Variant #0000298444 (NC_000002.11:g.32289031C>T, NM_014946.3:c.131C>T (SPAST))

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.32289031C>T
DNA change (hg38) g.32063962C>T
Published as SPAST(NM_014946.3):c.131C>T (p.S44L), SPAST(NM_014946.4):c.131C>T (p.(Ser44Leu), p.S44L)
ISCN -
DB-ID SPAST_000017 See all 5 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) 0.00461 View details
Owner VKGL-NL_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPAST NM_014946.3 -?/. - c.131C>T r.(?) p.(Ser44Leu)


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