Variant #0000607884 (NC_000002.11:g.27306726C>T, NM_007046.3:c.2287C>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.27306726C>T
DNA change (hg38) g.27083858C>T
Published as -
ISCN -
DB-ID CGREF1_000007
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) 1.0E-5 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2019-12-04 14:54:23 +01:00 (CET)
Date last edited 2020-03-23 16:13:27 +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.-3402C>T r.(?) p.(=)
CGREF1 NM_006569.5 ?/. - c.*17416G>A r.(=) p.(=)
EMILIN1 NM_007046.3 ?/. - c.2287C>T r.(?) p.(Arg763Trp)


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