"Ambry Genetics"[submitter] AND "RPL12"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2334868	NM_000976.4(RPL12):c.485G>A (p.Cys162Tyr)	RPL12 (C162Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2220624	NM_000976.4(RPL12):c.436C>T (p.Arg146Cys)	RPL12 (R146C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2617243	NM_000976.4(RPL12):c.396C>G (p.Ile132Met)	RPL12 (I132M)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2519713	NM_000976.4(RPL12):c.335T>C (p.Ile112Thr)	RPL12 (I112T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3315172	NM_000976.4(RPL12):c.251C>G (p.Ala84Gly)	RPL12 (A84G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2535212	NM_000976.4(RPL12):c.34G>C (p.Val12Leu)	LOC130002648, RPL12 (V12L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar