Siglec15 Variant Search Result - Rat Genome Database

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47 records found for search term Siglec15

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
407451407	CV3480721	single nucleotide variant	NM_213602.3(SIGLEC15):c.11C>A (p.Ser4Tyr)	not specified [RCV004676423]	uncertain significance	18	45825739	45825739	Human		name
155954052	CV1936232	single nucleotide variant	NM_213602.3(SIGLEC15):c.606G>A (p.Pro202=)	not provided [RCV002511893]	likely benign	18	45838827	45838827	Human		name
155954073	CV1936233	single nucleotide variant	NM_213602.3(SIGLEC15):c.642G>A (p.Pro214=)	not provided [RCV002511894]	benign	18	45838863	45838863	Human		name
156050084	CV2242029	single nucleotide variant	NM_213602.3(SIGLEC15):c.93G>C (p.Leu31Phe)	not specified [RCV004108967]	uncertain significance	18	45837069	45837069	Human		name
329349799	CV2447843	single nucleotide variant	NM_213602.3(SIGLEC15):c.90C>G (p.Asn30Lys)	not specified [RCV004258616]	uncertain significance	18	45837066	45837066	Human		name
401746052	CV2674566	single nucleotide variant	NM_213602.3(SIGLEC15):c.35C>T (p.Ala12Val)	not specified [RCV004291442]	likely benign	18	45825763	45825763	Human		name
401903549	CV2818332	single nucleotide variant	NM_213602.3(SIGLEC15):c.855C>T (p.Arg285=)	not provided [RCV003413447]	likely benign	18	45839076	45839076	Human		name
405270081	CV3185115	single nucleotide variant	NM_213602.3(SIGLEC15):c.984G>A (p.Pro328=)	not provided [RCV003885679]	likely benign	18	45842184	45842184	Human		name
155912638	CV2308931	single nucleotide variant	NM_213602.3(SIGLEC15):c.170G>A (p.Gly57Asp)	not specified [RCV004169219]	uncertain significance	18	45837570	45837570	Human		name
156342516	CV2343963	single nucleotide variant	NM_213602.3(SIGLEC15):c.239T>C (p.Ile80Thr)	not specified [RCV004195582]	uncertain significance	18	45837639	45837639	Human		name
156156491	CV2368047	single nucleotide variant	NM_213602.3(SIGLEC15):c.185T>G (p.Leu62Arg)	not specified [RCV004223129]	uncertain significance	18	45837585	45837585	Human		name
329349846	CV2449584	single nucleotide variant	NM_213602.3(SIGLEC15):c.296G>C (p.Arg99Pro)	not specified [RCV004268510]	uncertain significance	18	45837696	45837696	Human		name
401748477	CV2718907	single nucleotide variant	NM_213602.3(SIGLEC15):c.113G>T (p.Ser38Ile)	not specified [RCV004322509]	uncertain significance	18	45837513	45837513	Human		name
405749806	CV3311499	single nucleotide variant	NM_213602.3(SIGLEC15):c.158G>C (p.Ser53Thr)	not specified [RCV004453611]	uncertain significance	18	45837558	45837558	Human		name
405749813	CV3311500	single nucleotide variant	NM_213602.3(SIGLEC15):c.190T>G (p.Cys64Gly)	not specified [RCV004453612]	uncertain significance	18	45837590	45837590	Human		name
405749821	CV3311501	single nucleotide variant	NM_213602.3(SIGLEC15):c.293C>T (p.Ala98Val)	not specified [RCV004453613]	uncertain significance	18	45837693	45837693	Human		name
596938983	CV3547526	single nucleotide variant	NM_213602.3(SIGLEC15):c.128G>T (p.Arg43Leu)	not provided [RCV004811830]	likely benign	18	45837528	45837528	Human		name
597687198	CV3599170	single nucleotide variant	NM_213602.3(SIGLEC15):c.206C>G (p.Pro69Arg)	not specified [RCV004862095]	uncertain significance	18	45837606	45837606	Human		name
597687213	CV3599172	single nucleotide variant	NM_213602.3(SIGLEC15):c.163G>C (p.Glu55Gln)	not specified [RCV004862097]	uncertain significance	18	45837563	45837563	Human		name
598257168	CV3914497	single nucleotide variant	NM_213602.3(SIGLEC15):c.233C>T (p.Thr78Met)	not specified [RCV005279151]	uncertain significance	18	45837633	45837633	Human		name
150463442	CV1235056	single nucleotide variant	NM_213602.3(SIGLEC15):c.817T>C (p.Phe273Leu)	not provided [RCV001649638]	benign	18	45839038	45839038	Human		name
156376565	CV2206751	single nucleotide variant	NM_213602.3(SIGLEC15):c.605C>A (p.Pro202Gln)	not specified [RCV004083439]	uncertain significance	18	45838826	45838826	Human		name
155925373	CV2211820	single nucleotide variant	NM_213602.3(SIGLEC15):c.382C>A (p.Arg128Ser)	not specified [RCV004086647]	uncertain significance	18	45837782	45837782	Human		name
