Variant #0001032883 (NC_000002.11:g.198270013del, NM_012433.4:c.1425del (SF3B1))

Chromosome 2
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.198270013del
DNA change (hg38) g.197405289del
Published as SF3B1(NM_012433.4):c.1425del (p.(Phe475Leufs*23))
ISCN -
DB-ID SF3B1_000018
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +02:00 (CEST)
Date last edited 2025-10-09 18:26:12 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SF3B1 NM_012433.4 ./. - c.1425del r.(?) p.(Phe475LeufsTer23)


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