"Ambry Genetics"[submitter] AND "RASA2"[gene] - ClinVar - NCBI

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1747076	NM_006506.5(RASA2):c.11C>T (p.Ala4Val)	LOC129937686, RASA2 (A4V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1769363	NM_006506.5(RASA2):c.12G>A (p.Ala4=)	LOC129937686, RASA2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3225602	NM_006506.5(RASA2):c.13G>A (p.Ala5Thr)	LOC129937686, RASA2 (A5T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2562694	NM_006506.5(RASA2):c.13G>C (p.Ala5Pro)	LOC129937686, RASA2 (A5P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 218684	NM_006506.5(RASA2):c.17C>T (p.Pro6Leu)	LOC129937686, RASA2 (P6L)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 1792239	NM_006506.5(RASA2):c.24T>G (p.Ala8=)	LOC129937686, RASA2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1793656	NM_006506.5(RASA2):c.25G>T (p.Ala9Ser)	LOC129937686, RASA2 (A9S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 929175	NM_006506.5(RASA2):c.26C>T (p.Ala9Val)	LOC129937686, RASA2 (A9V)	Single nucleotide variant (missense variant)	not specified +1 more	GBenign/Likely benign
Select item 3312837	NM_006506.5(RASA2):c.27G>C (p.Ala9=)	LOC129937686, RASA2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1796200	NM_006506.5(RASA2):c.27G>T (p.Ala9=)	LOC129937686, RASA2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1796182	NM_006506.5(RASA2):c.27G>A (p.Ala9=)	LOC129937686, RASA2	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 1732058	NM_006506.5(RASA2):c.34T>A (p.Ser12Thr)	LOC129937686, RASA2 (S12T)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1492892	NM_006506.5(RASA2):c.35C>T (p.Ser12Phe)	LOC129937686, RASA2 (S12F)	Single nucleotide variant (missense variant)	not provided +1 more	GConflicting classifications of pathogenicity
Select item 933185	NM_006506.5(RASA2):c.38C>T (p.Ser13Phe)	LOC129937686, RASA2 (S13F)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 1743924	NM_006506.5(RASA2):c.48A>G (p.Pro16=)	LOC129937686, RASA2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1745337	NM_006506.5(RASA2):c.50C>T (p.Ala17Val)	LOC129937686, RASA2 (A17V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2534517	NM_006506.5(RASA2):c.56G>C (p.Ser19Thr)	LOC129937686, RASA2 (S19T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1753336	NM_006506.5(RASA2):c.63T>G (p.Thr21=)	LOC129937686, RASA2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1758180	NM_006506.5(RASA2):c.72C>G (p.Pro24=)	LOC129937686, RASA2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1758178	NM_006506.5(RASA2):c.72C>A (p.Pro24=)	LOC129937686, RASA2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2728112	NM_006506.5(RASA2):c.80G>T (p.Gly27Val)	LOC129937686, RASA2 (G27V)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1765051	NM_006506.5(RASA2):c.88G>T (p.Asp30Tyr)	LOC129937686, RASA2 (D30Y)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1765788	NM_006506.5(RASA2):c.90C>T (p.Asp30=)	LOC129937686, RASA2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2447625	NM_006506.5(RASA2):c.93T>G (p.Ser31Arg)	LOC129937686, RASA2 (S31R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1744524	NM_006506.5(RASA2):c.118C>T (p.Leu40=)	LOC129937686, RASA2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2625076	NM_006506.5(RASA2):c.124G>A (p.Gly42Ser)	LOC129937686, RASA2 (G42S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1352435	NM_006506.5(RASA2):c.124G>T (p.Gly42Cys)	LOC129937686, RASA2 (G42C)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3225601	NM_006506.5(RASA2):c.131T>C (p.Ile44Thr)	LOC129937686, RASA2 (I44T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1773757	NM_006506.5(RASA2):c.148T>G (p.Leu50Val)	RASA2 (L50V)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1774150	NM_006506.5(RASA2):c.150A>G (p.Leu50=)	RASA2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1177273	NM_006506.5(RASA2):c.156A>G (p.Pro52=)	RASA2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1775676	NM_006506.5(RASA2):c.157T>G (p.Tyr53Asp)	RASA2 (Y53D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1777427	NM_006506.5(RASA2):c.165A>G (p.Gly55=)	RASA2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2496762	NM_006506.5(RASA2):c.195C>T (p.Thr65=)	RASA2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1785036	NM_006506.5(RASA2):c.204G>A (p.Leu68=)	RASA2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2976785	NM_006506.5(RASA2):c.211G>A (p.Glu71Lys)	RASA2 (E71K)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1788248	NM_006506.5(RASA2):c.223C>T (p.Arg75Cys)	RASA2 (R75C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 992229	NM_006506.5(RASA2):c.255A>G (p.Pro85=)	RASA2	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 3225605	NM_006506.5(RASA2):c.277T>C (p.Phe93Leu)	RASA2 (F93L)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1797780	NM_006506.5(RASA2):c.292A>G (p.Thr98Ala)	RASA2 (T98A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2562702	NM_006506.5(RASA2):c.296T>C (p.Phe99Ser)	RASA2 (F99S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1467697	NM_006506.5(RASA2):c.316G>A (p.Val106Ile)	RASA2 (V106I)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3225606	NM_006506.5(RASA2):c.320A>G (p.Tyr107Cys)	RASA2 (Y107C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225607	NM_006506.5(RASA2):c.336A>G (p.Leu112=)	RASA2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 992788	NM_006506.5(RASA2):c.345T>A (p.Asp115Glu)	RASA2 (D115E)	Single nucleotide variant (missense variant)	not provided +3 more	GUncertain significance
Select item 1317888	NM_006506.5(RASA2):c.349C>T (p.Arg117Cys)	RASA2 (R117C)	Single nucleotide variant (missense variant)	not specified +1 more	GConflicting classifications of pathogenicity
Select item 2261022	NM_006506.5(RASA2):c.364G>A (p.Ala122Thr)	RASA2 (A122T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2562701	NM_006506.5(RASA2):c.366C>T (p.Ala122=)	RASA2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1734534	NM_006506.5(RASA2):c.374A>G (p.Lys125Arg)	RASA2 (K125R)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 984507	NM_006506.5(RASA2):c.382T>C (p.Leu128=)	RASA2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 2561488	NM_006506.5(RASA2):c.388A>G (p.Asn130Asp)	RASA2 (N130D)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1736761	NM_006506.5(RASA2):c.398G>A (p.Gly133Asp)	RASA2 (G133D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1737732	NM_006506.5(RASA2):c.408T>C (p.Thr136=)	RASA2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1634408	NM_006506.5(RASA2):c.414T>C (p.Phe138=)	RASA2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1738467	NM_006506.5(RASA2):c.417A>G (p.Ser139=)	RASA2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1738986	NM_006506.5(RASA2):c.423G>T (p.Gln141His)	RASA2 (Q141H)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1738978	NM_006506.5(RASA2):c.423G>A (p.Gln141=)	RASA2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1740132	NM_006506.5(RASA2):c.437A>G (p.Asn146Ser)	RASA2 (N146S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225608	NM_006506.5(RASA2):c.449A>G (p.Gln150Arg)	RASA2 (Q150R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1741198	NM_006506.5(RASA2):c.451G>A (p.Gly151Ser)	RASA2 (G151S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312842	NM_006506.5(RASA2):c.452G>A (p.Gly151Asp)	RASA2 (G151D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151695	NM_006506.5(RASA2):c.461A>C (p.His154Pro)	RASA2 (H154P)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1743277	NM_006506.5(RASA2):c.480T>G (p.Asn160Lys)	RASA2 (N160K)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1375090	NM_006506.5(RASA2):c.491C>T (p.Thr164Met)	RASA2 (T164M)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1744393	NM_006506.5(RASA2):c.495G>A (p.Glu165=)	RASA2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1744877	NM_006506.5(RASA2):c.502A>G (p.Thr168Ala)	RASA2 (T168A)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 3225609	NM_006506.5(RASA2):c.503C>G (p.Thr168Ser)	RASA2 (T168S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 917599	NM_006506.5(RASA2):c.519T>C (p.Leu173=)	RASA2	Single nucleotide variant (synonymous variant)	not specified +1 more	GLikely benign
