Variant #0001040364 (NC_000015.9:g.44861661_44861664del, NM_025137.3:c.6522_6525del (SPG11))

Chromosome 15
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.44861661_44861664del
DNA change (hg38) -
Published as SPG11(NM_025137.4):c.6522_6525del (p.(Ile2175Leufs*13))
ISCN -
DB-ID EIF3J_000118
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-05-05 21:14:00 +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.*8314_*8317del r.(=) p.(=)
SPG11 NM_025137.3 ?/. - c.6522_6525del r.(?) p.(Ile2175Leufs*13)


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