NM_014737.3:c.692-77_692-76insAGTCCCT

Variant names:

• chr20-4787830-A-AAGGGACT
• rs67164330
• NM_014737.3:c.692-77_692-76insAGTCCCT

Variant summary

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

The NM_014737.3(RASSF2):​c.692-77_692-76insAGTCCCT variant causes a intron change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: not found (cov: 32)
• Consequence: RASSF2 NM_014737.3 intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 0.0940
• Publications: 1 publications found

Genes affected

RASSF2 (HGNC:9883): (Ras association domain family member 2) This gene encodes a protein that contains a Ras association domain. Similar to its cattle and sheep counterparts, this gene is located near the prion gene. Two alternatively spliced transcripts encoding the same isoform have been reported. [provided by RefSeq, Jul 2008]

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_014737.3. You can select a different transcript below to see updated ACMG assignments.

RefSeq Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	RASSF2	NM_014737.3	MANE Select	c.692-77_692-76insAGTCCCT		intron	N/A	NP_055552.1
	RASSF2	NM_170774.2		c.692-77_692-76insAGTCCCT		intron	N/A	NP_739580.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	RASSF2	ENST00000379400.8	TSL:1 MANE Select	c.692-77_692-76insAGTCCCT		intron	N/A	ENSP00000368710.3
	RASSF2	ENST00000379376.2	TSL:1	c.692-77_692-76insAGTCCCT		intron	N/A	ENSP00000368684.2
	RASSF2	ENST00000478553.1	TSL:1	n.715-130_715-129insAGTCCCT		intron	N/A

Frequencies

GnomAD3 genomes Cov.: 32

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

GnomAD4 genome Cov.: 32

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
PhyloP100		0.094

Splicing

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

Other links and lift over

dbSNP: rs67164330; hg19: chr20-4768476;