Variant #0000926257 (NC_000016.9:g.28884961G>A, NM_004320.4:c.-5032G>A (ATP2A1))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.28884961G>A
DNA change (hg38) -
Published as SH2B1(NM_001387430.1):c.2091G>A (p.E697=)
ISCN -
DB-ID ATP2A1_000048
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) 2.0E-5 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2023-04-16 21:50:28 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP2A1 NM_004320.4 -?/. - c.-5032G>A r.(?) p.(=)
SH2B1 NM_015503.2 -?/. - c.*175G>A r.(=) p.(=)
RABEP2 NM_024816.2 -?/. - c.*31303C>T r.(=) p.(=)


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