Acp1 Variant Search Result - Rat Genome Database

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21 records found for search term Acp1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15164833	CV779028	single nucleotide variant	NM_004300.4(ACP1):c.43+8G>A	not provided [RCV000970816]	benign	2	265015	265015	Human		name
15174597	CV730132	single nucleotide variant	NM_004300.4(ACP1):c.43+10C>T	not provided [RCV000884166]	benign	2	265017	265017	Human		name
11641195	CV271700	single nucleotide variant	NM_004300.4(ACP1):c.231+73G>A	not provided [RCV000351394]	uncertain significance	2	272223	272223	Human		name
405769431	CV3299180	single nucleotide variant	NM_004300.4(ACP1):c.231+57G>A	not specified [RCV004435022]	uncertain significance	2	272207	272207	Human		name
597774492	CV3640090	single nucleotide variant	NM_004300.4(ACP1):c.231+49T>C	not specified [RCV004898031]	uncertain significance	2	272199	272199	Human		name
597774496	CV3640095	single nucleotide variant	NM_004300.4(ACP1):c.231+77C>T	not specified [RCV004898032]	likely benign	2	272227	272227	Human		name
598162335	CV3946055	single nucleotide variant	NM_004300.4(ACP1):c.231+68T>G	not specified [RCV005307195]	likely benign	2	272218	272218	Human		name
616938797	CV4015877	single nucleotide variant	NM_004300.4(ACP1):c.231+53C>T	Thalidomide response [RCV005414429]	drug response	2	272203	272203	Human		name
401780254	CV2725956	single nucleotide variant	NM_004300.4(ACP1):c.231+100G>T	not specified [RCV004324326]	uncertain significance	2	272250	272250	Human		name
15194370	CV763153	single nucleotide variant	NM_004300.4(ACP1):c.96C>T (p.Thr32=)	not provided [RCV000933625]	likely benign	2	271918	271918	Human		name
329390927	CV2455603	single nucleotide variant	NM_004300.4(ACP1):c.23C>T (p.Ser8Phe)	not specified [RCV004276852]	uncertain significance	2	264987	264987	Human		name
15196848	CV719795	single nucleotide variant	NM_004300.4(ACP1):c.21G>T (p.Lys7Asn)	not provided [RCV000889886]	benign	2	264985	264985	Human		name
15175892	CV719826	single nucleotide variant	NM_004300.4(ACP1):c.402G>A (p.Gly134=)	not provided [RCV000884468]	benign	2	277229	277229	Human		name
15166970	CV719827	single nucleotide variant	NM_004300.4(ACP1):c.423G>A (p.Thr141=)	not provided [RCV000882750]	benign	2	277250	277250	Human		name
8625338	CV80461	single nucleotide variant	NM_004300.3(ACP1):c.393C>A (p.Pro131=)	Malignant melanoma [RCV000060538]	not provided	2	277079	277079	Human		name
156311434	CV2260175	single nucleotide variant	NM_004300.4(ACP1):c.272G>T (p.Cys91Phe)	not specified [RCV004120952]	uncertain significance	2	275180	275180	Human		name
329380217	CV2466485	single nucleotide variant	NM_004300.4(ACP1):c.116A>T (p.Asn39Ile)	not specified [RCV004274035]	uncertain significance	2	271938	271938	Human		name
8563833	CV28724	single nucleotide variant	NM_004300.4(ACP1):c.317A>G (p.Gln106Arg)	ACP1 A/B POLYMORPHISM [RCV000014681]\|not provided [RCV004713171]	benign	2	277003	277003	Human	31	name , trait
8563833	CV28724	single nucleotide variant	NM_004300.4(ACP1):c.317A>G (p.Gln106Arg)	ACP1 A/B POLYMORPHISM [RCV000014681]\|not provided [RCV004713171]	benign	2	277003	277004	Human	31	name , trait
405769525	CV3299195	single nucleotide variant	NM_004300.4(ACP1):c.428A>G (p.Tyr143Cys)	not specified [RCV004435037]	uncertain significance	2	277255	277255	Human		name
407490290	CV3418101	single nucleotide variant	NM_004300.4(ACP1):c.343G>A (p.Glu115Lys)	not specified [RCV004604399]	uncertain significance	2	277029	277029	Human		name

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