Variant #0000340100 (NC_000015.9:g.44855454C>T, NM_025137.3:c.7197G>A (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.44855454C>T
DNA change (hg38) g.44563256C>T
Published as SPG11(NM_025137.4):c.7197G>A (p.K2399=, p.(Lys2399=))
ISCN -
DB-ID SPG11_000028 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) 0.00682 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +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.*2107C>T r.(=) p.(=)
SPG11 NM_025137.3 -/. - c.7197G>A r.(?) p.(Lys2399=)


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