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

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Items: 8

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2631938	NM_006372.5(SYNCRIP):c.1864T>C (p.Trp622Arg)	SYNCRIP (W524R +2 more)	Single nucleotide variant (missense variant +1 more)	SYNCRIP-related disorder	GUncertain significance
Select item 3040778	NM_006372.5(SYNCRIP):c.1788A>G (p.Gln596=)	SYNCRIP	Single nucleotide variant (synonymous variant +1 more)	SYNCRIP-related disorder	GLikely benign
Select item 3046652	NM_006372.5(SYNCRIP):c.1776G>A (p.Gln592=)	SYNCRIP	Single nucleotide variant (synonymous variant +1 more)	SYNCRIP-related disorder	GLikely benign
Select item 2635401	NM_006372.5(SYNCRIP):c.1682T>G (p.Val561Gly)	SYNCRIP (V463G +2 more)	Single nucleotide variant (missense variant +1 more)	SYNCRIP-related disorder	GUncertain significance
Select item 3052971	NM_006372.5(SYNCRIP):c.1644C>T (p.Arg548=)	SYNCRIP	Single nucleotide variant (synonymous variant)	SYNCRIP-related disorder	GLikely benign
Select item 2656734	NM_006372.5(SYNCRIP):c.1554C>T (p.Arg518=)	SYNCRIP	Single nucleotide variant (synonymous variant)	SYNCRIP-related disorder +1 more	GBenign
Select item 2635369	NM_006372.5(SYNCRIP):c.1523C>T (p.Pro508Leu)	SYNCRIP (P356L +3 more)	Single nucleotide variant (missense variant)	SYNCRIP-related disorder	GUncertain significance
Select item 3032201	NM_006372.5(SYNCRIP):c.302C>T (p.Thr101Ile)	SYNCRIP (T101I +1 more)	Single nucleotide variant (missense variant +1 more)	SYNCRIP-related disorder	GUncertain significance