Variant #0000809171 (NC_000020.10:g.17950988del, NM_052865.2:c.486del (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.17950988del
DNA change (hg38) -
Published as MGME1(NM_001310338.1):c.486delA (p.D163Mfs*18)
ISCN -
DB-ID SNX5_000001
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_Rotterdam
Database submission license Creative Commons Attribution-NonCommercial-ShareAlike 4.0 InternationalCreative Commons License
Created by VKGL-NL_Rotterdam
Date created 2021-09-17 14:40:49 +02:00 (CEST)
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.-1919del r.(?) p.(=)
MGME1 NM_052865.2 ?/. - c.486del r.(?) p.(Asp163Metfs*31)


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