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

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 423392	NM_001379228.1(MRAP):c.206+5G>T	LOC125418060, MRAP +1 more	Single nucleotide variant (intron variant)	MRAP-related disorder +1 more	GLikely pathogenic
Select item 339686	NM_001379228.1(MRAP):c.508T>A (p.Leu170Met)	URB1, MRAP (L170M +1 more)	Single nucleotide variant (missense variant +2 more)	MRAP-related disorder +1 more	GConflicting classifications of pathogenicity