Variant #0000551071 (NC_000013.10:g.77575065C>T, NM_006493.2:c.1185C>T (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.77575065C>T
DNA change (hg38) g.77000930C>T
Published as CLN5(NM_006493.2):c.1185C>T (p.I395=)
ISCN -
DB-ID CLN5_000033
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) 3.0E-5 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 2020-07-04 14:02:29 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLN5 NM_006493.2 -?/. - c.1185C>T r.(?) p.(Ile395=)
FBXL3 NM_012158.2 -?/. - c.*6215G>A r.(=) p.(=)


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