Variant #0000608922 (NC_000003.11:g.9988221_9988226dup, NM_015513.4:c.*1958_*1963dup (CRELD1))

Chromosome 3
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.9988221_9988226dup
DNA change (hg38) g.9946537_9946542dup
Published as PRRT3(NM_207351.3):c.2644_2645insTGCGCG (p.(Val880_Arg881dup))
ISCN -
DB-ID CRELD1_000037
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 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CRELD1 NM_015513.4 -?/. - c.*1958_*1963dup r.(=) p.(=)
PRRT3 NM_207351.3 -?/. - c.2639_2644dup r.(?) p.(Val880_Arg881dup)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.