"Ambry Genetics"[submitter] AND "RAET1G"[gene] - ClinVar - NCBI

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Items: 19

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3312542	NM_001001788.4(RAET1G):c.778C>T (p.Pro260Ser)	RAET1E-AS1, RAET1G (P260S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2293131	NM_001001788.4(RAET1G):c.710T>C (p.Met237Thr)	RAET1E-AS1, RAET1G (M237T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151173	NM_001001788.4(RAET1G):c.599G>A (p.Gly200Asp)	RAET1E-AS1, RAET1G (G200D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2385442	NM_001001788.4(RAET1G):c.535A>G (p.Thr179Ala)	RAET1E-AS1, RAET1G (T179A)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2463485	NM_001001788.4(RAET1G):c.532A>G (p.Met178Val)	RAET1E-AS1, RAET1G (M178V)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 2477645	NM_001001788.4(RAET1G):c.470T>C (p.Met157Thr)	RAET1E-AS1, RAET1G (M157T)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2267735	NM_001001788.4(RAET1G):c.434G>A (p.Gly145Glu)	RAET1E-AS1, RAET1G (G145E)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3151172	NM_001001788.4(RAET1G):c.406A>T (p.Ser136Cys)	RAET1E-AS1, RAET1G (S136C)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2520173	NM_001001788.4(RAET1G):c.403G>A (p.Gly135Ser)	RAET1E-AS1, RAET1G (G135S)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GLikely benign
Select item 2311722	NM_001001788.4(RAET1G):c.386A>G (p.Gln129Arg)	RAET1E-AS1, RAET1G (Q129R)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 3312541	NM_001001788.4(RAET1G):c.355C>G (p.Leu119Val)	RAET1E-AS1, RAET1G (L119V)	Single nucleotide variant (non-coding transcript variant +1 more)	not specified	GUncertain significance
Select item 2242843	NM_001001788.4(RAET1G):c.338A>G (p.Tyr113Cys)	RAET1G (Y113C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3151171	NM_001001788.4(RAET1G):c.317T>G (p.Leu106Arg)	RAET1G (L106R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3151170	NM_001001788.4(RAET1G):c.301C>T (p.Leu101Phe)	RAET1G (L101F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3151169	NM_001001788.4(RAET1G):c.292G>C (p.Val98Leu)	RAET1G (V98L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3312544	NM_001001788.4(RAET1G):c.226C>A (p.Pro76Thr)	RAET1G (P76T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2569116	NM_001001788.4(RAET1G):c.101G>C (p.Cys34Ser)	RAET1G (C34S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3312543	NM_001001788.4(RAET1G):c.76G>A (p.Gly26Arg)	RAET1G (G26R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3312540	NM_001001788.4(RAET1G):c.49C>A (p.Leu17Ile)	RAET1G (L17I)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance