Ramp2 Variant Search Result - Rat Genome Database

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17 records found for search term Ramp2

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405273993	CV3198354	single nucleotide variant	NM_005854.3(RAMP2):c.97+8C>T	RAMP2-related disorder [RCV003902120]	likely benign	17	42761366	42761366	Human		name , trait , alternate_id
155980614	CV2336937	single nucleotide variant	NM_005854.3(RAMP2):c.16G>A (p.Val6Met)	not specified [RCV004190548]	uncertain significance	17	42761277	42761277	Human		name
401757400	CV2734995	single nucleotide variant	NM_005854.3(RAMP2):c.25G>A (p.Ala9Thr)	not specified [RCV004333699]	uncertain significance	17	42761286	42761286	Human		name
598175226	CV3905293	single nucleotide variant	NM_005854.3(RAMP2):c.19G>C (p.Glu7Gln)	not specified [RCV005263974]	uncertain significance	17	42761280	42761280	Human		name
156184346	CV2222493	single nucleotide variant	NM_005854.3(RAMP2):c.37C>G (p.Arg13Gly)	not specified [RCV004099339]	uncertain significance	17	42761298	42761298	Human		name
156001817	CV2284524	single nucleotide variant	NM_005854.3(RAMP2):c.31G>T (p.Gly11Cys)	not specified [RCV004140701]	uncertain significance	17	42761292	42761292	Human		name
329380616	CV2464252	single nucleotide variant	NM_005854.3(RAMP2):c.40C>T (p.Leu14Phe)	not specified [RCV004276218]	uncertain significance	17	42761301	42761301	Human		name
405693208	CV3315413	single nucleotide variant	NM_005854.3(RAMP2):c.52C>G (p.Arg18Gly)	not specified [RCV004445743]	uncertain significance	17	42761313	42761313	Human		name
15168020	CV755866	single nucleotide variant	NM_005854.3(RAMP2):c.420C>T (p.Asp140=)	not provided [RCV000927207]	likely benign	17	42762744	42762744	Human		name
156107073	CV2303884	single nucleotide variant	NM_005854.3(RAMP2):c.170C>T (p.Thr57Met)	not specified [RCV004168168]	likely benign	17	42762361	42762361	Human		name
598175240	CV3905295	single nucleotide variant	NM_005854.3(RAMP2):c.164G>C (p.Gly55Ala)	not specified [RCV005263976]	uncertain significance	17	42762355	42762355	Human		name
156198656	CV2312938	single nucleotide variant	NM_005854.3(RAMP2):c.446T>C (p.Met149Thr)	not specified [RCV004159449]	uncertain significance	17	42762770	42762770	Human		name
401880502	CV2763064	single nucleotide variant	NM_005854.3(RAMP2):c.375G>C (p.Gln125His)	not specified [RCV004336118]	uncertain significance	17	42762699	42762699	Human		name
401874521	CV2774014	single nucleotide variant	NM_005854.3(RAMP2):c.410C>G (p.Thr137Ser)	not specified [RCV004358422]	uncertain significance	17	42762734	42762734	Human		name
597753657	CV3582691	single nucleotide variant	NM_005854.3(RAMP2):c.488T>C (p.Leu163Pro)	not specified [RCV004847168]	uncertain significance	17	42762812	42762812	Human		name
597704425	CV3582692	single nucleotide variant	NM_005854.3(RAMP2):c.364G>C (p.Glu122Gln)	not specified [RCV004860297]	uncertain significance	17	42762688	42762688	Human		name
598175232	CV3905294	single nucleotide variant	NM_005854.3(RAMP2):c.503G>A (p.Ser168Asn)	not specified [RCV005263975]	uncertain significance	17	42762827	42762827	Human		name