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

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Items: 30

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2238882	NM_152869.4(RGN):c.43C>T (p.Arg15Trp)	RGN (R15W)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 3314000	NM_152869.4(RGN):c.122G>A (p.Arg41Gln)	RGN (R41Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2212746	NM_152869.4(RGN):c.152G>A (p.Arg51Gln)	RGN (R51Q)	Single nucleotide variant (5 prime UTR variant +1 more)	not specified	GUncertain significance
Select item 2397561	NM_152869.4(RGN):c.181G>C (p.Val61Leu)	RGN (V8L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206846	NM_152869.4(RGN):c.181G>A (p.Val61Met)	RGN (V61M +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3313999	NM_152869.4(RGN):c.191G>T (p.Arg64Leu)	RGN (R64L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325930	NM_152869.4(RGN):c.194A>C (p.Gln65Pro)	RGN (Q12P +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2392974	NM_152869.4(RGN):c.218T>C (p.Ile73Thr)	RGN (I73T +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2570305	NM_152869.4(RGN):c.308A>G (p.Asn103Ser)	RGN (N103S +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2282484	NM_152869.4(RGN):c.331G>A (p.Gly111Arg)	RGN (G111R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468295	NM_152869.4(RGN):c.344C>G (p.Ala115Gly)	RGN (A115G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153611	NM_152869.4(RGN):c.349A>G (p.Thr117Ala)	RGN (T117A +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3314001	NM_152869.4(RGN):c.362A>G (p.Glu121Gly)	RGN (E68G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2549175	NM_152869.4(RGN):c.383A>G (p.Glu128Gly)	RGN (E128G +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2549268	NM_152869.4(RGN):c.404A>T (p.Tyr135Phe)	RGN (Y135F +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3313998	NM_152869.4(RGN):c.406T>C (p.Ser136Pro)	RGN (S136P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3153612	NM_152869.4(RGN):c.434A>G (p.Lys145Arg)	RGN (K145R +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3153613	NM_152869.4(RGN):c.530C>T (p.Ala177Val)	RGN (A177V +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2384067	NM_152869.4(RGN):c.535G>A (p.Asp179Asn)	RGN (D179N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2386472	NM_152869.4(RGN):c.541G>A (p.Asp181Asn)	RGN (D181N +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2204067	NM_152869.4(RGN):c.561C>G (p.Ile187Met)	RGN (I134M +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3313997	NM_152869.4(RGN):c.569G>A (p.Arg190His)	RGN (R118H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534917	NM_152869.4(RGN):c.590A>G (p.Glu197Gly)	RGN (E125G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2475488	NM_152869.4(RGN):c.646G>A (p.Val216Met)	RGN (V163M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2466498	NM_152869.4(RGN):c.649G>T (p.Ala217Ser)	RGN (A217S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153615	NM_152869.4(RGN):c.662G>C (p.Gly221Ala)	RGN (G168A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2312180	NM_152869.4(RGN):c.685C>T (p.Pro229Ser)	RGN (P176S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2388845	NM_152869.4(RGN):c.787G>A (p.Ala263Thr)	RGN (A210T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153616	NM_152869.4(RGN):c.790C>T (p.Arg264Trp)	RGN (R192W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153617	NM_152869.4(RGN):c.827C>G (p.Pro276Arg)	RGN (P276R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 30