Variant #0000535263 (NC_000008.10:g.68102960A>G, NM_024790.6:c.3281A>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.68102960A>G
DNA change (hg38) g.67190725A>G
Published as CSPP1(NM_001291339.2):c.2246A>G (p.E749G)
ISCN -
DB-ID ARFGEF1_000005
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) 6.0E-5 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARFGEF1 NM_006421.4 ?/. - c.*8209T>C r.(=) p.(=)
CSPP1 NM_024790.6 ?/. - c.3281A>G r.(?) p.(Glu1094Gly)


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