Variant #0000508189 (NC_000001.10:g.6485305T>A, NM_031475.2:c.290T>A (ESPN))

Chromosome 1
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.6485305T>A
DNA change (hg38) g.6425245T>A
Published as ESPN(NM_031475.3):c.290T>A (p.V97E)
ISCN -
DB-ID ESPN_000013
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) 0.00135 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 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
HES2 NM_019089.4 -?/. - c.-5425A>T r.(?) p.(=)
ESPN NM_031475.2 -?/. - c.290T>A r.(?) p.(Val97Glu)


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