Variant #0000993488 (NC_000003.11:g.186509567G>A, NM_002916.3:c.748C>T (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.186509567G>A
DNA change (hg38) -
Published as RFC4(NM_002916.3):c.748C>T (p.(Arg250*))
ISCN -
DB-ID RFC4_000001
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 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +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.*2509G>A r.(=) p.(=)
RFC4 NM_002916.3 ?/. - c.748C>T r.(?) p.(Arg250*)


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