Variant #0000680177 (NC_000015.9:g.44858101C>T, NM_025137.3:c.6950G>A (SPG11))

Chromosome 15
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.44858101C>T
DNA change (hg38) -
Published as SPG11(NM_025137.3):c.6950G>A (p.G2317D), SPG11(NM_025137.4):c.6950G>A (p.G2317D)
ISCN -
DB-ID EIF3J_000005 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) 8.0E-5 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 2020-08-06 14:59:34 +02:00 (CEST)
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.*4754C>T r.(=) p.(=)
SPG11 NM_025137.3 -?/. - c.6950G>A r.(?) p.(Gly2317Asp)


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