Variant #0001014408 (NC_000008.10:g.141549529T>G, NM_001164623.1:c.2059A>C (EIF2C2))

Chromosome 8
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.141549529T>G
DNA change (hg38) -
Published as AGO2(NM_012154.5):c.2059A>C (p.I687L)
ISCN -
DB-ID EIF2C2_000033
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) 1.0E-5 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2024-10-29 21:08:56 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EIF2C2 NM_001164623.1 ?/. - c.2059A>C r.(?) p.(Ile687Leu)
EIF2C2 NM_012154.3 ?/. - c.2059A>C r.(?) p.(Ile687Leu)


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