Variant #0000283170 (NC_000023.10:g.54475682C>T, NM_004463.2:c.2168G>A (FGD1))

Chromosome X
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.54475682C>T
DNA change (hg38) g.54449249C>T
Published as FGD1(NM_004463.2):c.2168G>A (p.(Arg723Gln)), FGD1(NM_004463.3):c.2168G>A (p.R723Q)
ISCN -
DB-ID FGD1_000043 See all 3 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) Retrieve
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2018-01-15 20:58:59 +01:00 (CET)
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     
FGD1 NM_004463.2 ?/. - c.2168G>A r.(?) p.(Arg723Gln)
TSR2 NM_058163.1 ?/. - c.*4699C>T r.(=) p.(=)


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