Variant #0001040626 (NC_000015.9:g.82443866G>A, NM_024580.5:c.2929C>T (EFTUD1))

Chromosome 15
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.82443866G>A
DNA change (hg38) -
Published as EFL1(NM_001322845.1):c.2929C>T (p.P977S), EFL1(NM_024580.6):c.2929C>T (p.(Pro977Ser))
ISCN -
DB-ID EFTUD1_000014 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) 0.0001 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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EFTUD1 NM_024580.5 ?/. - c.2929C>T r.(?) p.(Pro977Ser)


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