Variant #0000572381 (NC_000022.10:g.50902775T>C, NM_002972.2:c.1732A>G (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.50902775T>C
DNA change (hg38) g.50464346T>C
Published as SBF1(NM_002972.4):c.1732A>G (p.M578V)
ISCN -
DB-ID PPP6R2_000033
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 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 2019-07-18 18:22:55 +02:00 (CEST)
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.1732A>G r.(?) p.(Met578Val)
PPP6R2 NM_014678.4 ?/. - c.*20099T>C r.(=) p.(=)


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