Chrna6 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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35 records found for search term Chrna6

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
329378714	CV2447093	single nucleotide variant	NM_004198.3(CHRNA6):c.49T>C (p.Trp17Arg)	not specified [RCV004259967]	uncertain significance	8	42768382	42768382	Human		name
597770549	CV3653365	single nucleotide variant	NM_004198.3(CHRNA6):c.78A>T (p.Lys26Asn)	not specified [RCV004896938]	uncertain significance	8	42768353	42768353	Human		name
597770566	CV3653369	single nucleotide variant	NM_004198.3(CHRNA6):c.43T>G (p.Cys15Gly)	not specified [RCV004896942]	uncertain significance	8	42768388	42768388	Human		name
15098654	CV700593	single nucleotide variant	NM_004198.3(CHRNA6):c.819G>A (p.Thr273=)	not provided [RCV000958610]	benign	8	42756380	42756380	Human		name
15167315	CV711540	single nucleotide variant	NM_004198.3(CHRNA6):c.798G>A (p.Ser266=)	not provided [RCV000971375]	benign	8	42756401	42756401	Human		name
15174719	CV711541	single nucleotide variant	NM_004198.3(CHRNA6):c.732G>A (p.Thr244=)	not provided [RCV000972776]	benign	8	42756467	42756467	Human		name
401746887	CV2678947	single nucleotide variant	NM_004198.3(CHRNA6):c.128C>T (p.Ser43Phe)	not specified [RCV004294961]	uncertain significance	8	42765156	42765156	Human		name
405672086	CV3297307	single nucleotide variant	NM_004198.3(CHRNA6):c.286C>T (p.Arg96Cys)	not specified [RCV004441488]	uncertain significance	8	42757016	42757016	Human		name
15187863	CV736682	single nucleotide variant	NM_004198.3(CHRNA6):c.107G>C (p.Arg36Thr)	not provided [RCV000909206]	benign	8	42765177	42765177	Human		name
156365808	CV2193276	single nucleotide variant	NM_004198.3(CHRNA6):c.989G>A (p.Arg330His)	not specified [RCV004071253]	uncertain significance	8	42756210	42756210	Human		name
156019723	CV2272676	single nucleotide variant	NM_004198.3(CHRNA6):c.887C>T (p.Thr296Ile)	not specified [RCV004135338]	uncertain significance	8	42756312	42756312	Human		name
156351628	CV2323797	single nucleotide variant	NM_004198.3(CHRNA6):c.992C>T (p.Thr331Ile)	not specified [RCV004176342]	uncertain significance	8	42756207	42756207	Human		name
156189368	CV2342411	single nucleotide variant	NM_004198.3(CHRNA6):c.997A>G (p.Thr333Ala)	not specified [RCV004194022]	likely benign	8	42756202	42756202	Human		name
405672090	CV3297308	single nucleotide variant	NM_004198.3(CHRNA6):c.884C>T (p.Ser295Phe)	not specified [RCV004441489]	uncertain significance	8	42756315	42756315	Human		name
405672095	CV3297309	single nucleotide variant	NM_004198.3(CHRNA6):c.923T>A (p.Leu308Gln)	not specified [RCV004441490]	uncertain significance	8	42756276	42756276	Human		name
597770557	CV3653367	single nucleotide variant	NM_004198.3(CHRNA6):c.355G>A (p.Asp119Asn)	not specified [RCV004896940]	uncertain significance	8	42756947	42756947	Human		name
597770562	CV3653368	single nucleotide variant	NM_004198.3(CHRNA6):c.913G>A (p.Glu305Lys)	not specified [RCV004896941]	uncertain significance	8	42756286	42756286	Human		name
597770571	CV3653370	single nucleotide variant	NM_004198.3(CHRNA6):c.326G>A (p.Arg109His)	not specified [RCV004896943]	uncertain significance	8	42756976	42756976	Human		name
598264418	CV3951760	single nucleotide variant	NM_004198.3(CHRNA6):c.919C>G (p.Leu307Val)	not specified [RCV005326126]	uncertain significance	8	42756280	42756280	Human		name
598215398	CV3951764	single nucleotide variant	NM_004198.3(CHRNA6):c.518C>T (p.Ser173Phe)	not specified [RCV005316744]	uncertain significance	8	42756681	42756681	Human		name
598215403	CV3951765	single nucleotide variant	NM_004198.3(CHRNA6):c.980T>C (p.Ile327Thr)	not specified [RCV005316745]	uncertain significance	8	42756219	42756219	Human		name
598215408	CV3951766	single nucleotide variant	NM_004198.3(CHRNA6):c.793C>T (p.Pro265Ser)	not specified [RCV005316746]	uncertain significance	8	42756406	42756406	Human		name
598215415	CV3951767	single nucleotide variant	NM_004198.3(CHRNA6):c.560A>C (p.Asp187Ala)	not specified [RCV005316747]	uncertain significance	8	42756639	42756639	Human		name
156066638	CV2317860	single nucleotide variant	NM_004198.3(CHRNA6):c.1025A>G (p.Lys342Arg)	not specified [RCV004175096]	uncertain significance	8	42756174	42756174	Human		name
156132641	CV2365830	single nucleotide variant	NM_004198.3(CHRNA6):c.1277C>G (p.Ser426Trp)	not specified [RCV004214365]	uncertain significance	8	42755922	42755922	Human		name
329387733	CV2446696	single nucleotide variant	NM_004198.3(CHRNA6):c.1244C>T (p.Pro415Leu)	not specified [RCV004253743]	uncertain significance	8	42755955	42755955	Human		name
329374437	CV2463552	single nucleotide variant	NM_004198.3(CHRNA6):c.1368G>T (p.Trp456Cys)	not specified [RCV004277362]	uncertain significance	8	42753296	42753296	Human		name
401880945	CV2763190	single nucleotide variant	NM_004198.3(CHRNA6):c.1006A>G (p.Thr336Ala)	not specified [RCV004336229]	uncertain significance	8	42756193	42756193	Human		name
407455864	CV3422864	single nucleotide variant	NM_004198.3(CHRNA6):c.1186T>C (p.Phe396Leu)	not specified [RCV004610493]	uncertain significance	8	42756013	42756013	Human		name
597770545	CV3653364	single nucleotide variant	NM_004198.3(CHRNA6):c.1310A>G (p.Gln437Arg)	not specified [RCV004896937]	uncertain significance	8	42755889	42755889	Human		name
597770554	CV3653366	single nucleotide variant	NM_004198.3(CHRNA6):c.1286T>C (p.Val429Ala)	not specified [RCV004896939]	uncertain significance	8	42755913	42755913	Human		name
597770575	CV3653371	single nucleotide variant	NM_004198.3(CHRNA6):c.1108G>A (p.Val370Met)	not specified [RCV004896944]	uncertain significance	8	42756091	42756091	Human		name
598215383	CV3951761	single nucleotide variant	NM_004198.3(CHRNA6):c.1388T>C (p.Val463Ala)	not specified [RCV005316741]	uncertain significance	8	42753276	42753276	Human		name
598215393	CV3951763	single nucleotide variant	NM_004198.3(CHRNA6):c.1052A>G (p.Gln351Arg)	not specified [RCV005316743]	uncertain significance	8	42756147	42756147	Human		name
8633019	CV88233	single nucleotide variant	NM_001199279.1(CHRNA6):c.508G>A (p.Glu170Lys)	Malignant melanoma [RCV000068325]	not provided	8	42756646	42756646	Human		name

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