Variant #0000693671 (NC_000023.10:g.54496615G>A, NM_004463.2:c.935C>T (FGD1))

Chromosome X
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.54496615G>A
DNA change (hg38) -
Published as FGD1(NM_004463.2):c.935C>T (p.P312L, p.(Pro312Leu)), FGD1(NM_004463.3):c.935C>T (p.P312L)
ISCN -
DB-ID FGD1_000004 See all 5 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) 0.0003 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FGD1 NM_004463.2 -?/. - c.935C>T r.(?) p.(Pro312Leu)


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