Variant #0000614678 (NC_000013.10:g.77574952T>C, NM_006493.2:c.1072T>C (CLN5))

Chromosome 13
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.77574952T>C
DNA change (hg38) g.77000817T>C
Published as CLN5(NM_006493.4):c.925T>C (p.L309=)
ISCN -
DB-ID CLN5_000034
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 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLN5 NM_006493.2 -?/. - c.1072T>C r.(?) p.(Leu358=)
FBXL3 NM_012158.2 -?/. - c.*6328A>G r.(=) p.(=)


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