Variant #0000807729 (NC_000016.9:g.89614464G>T, NM_003119.2:c.1606G>T (SPG7))

Chromosome 16
Allele Unknown
Affects function (as reported) Affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.89614464G>T
DNA change (hg38) -
Published as SPG7(NM_001363850.1):c.1606G>T (p.G536*)
ISCN -
DB-ID RPL13_000023
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_VUmc
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_VUmc
Date created 2021-09-17 14:40:49 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPL13 NM_000977.3 +/. - c.-12677G>T r.(?) p.(=)
SPG7 NM_003119.2 +/. - c.1606G>T r.(?) p.(Gly536*)


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