Variant #0000515522 (NC_000002.11:g.27306114C>T, NM_007046.3:c.1675C>T (EMILIN1))

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.27306114C>T
DNA change (hg38) g.27083246C>T
Published as EMILIN1(NM_007046.4):c.1675C>T (p.R559W)
ISCN -
DB-ID CGREF1_000003
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 2019-07-18 18:22:55 +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.-4014C>T r.(?) p.(=)
CGREF1 NM_006569.5 -?/. - c.*18028G>A r.(=) p.(=)
EMILIN1 NM_007046.3 -?/. - c.1675C>T r.(?) p.(Arg559Trp)


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