Variant #0001002811 (NC_000016.9:g.89620971G>A, NM_003119.2:c.2181G>A (SPG7))

Chromosome 16
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.89620971G>A
DNA change (hg38) -
Published as SPG7(NM_003119.2):c.2181G>A (p.(Ala727=)), SPG7(NM_003119.4):c.2181G>A (p.A727=)
ISCN -
DB-ID SPG7_000042 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) 1.0E-5 View details
Owner VKGL-NL_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2024-08-28 13:16:32 +02:00 (CEST)
Date last edited 2025-05-05 21:14:00 +02:00 (CEST)
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
RPL13 NM_000977.3 ?/. - c.-6170G>A r.(?) p.(=)
SPG7 NM_003119.2 ?/. - c.2181G>A r.(?) p.(Ala727=)


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