Variant #0000980961 (NC_000014.8:g.65268950G>A, NM_000347.5:c.560C>T (SPTB))

Chromosome 14
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.65268950G>A
DNA change (hg38) -
Published as SPTB(NM_001355436.2):c.560C>T (p.(Thr187Met))
ISCN -
DB-ID SPTB_000174
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) 8.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +02:00 (CEST)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPTB NM_000347.5 ?/. - c.560C>T r.(?) p.(Thr187Met)
SPTB NM_001024858.2 ?/. - c.560C>T r.(?) p.(Thr187Met)


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