Variant #0000322295 (NC_000011.9:g.64593946_64593947insGG, NM_017525.2:c.4594_4595insCC (CDC42BPG))

Chromosome 11
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.64593946_64593947insGG
DNA change (hg38) g.64826474_64826475insGG
Published as CDC42BPG(NM_017525.2):c.4594_4595insCC (p.?)
ISCN -
DB-ID CDC42BPG_000001
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-06-30 17:59:10 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
CDC42BPG NM_017525.2 ?/. - c.4594_4595insCC r.(?) p.(Met1532ThrfsTer26)


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