Related gene-specific medical variations for Gene (Select 100126784) - ClinVar - NCBI

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

Links from Gene

Items: 14

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3298524	NM_145117.5(NAV2):c.256T>C (p.Phe86Leu)	LEISA1, NAV2 (F86L)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3298521	NM_145117.5(NAV2):c.82C>A (p.Pro28Thr)	LEISA1, NAV2 (P28T)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3177057	NM_145117.5(NAV2):c.31A>G (p.Lys11Glu)	LEISA1, NAV2 (K11E)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3176970	NM_145117.5(NAV2):c.197T>A (p.Leu66Gln)	LEISA1, NAV2 (L66Q)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3176920	NM_145117.5(NAV2):c.151A>T (p.Thr51Ser)	LEISA1, NAV2 (T51S)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3176902	NM_145117.5(NAV2):c.128G>A (p.Ser43Asn)	LEISA1, NAV2 (S43N)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 3051618	NM_145117.5(NAV2):c.51C>G (p.Pro17=)	LEISA1, NAV2	Single nucleotide variant (non-coding transcript variant +2 more)	NAV2-related disorder	GBenign
Select item 3042108	NM_145117.5(NAV2):c.155A>G (p.Tyr52Cys)	LEISA1, NAV2 (Y52C)	Single nucleotide variant (non-coding transcript variant +2 more)	NAV2-related disorder	GLikely benign
Select item 3040987	NM_145117.5(NAV2):c.170C>G (p.Pro57Arg)	LEISA1, NAV2 (P57R)	Single nucleotide variant (non-coding transcript variant +2 more)	NAV2-related disorder	GBenign
Select item 3039323	NM_145117.5(NAV2):c.84C>A (p.Pro28=)	LEISA1, NAV2	Single nucleotide variant (non-coding transcript variant +2 more)	NAV2-related disorder	GBenign
Select item 2689530	NM_145117.5(NAV2):c.26A>C (p.Lys9Thr)	LEISA1, NAV2 (K9T)	Single nucleotide variant (non-coding transcript variant +2 more)	not provided	GUncertain significance
Select item 2641676	NM_145117.5(NAV2):c.39A>C (p.Gly13=)	LEISA1, NAV2	Single nucleotide variant (non-coding transcript variant +2 more)	not provided	GLikely benign
Select item 2559012	NM_145117.5(NAV2):c.52G>A (p.Val18Met)	LEISA1, NAV2 (V18M)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance
Select item 2489593	NM_145117.5(NAV2):c.107C>A (p.Pro36His)	LEISA1, NAV2 (P36H)	Single nucleotide variant (non-coding transcript variant +2 more)	not specified	GUncertain significance