Variant #0001026437 (NC_000015.9:g.44858448_44858449del, NM_025137.3:c.6811_6812del (SPG11))

Chromosome 15
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.44858448_44858449del
DNA change (hg38) -
Published as SPG11(NM_025137.4):c.6811_6812delCT (p.L2271Dfs*68)
ISCN -
DB-ID EIF3J_000116
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 2025-02-07 18:57:27 +01:00 (CET)
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.*5101_*5102del r.(=) p.(=)
SPG11 NM_025137.3 +/. - c.6811_6812del r.(?) p.(Leu2271Aspfs*68)


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