Variant #0000323085 (NC_000012.11:g.110784210A>G, NC_000012.11(NM_001681.3):c.2980+84A>G (ATP2A2))

Chromosome 12
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.110784210A>G
DNA change (hg38) g.110346405A>G
Published as ATP2A2(NM_001681.4):c.2980+84A>G, ATP2A2(NM_170665.3):c.3064A>G (p.(Ile1022Val)), ATP2A2(NM_170665.4):c.3064A>G (p.I1022V)
ISCN -
DB-ID ATP2A2_000298 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) 0.00093 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-07-07 10:10:56 +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.2980+84A>G r.(=) p.(=)
ATP2A2 NM_170665.3 ?/. - c.3064A>G r.(?) p.(Ile1022Val)


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