Ptgds Variant Search Result - Rat Genome Database

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17 records found for search term Ptgds

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15159176	CV777801	single nucleotide variant	NM_000954.6(PTGDS):c.115-9T>C	not provided [RCV000947221]	benign	9	136978984	136978984	Human		name
15159181	CV777812	single nucleotide variant	NM_000954.6(PTGDS):c.115-8C>T	not provided [RCV000947222]	benign	9	136978985	136978985	Human		name
15146348	CV779385	single nucleotide variant	NM_000954.6(PTGDS):c.448+4C>T	not provided [RCV000967147]	benign	9	136980066	136980066	Human		name
405673054	CV3377730	single nucleotide variant	NM_000954.6(PTGDS):c.58C>G (p.Leu20Val)	not specified [RCV004515590]	uncertain significance	9	136977636	136977636	Human		name
598172454	CV3908521	single nucleotide variant	NM_000954.6(PTGDS):c.88G>A (p.Val30Met)	not specified [RCV005263548]	uncertain significance	9	136977666	136977666	Human		name
15122392	CV711884	single nucleotide variant	NM_000954.6(PTGDS):c.564G>A (p.Thr188=)	not provided [RCV000963066]	benign	9	136980846	136980846	Human		name
405673034	CV3377726	single nucleotide variant	NM_000954.6(PTGDS):c.166C>T (p.Arg56Trp)	not specified [RCV004515586]	uncertain significance	9	136979044	136979044	Human		name
598172433	CV3908518	single nucleotide variant	NM_000954.6(PTGDS):c.109G>A (p.Asp37Asn)	not specified [RCV005263545]	uncertain significance	9	136977687	136977687	Human		name
401762694	CV2720029	single nucleotide variant	NM_000954.6(PTGDS):c.370G>A (p.Asp124Asn)	not specified [RCV004323606]	likely benign	9	136979984	136979984	Human		name
401879802	CV2755280	single nucleotide variant	NM_000954.6(PTGDS):c.537C>G (p.Phe179Leu)	not specified [RCV004337456]	uncertain significance	9	136980271	136980271	Human		name
405673045	CV3377728	single nucleotide variant	NM_000954.6(PTGDS):c.385G>A (p.Ala129Thr)	not specified [RCV004515588]	uncertain significance	9	136979999	136979999	Human		name
405673049	CV3377729	single nucleotide variant	NM_000954.6(PTGDS):c.454A>G (p.Thr152Ala)	not specified [RCV004515589]	uncertain significance	9	136980188	136980188	Human		name
407532067	CV3468264	single nucleotide variant	NM_000954.6(PTGDS):c.493G>A (p.Ala165Thr)	not specified [RCV004657951]	likely benign	9	136980227	136980227	Human		name
597751681	CV3588678	single nucleotide variant	NM_000954.6(PTGDS):c.358G>C (p.Val120Leu)	not specified [RCV004846652]	uncertain significance	9	136979972	136979972	Human		name
598172441	CV3908519	single nucleotide variant	NM_000954.6(PTGDS):c.431G>A (p.Arg144His)	not specified [RCV005263546]	uncertain significance	9	136980045	136980045	Human		name
598172448	CV3908520	single nucleotide variant	NM_000954.6(PTGDS):c.352G>A (p.Val118Met)	not specified [RCV005263547]	uncertain significance	9	136979966	136979966	Human		name
598172467	CV3908523	single nucleotide variant	NM_000954.6(PTGDS):c.421G>A (p.Glu141Lys)	not specified [RCV005263550]	uncertain significance	9	136980035	136980035	Human		name