Variant #0000800555 (NC_000002.11:g.27305314G>A, NM_007046.3:c.875G>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.27305314G>A
DNA change (hg38) -
Published as EMILIN1(NM_007046.4):c.875G>A (p.R292Q)
ISCN -
DB-ID CGREF1_000020
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) 0.00052 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 2021-09-17 14:40:49 +02:00 (CEST)
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     
KHK NM_000221.2 -/. - c.-4814G>A r.(?) p.(=)
CGREF1 NM_006569.5 -/. - c.*18828C>T r.(=) p.(=)
EMILIN1 NM_007046.3 -/. - c.875G>A r.(?) p.(Arg292Gln)


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