Variant #0000722080 (NC_000008.10:g.68102949C>T, NM_024790.6:c.3270C>T (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.68102949C>T
DNA change (hg38) -
Published as CSPP1(NM_001291339.2):c.2235C>T (p.P745=), CSPP1(NM_024790.6):c.3270C>T (p.P1090=)
ISCN -
DB-ID CSPP1_000044 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) 0.00048 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARFGEF1 NM_006421.4 -?/. - c.*8220G>A r.(=) p.(=)
CSPP1 NM_024790.6 -?/. - c.3270C>T r.(?) p.(Pro1090=)


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