Variant #0000983743 (NC_000020.10:g.17950772A>G, NM_052865.2:c.270A>G (MGME1))

Chromosome 20
Allele Unknown
Affects function (as reported) Probably does not affect function
Affects function (by curator) Not classified
Classification method -
Clinical classification likely benign
DNA change (genomic) (Relative to hg19 / GRCh37) g.17950772A>G
DNA change (hg38) -
Published as MGME1(NM_052865.4):c.270A>G (p.(Gln90=))
ISCN -
DB-ID SNX5_000004
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) 0.01709 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 2024-04-19 20:27:30 +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     
SNX5 NM_014426.2 -?/. - c.-1704T>C r.(?) p.(=)
MGME1 NM_052865.2 -?/. - c.270A>G r.(?) p.(=)


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