Variant #0000314042 (NC_000014.8:g.65253749C>T, NM_000347.5:c.2934G>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.65253749C>T
DNA change (hg38) g.64787031C>T
Published as SPTB(NM_001024858.3):c.2934G>A (p.E978=)
ISCN -
DB-ID SPTB_000065 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) 0.01273 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.2934G>A r.(?) p.(Glu978=)
SPTB NM_001024858.2 -/. - c.2934G>A r.(?) p.(Glu978=)


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