DUSP11[gene] and "single gene"[properties] - ClinVar - NCBI

Warning: The NCBI web site requires JavaScript to function. more...

Search results

Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2403406	NM_003584.3(DUSP11):c.925A>G (p.Arg309Gly)	DUSP11 (R309G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086252	NM_003584.3(DUSP11):c.911G>C (p.Arg304Pro)	DUSP11 (R304P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2329668	NM_003584.3(DUSP11):c.908G>T (p.Ser303Ile)	DUSP11 (S303I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215630	NM_003584.3(DUSP11):c.866A>G (p.Tyr289Cys)	DUSP11 (Y289C)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 727180	NM_003584.3(DUSP11):c.794+5C>G	DUSP11	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3086259	NM_003584.3(DUSP11):c.701A>T (p.Lys234Ile)	DUSP11 (K234I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2528683	NM_003584.3(DUSP11):c.664G>A (p.Ala222Thr)	DUSP11 (A222T)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2265410	NM_003584.3(DUSP11):c.637C>T (p.Pro213Ser)	DUSP11 (P213S)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2374876	NM_003584.3(DUSP11):c.586A>G (p.Ile196Val)	DUSP11 (I196V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086256	NM_003584.3(DUSP11):c.517G>A (p.Val173Met)	DUSP11 (V173M +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2306742	NM_003584.3(DUSP11):c.454T>C (p.Cys152Arg)	DUSP11 (C152R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 722350	NM_003584.3(DUSP11):c.178-7G>C	DUSP11	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 3086254	NM_003584.3(DUSP11):c.169T>A (p.Leu57Met)	DUSP11 (L104M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2607762	NM_003584.3(DUSP11):c.133A>G (p.Met45Val)	DUSP11 (M45V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3086253	NM_003584.3(DUSP11):c.-2A>T	DUSP11 (H47L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3274039	NM_003584.3(DUSP11):c.-12C>T	DUSP11 (L44F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2402633	NM_003584.3(DUSP11):c.-108G>T	DUSP11	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 2544977	NM_003584.3(DUSP11):c.-118G>T	DUSP11	Single nucleotide variant (5 prime UTR variant)	not specified	GUncertain significance
Select item 722351	NM_003584.3(DUSP11):c.-118G>A	DUSP11	Single nucleotide variant (5 prime UTR variant)	not provided	GBenign