Has2 Variant Search Result - Rat Genome Database

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24 records found for search term Has2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8649932	CV126506	single nucleotide variant	NM_005328.2(HAS2):c.-1+2516A>G	Lung cancer [RCV000106993]	uncertain significance	8	121638337	121638337	Human		name
598265421	CV3971394	single nucleotide variant	NM_005328.3(HAS2):c.22T>C (p.Cys8Arg)	not specified [RCV005349056]	uncertain significance	8	121629319	121629319	Human		name
407514184	CV3443988	single nucleotide variant	NM_005328.3(HAS2):c.38T>C (p.Ile13Thr)	not specified [RCV004627452]	uncertain significance	8	121629303	121629303	Human		name
401896627	CV2791804	single nucleotide variant	NM_005328.3(HAS2):c.246C>A (p.Asn82Lys)	not specified [RCV004353121]	uncertain significance	8	121629095	121629095	Human		name
407514182	CV3443987	single nucleotide variant	NM_005328.3(HAS2):c.152C>G (p.Ala51Gly)	not specified [RCV004627451]	uncertain significance	8	121629189	121629189	Human		name
597709428	CV3682125	single nucleotide variant	NM_005328.3(HAS2):c.158T>C (p.Leu53Ser)	not specified [RCV004917315]	uncertain significance	8	121629183	121629183	Human		name
15185981	CV700385	single nucleotide variant	NM_005328.3(HAS2):c.1239C>G (p.Val413=)	not provided [RCV000953144]	benign	8	121614529	121614529	Human		name
156031918	CV2239274	single nucleotide variant	NM_005328.3(HAS2):c.511G>A (p.Val171Ile)	not specified [RCV004112238]	uncertain significance	8	121628830	121628830	Human		name
156200989	CV2256119	single nucleotide variant	NM_005328.3(HAS2):c.998G>A (p.Arg333Gln)	not specified [RCV004116403]	uncertain significance	8	121614770	121614770	Human		name
329354543	CV2448385	single nucleotide variant	NM_005328.3(HAS2):c.667G>A (p.Val223Met)	not specified [RCV004256670]	uncertain significance	8	121617167	121617167	Human		name
401770282	CV2711045	single nucleotide variant	NM_005328.3(HAS2):c.421G>A (p.Asp141Asn)	not specified [RCV004310741]	uncertain significance	8	121628920	121628920	Human		name
405789069	CV3269964	single nucleotide variant	NM_005328.3(HAS2):c.541A>G (p.Ile181Val)	not specified [RCV004399140]	uncertain significance	8	121628800	121628800	Human		name
407514186	CV3443989	single nucleotide variant	NM_005328.3(HAS2):c.503C>T (p.Ser168Leu)	not specified [RCV004627453]	uncertain significance	8	121628838	121628838	Human		name
598246346	CV3971395	single nucleotide variant	NM_005328.3(HAS2):c.572G>A (p.Arg191Lys)	not specified [RCV005345141]	uncertain significance	8	121628769	121628769	Human		name
156193554	CV2223274	single nucleotide variant	NM_005328.3(HAS2):c.1283G>A (p.Arg428Lys)	not specified [RCV004105891]	uncertain significance	8	121614485	121614485	Human		name
156235982	CV2224088	single nucleotide variant	NM_005328.3(HAS2):c.1099A>T (p.Met367Leu)	not specified [RCV004095955]	uncertain significance	8	121614669	121614669	Human		name
156336527	CV2360755	single nucleotide variant	NM_005328.3(HAS2):c.1605T>A (p.Asn535Lys)	not specified [RCV004213538]	uncertain significance	8	121614163	121614163	Human		name
401889641	CV2766780	single nucleotide variant	NM_005328.3(HAS2):c.1000T>G (p.Ser334Ala)	not specified [RCV004349169]	uncertain significance	8	121614768	121614768	Human		name
405789060	CV3269962	single nucleotide variant	NM_005328.3(HAS2):c.1026A>G (p.Ile342Met)	not specified [RCV004399138]	uncertain significance	8	121614742	121614742	Human		name
405789067	CV3269963	single nucleotide variant	NM_005328.3(HAS2):c.1570G>T (p.Val524Phe)	not specified [RCV004399139]	uncertain significance	8	121614198	121614198	Human		name
597709436	CV3682126	single nucleotide variant	NM_005328.3(HAS2):c.1508C>T (p.Pro503Leu)	not specified [RCV004917316]	uncertain significance	8	121614260	121614260	Human		name
597781185	CV3682127	single nucleotide variant	NM_005328.3(HAS2):c.1196A>T (p.Tyr399Phe)	not specified [RCV004930830]	uncertain significance	8	121614572	121614572	Human		name
597709445	CV3682128	single nucleotide variant	NM_005328.3(HAS2):c.1414G>A (p.Val472Ile)	not specified [RCV004917317]	uncertain significance	8	121614354	121614354	Human		name
28889090	CV859648	single nucleotide variant	NM_005328.3(HAS2):c.1590T>A (p.Tyr530Ter)	not provided [RCV001092147]	uncertain significance	8	121614178	121614178	Human		name

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