rs879182710

Variant names:

• chrM-15777-G-A
• rs879182710
• ENST00000361789.2:c.1031G>A
• MT-CYB p.Ser344Asn

Your query was ambiguous. Multiple possible variants found:

• chrM-15777-G-A
• chrM-15777-G-C

Variant summary

Our verdict is Benign. The variant received -13 ACMG points: 0P and 13B. BP4 BP6_Very_Strong BS2

The ENST00000361789.2(MT-CYB):​c.1031G>A​(p.Ser344Asn) variant causes a missense change. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Likely benign (★★). Another variant affecting the same amino acid position, but resulting in a different missense (i.e. S344T) has been classified as Benign.

• Frequency: Mitomap GenBank: 𝑓 0.0018 (AC: 112)
• Consequence: MT-CYB ENST00000361789.2 missense
• Scores: Apogee2 Benign 0.015
• Clinical Significance: Benign/Likely benign criteria provided, multiple submitters, no conflicts B:2 No linked disesase in Mitomap
• Conservation: PhyloP100: 4.74
• Publications: 2 publications found

Genes affected

MT-CYB (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]

TRNT (HGNC:7499): (mitochondrially encoded tRNA threonine)

TRNP (HGNC:7494): (mitochondrially encoded tRNA proline)

TRNP Gene-Disease associations (from GenCC):

• MERRF syndrome

  Inheritance: Mitochondrial Classification: DEFINITIVE, SUPPORTIVE Submitted by: G2P, Orphanet
• mitochondrial disease

  Inheritance: Mitochondrial Classification: DEFINITIVE Submitted by: ClinGen

ACMG classification

Our verdict: Benign. The variant received -13 ACMG points.

• BP4: Apogee2 supports a benign effect, 0.014891338 < 0.5 .
• BP6: Variant M-15777-G-A is Benign according to our data. Variant chrM-15777-G-A is described in ClinVar as Benign/Likely_benign. ClinVar VariationId is 377195.Status of the report is criteria_provided_multiple_submitters_no_conflicts, 2 stars.
• BS2: High AC in GnomadMitoHomoplasmic at 38

Variant Effect in Transcripts

ACMG analysis was done for transcript: ENST00000361789.2. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
There are no transcript annotations for this variant.

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	MT-CYB	ENST00000361789.2	TSL:6	c.1031G>A	p.Ser344Asn	missense	Exon 1 of 1	ENSP00000354554.2	P00156
	MT-TT	ENST00000387460.2	TSL:6	n.-111G>A		upstream_gene	N/A
	MT-TP	ENST00000387461.2	TSL:6	n.*179C>T		downstream_gene	N/A

Frequencies

Mitomap GenBank AF: 0.0018 AC: 112

Gnomad homoplasmic AF: 0.00067 AC: 38 AN: 56414

Gnomad heteroplasmic AF: 0.00014 AC: 8 AN: 56414

Alfa AF: 0.000891 Hom.: 4

Mitomap

No disease associated.

ClinVar

ClinVar submissions

Significance: Benign/Likely benign

Revision: criteria provided, multiple submitters, no conflicts

Pathogenic	VUS	Benign	Condition
-	-	1	Leigh syndrome (1)
-	-	1	not provided (1)

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
Apogee2	Benign	0.015
Hmtvar	Benign	0.19
AlphaMissense	Benign	0.10
PhyloP100		4.7
Mutation Taster		=15/185	disease causing

MaxEntScan Visualizer can be used to analyze the impact of this mutation on the neighboring sequence.

Other links and lift over

dbSNP: rs879182710;

hg19: chrM-15778;

COSMIC: COSV104670485;

COSMIC: COSV104670485;