Select item 997880	NM_006506.5(RASA2):c.540C>T (p.Cys180=)	RASA2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 3225610	NM_006506.5(RASA2):c.542A>G (p.His181Arg)	RASA2 (H181R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2562698	NM_006506.5(RASA2):c.552T>C (p.Pro184=)	RASA2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1748833	NM_006506.5(RASA2):c.564C>A (p.Gly188=)	RASA2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3312839	NM_006506.5(RASA2):c.567A>G (p.Gln189=)	RASA2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 2496761	NM_006506.5(RASA2):c.587C>T (p.Thr196Ile)	RASA2 (T196I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1750718	NM_006506.5(RASA2):c.595C>T (p.Leu199=)	RASA2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1751171	NM_006506.5(RASA2):c.602G>A (p.Gly201Asp)	RASA2 (G201D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2562696	NM_006506.5(RASA2):c.604C>T (p.Pro202Ser)	RASA2 (P202S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3312836	NM_006506.5(RASA2):c.609T>C (p.Ser203=)	RASA2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1752148	NM_006506.5(RASA2):c.619C>G (p.Gln207Glu)	RASA2 (Q207E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1753056	NM_006506.5(RASA2):c.635T>C (p.Val212Ala)	RASA2 (V212A)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1754298	NM_006506.5(RASA2):c.657G>C (p.Pro219=)	RASA2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 496328	NM_006506.5(RASA2):c.657G>A (p.Pro219=)	RASA2	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1434149	NM_006506.5(RASA2):c.675T>G (p.Phe225Leu)	RASA2 (F225L)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1755831	NM_006506.5(RASA2):c.685G>A (p.Val229Ile)	RASA2 (V229I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3151696	NM_006506.5(RASA2):c.698G>A (p.Ser233Asn)	RASA2 (S233N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3225611	NM_006506.5(RASA2):c.716C>G (p.Ser239Cys)	RASA2 (S239C)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1760009	NM_006506.5(RASA2):c.765C>T (p.Ile255=)	RASA2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 1760139	NM_006506.5(RASA2):c.768C>G (p.Asp256Glu)	RASA2 (D256E)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1931300	NM_006506.5(RASA2):c.772T>C (p.Trp258Arg)	RASA2 (W258R)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 1760584	NM_006506.5(RASA2):c.777C>T (p.Asn259=)	RASA2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1760660	NM_006506.5(RASA2):c.779A>G (p.Asn260Ser)	RASA2 (N260S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1760739	NM_006506.5(RASA2):c.780T>C (p.Asn260=)	RASA2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 1172892	NM_006506.5(RASA2):c.792C>G (p.Val264=)	RASA2	Single nucleotide variant (synonymous variant)	not provided +1 more	GLikely benign
Select item 707194	NM_006506.5(RASA2):c.807A>T (p.Leu269=)	RASA2	Single nucleotide variant (synonymous variant)	Hereditary cancer-predisposing syndrome +2 more	GLikely benign
Select item 1762792	NM_006506.5(RASA2):c.829A>T (p.Asn277Tyr)	RASA2 (N277Y)	Single nucleotide variant (missense variant)	not provided +1 more	GUncertain significance
Select item 1762898	NM_006506.5(RASA2):c.831C>G (p.Asn277Lys)	RASA2 (N277K)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1763014	NM_006506.5(RASA2):c.834A>G (p.Val278=)	RASA2	Single nucleotide variant (synonymous variant)	not specified	GLikely benign
Select item 3312840	NM_006506.5(RASA2):c.836T>C (p.Leu279Ser)	RASA2 (L279S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1683320	NM_006506.5(RASA2):c.847T>G (p.Ser283Ala)	RASA2 (S283A)	Single nucleotide variant (missense variant)	not specified +1 more	GUncertain significance
Select item 3225612	NM_006506.5(RASA2):c.854A>G (p.His285Arg)	RASA2 (H285R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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