Variant #0000949836 (NC_000012.11:g.110777408_110777412del, NM_001681.3:c.1643_1647del (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.110777408_110777412del
DNA change (hg38) -
Published as ATP2A2(NM_001681.4):c.1643_1647delTTCGA (p.I548Rfs*4)
ISCN -
DB-ID ATP2A2_000322
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 2023-11-27 17:35:39 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP2A2 NM_001681.3 ?/. - c.1643_1647del r.(?) p.(Ile548Argfs*4)
ATP2A2 NM_170665.3 ?/. - c.1643_1647del r.(?) p.(Ile548Argfs*4)


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