Variant #0000914209 (NC_000014.8:g.65259819_65259820insTGTACAGG, NM_000347.5:c.2562_2563insCTGTACAC (SPTB))

Chromosome 14
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.65259819_65259820insTGTACAGG
DNA change (hg38) -
Published as SPTB(NM_001355436.2):c.2562_2563insCTGTACAC (p.G855Lfs*46)
ISCN -
DB-ID SPTB_000166
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_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2023-01-11 15:44:22 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPTB NM_000347.5 +/. - c.2562_2563insCTGTACAC r.(?) p.(Gly855Leufs*46)
SPTB NM_001024858.2 +/. - c.2562_2563insCTGTACAC r.(?) p.(Gly855Leufs*46)


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