Variant #0000894760 (NC_000019.9:g.11489146C>T, EPOR(NM_000121.3):c.1041G>A)

Chromosome 19
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.11489146C>T
DNA change (hg38) -
Published as EPOR(NM_000121.4):c.1041G>A (p.P347=)
ISCN -
DB-ID EPOR_000019
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) 0.00126 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EPOR NM_000121.3 -/. - c.1041G>A r.(?) p.(Pro347=)
SWSAP1 NM_175871.3 -/. - c.*2454C>T r.(=) p.(=)