Variant #0001001430 (NC_000015.9:g.44955802C>T, NM_025137.3:c.44G>A (SPG11))

Chromosome 15
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.44955802C>T
DNA change (hg38) -
Published as SPG11(NM_025137.3):c.44G>A (p.(Gly15Asp))
ISCN -
DB-ID EIF3J_000115
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) 0.00011 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 N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
PATL2 NM_001145112.1 ?/. - c.*2349G>A r.(=) p.(=)
EIF3J NM_003758.2 ?/. - c.*102455C>T r.(=) p.(=)
SPG11 NM_025137.3 ?/. - c.44G>A r.(?) p.(Gly15Asp)


Screenscraping/webscraping (downloading large amounts of data using scripts) is strictly prohibited.
Use our APIs to retrieve data.