1-111477409-C-A

Variant names:

• chr1-111477409-C-A
• NM_001300834.2:c.183C>A
• C1orf162 p.Ile61Ile

Variant summary

Our verdict is Uncertain significance. The variant received 2 ACMG points: 2P and 0B. PM2

The NM_001300834.2(C1orf162):​c.183C>A​(p.Ile61Ile) variant causes a synonymous change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. In-silico tool predicts a benign outcome for this variant. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: not found (cov: 32)
• Consequence: C1orf162 NM_001300834.2 synonymous
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.746
• Publications: 0 publications found

Genes affected

C1orf162 (HGNC:28344): (chromosome 1 open reading frame 162) Predicted to be integral component of membrane. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Our verdict: Uncertain_significance. The variant received 2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001300834.2. 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
	C1orf162	NM_001300834.2	MANE Select	c.183C>A	p.Ile61Ile	synonymous	Exon 4 of 6	NP_001287763.1	Q8NEQ5-2
	C1orf162	NM_174896.4		c.183C>A	p.Ile61Ile	synonymous	Exon 4 of 6	NP_777556.1	Q8NEQ5-1
	C1orf162	NM_001300835.2		c.116-242C>A		intron	N/A	NP_001287764.1

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	C1orf162	ENST00000369718.4	TSL:2 MANE Select	c.183C>A	p.Ile61Ile	synonymous	Exon 4 of 6	ENSP00000358732.3	Q8NEQ5-2
	C1orf162	ENST00000343534.9	TSL:1	c.183C>A	p.Ile61Ile	synonymous	Exon 4 of 6	ENSP00000344218.5	Q8NEQ5-1
	C1orf162	ENST00000868017.1		c.183C>A	p.Ile61Ile	synonymous	Exon 4 of 6	ENSP00000538076.1

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 31

GnomAD4 genome Cov.: 32

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.52
CADD	Benign	6.5
DANN	Benign	0.57
PhyloP100		0.75
Mutation Taster		=100/0	polymorphism

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.25		Details are displayed if max score is > 0.2
DS_DL_spliceai		0.25		Position offset: 19

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

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

Other links and lift over

hg19: chr1-112020031;