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

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Items: 39

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2214581	NM_020211.3(RGMA):c.1322C>T (p.Pro441Leu)	RGMA (P425L +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2461603	NM_020211.3(RGMA):c.1318G>A (p.Val440Ile)	RGMA (V448I +2 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 3153603	NM_020211.3(RGMA):c.1298G>T (p.Arg433Leu)	RGMA (R433L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520303	NM_020211.3(RGMA):c.1238T>C (p.Leu413Pro)	RGMA (L421P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3313987	NM_020211.3(RGMA):c.1217C>T (p.Ser406Phe)	RGMA (S390F +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2525147	NM_020211.3(RGMA):c.1166A>G (p.Asn389Ser)	RGMA (N373S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2309371	NM_020211.3(RGMA):c.1058A>G (p.Glu353Gly)	RGMA (E337G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2510499	NM_020211.3(RGMA):c.1057G>A (p.Glu353Lys)	RGMA (E353K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2249761	NM_020211.3(RGMA):c.1037G>T (p.Ser346Ile)	RGMA (S346I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3313989	NM_020211.3(RGMA):c.1028C>G (p.Ala343Gly)	RGMA (A343G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3313990	NM_020211.3(RGMA):c.977A>C (p.Asp326Ala)	RGMA (D334A +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2620567	NM_020211.3(RGMA):c.970C>G (p.Gln324Glu)	RGMA (Q332E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153605	NM_020211.3(RGMA):c.754G>A (p.Asp252Asn)	RGMA (D260N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2260640	NM_020211.3(RGMA):c.748G>A (p.Gly250Ser)	RGMA (G234S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2406779	NM_020211.3(RGMA):c.711C>G (p.Asp237Glu)	RGMA (D245E +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2275725	NM_020211.3(RGMA):c.706A>G (p.Met236Val)	RGMA (M236V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3153604	NM_020211.3(RGMA):c.619G>A (p.Gly207Ser)	RGMA (G191S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2356859	NM_020211.3(RGMA):c.530G>A (p.Arg177His)	RGMA (R161H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2477911	NM_020211.3(RGMA):c.515G>A (p.Arg172Lys)	RGMA (R172K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3313991	NM_020211.3(RGMA):c.493C>G (p.Leu165Val)	RGMA (L149V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2399036	NM_020211.3(RGMA):c.482C>T (p.Thr161Met)	RGMA (T169M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2286242	NM_020211.3(RGMA):c.464C>T (p.Ser155Leu)	RGMA (S139L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2491826	NM_020211.3(RGMA):c.383C>T (p.Thr128Met)	RGMA (T136M +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2518647	NM_020211.3(RGMA):c.371C>T (p.Pro124Leu)	RGMA (P108L +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3313988	NM_020211.3(RGMA):c.370C>T (p.Pro124Ser)	RGMA (P124S +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2291906	NM_020211.3(RGMA):c.316A>G (p.Ile106Val)	RGMA (I114V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3313986	NM_020211.3(RGMA):c.310C>A (p.His104Asn)	RGMA (H112N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2366687	NM_020211.3(RGMA):c.307G>A (p.Val103Ile)	RGMA (V87I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2494132	NM_020211.3(RGMA):c.220G>A (p.Glu74Lys)	RGMA (E58K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3313985	NM_020211.3(RGMA):c.178G>A (p.Ala60Thr)	RGMA (A68T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2476153	NM_020211.3(RGMA):c.154A>C (p.Lys52Gln)	RGMA (K36Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2233872	NM_020211.3(RGMA):c.74G>C (p.Arg25Pro)	RGMA (R33P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2345098	NM_020211.3(RGMA):c.67G>A (p.Ala23Thr)	RGMA (A23T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2549431	NM_020211.3(RGMA):c.62G>A (p.Arg21Lys)	RGMA (R29K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2482886	NM_020211.3(RGMA):c.55A>G (p.Met19Val)	RGMA (M27V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2288852	NM_020211.3(RGMA):c.40G>A (p.Ala14Thr)	RGMA (A22T +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2298077	NM_020211.3(RGMA):c.23T>C (p.Leu8Pro)	RGMA (L8P +1 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2283122	NM_020211.3(RGMA):c.15-695A>C	RGMA (T11P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2396978	NM_020211.3(RGMA):c.15-713G>A	RGMA (G5R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance

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Items: 39