Variant #0000275942 (NC_000011.9:g.65635437G>T, NM_016938.4:c.1065C>A (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.65635437G>T
DNA change (hg38) g.65867966G>T
Published as EFEMP2(NM_016938.4):c.1065C>A (p.S355R), EFEMP2(NM_016938.5):c.1065C>A (p.S355R)
ISCN -
DB-ID EFEMP2_000005 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) 6.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
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.1065C>A r.(?) p.(Ser355Arg)
MUS81 NM_025128.4 ?/. - c.*1914G>T r.(=) p.(=)


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