Variant #0001035893 (NC_000006.11:g.74207487A>G, NM_133645.2:c.1860A>G (MTO1))

Chromosome 6
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.74207487A>G
DNA change (hg38) -
Published as MTO1(NM_012123.4):c.1785A>G (p.(Gln595=))
ISCN -
DB-ID MTO1_000027
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) 0.00493 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 2025-05-05 21:14:00 +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     
MTO1 NM_012123.4 -?/. - c.1785A>G r.(?) p.(Gln595=)
MTO1 NM_133645.2 -?/. - c.1860A>G r.(?) p.(=)


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