Variant #0001055741 (NC_000016.9:g.89619468C>T, NM_003119.2:c.1861C>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.89619468C>T
DNA change (hg38) -
Published as SPG7(NM_003119.4):c.1861C>T (p.(Gln621*))
ISCN -
DB-ID RPL13_000064
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2025-11-01 13:22:20 +01:00 (CET)
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.-7673C>T r.(?) p.(=)
SPG7 NM_003119.2 +/. - c.1861C>T r.(?) p.(Gln621*)


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