Variant #0000615557 (NC_000015.9:g.82555229C>A, NM_024580.5:c.-294G>T (EFTUD1))

Chromosome 15
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.82555229C>A
DNA change (hg38) g.82262888C>A
Published as SAXO2(NM_001008226.1):c.9C>A (p.A3=)
ISCN -
DB-ID EFTUD1_000009
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) Retrieve
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-07-06 17:33:40 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
FAM154B NM_001008226.1 -?/. - c.9C>A r.(?) p.(Ala3=)
EFTUD1 NM_024580.5 -?/. - c.-294G>T r.(?) p.(=)


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