Variant #0000248257 (NC_000012.11:g.110734406A>G, NM_001681.3:c.327A>G (ATP2A2))

Chromosome 12
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.110734406A>G
DNA change (hg38) g.110296601A>G
Published as ATP2A2(NM_170665.3):c.327A>G (p.(Glu109Glu)), ATP2A2(NM_170665.4):c.327A>G (p.E109=)
ISCN -
DB-ID ATP2A2_000293 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) 0.00761 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +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.327A>G r.(?) p.(Glu109=)
ATP2A2 NM_170665.3 -/. - c.327A>G r.(?) p.(Glu109=)


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