Variant #0000801379 (NC_000003.11:g.73111813C>T, NM_018029.3:c.581C>T (EBLN2))

Chromosome 3
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.73111813C>T
DNA change (hg38) -
Published as EBLN2(NM_018029.4):c.581C>T (p.A194V)
ISCN -
DB-ID EBLN2_000002
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) 2.0E-5 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EBLN2 NM_018029.3 ?/. - c.581C>T r.(?) p.(Ala194Val)
PPP4R2 NM_174907.2 ?/. - c.420-1011C>T r.(=) p.(=)


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