"PreventionGenetics, part of Exact Sciences"[submitter] AND "SYNE4"[ge - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 227083	NM_001039876.3(SYNE4):c.*5T>C	SYNE4	Single nucleotide variant (3 prime UTR variant)	SYNE4-related condition +2 more	GBenign/Likely benign
Select item 235735	NM_001039876.3(SYNE4):c.1102G>A (p.Val368Met)	SYNE4 (V368M +1 more)	Single nucleotide variant (missense variant)	SYNE4-related condition +2 more	GConflicting classifications of pathogenicity
Select item 682357	NM_001039876.3(SYNE4):c.916G>C (p.Gly306Arg)	SYNE4 (G193R +1 more)	Single nucleotide variant (missense variant)	SYNE4-related condition +1 more	GLikely benign
Select item 227089	NM_001039876.3(SYNE4):c.805C>T (p.Leu269=)	SYNE4	Single nucleotide variant (synonymous variant)	SYNE4-related condition +2 more	GBenign/Likely benign
Select item 504863	NM_001039876.3(SYNE4):c.764T>C (p.Ile255Thr)	SYNE4 (I255T +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 514699	NM_001039876.3(SYNE4):c.756G>A (p.Ala252=)	SYNE4	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 228294	NM_001039876.3(SYNE4):c.699G>A (p.Trp233Ter)	SYNE4 (W233* +1 more)	Single nucleotide variant (nonsense)	SYNE4-related condition +4 more	GConflicting classifications of pathogenicity
Select item 1909197	NM_001039876.3(SYNE4):c.669C>T (p.Asp223=)	SYNE4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 666764	NM_001039876.3(SYNE4):c.638C>T (p.Thr213Met)	SYNE4 (T100M +1 more)	Single nucleotide variant (missense variant)	not specified +2 more	GConflicting classifications of pathogenicity
Select item 725651	NM_001039876.3(SYNE4):c.391G>A (p.Ala131Thr)	SYNE4 (A131T)	Single nucleotide variant (missense variant +1 more)	SYNE4-related condition +1 more	GBenign/Likely benign
Select item 504864	NM_001039876.3(SYNE4):c.257C>T (p.Pro86Leu)	SYNE4 (P86L)	Single nucleotide variant (missense variant)	not provided +2 more	GLikely benign
Select item 682172	NM_001039876.3(SYNE4):c.249C>T (p.Tyr83=)	SYNE4	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 594209	NM_001039876.3(SYNE4):c.243T>C (p.Ser81=)	SYNE4	Single nucleotide variant (synonymous variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 227092	NM_001039876.3(SYNE4):c.96C>T (p.Thr32=)	SYNE4	Single nucleotide variant (synonymous variant)	not specified +2 more	GBenign/Likely benign
Select item 504816	NM_001039876.3(SYNE4):c.7C>T (p.Leu3=)	SYNE4	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign