Variant #0000547828 (NC_000012.11:g.32772659C>A, NM_139241.2:c.1366C>A (FGD4))

Chromosome 12
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.32772659C>A
DNA change (hg38) g.32619725C>A
Published as FGD4(NM_001304484.2):c.334C>A (p.P112T), FGD4(NM_139241.3):c.1366C>A (p.P456T)
ISCN -
DB-ID FGD4_000049 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) 0.00141 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FGD4 NM_139241.2 ?/. - c.1366C>A r.(?) p.(Pro456Thr)


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