Variant #0000557758 (NC_000016.9:g.28503036C>T, NM_001042432.1:c.45G>A (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.28503036C>T
DNA change (hg38) g.28491715C>T
Published as CLN3(NM_001042432.1):c.45G>A (p.E15=), CLN3(NM_001042432.2):c.45G>A (p.E15=)
ISCN -
DB-ID CLN3_000096 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) 0.00235 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLN3 NM_001042432.1 -?/. - c.45G>A r.(?) p.(Glu15=)
APOBR NM_018690.3 -?/. - c.-2967C>T r.(?) p.(=)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.