chrX-51710560-C-A

Variant names:

• chrX-51710560-C-A
• rs1557347412
• NM_001355277.1:c.49C>A

Variant summary

Our verdict is Benign. The variant received -7 ACMG points: 0P and 7B. BP4_Strong BP6_Moderate BP7

The NM_001355277.1(CENPVL1):​c.49C>A​(p.Arg17Arg) variant causes a synonymous change involving the alteration of a non-conserved nucleotide. In-silico tool predicts a benign outcome for this variant. Variant has been reported in ClinVar as Likely benign (★).

• Frequency: Genomes: not found (cov: 0)
• Consequence: CENPVL1 NM_001355277.1 synonymous
• Clinical Significance: Likely benign criteria provided, single submitter B:1
• Conservation: PhyloP100: -0.617
• Publications: 0 publications found

Genes affected

CENPVL1 (HGNC:31851): (centromere protein V like 1) Predicted to enable carbon-sulfur lyase activity and metal ion binding activity. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Our verdict: Benign. The variant received -7 ACMG points.

• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.89).
• BP6: Variant X-51710560-C-A is Benign according to our data. Variant chrX-51710560-C-A is described in ClinVar as Likely_benign. ClinVar VariationId is 2660570.Status of the report is criteria_provided_single_submitter, 1 stars.
• BP7: Synonymous conserved (PhyloP=-0.617 with no splicing effect.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001355277.1. 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
	CENPVL1	NM_001355277.1	MANE Select	c.49C>A	p.Arg17Arg	synonymous	Exon 1 of 1	NP_001342206.1	A0A0U1RR11

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	CENPVL1	ENST00000602548.2	TSL:6 MANE Select	c.49C>A	p.Arg17Arg	synonymous	Exon 1 of 1	ENSP00000489273.1	A0A0U1RR11

Frequencies

GnomAD3 genomes Cov.: 0

GnomAD4 exome Cov.: 0

GnomAD4 genome Cov.: 0

ClinVar

ClinVar submissions

Significance: Likely benign

Revision: criteria provided, single submitter

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

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.89
CADD	Benign	7.5
DANN	Benign	0.83
PhyloP100		-0.62
PromoterAI		-0.054	Neutral

Splicing

Name	Calibrated prediction	Score	Prediction
SpliceAI score (max)		0.0		Details are displayed if max score is > 0.2

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

Other links and lift over

dbSNP: rs1557347412; hg19: chrX-51453656;