Variant #0000680179 (NC_000015.9:g.44865850G>A, NM_025137.3:c.6100C>T (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.44865850G>A
DNA change (hg38) -
Published as SPG11(NM_025137.3):c.6100C>T (p.R2034*), SPG11(NM_025137.4):c.6100C>T (p.(Arg2034*))
ISCN -
DB-ID SPG11_000113 See all 4 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 View details
Owner VKGL-NL_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2020-08-06 14:59:34 +02:00 (CEST)
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.*12503G>A r.(=) p.(=)
SPG11 NM_025137.3 +/. - c.6100C>T r.(?) p.(Arg2034Ter)


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