"PreventionGenetics, part of Exact Sciences"[submitter] AND "VPS37A"[g - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 540285	NM_152415.3(VPS37A):c.96G>C (p.Leu32=)	VPS37A	Single nucleotide variant (synonymous variant +1 more)	Hereditary spastic paraplegia 53 +1 more	GLikely benign
Select item 3042315	NM_152415.3(VPS37A):c.174A>T (p.Ile58=)	VPS37A	Single nucleotide variant (synonymous variant +2 more)	VPS37A-related disorder	GLikely benign
Select item 696358	NM_152415.3(VPS37A):c.297C>G (p.Thr99=)	VPS37A	Single nucleotide variant (synonymous variant)	VPS37A-related disorder +1 more	GLikely benign
Select item 2421066	NM_152415.3(VPS37A):c.417-9T>C	VPS37A	Single nucleotide variant (intron variant)	Hereditary spastic paraplegia 53 +1 more	GLikely benign
Select item 696204	NM_152415.3(VPS37A):c.446C>T (p.Pro149Leu)	VPS37A (P124L +2 more)	Single nucleotide variant (missense variant)	VPS37A-related disorder +1 more	GLikely benign
Select item 2195472	NM_152415.3(VPS37A):c.1168C>T (p.His390Tyr)	VPS37A (H365Y +4 more)	Single nucleotide variant (missense variant)	VPS37A-related disorder +1 more	GConflicting classifications of pathogenicity
Select item 3044627	NM_004686.5(MTMR7):c.1749T>G (p.Ser583Arg)	MTMR7, VPS37A (S583R)	Single nucleotide variant (missense variant +1 more)	MTMR7-related disorder	GLikely benign
Select item 3042663	NM_004686.5(MTMR7):c.1565T>C (p.Met522Thr)	MTMR7, VPS37A (M522T)	Single nucleotide variant (missense variant +1 more)	MTMR7-related disorder	GLikely benign
Select item 3034900	NM_004686.5(MTMR7):c.1185C>T (p.Ile395=)	MTMR7, VPS37A	Single nucleotide variant (synonymous variant +1 more)	MTMR7-related disorder	GLikely benign
Select item 3035557	NM_004686.5(MTMR7):c.1036G>A (p.Ala346Thr)	MTMR7, VPS37A (A346T)	Single nucleotide variant (missense variant +1 more)	MTMR7-related disorder	GLikely benign