"Ambry Genetics"[submitter] AND "RPL18"[gene] - ClinVar - NCBI

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

Search results

Items: 11

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3156045	NM_000979.4(RPL18):c.541C>T (p.Arg181Trp)	RPL18 (R152W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2776002	NM_000979.4(RPL18):c.476C>T (p.Pro159Leu)	RPL18 (P130L +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2600658	NM_000979.4(RPL18):c.457G>A (p.Gly153Ser)	RPL18 (G124S +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2293393	NM_000979.4(RPL18):c.448C>T (p.Arg150Trp)	RPL18 (R150W +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2549899	NM_000979.4(RPL18):c.341T>G (p.Leu114Arg)	RPL18 (L114R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2535973	NM_000979.4(RPL18):c.334C>T (p.Arg112Cys)	RPL18 (R83C +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2869957	NM_000979.4(RPL18):c.329G>A (p.Arg110His)	RPL18 (R110H +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2198214	NM_000979.4(RPL18):c.323G>A (p.Arg108Gln)	RPL18 (R79Q +1 more)	Single nucleotide variant (missense variant +1 more)	not specified +1 more	GUncertain significance
Select item 2210444	NM_000979.4(RPL18):c.236C>T (p.Thr79Met)	RPL18 (T50M +1 more)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GUncertain significance
Select item 2268815	NM_000979.4(RPL18):c.227A>G (p.Glu76Gly)	RPL18 (E47G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2532570	NM_000979.4(RPL18):c.16C>T (p.Arg6Cys)	RPL18 (R6C)	Single nucleotide variant (missense variant +2 more)	not specified +1 more	GUncertain significance