Variant #0000945248 (NC_000002.11:g.54843415_54843417del, NM_003128.2:c.546_548del (SPTBN1))

Chromosome 2
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.54843415_54843417del
DNA change (hg38) -
Published as -
ISCN -
DB-ID SPTBN1_000029
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs2103829011
Origin CLASSIFICATION record
Segregation -
Frequency -
Re-site -
VIP -
Methylation -
Average frequency (gnomAD v.2.1.1) Retrieve
Owner MobiDetails
Database submission license Creative Commons Attribution 4.0 InternationalCreative Commons License
Created by MobiDetails
Date created 2023-11-18 10:37:01 +01:00 (CET)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPTBN1 NM_003128.2 +?/. - c.546_548del r.(?) p.(Trp182del)


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