Variant #0000688994 (NC_000003.11:g.186507009A>C, NM_002916.3:c.*749T>G (RFC4))

Chromosome 3
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.186507009A>C
DNA change (hg38) -
Published as EIF4A2(NM_001967.4):c.1175A>C (p.Y392S)
ISCN -
DB-ID EIF4A2_000002
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 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2024-10-29 20:49:11 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EIF4A2 NM_001967.3 ?/. - c.1175A>C r.(?) p.(Tyr392Ser)
RFC4 NM_002916.3 ?/. - c.*749T>G r.(=) p.(=)


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