Variant #0000324070 (NC_000015.9:g.44952826del, NC_000015.9(NM_025137.3):c.258-6del (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.44952826del
DNA change (hg38) g.44660628del
Published as SPG11(NM_001160227.1):c.258-6delT (p.(=)), SPG11(NM_025137.3):c.258-6delT
ISCN -
DB-ID SPG11_000099 See all 2 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) Retrieve
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2020-08-06 14:59:34 +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.*99479del r.(?) p.(=)
SPG11 NM_025137.3 ?/. - c.258-6del r.(=) p.(=)


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