Tmem150a Variant Search Result - Rat Genome Database

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15 records found for search term Tmem150a

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
405794406	CV3335991	single nucleotide variant	NM_001031738.3(TMEM150A):c.7G>A (p.Ala3Thr)	not specified [RCV004475236]	uncertain significance	2	85601942	85601942	Human		name
405794409	CV3335992	single nucleotide variant	NM_001031738.3(TMEM150A):c.86A>G (p.Asn29Ser)	not specified [RCV004475237]	uncertain significance	2	85601462	85601462	Human		name
155980204	CV2222992	single nucleotide variant	NM_001031738.3(TMEM150A):c.272C>T (p.Ala91Val)	not specified [RCV004103582]	uncertain significance	2	85600015	85600015	Human		name
401876445	CV2761052	single nucleotide variant	NM_001031738.3(TMEM150A):c.134C>T (p.Pro45Leu)	not specified [RCV004338717]	uncertain significance	2	85601087	85601087	Human		name
401863142	CV2776718	single nucleotide variant	NM_001031738.3(TMEM150A):c.103G>A (p.Val35Met)	not specified [RCV004357876]	uncertain significance	2	85601445	85601445	Human		name
597752845	CV3616876	single nucleotide variant	NM_001031738.3(TMEM150A):c.290G>T (p.Arg97Leu)	not specified [RCV004867246]	uncertain significance	2	85599997	85599997	Human		name
597752850	CV3616877	single nucleotide variant	NM_001031738.3(TMEM150A):c.232C>T (p.Leu78Phe)	not specified [RCV004867247]	uncertain significance	2	85600381	85600381	Human		name
401772265	CV2712625	single nucleotide variant	NM_001031738.3(TMEM150A):c.767G>C (p.Ser256Thr)	not specified [RCV004307951]	uncertain significance	2	85599125	85599125	Human		name
405794397	CV3335988	single nucleotide variant	NM_001031738.3(TMEM150A):c.449C>T (p.Ala150Val)	not specified [RCV004475233]	uncertain significance	2	85599650	85599650	Human		name
405794400	CV3335989	single nucleotide variant	NM_001031738.3(TMEM150A):c.727C>T (p.Pro243Ser)	not specified [RCV004475234]	uncertain significance	2	85599165	85599165	Human		name
405794403	CV3335990	single nucleotide variant	NM_001031738.3(TMEM150A):c.757G>A (p.Gly253Arg)	not specified [RCV004475235]	uncertain significance	2	85599135	85599135	Human		name
407453331	CV3486402	single nucleotide variant	NM_001031738.3(TMEM150A):c.739C>T (p.Arg247Trp)	not specified [RCV004684500]	uncertain significance	2	85599153	85599153	Human		name
407453332	CV3486403	single nucleotide variant	NM_001031738.3(TMEM150A):c.338C>T (p.Thr113Met)	not specified [RCV004684501]	uncertain significance	2	85599949	85599949	Human		name
597752840	CV3616875	single nucleotide variant	NM_001031738.3(TMEM150A):c.589G>A (p.Val197Ile)	not specified [RCV004867245]	likely benign	2	85599303	85599303	Human		name
598213134	CV3917415	single nucleotide variant	NM_001031738.3(TMEM150A):c.796G>A (p.Glu266Lys)	not specified [RCV005292258]	uncertain significance	2	85599096	85599096	Human		name