Variant #0001053032 (NC_000008.10:g.68150608C>G, NM_024790.6:c.*42780C>G (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.68150608C>G
DNA change (hg38) -
Published as ARFGEF1(NM_006421.5):c.3259G>C (p.(Ala1087Pro))
ISCN -
DB-ID ARFGEF1_000048
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) 3.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +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     
ARFGEF1 NM_006421.4 ?/. - c.3259G>C r.(?) p.(Ala1087Pro)
CSPP1 NM_024790.6 ?/. - c.*42780C>G r.(=) p.(=)


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