Variant #0000557760 (NC_000016.9:g.28506822G>A, NM_001042432.1:c.-3558C>T (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.28506822G>A
DNA change (hg38) g.28495501G>A
Published as APOBR(NM_018690.3):c.460G>A (p.(Gly154Ser))
ISCN -
DB-ID CLN3_000108
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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLN3 NM_001042432.1 -?/. - c.-3558C>T r.(?) p.(=)
APOBR NM_018690.3 -?/. - c.460G>A r.(?) p.(Gly154Ser)
IL27 NM_145659.3 -?/. - c.*4150C>T r.(=) p.(=)


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