156162676	CV2246544	single nucleotide variant	NM_213602.3(SIGLEC15):c.533G>C (p.Ser178Thr)	not specified [RCV004110297]	uncertain significance	18	45838754	45838754	Human		name
155977602	CV2266427	single nucleotide variant	NM_213602.3(SIGLEC15):c.538G>A (p.Ala180Thr)	not specified [RCV004131012]	uncertain significance	18	45838759	45838759	Human		name
156290254	CV2299476	single nucleotide variant	NM_213602.3(SIGLEC15):c.388G>C (p.Glu130Gln)	not specified [RCV004154551]	uncertain significance	18	45837788	45837788	Human		name
156395188	CV2325236	single nucleotide variant	NM_213602.3(SIGLEC15):c.535C>G (p.Pro179Ala)	not specified [RCV004177642]	uncertain significance	18	45838756	45838756	Human		name
156067762	CV2345832	single nucleotide variant	NM_213602.3(SIGLEC15):c.631G>A (p.Val211Met)	not specified [RCV004198878]	uncertain significance	18	45838852	45838852	Human		name
155927794	CV2349786	single nucleotide variant	NM_213602.3(SIGLEC15):c.333C>G (p.His111Gln)	not specified [RCV004204198]	uncertain significance	18	45837733	45837733	Human		name
156347360	CV2382882	single nucleotide variant	NM_213602.3(SIGLEC15):c.673G>A (p.Glu225Lys)	not specified [RCV004217481]	uncertain significance	18	45838894	45838894	Human		name
155966046	CV2396023	single nucleotide variant	NM_213602.3(SIGLEC15):c.700C>G (p.Arg234Gly)	not specified [RCV004237567]	uncertain significance	18	45838921	45838921	Human		name
329349995	CV2451220	single nucleotide variant	NM_213602.3(SIGLEC15):c.551G>A (p.Arg184His)	not specified [RCV004270134]	uncertain significance	18	45838772	45838772	Human		name
401743632	CV2684148	single nucleotide variant	NM_213602.3(SIGLEC15):c.824C>T (p.Ala275Val)	not specified [RCV004288823]	uncertain significance	18	45839045	45839045	Human		name
401746637	CV2705011	single nucleotide variant	NM_213602.3(SIGLEC15):c.472C>T (p.His158Tyr)	not specified [RCV004309610]	uncertain significance	18	45837872	45837872	Human		name
401904357	CV2818331	single nucleotide variant	NM_213602.3(SIGLEC15):c.503C>G (p.Pro168Arg)	not provided [RCV003421634]	uncertain significance	18	45838724	45838724	Human		name
405749828	CV3311502	single nucleotide variant	NM_213602.3(SIGLEC15):c.613G>T (p.Gly205Cys)	not specified [RCV004453614]	uncertain significance	18	45838834	45838834	Human		name
407451404	CV3480719	single nucleotide variant	NM_213602.3(SIGLEC15):c.482G>A (p.Arg161Gln)	not specified [RCV004676422]	uncertain significance	18	45837882	45837882	Human		name
407450965	CV3480720	single nucleotide variant	NM_213602.3(SIGLEC15):c.418T>C (p.Tyr140His)	not specified [RCV004669824]	uncertain significance	18	45837818	45837818	Human		name
597687206	CV3599171	single nucleotide variant	NM_213602.3(SIGLEC15):c.383G>C (p.Arg128Pro)	not specified [RCV004862096]	uncertain significance	18	45837783	45837783	Human		name
597687222	CV3599173	single nucleotide variant	NM_213602.3(SIGLEC15):c.896C>A (p.Thr299Asn)	not specified [RCV004862098]	uncertain significance	18	45840232	45840232	Human		name
597687232	CV3599174	single nucleotide variant	NM_213602.3(SIGLEC15):c.545C>A (p.Ala182Asp)	not specified [RCV004862099]	uncertain significance	18	45838766	45838766	Human		name
597687243	CV3599175	single nucleotide variant	NM_213602.3(SIGLEC15):c.643C>T (p.Arg215Cys)	not specified [RCV004862100]	uncertain significance	18	45838864	45838864	Human		name
598199465	CV3914492	single nucleotide variant	NM_213602.3(SIGLEC15):c.337C>T (p.Arg113Cys)	not specified [RCV005268398]	uncertain significance	18	45837737	45837737	Human		name
598257150	CV3914493	single nucleotide variant	NM_213602.3(SIGLEC15):c.489C>A (p.His163Gln)	not specified [RCV005279148]	uncertain significance	18	45837889	45837889	Human		name
598257156	CV3914494	single nucleotide variant	NM_213602.3(SIGLEC15):c.868C>A (p.Arg290Ser)	not specified [RCV005279149]	uncertain significance	18	45839089	45839089	Human		name
598257161	CV3914495	single nucleotide variant	NM_213602.3(SIGLEC15):c.904C>G (p.Arg302Gly)	not specified [RCV005279150]	uncertain significance	18	45840240	45840240	Human		name
598257173	CV3914498	single nucleotide variant	NM_213602.3(SIGLEC15):c.707C>A (p.Thr236Lys)	not specified [RCV005279152]	uncertain significance	18	45838928	45838928	Human		name

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