Variant #0000803733 (NC_000008.10:g.68066372G>T, NC_000008.10(NM_024790.6):c.2226+1G>T (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.68066372G>T
DNA change (hg38) -
Published as CSPP1(NM_001363131.1):c.2160+1G>T, CSPP1(NM_024790.6):c.2226+1G>T
ISCN -
DB-ID CSPP1_000085
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 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited 2024-02-26 20:06:56 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CSPP1 NM_024790.6 +?/. - c.2226+1G>T r.spl? p.?


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