7-117129846-CGG-AGA

Variant names:

• chr7-117129846-CGG-AGA
• NM_001369598.1:c.448_449+1delCGGinsAGA
• ST7 p.151

Variant summary

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

The NM_001369598.1(ST7):​c.448_449+1delCGGinsAGA​(p.151) variant causes a splice donor, splice region, synonymous, intron change involving the alteration of a 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 MNV, and the frequency of such variant types in population databases may be underestimated and unreliable. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar. Synonymous variant affecting the same amino acid position (i.e. R150R) has been classified as Likely benign.

• Frequency: Genomes: not found (cov: 32)
• Consequence: ST7 NM_001369598.1 splice_donor, splice_region, synonymous, intron
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: 9.63
• Publications: 0 publications found

Genes affected

ST7 (HGNC:11351): (suppression of tumorigenicity 7) The gene for this product maps to a region on chromosome 7 identified as an autism-susceptibility locus. Mutation screening of the entire coding region in autistic individuals failed to identify phenotype-specific variants, suggesting that coding mutations for this gene are unlikely to be involved in the etiology of autism. The function of this gene product has not been determined. Transcript variants encoding different isoforms of this protein have been described. [provided by RefSeq, Jul 2008]

ST7-AS2 (HGNC:16044): (ST7 antisense RNA 2)

ACMG classification

Our verdict: Uncertain_significance. The variant received 0 ACMG points.

Variant Effect in Transcripts

ACMG analysis was done for transcript: NM_001369598.1. 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
	ST7	NM_001369598.1	MANE Select	c.448_449+1delCGGinsAGA	p.151	splice_donor splice_region synonymous intron	N/A	NP_001356527.1	H7BXS2
	ST7	NM_021908.3		c.448_449+1delCGGinsAGA	p.151	splice_donor splice_region synonymous intron	N/A	NP_068708.1	X5DRA0
	ST7	NM_001369601.1		c.448_449+1delCGGinsAGA	p.151	splice_donor splice_region synonymous intron	N/A	NP_001356530.1	E7EPD9

Ensembl Transcripts

Sel.	Gene	Transcript	Tags	HGVSc	HGVSp	Effect	Exon Rank	Protein	UniProt
	ST7	ENST00000323984.8	TSL:5 MANE Select	c.448_449+1delCGGinsAGA	p.151	splice_donor splice_region synonymous intron	N/A	ENSP00000325673.3	H7BXS2
	ST7	ENST00000265437.9	TSL:1	c.448_449+1delCGGinsAGA	p.151	splice_donor splice_region synonymous intron	N/A	ENSP00000265437.5	Q9NRC1-1
	ST7	ENST00000393451.7	TSL:1	c.448_449+1delCGGinsAGA	p.151	splice_donor splice_region synonymous intron	N/A	ENSP00000377097.3	Q9NRC1-2

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		9.6

Splicing

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: chr7-116769900;