Sult4a1 Variant Search Result - Rat Genome Database

Submit Data | Help | Video Tutorials | News | Publications | Download | REST API | Citing RGD | Contact

Advanced Search (OLGA)

Variants search result for Homo sapiens
(View Results for all Objects and Ontologies)

15 records found for search term Sult4a1

Refine Term:

Assembly:

Chr

Sort By:

Export

RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8586936	CV121559	single nucleotide variant	NM_014351.3(SULT4A1):c.170-7547T>G	Lung cancer [RCV000102079]	uncertain significance	22	43849479	43849479	Human		name
15153623	CV758125	single nucleotide variant	NM_014351.4(SULT4A1):c.258C>T (p.Leu86=)	not provided [RCV000924095]	likely benign	22	43841844	43841844	Human		name
597759765	CV3612033	single nucleotide variant	NM_014351.4(SULT4A1):c.717C>T (p.Asn239=)	not specified [RCV004869055]	likely benign	22	43829085	43829085	Human		name
597759761	CV3612032	single nucleotide variant	NM_014351.4(SULT4A1):c.250G>A (p.Glu84Lys)	not specified [RCV004869054]	uncertain significance	22	43841852	43841852	Human		name
156131262	CV2235224	single nucleotide variant	NM_014351.4(SULT4A1):c.488G>A (p.Arg163Gln)	not specified [RCV004107272]	uncertain significance	22	43838887	43838887	Human		name
156349383	CV2305576	single nucleotide variant	NM_014351.4(SULT4A1):c.571G>A (p.Val191Met)	not specified [RCV004165598]	uncertain significance	22	43833672	43833672	Human		name
156079339	CV2351177	single nucleotide variant	NM_014351.4(SULT4A1):c.602G>A (p.Arg201Gln)	not specified [RCV004214029]	uncertain significance	22	43833641	43833641	Human		name
401719770	CV2705514	single nucleotide variant	NM_014351.4(SULT4A1):c.740G>A (p.Arg247Gln)	not specified [RCV004318387]	uncertain significance	22	43829062	43829062	Human		name
405705731	CV3327436	single nucleotide variant	NM_014351.4(SULT4A1):c.368A>G (p.Asn123Ser)	not specified [RCV004461028]	uncertain significance	22	43839958	43839958	Human		name
407497280	CV3481887	single nucleotide variant	NM_014351.4(SULT4A1):c.784A>C (p.Asn262His)	not specified [RCV004668349]	uncertain significance	22	43826072	43826072	Human		name
597759770	CV3612035	single nucleotide variant	NM_014351.4(SULT4A1):c.531G>T (p.Glu177Asp)	not specified [RCV004869056]	uncertain significance	22	43833712	43833712	Human		name
598221760	CV3912458	single nucleotide variant	NM_014351.4(SULT4A1):c.680C>T (p.Thr227Met)	not specified [RCV005293673]	uncertain significance	22	43829122	43829122	Human		name
598221765	CV3912459	single nucleotide variant	NM_014351.4(SULT4A1):c.415G>A (p.Val139Met)	not specified [RCV005293674]	uncertain significance	22	43838960	43838960	Human		name
598221770	CV3912460	single nucleotide variant	NM_014351.4(SULT4A1):c.814A>C (p.Lys272Gln)	not specified [RCV005293675]	uncertain significance	22	43826042	43826042	Human		name
598263476	CV3912461	single nucleotide variant	NM_014351.4(SULT4A1):c.316C>T (p.Arg106Cys)	not specified [RCV005280524]	uncertain significance	22	43840010	43840010	Human		name