Variant #0000613567 (NC_000011.9:g.65635855G>A, NM_016938.4:c.885C>T (EFEMP2))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.65635855G>A
DNA change (hg38) g.65868384G>A
Published as EFEMP2(NM_016938.4):c.885C>T (p.S295=), EFEMP2(NM_016938.5):c.885C>T (p.S295=)
ISCN -
DB-ID EFEMP2_000008 See all 3 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) 0.00013 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EFEMP2 NM_016938.4 -?/. - c.885C>T r.(?) p.(Ser295=)
MUS81 NM_025128.4 -?/. - c.*2332G>A r.(=) p.(=)


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