Variant #0000947822 (NC_000002.11:g.27306224T>C, NM_007046.3:c.1785T>C (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.27306224T>C
DNA change (hg38) -
Published as EMILIN1(NM_007046.4):c.1785T>C (p.L595=)
ISCN -
DB-ID CGREF1_000027
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2023-11-27 17:35:39 +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.-3904T>C r.(?) p.(=)
CGREF1 NM_006569.5 -?/. - c.*17918A>G r.(=) p.(=)
EMILIN1 NM_007046.3 -?/. - c.1785T>C r.(?) p.(=)


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