Variant #0000567297 (NC_000019.9:g.3976699G>A, NM_001961.3:c.2430C>T (EEF2))

Chromosome 19
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.3976699G>A
DNA change (hg38) g.3976701G>A
Published as EEF2(NM_001961.3):c.2430C>T (p.P810=), EEF2(NM_001961.4):c.2430C>T (p.(Pro810=))
ISCN -
DB-ID EEF2_000027 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) 0.00019 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 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EEF2 NM_001961.3 -?/. - c.2430C>T r.(?) p.(Pro810=)


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