NC_012920.1(MT-CYB):m.14825A>G AND Leigh syndrome

Germline classification:: Uncertain significance (1 submission)
Last evaluated:: Oct 17, 2019
Review status:: 1 star out of maximum of 4 stars
criteria provided, single submitter

Somatic classification of clinical impact:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Somatic classification of oncogenicity:: None
Review status:: (0/4) 0 stars out of maximum of 4 stars
no assertion criteria provided

Record status:: current
Accession:: RCV000855162.1

Allele description [Variation Report for NC_012920.1(MT-CYB):m.14825A>G]

NC_012920.1(MT-CYB):m.14825A>G

Gene:

MT-CYB:mitochondrially encoded cytochrome b [Gene - OMIM - HGNC]

Variant type:

single nucleotide variant

Genomic location:

Preferred name:

NC_012920.1(MT-CYB):m.14825A>G

HGVS:

NC_012920.1:m.14825A>G

Links:

dbSNP: rs1603224912

NCBI 1000 Genomes Browser:

rs1603224912

Condition(s)

Name:: Leigh syndrome (NULS)
Synonyms:: Leigh Disease; Subacute necrotizing encephalopathy; Necrotizing encephalopathy infantile subacute of Leigh; See all synonyms [MedGen]
Identifiers:: MONDO: MONDO:0009723; MedGen: C0023264; Orphanet: 506; OMIM: 256000

Recent activity

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protein lin-9 homolog isoform 3 [Homo sapiens]
protein lin-9 homolog isoform 3 [Homo sapiens]
gi|394582075|ref|NP_001257339.1|

Protein
Homo sapiens lin-9 DREAM MuvB core complex component (LIN9), transcript variant ...
Homo sapiens lin-9 DREAM MuvB core complex component (LIN9), transcript variant 2, mRNA
gi|394582064|ref|NM_001270409.1|

Nucleotide
Caenorhabditis elegans Peptidase S1 domain-containing protein (C50D2.1), mRNA
Caenorhabditis elegans Peptidase S1 domain-containing protein (C50D2.1), mRNA
gi|1845971434|ref|NM_061262.6|

Nucleotide
Caenorhabditis elegans Neuralized-like protein 2 (F10D7.5), mRNA
Caenorhabditis elegans Neuralized-like protein 2 (F10D7.5), mRNA
gi|1734341991|ref|NM_078417.6|

Nucleotide

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Submission Accession	Submitter	Review Status (Assertion method)	Clinical Significance (Last evaluated)	Origin	Method	Citations
SCV000998212	Wong Mito Lab, Molecular and Human Genetics, Baylor College of Medicine	criteria provided, single submitter (Modified ACMG Guidelines (Unpublished))	Uncertain significance (Oct 17, 2019)	germline	clinical testing	Citation Link

Submission Accession

Submitter

Review Status
(Assertion method)

Clinical Significance
(Last evaluated)

Origin

Method

Citations

SCV000998212

Wong Mito Lab, Molecular and Human Genetics, Baylor College of Medicine

criteria provided, single submitter

(Modified ACMG Guidelines (Unpublished))

Uncertain significance
(Oct 17, 2019)

germline

clinical testing

Citation Link

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Summary from all submissions

Ethnicity	Origin	Affected	Individuals	Families	Chromosomes tested	Number Tested	Family history	Method
not provided	germline	unknown	not provided	not provided	not provided	not provided	not provided	clinical testing

Details of each submission

From Wong Mito Lab, Molecular and Human Genetics, Baylor College of Medicine, SCV000998212.1

#	Ethnicity	Individuals	Chromosomes Tested	Family History	Method	Citations
1	not provided	not provided	not provided	not provided	clinical testing	not provided

Description

The NC_012920.1:m.14825A>G (YP_003024038.1:p.Ile27Val) variant in MTCYB gene is interpretated to be a Uncertain Significance variant based on the modified ACMG guidelines (unpublished). This variant meets the following evidence codes: PP6

#	Sample				Method		Observation
#	Origin	Affected	Number tested	Tissue	Purpose	Method	Individuals	Allele frequency	Families	Co-occurrences
1	germline	unknown	not provided	not provided	not provided		not provided	not provided	not provided	not provided

Last Updated: May 19, 2024

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