Variant #0000557753 (NC_000016.9:g.28499936A>G, NM_001042432.1:c.270T>C (CLN3))

Chromosome 16
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.28499936A>G
DNA change (hg38) g.28488615A>G
Published as CLN3(NM_001042432.1):c.270T>C (p.F90=), CLN3(NM_001042432.2):c.270T>C (p.F90=), CLN3(NM_001286105.1):c.50T>C (p.L17S)
ISCN -
DB-ID CLN3_000106 See all 3 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) 0.0003 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLN3 NM_001042432.1 -?/. - c.270T>C r.(?) p.(Phe90=)


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