Variant #0000559104 (NC_000016.9:g.74760199C>T, NM_024306.4:c.537G>A (FA2H))

Chromosome 16
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.74760199C>T
DNA change (hg38) g.74726301C>T
Published as FA2H(NM_024306.4):c.537G>A (p.L179=), FA2H(NM_024306.5):c.537G>A (p.L179=)
ISCN -
DB-ID FA2H_000011 See all 2 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) 0.00222 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FA2H NM_024306.4 -/. - c.537G>A r.(?) p.(Leu179=)


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