Variant #0001037035 (NC_000008.10:g.68115482T>C, NM_024790.6:c.*7654T>C (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.68115482T>C
DNA change (hg38) -
Published as ARFGEF1(NM_006421.5):c.4964A>G (p.(Asp1655Gly), p.D1655G)
ISCN -
DB-ID ARFGEF1_000025 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) 9.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-05-05 21:14:00 +02:00 (CEST)
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.4964A>G r.(?) p.(Asp1655Gly)
CSPP1 NM_024790.6 -?/. - c.*7654T>C r.(=) p.(=)


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