Variant #0000623228 (NC_000015.9:g.44864966C>A, NM_025137.3:c.6258G>T (SPG11))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.44864966C>A
DNA change (hg38) g.44572768C>A
Published as SPG11(NM_025137.3):c.6258G>T (p.L2086=), SPG11(NM_025137.4):c.6258G>T (p.L2086=, p.(Leu2086=))
ISCN -
DB-ID SPG11_000045 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) 0.00668 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 2019-12-06 12:43:26 +01:00 (CET)
Date last edited 2025-02-07 18:57:27 +01:00 (CET)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
EIF3J NM_003758.2 -?/. - c.*11619C>A r.(=) p.(=)
SPG11 NM_025137.3 -?/. - c.6258G>T r.(?) p.(Leu2086=)


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