rs2733285

Variant names:

• chr12-41504058-T-A
• rs2733285
• NM_001164595.2:c.844-2398T>A

Your query was ambiguous. Multiple possible variants found:

• chr12-41504058-T-A
• chr12-41504058-T-C

Variant summary

Our verdict is Likely benign. Variant got -2 ACMG points: 2P and 4B. PM2 BP4_Strong

The NM_001164595.2(PDZRN4):​c.844-2398T>A variant causes a intron 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: 31)
• Consequence: PDZRN4 NM_001164595.2 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.86

Genes affected

PDZRN4 (HGNC:30552): (PDZ domain containing ring finger 4) Predicted to enable metal ion binding activity. [provided by Alliance of Genome Resources, Apr 2022]

ACMG classification

Verdict is Likely_benign. Variant got -2 ACMG points.

• PM2: Very rare variant in population databases, with high coverage
• BP4: Computational evidence support a benign effect (BayesDel_noAF=-0.94).

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
PDZRN4	NM_001164595.2	c.844-2398T>A		intron_variant	Intron 3 of 9	ENST00000402685.7	NP_001158067.1
PDZRN4	NM_013377.4	c.70-2398T>A		intron_variant	Intron 1 of 7		NP_037509.3

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
PDZRN4	ENST00000402685.7	c.844-2398T>A		intron_variant	Intron 3 of 9	2	NM_001164595.2	ENSP00000384197.2
PDZRN4	ENST00000539469.6	c.70-2398T>A		intron_variant	Intron 1 of 7	1		ENSP00000439990.2
PDZRN4	ENST00000298919.7	c.64-2398T>A		intron_variant	Intron 3 of 9	2		ENSP00000298919.7
PDZRN4	ENST00000649474.1	c.-123-2398T>A		intron_variant	Intron 2 of 8			ENSP00000497437.1

Frequencies

GnomAD3 genomes Cov.: 31

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

GnomAD4 genome Cov.: 31

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Name	Calibrated prediction	Score	Prediction
BayesDel_noAF	Benign	-0.94
CADD	Benign	1.5
DANN	Benign	0.69

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

Publications

LitVar

Other links and lift over

dbSNP: rs2733285; hg19: chr12-41897860;