Variant #0000893286 (NC_000016.9:g.89620238C>T, NM_003119.2:c.1973C>T (SPG7))

Chromosome 16
Allele Unknown
Affects function (as reported) Probably affects function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely pathogenic
DNA change (genomic) (Relative to hg19 / GRCh37) g.89620238C>T
DNA change (hg38) -
Published as SPG7(NM_001363850.1):c.1973C>T (p.A658V)
ISCN -
DB-ID RPL13_000042
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 2022-11-01 13:41:49 +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.-6903C>T r.(?) p.(=)
SPG7 NM_003119.2 +?/. - c.1973C>T r.(?) p.(Ala658Val)


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