Variant #0000725728 (NC_000016.9:g.28884936C>T, NM_004320.4:c.-5057C>T (ATP2A1))

Chromosome 16
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.28884936C>T
DNA change (hg38) -
Published as SH2B1(NM_001387430.1):c.2066C>T (p.P689L)
ISCN -
DB-ID ATP2A1_000032
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 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2024-04-19 20:27:30 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
ATP2A1 NM_004320.4 ?/. - c.-5057C>T r.(?) p.(=)
SH2B1 NM_015503.2 ?/. - c.*150C>T r.(=) p.(=)
RABEP2 NM_024816.2 ?/. - c.*31328G>A r.(=) p.(=)


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