Related gene-specific medical variations for Gene (Select 135250) - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3151168	NM_001394057.1(RAET1E):c.650A>C (p.His217Pro)	RAET1E, RAET1E-AS1 +1 more (H217P +1 more)	Single nucleotide variant (non-coding transcript variant +3 more)	not specified	GUncertain significance
Select item 3151167	NM_001394057.1(RAET1E):c.480T>G (p.Ile160Met)	RAET1E, RAET1E-AS1 +1 more (I124M +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3151166	NM_001394057.1(RAET1E):c.394C>T (p.Arg132Trp)	RAET1E, RAET1E-AS1 +1 more (R132W +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3151165	NM_001394057.1(RAET1E):c.34C>T (p.Arg12Cys)	RAET1E, RAET1E-AS1 +1 more (R12C)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3151164	NM_001394057.1(RAET1E):c.260G>T (p.Trp87Leu)	RAET1E, RAET1E-AS1 +1 more (W87L +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3151163	NM_001394057.1(RAET1E):c.248C>T (p.Ala83Val)	RAET1E, RAET1E-AS1 +1 more (A83V +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3151162	NM_001394057.1(RAET1E):c.247G>T (p.Ala83Ser)	RAET1E, RAET1E-AS1 +1 more (A47S +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2615907	NM_001394057.1(RAET1E):c.538T>A (p.Tyr180Asn)	RAET1E, RAET1E-AS1 +1 more (Y180N +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2612428	NM_001394057.1(RAET1E):c.465G>A (p.Met155Ile)	RAET1E, RAET1E-AS1 +1 more (M119I +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2604333	NM_001394057.1(RAET1E):c.208A>T (p.Met70Leu)	RAET1E, RAET1E-AS1 +1 more (M34L +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2535582	NM_001394057.1(RAET1E):c.742T>G (p.Trp248Gly)	RAET1E, RAET1E-AS1 +1 more (W212G +1 more)	Single nucleotide variant (non-coding transcript variant +3 more)	not specified	GUncertain significance
Select item 2385433	NM_001394057.1(RAET1E):c.395G>A (p.Arg132Gln)	RAET1E, RAET1E-AS1 +1 more (R132Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2379203	NM_001394057.1(RAET1E):c.562G>A (p.Asp188Asn)	RAET1E, RAET1E-AS1 +1 more (D188N +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366711	NM_001394057.1(RAET1E):c.428A>G (p.Asn143Ser)	RAET1E, RAET1E-AS1 +1 more (N107S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366632	NM_001394057.1(RAET1E):c.302T>C (p.Leu101Pro)	RAET1E, RAET1E-AS1 +1 more (L101P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366151	NM_001394057.1(RAET1E):c.454G>T (p.Ala152Ser)	RAET1E, RAET1E-AS1 +1 more (A116S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2305173	NM_001394057.1(RAET1E):c.638C>T (p.Ala213Val)	RAET1E, RAET1E-AS1 +1 more (A177V +1 more)	Single nucleotide variant (missense variant +2 more)	not specified	GLikely benign