Variant #0000861280 (NC_000008.10:g.68089943A>G, NM_024790.6:c.3123A>G (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.68089943A>G
DNA change (hg38) -
Published as CSPP1(NM_001382391.1):c.3138A>G (p.(Lys1046=)), CSPP1(NM_024790.6):c.3123A>G (p.K1041=)
ISCN -
DB-ID ARFGEF1_000013 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) 0.00362 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2022-05-09 15:51:19 +02:00 (CEST)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ARFGEF1 NM_006421.4 -?/. - c.*21226T>C r.(=) p.(=)
CSPP1 NM_024790.6 -?/. - c.3123A>G r.(?) p.(Lys1041=)


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