Variant #0001045828 (NC_000002.11:g.27306788G>C, NM_007046.3:c.2349G>C (EMILIN1))

Chromosome 2
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.27306788G>C
DNA change (hg38) -
Published as EMILIN1(NM_007046.4):c.2349G>C (p.Q783H)
ISCN -
DB-ID CGREF1_000038
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2025-07-08 13:22:38 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
KHK NM_000221.2 ?/. - c.-3340G>C r.(?) p.(=)
CGREF1 NM_006569.5 ?/. - c.*17354C>G r.(=) p.(=)
EMILIN1 NM_007046.3 ?/. - c.2349G>C r.(?) p.(Gln783His)


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