M-14766-C-T

Variant names:

• chrM-14766-C-T
• rs193302980
• unassigned_transcript_4818:c.20C>T

Variant summary

Our verdict is Benign. Variant got -10 ACMG points: 0P and 10B. BP6_Moderate BA1

In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Benign (★).

• Frequency: Mitomap GenBank: 𝑓 0.76 (AC: 46208)
• Consequence: CYTB missense
• Scores: Apogee2 Benign 0.042
• Clinical Significance: Benign criteria provided, single submitter P:2 B:1 No linked disesase in Mitomap
• Conservation: PhyloP100: 0.116

Genes affected

CYTB (HGNC:7427): (mitochondrially encoded cytochrome b) Predicted to enable metal ion binding activity. Predicted to be involved in several processes, including electron transport coupled proton transport; response to cobalamin; and response to glucagon. Located in mitochondrion. Implicated in ovarian carcinoma and urinary bladder cancer. [provided by Alliance of Genome Resources, Apr 2022]

ND6 (HGNC:7462): (mitochondrially encoded NADH dehydrogenase 6) Enables NADH dehydrogenase (ubiquinone) activity. Involved in mitochondrial electron transport, NADH to ubiquinone and mitochondrial respiratory chain complex I assembly. Predicted to be located in mitochondrial inner membrane. Implicated in Leber hereditary optic neuropathy; Leigh disease; and spinal muscular atrophy with lower extremity predominante 2B. [provided by Alliance of Genome Resources, Apr 2022]

TRNE (HGNC:7479): (mitochondrially encoded tRNA glutamic acid)

ACMG classification

Verdict is Benign. Variant got -10 ACMG points.

• BP6: Variant M-14766-C-T is Benign according to our data. Variant chrM-14766-C-T is described in ClinVar as [Benign]. Clinvar id is 140587.Status of the report is criteria_provided_single_submitter, 1 stars.
• BA1: High frequency in mitomap database: 0.7558

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
CYTB	unassigned_transcript_4818	c.20C>T	p.Thr7Ile	missense_variant	Exon 1 of 1
ND6	unassigned_transcript_4816	c.-93G>A		upstream_gene_variant
TRNE	unassigned_transcript_4817	c.-24G>A		upstream_gene_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt

Frequencies

GnomAD4 exome Cov.: 0

We have no GnomAD4 genomes data on this position. Probably position not covered by the project.

Mitomap GenBank AF: 0.76 AC: 46208

Gnomad homoplasmic AF: 0.71 AC: 39641 AN: 56086

Gnomad heteroplasmic AF: 0.000053 AC: 3 AN: 56086

Alfa AF: 0.651 Hom.: 8136

Mitomap

No disease associated.

ClinVar

Significance: Benign

Submissions summary: Pathogenic:2 Benign:1

Revision: criteria provided, single submitter

Submissions by phenotype

Venous thromboembolism Pathogenic:1

-

Genomics Division, Defence Institute of Physiology and Allied Sciences

Significance: Likely risk allele

Review Status: no assertion criteria provided

Collection Method: case-control

- -

Familial cancer of breast Pathogenic:1

-

Department of Zoology Govt. MVM College

Significance: Likely pathogenic

Review Status: no assertion criteria provided

Collection Method: literature only

- -

Leigh syndrome Benign:1

Oct 17, 2019

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

Significance: Benign

Review Status: criteria provided, single submitter

Collection Method: clinical testing

The NC_012920.1:m.14766C>T (YP_003024038.1:p.Thr7Ile) variant in MTCYB gene is interpretated to be a Benign variant based on the modified ACMG guidelines (unpublished). This variant meets the following evidence codes: BA1 -

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
Apogee2	Benign	0.042
Hmtvar	Benign	0.090
AlphaMissense	Benign	0.14

Splicing

Find out detailed SpliceAI scores and Pangolin per-transcript scores at spliceailookup.broadinstitute.org

Publications

LitVar

Other links and lift over

dbSNP: rs193302980; hg19: chrM-14767;