chr15-89776891-G-GGGGCAGGGGCAAGGGCAGGGGCAAGGGCAGGGGCAA

Position:

• chr15-89776891-G-GGGGCAGGGGCAAGGGCAGGGGCAAGGGCAGGGGCAA

Variant summary

Our verdict is Uncertain significance. Variant got 0 ACMG points: 0P and 0B.

The NM_001039958.2(MESP2):​c.557_558insAGGGCAGGGGCAAGGGCAGGGGCAAGGGCAGGGGCA​(p.Gln194_Gly205dup) variant causes a inframe insertion change involving the alteration of a non-conserved nucleotide. No clinical diagnostic laboratories have submitted clinical-significance assessments for this variant to ClinVar.

• Frequency: Genomes: not found (cov: 0)
• Consequence: MESP2 NM_001039958.2 inframe_insertion
• Clinical Significance: Not reported in ClinVar
• Conservation: PhyloP100: -1.32

Genes affected

MESP2 (HGNC:29659): (mesoderm posterior bHLH transcription factor 2) This gene encodes a member of the bHLH family of transcription factors and plays a key role in defining the rostrocaudal patterning of somites via interactions with multiple Notch signaling pathways. This gene is expressed in the anterior presomitic mesoderm and is downregulated immediately after the formation of segmented somites. This gene also plays a role in the formation of epithelial somitic mesoderm and cardiac mesoderm. Mutations in the MESP2 gene cause autosomal recessive spondylocostal dystosis 2 (SCD02). [provided by RefSeq, Oct 2008]

ACMG classification

Verdict is Uncertain_significance. Variant got 0 ACMG points.

Transcripts

RefSeq

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	MANE	Protein	UniProt
MESP2	NM_001039958.2	c.557_558insAGGGCAGGGGCAAGGGCAGGGGCAAGGGCAGGGGCA	p.Gln194_Gly205dup	inframe_insertion	1/2	ENST00000341735.5	NP_001035047.1

Ensembl

Gene	Transcript	HGVSc	HGVSp	Effect	#exon/exons	TSL	MANE	Protein	Appris	UniProt
MESP2	ENST00000341735.5	c.557_558insAGGGCAGGGGCAAGGGCAGGGGCAAGGGCAGGGGCA	p.Gln194_Gly205dup	inframe_insertion	1/2	1	NM_001039958.2	ENSP00000342392	P1
MESP2	ENST00000560219.2	c.31-1151_31-1150insAGGGCAGGGGCAAGGGCAGGGGCAAGGGCAGGGGCA		intron_variant		1		ENSP00000452998
MESP2	ENST00000558723.1	n.39-1151_39-1150insAGGGCAGGGGCAAGGGCAGGGGCAAGGGCAGGGGCA		intron_variant, non_coding_transcript_variant		3

Frequencies

GnomAD3 genomes Cov.: 0

GnomAD4 exome Cov.: 0

GnomAD4 genome Cov.: 0

ClinVar

Not reported in ClinVar

Computational scores

Source: dbNSFP v4.3

Splicing

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

Publications

LitVar

Other links and lift over

dbSNP: rs397507446; hg19: chr15-90320122;