Variant #0000507631 (NC_000001.10:g.45341360T>C, NM_020365.4:c.983A>G (EIF2B3))

Chromosome 1
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.45341360T>C
DNA change (hg38) g.44875688T>C
Published as EIF2B3(NM_001166588.2):c.983A>G (p.(Lys328Arg)), EIF2B3(NM_020365.4):c.983A>G (p.K328R)
ISCN -
DB-ID EIF2B3_000010 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) 0.0012 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 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EIF2B3 NM_020365.4 ?/. - c.983A>G r.(?) p.(Lys328Arg)


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