Variant #0000861193 (NC_000008.10:g.27646357A>G, NC_000008.10(NM_001017420.2):c.1132-7A>G (ESCO2))

Chromosome 8
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.27646357A>G
DNA change (hg38) -
Published as ESCO2(NM_001017420.2):c.1132-7A>G, ESCO2(NM_001017420.3):c.1132-7A>G
ISCN -
DB-ID ESCO2_000015 See all 6 reported entries
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 2022-05-09 15:51:19 +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     
ESCO2 NM_001017420.2 +/. - c.1132-7A>G r.(=) p.(=)


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