Variant #0000346199 (NC_000016.9:g.89619501G>A, NM_003119.2:c.1894G>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.89619501G>A
DNA change (hg38) g.89553093G>A
Published as SPG7(NM_003119.3):c.1894G>A (p.G632R)
ISCN -
DB-ID SPG7_000063 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) 0 View details
Owner VKGL-NL_Nijmegen
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Nijmegen
Date created 2018-01-15 20:58:59 +01:00 (CET)
Date last edited 2022-05-09 15:51:19 +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.-7640G>A r.(?) p.(=)
SPG7 NM_003119.2 ?/. - c.1894G>A r.(?) p.(Gly632Arg)


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