Variant #0000546483 (NC_000012.11:g.110734514dup, NM_001681.3:c.435dup (ATP2A2))

Chromosome 12
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.110734514dup
DNA change (hg38) g.110296709dup
Published as ATP2A2(NM_170665.4):c.435dupA (p.V146Sfs*4)
ISCN -
DB-ID ATP2A2_000300
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) Retrieve
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-08-06 14:59:34 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP2A2 NM_001681.3 +/. - c.435dup r.(?) p.(Val146SerfsTer4)
ATP2A2 NM_170665.3 +/. - c.435dup r.(?) p.(Val146SerfsTer4)


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