Variant #0000552840 (NC_000014.8:g.65261215C>T, NM_000347.5:c.1765G>A (SPTB))

Chromosome 14
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.65261215C>T
DNA change (hg38) g.64794497C>T
Published as SPTB(NM_001024858.3):c.1765G>A (p.A589T)
ISCN -
DB-ID SPTB_000129
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) 0.00171 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPTB NM_000347.5 -/. - c.1765G>A r.(?) p.(Ala589Thr)
SPTB NM_001024858.2 -/. - c.1765G>A r.(?) p.(Ala589Thr)


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