Variant #0000930078 (NC_000012.11:g.32777902T>C, NC_000012.11(NM_139241.2):c.1543-8T>C (FGD4))

Chromosome 12
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.32777902T>C
DNA change (hg38) -
Published as FGD4(NM_001304484.2):c.511-8T>C, FGD4(NM_139241.3):c.1543-8T>C
ISCN -
DB-ID FGD4_000050 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) 0.00353 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 2023-07-07 10:10:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FGD4 NM_139241.2 -/. - c.1543-8T>C r.(=) p.(=)


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