Variant #0000978270 (NC_000008.10:g.68107597G>T, NC_000008.10(NM_024790.6):c.3455-20G>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.68107597G>T
DNA change (hg38) -
Published as CSPP1(NM_001382391.1):c.3470-20G>T
ISCN -
DB-ID ARFGEF1_000018
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) 0.00019 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 2024-04-19 20:27:30 +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.*3572C>A r.(=) p.(=)
CSPP1 NM_024790.6 -?/. - c.3455-20G>T r.(=) p.(=)


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