Variant #0000993387 (NC_000003.11:g.15471471T>C, NM_033083.6:c.155T>C (EAF1))

Chromosome 3
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.15471471T>C
DNA change (hg38) -
Published as EAF1(NM_033083.6):c.155T>C (p.(Val52Ala))
ISCN -
DB-ID EAF1_000001
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) 0.00109 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EAF1 NM_033083.6 ?/. - c.155T>C r.(?) p.(Val52Ala)
METTL6 NM_152396.2 ?/. - c.-2687A>G r.(?) p.(=)


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