Variant #0000865025 (NC_000016.9:g.89598369G>A, NM_003119.2:c.1045G>A (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.89598369G>A
DNA change (hg38) -
Published as SPG7(NM_003119.2):c.1045G>A (p.(Gly349Ser)), SPG7(NM_003119.3):c.1045G>A (p.G349S), SPG7(NM_003119.4):c.1045G>A (p.G349S)
ISCN -
DB-ID SPG7_000025 See all 12 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) 0.00082 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 2022-05-09 16:01:56 +02:00 (CEST)
Date last edited N/A
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Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SPG7 NM_003119.2 +/. - c.1045G>A r.(?) p.(Gly349Ser)


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