Variant #0000950778 (NC_000016.9:g.89613145C>T, NM_003119.2:c.1529C>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.89613145C>T
DNA change (hg38) -
Published as SPG7(NM_001363850.1):c.1529C>T (p.A510V), SPG7(NM_003119.2):c.1529C>T (p.(Ala510Val)), SPG7(NM_003119.4):c.1529C>T (p.A510V)
ISCN -
DB-ID SPG7_000003 See all 17 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) 0.00288 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 2023-11-27 17:35:39 +01:00 (CET)
Date last edited 2024-08-28 13:16:32 +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.-13996C>T r.(?) p.(=)
SPG7 NM_003119.2 +/. - c.1529C>T r.(?) p.(Ala510Val)


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