"PreventionGenetics, part of Exact Sciences"[submitter] AND "MOBP"[gen - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2631821	NM_001393704.1(MOBP):c.206+5G>C	MOBP	Single nucleotide variant (intron variant)	MOBP-related disorder	GUncertain significance
Select item 3057625	NM_001393704.1(MOBP):c.207-27G>A	MOBP	Single nucleotide variant (synonymous variant +1 more)	MOBP-related disorder	GLikely benign
Select item 2634486	NM_001393704.1(MOBP):c.250C>T (p.Pro84Ser)	MOBP (P108S +1 more)	Single nucleotide variant (missense variant +2 more)	MOBP-related disorder	GUncertain significance
Select item 2636755	NM_001393704.1(MOBP):c.260C>T (p.Pro87Leu)	MOBP (P111L +1 more)	Single nucleotide variant (missense variant +2 more)	MOBP-related disorder	GUncertain significance
Select item 3052120	NM_001393704.1(MOBP):c.294GTCCCCTCCGAGGTCTGAGCGTCAGCCACG[3] (p.99SPPRSERQPR[3])	MOBP	Microsatellite (inframe deletion +3 more)	MOBP-related disorder	GLikely benign
Select item 2634225	NM_001393704.1(MOBP):c.361C>T (p.Pro121Ser)	MOBP (P121S +1 more)	Single nucleotide variant (missense variant +2 more)	MOBP-related disorder	GUncertain significance

ClinVar