Variant #0000322653 (NC_000012.11:g.6981466A>T, NM_000365.5:c.*1919A>T (TPI1))

Chromosome 12
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.6981466A>T
DNA change (hg38) g.6872302A>T
Published as SPSB2(NM_001146316.1):c.600T>A (p.(Tyr200Ter))
ISCN -
DB-ID SPSB2_000001
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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-07-02 13:15:42 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
TPI1 NM_000365.5 ?/. - c.*1919A>T r.(=) p.(=)
SPSB2 NM_032641.3 ?/. - c.600T>A r.(?) p.(Tyr200Ter)


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