)


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