Baalc Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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17 records found for search term Baalc

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401886072	CV2771059	single nucleotide variant	NM_024812.3(BAALC):c.26A>T (p.Asp9Val)	not specified [RCV004346068]	uncertain significance	8	103140923	103140923	Human		name
156397707	CV2197449	single nucleotide variant	NM_024812.3(BAALC):c.54C>G (p.Ser18Arg)	not specified [RCV004081184]	uncertain significance	8	103140951	103140951	Human		name
329362178	CV2466086	single nucleotide variant	NM_024812.3(BAALC):c.40C>G (p.Arg14Gly)	not specified [RCV004277969]	uncertain significance	8	103140937	103140937	Human		name
405690929	CV3290735	single nucleotide variant	NM_024812.3(BAALC):c.61C>G (p.Arg21Gly)	not specified [RCV004423648]	uncertain significance	8	103140958	103140958	Human		name
156302329	CV2258645	single nucleotide variant	NM_024812.3(BAALC):c.223C>A (p.Pro75Thr)	not specified [RCV004117900]	uncertain significance	8	103212981	103212981	Human		name
156295355	CV2321498	single nucleotide variant	NM_024812.3(BAALC):c.125C>G (p.Pro42Arg)	not specified [RCV004177467]	uncertain significance	8	103141022	103141022	Human		name
155904600	CV2385554	single nucleotide variant	NM_024812.3(BAALC):c.280A>G (p.Ser94Gly)	not specified [RCV004233194]	uncertain significance	8	103213038	103213038	Human		name
401763193	CV2720229	single nucleotide variant	NM_024812.3(BAALC):c.212C>T (p.Pro71Leu)	not specified [RCV004325566]	uncertain significance	8	103212970	103212970	Human		name
401860492	CV2758501	single nucleotide variant	NM_024812.3(BAALC):c.275G>A (p.Ser92Asn)	not specified [RCV004335553]	uncertain significance	8	103213033	103213033	Human		name
407485683	CV3423688	single nucleotide variant	NM_024812.3(BAALC):c.242C>T (p.Thr81Met)	not specified [RCV004603457]	likely benign	8	103213000	103213000	Human		name
407485752	CV3423699	single nucleotide variant	NM_024812.3(BAALC):c.104C>T (p.Ala35Val)	not specified [RCV004603467]	uncertain significance	8	103141001	103141001	Human		name
597700965	CV3625137	single nucleotide variant	NM_024812.3(BAALC):c.253A>G (p.Thr85Ala)	not specified [RCV004885674]	uncertain significance	8	103213011	103213011	Human		name
329373857	CV2452535	single nucleotide variant	NM_024812.3(BAALC):c.428G>A (p.Cys143Tyr)	not specified [RCV004273127]	uncertain significance	8	103228089	103228089	Human		name
401755718	CV2728671	single nucleotide variant	NM_024812.3(BAALC):c.410G>A (p.Arg137Gln)	not specified [RCV004333523]	uncertain significance	8	103228071	103228071	Human		name
401896693	CV2791949	single nucleotide variant	NM_024812.3(BAALC):c.398T>C (p.Met133Thr)	not specified [RCV004359373]	uncertain significance	8	103228059	103228059	Human		name
405690920	CV3290734	single nucleotide variant	NM_024812.3(BAALC):c.336A>T (p.Arg112Ser)	not specified [RCV004423647]	uncertain significance	8	103227997	103227997	Human		name
597701042	CV3625148	single nucleotide variant	NM_024812.3(BAALC):c.397A>G (p.Met133Val)	not specified [RCV004885685]	likely benign	8	103228058	103228058	Human		name