rs1555618025

Variant names:

• chr17-39724733-A-ACGTGATGGCTTC
• rs1555618025
• NM_004448.4:c.2325_2326insTCCGTGATGGCT

Variant summary

Our verdict is Uncertain significance. The variant received 4 ACMG points: 4P and 0B. PM4 PP5_Moderate

The NM_004448.4(ERBB2):​c.2325_2326insTCCGTGATGGCT​(p.Ala775_Gly776insSerValMetAla) variant causes a conservative inframe insertion change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. It is difficult to determine the true allele frequency of this variant because it is of type INS_BIG, and the frequency of such variant types in population databases may be underestimated and unreliable. Variant has been reported in ClinVar as Likely pathogenic (★).

• Frequency: Genomes: not found (cov: 31)
• Consequence: ERBB2 NM_004448.4 conservative_inframe_insertion
• Clinical Significance: Likely pathogenic criteria provided, single submitter P:1
• Conservation: PhyloP100: -0.923
• Publications: 0 publications found

Genes affected

ERBB2 (HGNC:3430): (erb-b2 receptor tyrosine kinase 2) This gene encodes a member of the epidermal growth factor (EGF) receptor family of receptor tyrosine kinases. This protein has no ligand binding domain of its own and therefore cannot bind growth factors. However, it does bind tightly to other ligand-bound EGF receptor family members to form a heterodimer, stabilizing ligand binding and enhancing kinase-mediated activation of downstream signalling pathways, such as those involving mitogen-activated protein kinase and phosphatidylinositol-3 kinase. Allelic variations at amino acid positions 654 and 655 of isoform a (positions 624 and 625 of isoform b) have been reported, with the most common allele, Ile654/Ile655, shown here. Amplification and/or overexpression of this gene has been reported in numerous cancers, including breast and ovarian tumors. Alternative splicing results in several additional transcript variants, some encoding different isoforms and others that have not been fully characterized. [provided by RefSeq, Jul 2008]

ERBB2 Gene-Disease associations (from GenCC):

• Hirschsprung disease

  Inheritance: AD Classification: SUPPORTIVE Submitted by: Orphanet
• lung cancer

  Inheritance: AD Classification: LIMITED Submitted by: Ambry Genetics
• glioma susceptibility 1

  Inheritance: Unknown Classification: LIMITED Submitted by: Labcorp Genetics (formerly Invitae)
• visceral neuropathy, familial, 2, autosomal recessive

  Inheritance: Unknown Classification: LIMITED Submitted by: Labcorp Genetics (formerly Invitae)

ACMG classification

Our verdict: Uncertain_significance. The variant received 4 ACMG points.

• PM4: Nonframeshift variant in NON repetitive region in NM_004448.4.
• PP5: Variant 17-39724733-A-ACGTGATGGCTTC is Pathogenic according to our data. Variant chr17-39724733-A-ACGTGATGGCTTC is described in ClinVar as Likely_pathogenic. ClinVar VariationId is 163409.Status of the report is criteria_provided_single_submitter, 1 stars.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_004448.4. 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
	ERBB2	NM_004448.4	MANE Select	c.2325_2326insTCCGTGATGGCT	p.Ala775_Gly776insSerValMetAla	conservative_inframe_insertion	Exon 20 of 27	NP_004439.2
	ERBB2	NM_001382784.1		c.2442_2443insTCCGTGATGGCT	p.Ala814_Gly815insSerValMetAla	conservative_inframe_insertion	Exon 21 of 28	NP_001369713.1
	ERBB2	NM_001382785.1		c.2427_2428insTCCGTGATGGCT	p.Ala809_Gly810insSerValMetAla	conservative_inframe_insertion	Exon 21 of 28	NP_001369714.1

Ensembl Transcripts

Selected	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ERBB2	ENST00000269571.10	TSL:1 MANE Select	c.2325_2326insTCCGTGATGGCT	p.Ala775_Gly776insSerValMetAla	conservative_inframe_insertion	Exon 20 of 27	ENSP00000269571.4
	ERBB2	ENST00000584450.5	TSL:1	c.2325_2326insTCCGTGATGGCT	p.Ala775_Gly776insSerValMetAla	conservative_inframe_insertion	Exon 20 of 26	ENSP00000463714.1
	ERBB2	ENST00000578373.5	TSL:1	n.*2115_*2116insTCCGTGATGGCT		non_coding_transcript_exon	Exon 20 of 27	ENSP00000463427.1

Frequencies

GnomAD3 genomes Cov.: 31

GnomAD4 exome Cov.: 33

GnomAD4 genome Cov.: 31

ClinVar

ClinVar submissions as Germline

Significance: Likely pathogenic

Revision: criteria provided, single submitter

Pathogenic	VUS	Benign	Condition
1	-	-	Non-small cell lung carcinoma (1)

Computational scores

Source: dbNSFP v4.9

Name	Calibrated prediction	Score	Prediction
PhyloP100		-0.92

Splicing

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

Other links and lift over

dbSNP: rs1555618025; hg19: chr17-37880986;