Variant #0000609098 (NC_000004.11:g.155507164C>T, NM_000508.3:c.1417G>A (FGA))

Chromosome 4
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.155507164C>T
DNA change (hg38) g.154586012C>T
Published as FGA(NM_000508.3):c.1417G>A (p.D473N), FGA(NM_021871.4):c.1417G>A (p.(Asp473Asn), p.D473N)
ISCN -
DB-ID FGA_000015 See all 4 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) 0.00042 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 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2025-11-01 13:22:20 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     

Haplotype     
FGA NM_000508.3 ?/. - c.1417G>A r.(?) p.(Asp473Asn) -


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