Variant #0000611600 (NC_000008.10:g.27660819_27660820del, NC_000008.10(NM_001017420.2):c.1674-4_1674-3del (ESCO2))

Chromosome 8
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.27660819_27660820del
DNA change (hg38) g.27803302_27803303del
Published as ESCO2(NM_001017420.2):c.1674-6_1674-5del (p.?)
ISCN -
DB-ID ESCO2_000057
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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2020-06-23 18:17:44 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ESCO2 NM_001017420.2 -?/. - c.1674-4_1674-3del r.spl? p.?


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