Variant #0000981231 (NC_000015.9:g.44944341G>A, NM_025137.3:c.993C>T (SPG11))

Chromosome 15
Allele Unknown
Affects function (as reported) Does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.44944341G>A
DNA change (hg38) -
Published as SPG11(NM_025137.4):c.993C>T (p.S331=, p.(Ser331=))
ISCN -
DB-ID EIF3J_000046 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) 0.00848 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-04-19 20:27:30 +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     
EIF3J NM_003758.2 -/. - c.*90994G>A r.(=) p.(=)
SPG11 NM_025137.3 -/. - c.993C>T r.(?) p.(Ser331=)


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