"Ambry Genetics"[submitter] AND "LOC130066397"[gene] - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3164151	NM_020062.4(SLC2A4RG):c.133T>A (p.Ser45Thr)	LOC130066397, SLC2A4RG (S45T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3164152	NM_020062.4(SLC2A4RG):c.134C>A (p.Ser45Tyr)	LOC130066397, SLC2A4RG (S45Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3319473	NM_020062.4(SLC2A4RG):c.209C>T (p.Ala70Val)	LOC130066397, SLC2A4RG (A70V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404969	NM_020062.4(SLC2A4RG):c.223A>C (p.Thr75Pro)	LOC130066397, SLC2A4RG (T75P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275058	NM_020062.4(SLC2A4RG):c.245G>C (p.Arg82Pro)	LOC130066397, SLC2A4RG (R82P)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2241918	NM_020062.4(SLC2A4RG):c.247A>C (p.Thr83Pro)	LOC130066397, SLC2A4RG (T83P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2619307	NM_020062.4(SLC2A4RG):c.268G>A (p.Val90Ile)	LOC130066397, SLC2A4RG (V90I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar