Variant #0001048979 (NC_000002.11:g.46603640A>C, NC_000002.11(NM_001430.4):c.1035-38A>C (EPAS1))

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.46603640A>C
DNA change (hg38) -
Published as -
ISCN -
DB-ID EPAS1_000045
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs116083076
Origin Unknown
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) 0.00425 View details
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2025-10-09 16:51:01 +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     
EPAS1 NM_001430.4 -?/. - c.1035-38A>C r.(?) p.(?)


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