Variant #0000554353 (NC_000015.9:g.44856764A>G, NM_025137.3:c.7132T>C (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.44856764A>G
DNA change (hg38) g.44564566A>G
Published as SPG11(NM_025137.3):c.7132T>C (p.F2378L), SPG11(NM_025137.4):c.7132T>C (p.F2378L)
ISCN -
DB-ID EIF3J_000003 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) 0.00021 View details
Owner VKGL-NL_AMC
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_AMC
Date created 2019-07-18 18:22:55 +02:00 (CEST)
Date last edited 2021-09-17 14:40:49 +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.*3417A>G r.(=) p.(=)
SPG11 NM_025137.3 ?/. - c.7132T>C r.(?) p.(Phe2378Leu)


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