Variant #0000314035 (NC_000014.8:g.65260543C>A, NM_000347.5:c.1838G>T (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.65260543C>A
DNA change (hg38) g.64793825C>A
Published as SPTB(NM_001024858.3):c.1838G>T (p.S613I)
ISCN -
DB-ID SPTB_000073 See all 2 reported entries
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) 0.00275 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 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2021-09-17 14:40:49 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPTB NM_000347.5 -/. - c.1838G>T r.(?) p.(Ser613Ile)
SPTB NM_001024858.2 -/. - c.1838G>T r.(?) p.(Ser613Ile)


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