Slc29a1 Variant Search Result - Rat Genome Database

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34 records found for search term Slc29a1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405275433	CV3211196	single nucleotide variant	NM_001304462.2(SLC29A1):c.87-8T>A	SLC29A1-related disorder [RCV003937180]	likely benign	6	44221578	44221578	Human		name , trait , alternate_id
405274646	CV3207694	single nucleotide variant	NM_001372327.1(SLC29A1):c.-52+8C>T	SLC29A1-related disorder [RCV003929388]	likely benign	6	44223649	44223649	Human		name , trait , alternate_id
15114680	CV779206	single nucleotide variant	NM_001372327.1(SLC29A1):c.590-9C>T	not provided [RCV000961718]	benign	6	44230559	44230559	Human		name
15114693	CV779210	single nucleotide variant	NM_001372327.1(SLC29A1):c.864+4C>T	not provided [RCV000961720]	benign	6	44231465	44231465	Human		name
15114686	CV779363	single nucleotide variant	NM_001372327.1(SLC29A1):c.767-5C>T	not provided [RCV000961719]	benign	6	44231359	44231359	Human		name
15139598	CV744272	single nucleotide variant	NM_001372327.1(SLC29A1):c.1260-7C>T	not provided [RCV000899172]	likely benign	6	44233410	44233410	Human		name
15176628	CV722053	single nucleotide variant	NM_001372327.1(SLC29A1):c.84G>A (p.Pro28=)	not provided [RCV000884626]	benign	6	44229444	44229444	Human		name
21067999	CV681925	single nucleotide variant	NM_001372327.1(SLC29A1):c.20C>T (p.Pro7Leu)	Squamous cell carcinoma of the head and neck [RCV000993801]	uncertain significance	6	44227333	44227333	Human		name
597701284	CV3602787	single nucleotide variant	NM_001372327.1(SLC29A1):c.74C>T (p.Thr25Met)	not specified [RCV004859966]	uncertain significance	6	44229434	44229434	Human		name
15135778	CV765707	single nucleotide variant	NM_001372327.1(SLC29A1):c.618C>T (p.Phe206=)	not provided [RCV000942973]	likely benign	6	44230596	44230596	Human		name
8626217	CV81361	single nucleotide variant	NM_001078177.1(SLC29A1):c.927C>T (p.Ala309=)	Malignant melanoma [RCV000061439]	not provided	6	44232060	44232060	Human		name
156255409	CV2194496	single nucleotide variant	NM_001372327.1(SLC29A1):c.194C>T (p.Ala65Val)	not specified [RCV004081567]	uncertain significance	6	44229671	44229671	Human		name
156247427	CV2202883	single nucleotide variant	NM_001372327.1(SLC29A1):c.565G>A (p.Val189Met)	not specified [RCV004069159]	uncertain significance	6	44230457	44230457	Human		name
156247996	CV2276942	single nucleotide variant	NM_001372327.1(SLC29A1):c.977G>A (p.Arg326His)	not specified [RCV004140276]	uncertain significance	6	44232346	44232346	Human		name
156100608	CV2392957	single nucleotide variant	NM_001372327.1(SLC29A1):c.442G>A (p.Val148Met)	not specified [RCV004242812]	likely benign	6	44230034	44230034	Human		name
329350293	CV2463616	single nucleotide variant	NM_001372327.1(SLC29A1):c.440T>C (p.Ile147Thr)	not specified [RCV004277413]	uncertain significance	6	44230032	44230032	Human		name
401743599	CV2680000	single nucleotide variant	NM_001372327.1(SLC29A1):c.902C>A (p.Thr301Asn)	not specified [RCV004284270]	uncertain significance	6	44232035	44232035	Human		name
401857403	CV2761608	single nucleotide variant	NM_001372327.1(SLC29A1):c.326C>T (p.Ser109Phe)	not specified [RCV004337234]	uncertain significance	6	44229918	44229918	Human		name
405782721	CV3322050	single nucleotide variant	NM_001372327.1(SLC29A1):c.441C>G (p.Ile147Met)	not specified [RCV004458940]	uncertain significance	6	44230033	44230033	Human		name
405782727	CV3322051	single nucleotide variant	NM_001372327.1(SLC29A1):c.673G>A (p.Gly225Ser)	not specified [RCV004458941]	uncertain significance	6	44230651	44230651	Human		name
407451094	CV3474180	single nucleotide variant	NM_001372327.1(SLC29A1):c.661A>G (p.Ile221Val)	not specified [RCV004672458]	uncertain significance	6	44230639	44230639	Human		name
407451864	CV3474181	single nucleotide variant	NM_001372327.1(SLC29A1):c.325T>C (p.Ser109Pro)	not specified [RCV004683659]	uncertain significance	6	44229917	44229917	Human		name
597755392	CV3602788	single nucleotide variant	NM_001372327.1(SLC29A1):c.815A>G (p.Asn272Ser)	not specified [RCV004868138]	likely benign	6	44231412	44231412	Human		name
598169805	CV3918453	single nucleotide variant	NM_001372327.1(SLC29A1):c.518C>T (p.Thr173Met)	not specified [RCV005284373]	uncertain significance	6	44230410	44230410	Human		name
598236987	CV3918455	single nucleotide variant	NM_001372327.1(SLC29A1):c.346C>G (p.Leu116Val)	not specified [RCV005275563]	uncertain significance	6	44229938	44229938	Human		name
598169811	CV3918456	single nucleotide variant	NM_001372327.1(SLC29A1):c.692T>C (p.Phe231Ser)	not specified [RCV005284375]	uncertain significance	6	44230815	44230815	Human		name
156064898	CV2340796	single nucleotide variant	NM_001372327.1(SLC29A1):c.1205C>T (p.Ala402Val)	not specified [RCV004188156]	uncertain significance	6	44232952	44232952	Human		name
156009891	CV2362050	single nucleotide variant	NM_001372327.1(SLC29A1):c.1087A>G (p.Ser363Gly)	not specified [RCV004209861]	uncertain significance	6	44232834	44232834	Human		name
405782709	CV3322048	single nucleotide variant	NM_001372327.1(SLC29A1):c.1147C>T (p.Arg383Cys)	not specified [RCV004458938]	uncertain significance	6	44232894	44232894	Human		name
405782715	CV3322049	single nucleotide variant	NM_001372327.1(SLC29A1):c.1337C>T (p.Ala446Val)	not specified [RCV004458939]	uncertain significance	6	44233494	44233494	Human		name
407451098	CV3474183	single nucleotide variant	NM_001372327.1(SLC29A1):c.1029G>C (p.Leu343Phe)	not specified [RCV004672459]	uncertain significance	6	44232398	44232398	Human		name
597755396	CV3602789	single nucleotide variant	NM_001372327.1(SLC29A1):c.1136A>T (p.Asn379Ile)	not specified [RCV004868139]	uncertain significance	6	44232883	44232883	Human		name
597755400	CV3602790	single nucleotide variant	NM_001372327.1(SLC29A1):c.1061C>T (p.Pro354Leu)	not specified [RCV004868140]	uncertain significance	6	44232808	44232808	Human		name
12912627	CV421143	single nucleotide variant	NM_001372327.1(SLC29A1):c.1159A>C (p.Thr387Pro)	Hemolytic disease of fetus OR newborn due to isoimmunization [RCV000492821]	pathogenic	6	44232906	44232906	Human	1	name

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