Variant #0000912981 (NC_000008.10:g.67988704A>G, NC_000008.10(NM_024790.6):c.208-13A>G (CSPP1))

Chromosome 8
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.67988704A>G
DNA change (hg38) -
Published as CSPP1(NM_001382391.1):c.100-13A>G, CSPP1(NM_024790.6):c.208-13A>G
ISCN -
DB-ID CSPP1_000092 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) 0.00076 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-01-11 15:44:22 +01:00 (CET)
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.208-13A>G r.(=) p.(=)


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