Nanog Variant Search Result - Rat Genome Database

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32 records found for search term Nanog

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597654107	CV3565125	single nucleotide variant	NM_024865.4(NANOG):c.22C>A (p.Pro8Thr)	not specified [RCV004834035]	uncertain significance	12	7789636	7789636	Human		name
401929237	CV2810160	single nucleotide variant	NM_024865.4(NANOG):c.912C>T (p.Asp304=)	not provided [RCV003390168]	likely benign	12	7795089	7795089	Human		name
156175047	CV2254629	single nucleotide variant	NM_024865.4(NANOG):c.154T>C (p.Ser52Pro)	not specified [RCV004115117]	uncertain significance	12	7792952	7792952	Human		name
598205102	CV3987204	single nucleotide variant	NM_024865.4(NANOG):c.205T>C (p.Ser69Pro)	not specified [RCV005376706]	uncertain significance	12	7793003	7793003	Human		name
598205115	CV3987206	single nucleotide variant	NM_024865.4(NANOG):c.172A>G (p.Met58Val)	not specified [RCV005376708]	uncertain significance	12	7792970	7792970	Human		name
15162300	CV753615	single nucleotide variant	NM_024865.4(NANOG):c.115C>A (p.Gln39Lys)	not provided [RCV000925862]	likely benign	12	7789729	7789729	Human		name
156082506	CV2244410	single nucleotide variant	NM_024865.4(NANOG):c.643T>G (p.Ser215Ala)	not specified [RCV004100381]	uncertain significance	12	7794820	7794820	Human		name
156082539	CV2244412	single nucleotide variant	NM_024865.4(NANOG):c.644C>A (p.Ser215Tyr)	not specified [RCV004100383]	uncertain significance	12	7794821	7794821	Human		name
329356505	CV2430782	single nucleotide variant	NM_024865.4(NANOG):c.844A>G (p.Arg282Gly)	not specified [RCV004253959]	uncertain significance	12	7795021	7795021	Human		name
405790533	CV3335145	single nucleotide variant	NM_024865.4(NANOG):c.656A>G (p.His219Arg)	not specified [RCV004473907]	uncertain significance	12	7794833	7794833	Human		name
407520713	CV3447923	single nucleotide variant	NM_024865.4(NANOG):c.370C>A (p.Gln124Lys)	not specified [RCV004652278]	uncertain significance	12	7793168	7793168	Human		name
597654093	CV3565123	single nucleotide variant	NM_024865.4(NANOG):c.380A>G (p.Glu127Gly)	not specified [RCV004834033]	uncertain significance	12	7793178	7793178	Human		name
597654101	CV3565124	single nucleotide variant	NM_024865.4(NANOG):c.528C>A (p.Ser176Arg)	not specified [RCV004834034]	uncertain significance	12	7794705	7794705	Human		name
597654113	CV3565126	single nucleotide variant	NM_024865.4(NANOG):c.721T>C (p.Tyr241His)	not specified [RCV004834036]	uncertain significance	12	7794898	7794898	Human		name
598159228	CV3987207	single nucleotide variant	NM_001145465.1(NANOGNB):c.8G>A (p.Arg3Gln)	not specified [RCV005390107]	uncertain significance	12	7765293	7765293	Human		name
401769389	CV2734984	single nucleotide variant	NM_001145465.1(NANOGNB):c.47A>G (p.Glu16Gly)	not specified [RCV004333688]	uncertain significance	12	7765332	7765332	Human		name
401876765	CV2767708	single nucleotide variant	NM_001145465.1(NANOGNB):c.68G>A (p.Arg23Gln)	not specified [RCV004345840]	uncertain significance	12	7765353	7765353	Human		name
401916309	CV2817394	single nucleotide variant	NM_001355281.2(NANOGP8):c.912C>T (p.Asp304=)	not provided [RCV003400852]	likely benign	15	35084199	35084199	Human		name
405790559	CV3335153	single nucleotide variant	NM_001145465.1(NANOGNB):c.37G>A (p.Ala13Thr)	not specified [RCV004473915]	uncertain significance	12	7765322	7765322	Human		name
405790582	CV3335161	single nucleotide variant	NM_001145465.1(NANOGNB):c.43T>C (p.Trp15Arg)	not specified [RCV004473923]	uncertain significance	12	7765328	7765328	Human		name
156007664	CV2392638	single nucleotide variant	NM_001145465.1(NANOGNB):c.140A>T (p.Gln47Leu)	not specified [RCV004245873]	uncertain significance	12	7770020	7770020	Human		name
329954608	CV2473322	single nucleotide variant	NM_001355281.2(NANOGP8):c.190G>T (p.Asp64Tyr)	Keratoconus [RCV003235811]	uncertain significance	15	35084921	35084921	Human	2	name
597654129	CV3565128	single nucleotide variant	NM_001145465.1(NANOGNB):c.109T>A (p.Ser37Thr)	not specified [RCV004834038]	uncertain significance	12	7769989	7769989	Human		name
156399317	CV2205050	single nucleotide variant	NM_001145465.1(NANOGNB):c.313G>A (p.Glu105Lys)	not specified [RCV004077662]	likely benign	12	7770193	7770193	Human		name
155964813	CV2282882	single nucleotide variant	NM_001145465.1(NANOGNB):c.472A>G (p.Asn158Asp)	not specified [RCV004143529]	uncertain significance	12	7770475	7770475	Human		name
401762925	CV2707367	single nucleotide variant	NM_001145465.1(NANOGNB):c.464A>G (p.Lys155Arg)	not specified [RCV004312761]	uncertain significance	12	7770467	7770467	Human		name
401895240	CV2789790	single nucleotide variant	NM_001145465.1(NANOGNB):c.383C>T (p.Thr128Ile)	not specified [RCV004361895]	uncertain significance	12	7770263	7770263	Human		name
405790564	CV3335155	single nucleotide variant	NM_001145465.1(NANOGNB):c.419A>G (p.Asp140Gly)	not specified [RCV004473917]	likely benign	12	7770299	7770299	Human		name
597654121	CV3565127	single nucleotide variant	NM_001145465.1(NANOGNB):c.371A>G (p.Asn124Ser)	not specified [RCV004834037]	uncertain significance	12	7770251	7770251	Human		name
597654135	CV3565129	single nucleotide variant	NM_001145465.1(NANOGNB):c.395G>A (p.Ser132Asn)	not specified [RCV004834039]	uncertain significance	12	7770275	7770275	Human		name
597654144	CV3565130	single nucleotide variant	NM_001145465.1(NANOGNB):c.430A>C (p.Lys144Gln)	not specified [RCV004834040]	uncertain significance	12	7770310	7770310	Human		name
597654154	CV3565131	single nucleotide variant	NM_001145465.1(NANOGNB):c.465G>T (p.Lys155Asn)	not specified [RCV004834041]	uncertain significance	12	7770468	7770468	Human		name

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