Variant #0000554442 (NC_000015.9:g.44952677C>T, NM_025137.3:c.395G>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.44952677C>T
DNA change (hg38) g.44660479C>T
Published as SPG11(NM_025137.3):c.395G>A (p.S132N), SPG11(NM_025137.4):c.395G>A (p.S132N)
ISCN -
DB-ID SPG11_000097 See all 4 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) 0.00022 View details
Owner VKGL-NL_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
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.*99330C>T r.(=) p.(=)
SPG11 NM_025137.3 -?/. - c.395G>A r.(?) p.(Ser132Asn)


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