Variant #0000554366 (NC_000015.9:g.44858439_44858440insTGT, NM_025137.3:c.6818_6819insACA (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.44858439_44858440insTGT
DNA change (hg38) g.44566241_44566242insTGT
Published as SPG11(NM_025137.3):c.6818_6819insACA (p.L2273_D2274insQ)
ISCN -
DB-ID EIF3J_000008
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2020-03-23 16:13:27 +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.*5092_*5093insTGT r.(=) p.(=)
SPG11 NM_025137.3 ?/. - c.6818_6819insACA r.(?) p.(Leu2273_Asp2274insGln)


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