Variant #0000618643 (NC_000022.10:g.50897935C>T, NM_002972.2:c.3652G>A (SBF1))

Chromosome 22
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.50897935C>T
DNA change (hg38) g.50459506C>T
Published as SBF1(NM_002972.4):c.3652G>A (p.V1218I)
ISCN -
DB-ID PPP6R2_000051
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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SBF1 NM_002972.2 ?/. - c.3652G>A r.(?) p.(Val1218Ile)
PPP6R2 NM_014678.4 ?/. - c.*15259C>T r.(=) p.(=)


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