rs879253776

Variant names:

• chr16-30086366-C-CG
• rs879253776
• NM_004608.4:c.1169dupC

Variant summary

Our verdict is Likely pathogenic. Variant got 8 ACMG points: 8P and 0B. PVS1_Strong PM2 PP5_Moderate

The NM_004608.4(TBX6):​c.1169dupC​(p.His391AlafsTer96) variant causes a frameshift change involving the alteration of a non-conserved nucleotide. The variant was absent in control chromosomes in GnomAD project. Variant has been reported in ClinVar as Pathogenic (★).

• Frequency: Genomes: not found (cov: 32)
• Consequence: TBX6 NM_004608.4 frameshift
• Clinical Significance: Pathogenic criteria provided, single submitter P:1
• Conservation: PhyloP100: 0.441

Genes affected

TBX6 (HGNC:11605): (T-box transcription factor 6) This gene is a member of a phylogenetically conserved family of genes that share a common DNA-binding domain, the T-box. T-box genes encode transcription factors involved in the regulation of developmental processes. Knockout studies in mice indicate that this gene is important for specification of paraxial mesoderm structures. [provided by RefSeq, Aug 2008]

ACMG classification

Verdict is Likely_pathogenic. Variant got 8 ACMG points.

• PVS1: Loss of function variant, product does not undergo nonsense mediated mRNA decay. Variant is located in the 3'-most exon, not predicted to undergo nonsense mediated mRNA decay. Fraction of 0.108 CDS is truncated, and there are 0 pathogenic variants in the truncated region.
• PM2: Very rare variant in population databases, with high coverage
• PP5: Variant 16-30086366-C-CG is Pathogenic according to our data. Variant chr16-30086366-C-CG is described in ClinVar as [Pathogenic]. Clinvar id is 243054.Status of the report is criteria_provided_single_submitter, 1 stars.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	MANE	Protein	UniProt
TBX6	NM_004608.4	c.1169dupC	p.His391AlafsTer96	frameshift_variant	Exon 9 of 9	ENST00000395224.7	NP_004599.2
TBX6	XM_011545926.4	c.1169dupC	p.His391AlafsTer96	frameshift_variant	Exon 9 of 9		XP_011544228.1
TBX6	XM_047434551.1	c.1169dupC	p.His391AlafsTer96	frameshift_variant	Exon 8 of 8		XP_047290507.1
TBX6	XR_007064904.1	n.*236dupC		downstream_gene_variant

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	Exon rank	TSL	MANE	Protein	Appris	UniProt
TBX6	ENST00000395224.7	c.1169dupC	p.His391AlafsTer96	frameshift_variant	Exon 9 of 9	1	NM_004608.4	ENSP00000378650.2
TBX6	ENST00000279386.6	c.1169dupC	p.His391AlafsTer96	frameshift_variant	Exon 8 of 8	1		ENSP00000279386.2
TBX6	ENST00000567664.5	n.*303dupC		non_coding_transcript_exon_variant	Exon 7 of 7	5		ENSP00000460425.1
TBX6	ENST00000567664.5	n.*303dupC		3_prime_UTR_variant	Exon 7 of 7	5		ENSP00000460425.1

Frequencies

GnomAD3 genomes Cov.: 32

GnomAD4 exome Cov.: 34

GnomAD4 genome Cov.: 32

ClinVar

Significance: Pathogenic

Submissions summary: Pathogenic:1

Revision: criteria provided, single submitter

Submissions by phenotype

Spondylocostal dysostosis 5 Pathogenic:1

Nov 15, 2015

Lupski Lab, Baylor-Hopkins CMG, Baylor College of Medicine

Significance: Pathogenic

Review Status: criteria provided, single submitter

Collection Method: research

This variant was observed in 1 individual with a vertebral malformation. The variant was found to be in trans with a high-risk TBX6 haplotype, T-C-A (rs2289292, rs3809624, rs3809627). -

Computational scores

Source: dbNSFP v4.3

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: rs879253776; hg19: chr16-30097687;