Variant #0000261197 (NC_000016.9:g.28898793T>C, NM_004320.4:c.678T>C (ATP2A1))

Chromosome 16
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.28898793T>C
DNA change (hg38) g.28887472T>C
Published as ATP2A1(NM_004320.5):c.678T>C (p.T226=), ATP2A1(NM_004320.6):c.678T>C (p.T226=)
ISCN -
DB-ID ATP2A1_000004 See all 3 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) 0.35125 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP2A1 NM_004320.4 -/. - c.678T>C r.(?) p.(Thr226=)
RABEP2 NM_024816.2 -/. - c.*17471A>G r.(=) p.(=)


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