Variant #0000251565 (NC_000014.8:g.65268605A>G, NC_000014.8(NM_000347.5):c.567-53T>C (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.65268605A>G
DNA change (hg38) g.64801887A>G
Published as SPTB(NM_001024858.3):c.567-53T>C
ISCN -
DB-ID SPTB_000093
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 2018-01-15 20:58:59 +01:00 (CET)
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.567-53T>C r.(=) p.(=)
SPTB NM_001024858.2 -/. - c.567-53T>C r.(=) p.(=)


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