Variant #0000265029 (NC_000008.10:g.67976622C>T, NM_024790.6:c.-12C>T (CSPP1))

Chromosome 8
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.67976622C>T
DNA change (hg38) g.67064387C>T
Published as CSPP1(NM_024790.6):c.-12C>T
ISCN -
DB-ID CSPP1_000022
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) 0.00106 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 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     
COPS5 NM_006837.2 -/. - c.-2391G>A r.(?) p.(=)
CSPP1 NM_024790.6 -/. - c.-12C>T r.(?) p.(=)


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