Variant #0000725104 (NC_000015.9:g.44855395T>C, NM_025137.3:c.7256A>G (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.44855395T>C
DNA change (hg38) -
Published as SPG11(NM_025137.4):c.7256A>G (p.K2419R, p.(Lys2419Arg))
ISCN -
DB-ID SPG11_000027 See all 5 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) 0.00296 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2021-02-08 18:36:18 +01:00 (CET)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EIF3J NM_003758.2 -/. - c.*2048T>C r.(=) p.(=)
SPG11 NM_025137.3 -/. - c.7256A>G r.(?) p.(Lys2419Arg)


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