Dsn1 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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28 records found for search term Dsn1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15202784	CV705464	single nucleotide variant	NM_001145315.2(DSN1):c.72A>G (p.Gln24=)	not provided [RCV000958033]	benign	20	36771156	36771156	Human		name
598189046	CV3957292	single nucleotide variant	NM_001145315.2(DSN1):c.82A>G (p.Ser28Gly)	not specified [RCV005334479]	uncertain significance	20	36771146	36771146	Human		name
15173138	CV716948	single nucleotide variant	NM_001145315.2(DSN1):c.894A>G (p.Ser298=)	not provided [RCV000972554]	benign	20	36754830	36754830	Human		name
329386999	CV2452773	single nucleotide variant	NM_001145315.2(DSN1):c.101T>C (p.Val34Ala)	not specified [RCV004275311]	uncertain significance	20	36771127	36771127	Human		name
401732604	CV2691055	single nucleotide variant	NM_001145315.2(DSN1):c.283T>C (p.Ser95Pro)	not specified [RCV004301063]	uncertain significance	20	36770945	36770945	Human		name
401735807	CV2692204	single nucleotide variant	NM_001145315.2(DSN1):c.104T>A (p.Phe35Tyr)	not specified [RCV004301900]	uncertain significance	20	36771124	36771124	Human		name
405716261	CV3244829	single nucleotide variant	NM_001145315.2(DSN1):c.289C>T (p.Arg97Trp)	not specified [RCV004377298]	uncertain significance	20	36770939	36770939	Human		name
598189061	CV3957294	single nucleotide variant	NM_001145315.2(DSN1):c.236A>G (p.His79Arg)	not specified [RCV005334481]	uncertain significance	20	36770992	36770992	Human		name
155921561	CV2276328	single nucleotide variant	NM_001145315.2(DSN1):c.933G>C (p.Gln311His)	not specified [RCV004144073]	uncertain significance	20	36754791	36754791	Human		name
155921489	CV2340462	single nucleotide variant	NM_001145315.2(DSN1):c.945G>T (p.Lys315Asn)	not specified [RCV004197189]	uncertain significance	20	36754779	36754779	Human	1	name
155921489	CV2340462	single nucleotide variant	NM_001145315.2(DSN1):c.945G>T (p.Lys315Asn)	not specified [RCV004197189]	uncertain significance	20	36754779	36754780	Human	1	name
155930410	CV2361142	single nucleotide variant	NM_001145315.2(DSN1):c.785C>A (p.Ser262Tyr)	not specified [RCV004216331]	uncertain significance	20	36755770	36755770	Human		name
156154560	CV2369516	single nucleotide variant	NM_001145315.2(DSN1):c.577G>A (p.Glu193Lys)	not specified [RCV004210451]	uncertain significance	20	36762474	36762474	Human		name
329366265	CV2438296	single nucleotide variant	NM_001145315.2(DSN1):c.638A>C (p.Glu213Ala)	not specified [RCV004257052]	uncertain significance	20	36758570	36758570	Human		name
329370708	CV2461837	single nucleotide variant	NM_001145315.2(DSN1):c.965A>G (p.Lys322Arg)	not specified [RCV004271753]	uncertain significance	20	36752894	36752894	Human		name
405716258	CV3244830	single nucleotide variant	NM_001145315.2(DSN1):c.311C>T (p.Thr104Met)	not specified [RCV004377299]	uncertain significance	20	36770917	36770917	Human		name
405716252	CV3244831	single nucleotide variant	NM_001145315.2(DSN1):c.320G>A (p.Arg107Gln)	not specified [RCV004377300]	uncertain significance	20	36770908	36770908	Human		name
405716245	CV3244832	single nucleotide variant	NM_001145315.2(DSN1):c.365G>A (p.Arg122Gln)	not specified [RCV004377301]	uncertain significance	20	36768033	36768033	Human		name
405716238	CV3244833	single nucleotide variant	NM_001145315.2(DSN1):c.619T>A (p.Ser207Thr)	not specified [RCV004377302]	uncertain significance	20	36758589	36758589	Human		name
405716231	CV3244834	single nucleotide variant	NM_001145315.2(DSN1):c.755T>G (p.Val252Gly)	not specified [RCV004377303]	uncertain significance	20	36755800	36755800	Human		name
407489645	CV3434818	single nucleotide variant	NM_001145315.2(DSN1):c.634A>C (p.Lys212Gln)	not specified [RCV004619969]	uncertain significance	20	36758574	36758574	Human		name
407489989	CV3434819	single nucleotide variant	NM_001145315.2(DSN1):c.647C>A (p.Thr216Lys)	not specified [RCV004619970]	uncertain significance	20	36758561	36758561	Human		name
597682621	CV3663149	single nucleotide variant	NM_001145315.2(DSN1):c.556G>A (p.Gly186Arg)	not specified [RCV004914474]	uncertain significance	20	36762495	36762495	Human		name
597682629	CV3663150	single nucleotide variant	NM_001145315.2(DSN1):c.622G>A (p.Val208Met)	not specified [RCV004914475]	uncertain significance	20	36758586	36758586	Human		name
597682639	CV3663151	single nucleotide variant	NM_001145315.2(DSN1):c.818A>C (p.Asp273Ala)	not specified [RCV004914476]	uncertain significance	20	36755737	36755737	Human		name
598189026	CV3957290	single nucleotide variant	NM_001145315.2(DSN1):c.557G>C (p.Gly186Ala)	not specified [RCV005334477]	uncertain significance	20	36762494	36762494	Human		name
598189036	CV3957291	single nucleotide variant	NM_001145315.2(DSN1):c.317G>A (p.Arg106Gln)	not specified [RCV005334478]	uncertain significance	20	36770911	36770911	Human		name
598189052	CV3957293	single nucleotide variant	NM_001145315.2(DSN1):c.379G>C (p.Asp127His)	not specified [RCV005334480]	uncertain significance	20	36768019	36768019	Human		name

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