Related gene-specific medical variations for Gene (Select 9271) - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3314330	NM_001393629.1(RIMBP2):c.3880A>G (p.Met1294Val)	PIWIL1, RIMBP2 (M1055V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3154330	NM_001393629.1(RIMBP2):c.3793G>C (p.Val1265Leu)	PIWIL1, RIMBP2 (V973L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3154328	NM_001393629.1(RIMBP2):c.3614G>A (p.Arg1205His)	PIWIL1, RIMBP2 (R913H +3 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3154327	NM_001393629.1(RIMBP2):c.3256C>T (p.Arg1086Cys)	PIWIL1, RIMBP2 (R847C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3154326	NM_001393629.1(RIMBP2):c.3236T>A (p.Ile1079Asn)	PIWIL1, RIMBP2 (I1079N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2643591	NM_001393629.1(RIMBP2):c.2910G>A (p.Val970=)	PIWIL1, RIMBP2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2643590	NM_001393629.1(RIMBP2):c.2988G>A (p.Pro996=)	PIWIL1, RIMBP2	Single nucleotide variant (synonymous variant +1 more)	not provided	GLikely benign
Select item 2523586	NM_001393629.1(RIMBP2):c.3314C>T (p.Pro1105Leu)	PIWIL1, RIMBP2 (P866L +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510471	NM_001393629.1(RIMBP2):c.3704C>T (p.Thr1235Ile)	PIWIL1, RIMBP2 (T943I +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2368453	NM_001393629.1(RIMBP2):c.3834A>C (p.Glu1278Asp)	PIWIL1, RIMBP2 (E1022D +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2360695	NM_001393629.1(RIMBP2):c.3251G>A (p.Arg1084Gln)	PIWIL1, RIMBP2 (R792Q +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338125	NM_001393629.1(RIMBP2):c.3900+527G>A	PIWIL1, RIMBP2 (V1064I +3 more)	Single nucleotide variant (missense variant +2 more)	not specified	GUncertain significance
Select item 2325759	NM_001393629.1(RIMBP2):c.3721A>G (p.Ile1241Val)	PIWIL1, RIMBP2 (I1002V +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2316176	NM_001393629.1(RIMBP2):c.3745G>A (p.Asp1249Asn)	PIWIL1, RIMBP2 (D1010N +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2297898	NM_001393629.1(RIMBP2):c.3716G>C (p.Gly1239Ala)	PIWIL1, RIMBP2 (G983A +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2215823	NM_001393629.1(RIMBP2):c.3691G>A (p.Glu1231Lys)	PIWIL1, RIMBP2 (E1231K +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2213822	NM_001393629.1(RIMBP2):c.3613C>T (p.Arg1205Cys)	PIWIL1, RIMBP2 (R913C +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance