Variant #0000275917 (NC_000019.9:g.3981320C>T, NC_000019.9(NM_001961.3):c.1011+17G>A (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.3981320C>T
DNA change (hg38) g.3981322C>T
Published as EEF2(NM_001961.3):c.1011+17G>A, EEF2(NM_001961.4):c.1011+17G>A
ISCN -
DB-ID EEF2_000017 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) 0.00415 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 2018-01-15 20:58:59 +01:00 (CET)
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     
EEF2 NM_001961.3 -?/. - c.1011+17G>A r.(=) p.(=)


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