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

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Items: 36

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2552838	NM_001366508.1(RGMB):c.37G>A (p.Ala13Thr)	RGMB (A54T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3313994	NM_001366508.1(RGMB):c.40G>T (p.Ala14Ser)	RGMB (A54S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3313993	NM_001366508.1(RGMB):c.52G>A (p.Glu18Lys)	RGMB (E18K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2362293	NM_001366508.1(RGMB):c.71G>A (p.Gly24Glu)	RGMB (G24E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153608	NM_001366508.1(RGMB):c.74T>C (p.Leu25Pro)	RGMB (L66P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2530088	NM_001366508.1(RGMB):c.80C>T (p.Pro27Leu)	RGMB (P67L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2293885	NM_001366508.1(RGMB):c.83C>G (p.Pro28Arg)	RGMB (P69R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233487	NM_001366508.1(RGMB):c.85C>A (p.Pro29Thr)	RGMB (P69T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2553793	NM_001366508.1(RGMB):c.88C>G (p.Leu30Val)	RGMB (L71V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2474501	NM_001366508.1(RGMB):c.167T>C (p.Ile56Thr)	LOC126807464, RGMB (I97T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2600810	NM_001366508.1(RGMB):c.220G>A (p.Val74Ile)	LOC126807464, RGMB (V114I +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3313995	NM_001366508.1(RGMB):c.343C>T (p.Leu115Phe)	LOC126807464, RGMB (L115F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2550617	NM_001366508.1(RGMB):c.346A>G (p.Met116Val)	LOC126807464, RGMB (M116V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153609	NM_001366508.1(RGMB):c.388A>G (p.Thr130Ala)	LOC126807464, RGMB (T171A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2372016	NM_001366508.1(RGMB):c.395C>G (p.Pro132Arg)	LOC126807464, RGMB (P132R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2324230	NM_001366508.1(RGMB):c.530A>T (p.Asn177Ile)	LOC126807464, RGMB (N217I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2622888	NM_001366508.1(RGMB):c.607C>A (p.Pro203Thr)	LOC126807464, RGMB (P243T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2485954	NM_001366508.1(RGMB):c.646A>G (p.Ile216Val)	RGMB (I216V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2236329	NM_001366508.1(RGMB):c.652A>G (p.Ile218Val)	RGMB (I218V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2486478	NM_001366508.1(RGMB):c.671A>G (p.His224Arg)	RGMB (H224R +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3313996	NM_001366508.1(RGMB):c.680C>T (p.Thr227Ile)	RGMB (T227I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153610	NM_001366508.1(RGMB):c.682G>T (p.Asp228Tyr)	RGMB (D269Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2404765	NM_001366508.1(RGMB):c.719C>T (p.Pro240Leu)	RGMB (P240L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2548563	NM_001366508.1(RGMB):c.880C>T (p.Arg294Cys)	RGMB (R294C +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549535	NM_001366508.1(RGMB):c.892G>A (p.Asp298Asn)	RGMB (D298N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2267261	NM_001366508.1(RGMB):c.937G>A (p.Val313Met)	RGMB (V313M +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2364974	NM_001366508.1(RGMB):c.962G>A (p.Arg321His)	RGMB (R361H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153606	NM_001366508.1(RGMB):c.967G>A (p.Asp323Asn)	RGMB (D363N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2513978	NM_001366508.1(RGMB):c.973G>A (p.Gly325Arg)	RGMB (G325R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2244913	NM_001366508.1(RGMB):c.979G>A (p.Gly327Ser)	RGMB (G367S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2364341	NM_001366508.1(RGMB):c.989C>T (p.Ser330Phe)	RGMB (S330F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153607	NM_001366508.1(RGMB):c.1042G>A (p.Gly348Ser)	RGMB (G389S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2355746	NM_001366508.1(RGMB):c.1126C>A (p.Leu376Met)	RGMB (L416M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2396908	NM_001366508.1(RGMB):c.1148A>G (p.Asn383Ser)	RGMB (N424S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592257	NM_001366508.1(RGMB):c.1195C>T (p.His399Tyr)	RGMB (H399Y +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2376755	NM_001366508.1(RGMB):c.1301T>C (p.Ile434Thr)	RGMB (I475T +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign

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Items: 36