Variant #0001066197 (NC_000015.9:g.44958658del, NM_025137.3:c.-2813del (SPG11))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.44958658del
DNA change (hg38) -
Published as -
ISCN -
DB-ID chr15_006432
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_Groningen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Groningen
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PATL2 NM_001145112.1 +?/. - c.1545del r.(?) p.(Ser515Argfs*42)
EIF3J NM_003758.2 +?/. - c.*105311del r.(?) p.(=)
SPG11 NM_025137.3 +?/. - c.-2813del r.(?) p.(=)


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