Pcp4 Variant Search Result - Rat Genome Database

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9 records found for search term Pcp4

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405762606	CV3364833	single nucleotide variant	NM_006198.3(PCP4):c.82G>A (p.Glu28Lys)	not specified [RCV004500848]	uncertain significance	21	39929004	39929004	Human		name
598165087	CV4006023	single nucleotide variant	NM_006198.3(PCP4):c.104A>G (p.Asp35Gly)	not specified [RCV005391272]	uncertain significance	21	39929026	39929026	Human		name
15153374	CV778742	single nucleotide variant	NM_001102566.2(PCP4L1):c.64+9G>T	not provided [RCV000968532]	benign	1	161283731	161283731	Human		name
15185516	CV696218	single nucleotide variant	NM_001102566.2(PCP4L1):c.192G>A (p.Lys64=)	not provided [RCV000953007]	benign	1	161284466	161284466	Human		name
156107141	CV2355304	single nucleotide variant	NM_001102566.2(PCP4L1):c.89C>T (p.Ala30Val)	not specified [RCV004203154]	uncertain significance	1	161284363	161284363	Human		name
597697523	CV3571944	single nucleotide variant	NM_001102566.2(PCP4L1):c.92A>C (p.Glu31Ala)	not specified [RCV004839337]	uncertain significance	1	161284366	161284366	Human		name
156326199	CV2335427	single nucleotide variant	NM_001102566.2(PCP4L1):c.169C>T (p.Arg57Trp)	not specified [RCV004186976]	uncertain significance	1	161284443	161284443	Human		name
405762446	CV3364834	single nucleotide variant	NM_001102566.2(PCP4L1):c.170G>A (p.Arg57Gln)	not specified [RCV004500849]	uncertain significance	1	161284444	161284444	Human		name
598165096	CV4006024	single nucleotide variant	NM_001102566.2(PCP4L1):c.158A>G (p.Gln53Arg)	not specified [RCV005391273]	uncertain significance	1	161284432	161284432	Human		name