Variant #0000894518 (NC_000018.9:g.33935574C>T, NM_025135.2:c.238C>T (FHOD3))

Chromosome 18
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.33935574C>T
DNA change (hg38) -
Published as FHOD3(NM_001281740.1):c.238C>T (p.(Arg80Trp)), FHOD3(NM_001281740.2):c.238C>T (p.R80W), FHOD3(NM_001281740.3):c.238C>T (p.R80W), FHOD3(NM_025135.5)...
ISCN -
DB-ID FHOD3_000063 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) 0.00019 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2022-11-01 13:41:49 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FHOD3 NM_025135.2 ?/. - c.238C>T r.(?) p.(Arg80Trp)


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