Variant #0000346657 (NC_000011.9:g.65636053T>C, NM_016938.4:c.775A>G (EFEMP2))

Chromosome 11
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.65636053T>C
DNA change (hg38) g.65868582T>C
Published as EFEMP2(NM_016938.4):c.775A>G (p.I259V), EFEMP2(NM_016938.5):c.775A>G (p.I259V)
ISCN -
DB-ID EFEMP2_000009 See all 4 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) 0.97554 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EFEMP2 NM_016938.4 -/. - c.775A>G r.(?) p.(Ile259Val)
MUS81 NM_025128.4 -/. - c.*2530T>C r.(=) p.(=)


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