Variant #0001068306 (NC_000023.10:g.54491965G>A, NM_004463.2:c.1555C>T (FGD1))

Chromosome X
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.54491965G>A
DNA change (hg38) -
Published as -
ISCN -
DB-ID FGD1_000108 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs1557189252
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2026-02-17 11:59:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FGD1 NM_004463.2 +?/. - c.1555C>T r.(?) p.(Arg519Cys)


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