Variant #0000302412 (NC_000015.9:g.44944037C>T, NM_025137.3:c.1108G>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.44944037C>T
DNA change (hg38) g.44651839C>T
Published as SPG11(NM_001160227.1):c.1108G>A (p.(Glu370Lys)), SPG11(NM_025137.4):c.1108G>A (p.E370K)
ISCN -
DB-ID SPG11_000093 See all 6 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) 0.01738 View details
Owner VKGL-NL_Utrecht
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Utrecht
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2023-01-11 15:44:22 +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.*90690C>T r.(=) p.(=)
SPG11 NM_025137.3 -/. - c.1108G>A r.(?) p.(Glu370Lys)


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