"Ambry Genetics"[submitter] AND "LOC126806140"[gene] - ClinVar - NCBI

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

Search results

Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
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 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 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 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 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
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 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 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 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