Variant #0000442938 (NC_000011.9:g.66475652C>T, NM_006946.2:c.1310G>A (SPTBN2))

Chromosome 11
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.66475652C>T
DNA change (hg38) g.66708181C>T
Published as -
ISCN -
DB-ID SPTBN2_000069
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin De novo
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner Ginevra Zanni
Database submission license No license selected
Created by Ginevra Zanni
Date created 2018-12-28 10:34:37 +01:00 (CET)
Date last edited 2023-01-31 09:26:24 +01:00 (CET)
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPTBN2 NM_006946.2 +?/. - c.1310G>A r.(?) p.(Arg437Gln)



Screenings

Stop! No screenings found!


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.