Variant #0000688729 (NC_000002.11:g.27308159G>A, NM_007046.3:c.2707G>A (EMILIN1))

Chromosome 2
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.27308159G>A
DNA change (hg38) -
Published as EMILIN1(NM_007046.4):c.2707G>A (p.E903K, p.(Glu903Lys))
ISCN -
DB-ID CGREF1_000016 See all 2 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) 0.01904 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2020-09-15 15:50:26 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KHK NM_000221.2 -/. - c.-1969G>A r.(?) p.(=)
CGREF1 NM_006569.5 -/. - c.*15983C>T r.(=) p.(=)
EMILIN1 NM_007046.3 -/. - c.2707G>A r.(?) p.(Glu903Lys)


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