"PreventionGenetics, part of Exact Sciences"[submitter] AND "LOC114803 - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3061592	NM_138711.6(PPARG):c.530-7T>A	LOC114803475, PPARG	Single nucleotide variant (intron variant)	PPARG-related disorder	GLikely benign
Select item 3057658	NM_138711.6(PPARG):c.618C>T (p.Ser206=)	LOC114803475, PPARG	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 1555861	NM_138711.6(PPARG):c.675G>A (p.Pro225=)	LOC114803475, PPARG	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder +1 more	GLikely benign
Select item 3054277	NM_138711.6(PPARG):c.693G>C (p.Ala231=)	LOC114803475, PPARG	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 2718555	NM_138711.6(PPARG):c.698C>T (p.Ala233Val)	LOC114803475, PPARG (A263V +2 more)	Single nucleotide variant (missense variant +1 more)	PPARG-related disorder +1 more	GUncertain significance
Select item 2631326	NM_138711.6(PPARG):c.701T>C (p.Ile234Thr)	LOC114803475, PPARG (I234T +2 more)	Single nucleotide variant (missense variant +1 more)	PPARG-related disorder	GUncertain significance
Select item 3040523	NM_138711.6(PPARG):c.729+25T>C	LOC114803475, PPARG	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 2632802	NM_138711.6(PPARG):c.729+31dup	LOC114803475, PPARG (E256fs +1 more)	Duplication (frameshift variant +1 more)	PPARG-related disorder	GUncertain significance
Select item 3042755	NM_138711.6(PPARG):c.729+36G>A	LOC114803475, PPARG	Single nucleotide variant (synonymous variant +1 more)	PPARG-related disorder	GLikely benign
Select item 3033685	NM_138711.6(PPARG):c.729+73G>A	LOC114803475, PPARG	Single nucleotide variant (3 prime UTR variant +1 more)	PPARG-related disorder	GLikely benign