Variant #0001024568 (NC_000002.11:g.27306590C>G, NM_007046.3:c.2151C>G (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.27306590C>G
DNA change (hg38) -
Published as EMILIN1(NM_007046.4):c.2151C>G (p.A717=)
ISCN -
DB-ID CGREF1_000036
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) 0.00069 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2025-02-07 18:57:27 +01:00 (CET)
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.-3538C>G r.(?) p.(=)
CGREF1 NM_006569.5 -?/. - c.*17552G>C r.(=) p.(=)
EMILIN1 NM_007046.3 -?/. - c.2151C>G r.(?) p.(=)


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