Variant #0001000646 (NC_000013.10:g.92560253_92560258dup, NM_004466.4:c.1343_1348dup (GPC5))

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.92560253_92560258dup
DNA change (hg38) -
Published as GPC5(NM_004466.4):c.1343_1348dupTCAAAG (p.(Val448_Lys449dup))
ISCN -
DB-ID GPC5_000007
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
GPC5 NM_004466.4 -?/. - c.1343_1348dup r.(?) p.(Val448_Lys449dup)


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