Variant #0000676606 (NC_000002.11:g.27305403C>T, NM_007046.3:c.964C>T (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.27305403C>T
DNA change (hg38) -
Published as EMILIN1(NM_007046.4):c.964C>T (p.R322W)
ISCN -
DB-ID CGREF1_000014
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) 4.0E-5 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2020-08-06 14:59:34 +02:00 (CEST)
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     
KHK NM_000221.2 ?/. - c.-4725C>T r.(?) p.(=)
CGREF1 NM_006569.5 ?/. - c.*18739G>A r.(=) p.(=)
EMILIN1 NM_007046.3 ?/. - c.964C>T r.(?) p.(Arg322Trp)


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