Related gene-specific medical variations for Gene (Select 51455) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3153215	NM_016316.4(REV1):c.3144C>A (p.His1048Gln)	LOC126806281, REV1 (H1047Q +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3153214	NM_016316.4(REV1):c.3067G>C (p.Ala1023Pro)	LOC126806281, REV1 (A1023P +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2460327	NM_016316.4(REV1):c.3115A>G (p.Arg1039Gly)	LOC126806281, REV1 (R968G +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2215506	NM_016316.4(REV1):c.2974C>A (p.Gln992Lys)	LOC126806281, REV1 (Q921K +5 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 708522	NM_016316.4(REV1):c.3033A>G (p.Pro1011=)	LOC126806281, REV1	Single nucleotide variant (synonymous variant +1 more)	not provided	GBenign
Select item 156801	NM_016316.4(REV1):c.351-3232_513dup	REV1	Duplication (splice acceptor variant +1 more)	Large for gestational age +1 more	Gnot provided
Select item 156800	NM_016316.4(REV1):c.351-3232_770dup	REV1	Duplication (splice acceptor variant +1 more)	Normal pregnancy	Gnot provided

ClinVar