Variant #0000949115 (NC_000008.10:g.68214696T>A, NM_024790.6:c.*106868T>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.68214696T>A
DNA change (hg38) -
Published as ARFGEF1(NM_006421.5):c.130A>T (p.I44L)
ISCN -
DB-ID ARFGEF1_000017
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) 4.0E-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 2023-11-27 17:35:39 +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.130A>T r.(?) p.(Ile44Leu)
CSPP1 NM_024790.6 ?/. - c.*106868T>A r.(=) p.(=)


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