Variant #0000339826 (NC_000002.11:g.32340779G>A, SPAST(NM_014946.3):c.879G>A)

Chromosome 2
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.32340779G>A
DNA change (hg38) g.32115710G>A
Published as SPAST(NM_014946.3):c.879G>A (p.P293=), SPAST(NM_014946.4):c.879G>A (p.P293=)
ISCN -
DB-ID SPAST_000019 See all 3 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) 0.00955 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPAST NM_014946.3 -?/. - c.879G>A r.(?) p.(Pro293=)