Variant #0000442988 (NC_000011.9:g.66483425G>A, NM_006946.2:c.185C>T (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.66483425G>A
DNA change (hg38) g.66715954G>A
Published as -
ISCN -
DB-ID SPTBN2_000072 See all 2 reported entries
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID -
Origin Unknown
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 10:49:34 +01:00 (CET)
Date last edited 2023-01-31 09:28:54 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPTBN2 NM_006946.2 +?/. - c.185C>T r.(?) p.(Thr62Ile)



Screenings

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