Variant #0000622090 (NC_000008.10:g.68107747G>A, NM_024790.6:c.3585G>A (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.68107747G>A
DNA change (hg38) g.67195512G>A
Published as CSPP1(NM_001363131.2):c.3519G>A (p.E1173=)
ISCN -
DB-ID ARFGEF1_000011
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) 1.0E-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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2020-06-23 20:22:48 +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.*3422C>T r.(=) p.(=)
CSPP1 NM_024790.6 -?/. - c.3585G>A r.(?) p.(Glu1195=)


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