Variant #0000261199 (NC_000012.11:g.110760727C>A, NC_000012.11(NM_001681.3):c.464-70C>A (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.110760727C>A
DNA change (hg38) g.110322922C>A
Published as ATP2A2(NM_170665.3):c.464-70C>A (p.?), ATP2A2(NM_170665.4):c.464-70C>A
ISCN -
DB-ID ATP2A2_000294 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) Retrieve
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 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.464-70C>A r.(=) p.(=)
ATP2A2 NM_170665.3 -/. - c.464-70C>A r.(=) p.(=)


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