Variant #0000615320 (NC_000015.9:g.44856827G>A, NM_025137.3:c.7069C>T (SPG11))

Chromosome 15
Allele Unknown
Affects function (as reported) Effect unknown
Affects function (by curator) Not classified
Classification method -
Clinical classification VUS
DNA change (genomic) (Relative to hg19 / GRCh37) g.44856827G>A
DNA change (hg38) g.44564629G>A
Published as SPG11(NM_025137.3):c.7069C>T (p.L2357F, p.(Leu2357Phe)), SPG11(NM_025137.4):c.7069C>T (p.L2357F)
ISCN -
DB-ID SPG11_000029 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) 0.0014 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 2019-12-04 15:24:38 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +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.*3480G>A r.(=) p.(=)
SPG11 NM_025137.3 ?/. - c.7069C>T r.(?) p.(Leu2357Phe)


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