Variant #0000975224 (NC_000002.11:g.32314683_32314686del, NC_000002.11(NM_014946.3):c.586+9_586+12del (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.32314683_32314686del
DNA change (hg38) -
Published as SPAST(NM_014946.3):c.586+9_586+12delTAAT, SPAST(NM_014946.4):c.586+9_586+12delTAAT
ISCN -
DB-ID SPAST_000042 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) Retrieve
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2024-04-19 20:20:39 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPAST NM_014946.3 -?/. - c.586+9_586+12del r.(=) p.(=)


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