Related gene-specific medical variations for Gene (Select 79954) - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3300253	NM_024894.4(NOL10):c.951T>A (p.Asp317Glu)	LOC126806141, NOL10 (D291E +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3201025	NM_024894.4(NOL10):c.1588C>T (p.Arg530Cys)	LOC126806140, NOL10 (R480C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2597271	NM_024894.4(NOL10):c.1639A>C (p.Ser547Arg)	LOC126806140, NOL10 (S521R +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2555747	NM_024894.4(NOL10):c.1655A>G (p.Asp552Gly)	LOC126806140, NOL10 (D502G +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2525205	NM_024894.4(NOL10):c.1693C>T (p.Arg565Cys)	LOC126806140, NOL10 (R515C +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2519476	NM_024894.4(NOL10):c.928G>A (p.Glu310Lys)	LOC126806141, NOL10 (E260K +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2491962	NM_024894.4(NOL10):c.1430C>T (p.Pro477Leu)	LOC126806140, NOL10 (P427L +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2357957	NM_024894.4(NOL10):c.53A>G (p.Lys18Arg)	LOC129933106, NOL10 (K18R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2327932	NM_024894.4(NOL10):c.1581A>C (p.Gln527His)	LOC126806140, NOL10 (Q477H +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2262636	NM_024894.4(NOL10):c.1649G>A (p.Ser550Asn)	LOC126806140, NOL10 (S500N +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2257387	NM_024894.4(NOL10):c.1613C>A (p.Pro538Gln)	LOC126806140, NOL10 (P488Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2239105	NM_024894.4(NOL10):c.1624C>T (p.Pro542Ser)	LOC126806140, NOL10 (P492S +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance