Variant #0000724580 (NC_000013.10:g.77575075_77575078dup, NM_006493.2:c.1195_1198dup (CLN5))

Chromosome 13
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.77575075_77575078dup
DNA change (hg38) -
Published as CLN5(NM_006493.2):c.1195_1198dupATCA (p.R400Nfs*131)
ISCN -
DB-ID CLN5_000049
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CLN5 NM_006493.2 ?/. - c.1195_1198dup r.(?) p.(Arg400Asnfs*131)
FBXL3 NM_012158.2 ?/. - c.*6202_*6205dup r.(=) p.(=)


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