Variant #0001038604 (NC_000011.9:g.65636038G>A, NM_016938.4:c.790C>T (EFEMP2))

Chromosome 11
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.65636038G>A
DNA change (hg38) -
Published as EFEMP2(NM_016938.5):c.790C>T (p.(Arg264Cys))
ISCN -
DB-ID EFEMP2_000062
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 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EFEMP2 NM_016938.4 ?/. - c.790C>T r.(?) p.(Arg264Cys)
MUS81 NM_025128.4 ?/. - c.*2515G>A r.(=) p.(=)


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