Variant #0000997305 (NC_000008.10:g.68204278C>A, NM_024790.6:c.*96450C>A (CSPP1))

Chromosome 8
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.68204278C>A
DNA change (hg38) -
Published as ARFGEF1(NM_006421.5):c.720G>T (p.E240D)
ISCN -
DB-ID ARFGEF1_000023
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARFGEF1 NM_006421.4 ?/. - c.720G>T r.(?) p.(Glu240Asp)
CSPP1 NM_024790.6 ?/. - c.*96450C>A r.(=) p.(=)


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