Variant #0000329492 (NC_000003.11:g.62860547_62860552dup, NM_003716.3:c.162_167dup (CADPS))

Chromosome 3
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.62860547_62860552dup
DNA change (hg38) g.62874872_62874877dup
Published as CADPS(NM_003716.3):c.167_168insCGCCGG (p.?)
ISCN -
DB-ID CADPS_000003
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 2018-01-15 20:58:59 +01:00 (CET)
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     
CADPS NM_003716.3 ?/. - c.162_167dup r.(?) p.(Ala57_Gly58dup)


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