Variant #0000807334 (NC_000016.9:g.28909414C>T, NM_004320.4:c.1513C>T (ATP2A1))

Chromosome 16
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.28909414C>T
DNA change (hg38) -
Published as ATP2A1(NM_004320.4):c.1513C>T (p.(Arg505Trp))
ISCN -
DB-ID ATP2A1_000039
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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2021-09-17 14:40:49 +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     
ATP2A1 NM_004320.4 ?/. - c.1513C>T r.(?) p.(Arg505Trp)
RABEP2 NM_024816.2 ?/. - c.*6850G>A r.(=) p.(=)


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