Variant #0001067300 (NC_000020.10:g.17949102T>A, NM_052865.2:c.-742T>A (MGME1))

Chromosome 20
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.17949102T>A
DNA change (hg38) -
Published as SNX5(NM_152227.3):c.-32-2A>T
ISCN -
DB-ID SNX5_000006
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_Leiden
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Leiden
Date created 2026-01-20 18:57:21 +01:00 (CET)
Date last edited N/A
Options




Variant on transcripts


Gene     

AscendingTranscript     

Affects function     

Exon     

DNA change (cDNA)     

RNA change     

Protein     
SNX5 NM_014426.2 ?/. - c.-34A>T r.(?) p.(=)
MGME1 NM_052865.2 ?/. - c.-742T>A r.(?) p.(=)


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