Variant #0001060405 (NC_000001.10:g.158651387_158651389dup, NM_003126.2:c.460_462dup (SPTA1))

Chromosome 1
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.158651387_158651389dup
DNA change (hg38) -
Published as -
ISCN -
DB-ID SPTA1_000233
Variant remarks -
Reference -
ClinVar ID -
dbSNP ID rs757679761
Origin Unknown
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 2025-12-01 15:53:01 +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     
SPTA1 NM_003126.2 +/. - c.460_462dup r.(?) p.(Leu155dup)


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