"GeneDx"[submitter] AND "DUSP6"[gene] - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1268548	NM_001946.4(DUSP6):c.*300A>G	DUSP6	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 3364485	NM_001946.4(DUSP6):c.1048A>T (p.Ser350Cys)	DUSP6 (S204C +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1309605	NM_001946.4(DUSP6):c.975G>A (p.Met325Ile)	DUSP6 (M179I +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1226329	NM_001946.4(DUSP6):c.839-251C>T	DUSP6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1237614	NM_001946.4(DUSP6):c.839-276T>C	DUSP6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1229511	NM_001946.4(DUSP6):c.839-299C>T	DUSP6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1218279	NM_001946.4(DUSP6):c.838+263G>A	DUSP6	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1225295	NM_001946.4(DUSP6):c.838+119A>C	DUSP6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1261506	NM_001946.4(DUSP6):c.430T>G (p.Ser144Ala)	DUSP6 (S144A)	Single nucleotide variant (missense variant +1 more)	not provided	GBenign
Select item 1292720	NM_001946.4(DUSP6):c.401-24T>C	DUSP6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1230916	NM_001946.4(DUSP6):c.401-113T>A	DUSP6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1250149	NM_001946.4(DUSP6):c.401-214G>A	DUSP6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1238764	NM_001946.4(DUSP6):c.400+298A>G	DUSP6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1230616	NM_001946.4(DUSP6):c.400+231T>C	DUSP6	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 802882	NM_001946.4(DUSP6):c.340G>T (p.Val114Leu)	DUSP6 (V114L)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1306581	NM_001946.4(DUSP6):c.306C>A (p.Ser102Arg)	DUSP6 (S102R)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 1260187	NM_001946.4(DUSP6):c.260C>T (p.Thr87Ile)	DUSP6 (T87I)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1190831	NM_001946.4(DUSP6):c.-316T>C	DUSP6	Single nucleotide variant (5 prime UTR variant)	not provided	GLikely benign