Variant #0000978264 (NC_000008.10:g.67986546_67986547del, NM_024790.6:c.167_168del (CSPP1))

Chromosome 8
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.67986546_67986547del
DNA change (hg38) -
Published as CSPP1(NM_001382391.1):c.59_60del (p.(Lys20SerfsTer6))
ISCN -
DB-ID CSPP1_000091 See all 2 reported entries
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 2024-04-19 20:27:30 +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     
CSPP1 NM_024790.6 +?/. - c.167_168del r.(?) p.(Lys56Serfs*6)


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