Cox5b Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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14 records found for search term Cox5b

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401916705	CV2812135	single nucleotide variant	NM_001862.3(COX5B):c.21C>T (p.Arg7=)	not provided [RCV003429193]	likely benign	2	97646107	97646107	Human		name
156357006	CV2318223	single nucleotide variant	NM_001862.3(COX5B):c.12G>C (p.Arg4Ser)	not specified [RCV004179408]	uncertain significance	2	97646098	97646098	Human		name
598234869	CV3945076	single nucleotide variant	NM_001862.3(COX5B):c.19C>T (p.Arg7Cys)	not specified [RCV005320145]	uncertain significance	2	97646105	97646105	Human		name
156278934	CV2325154	single nucleotide variant	NM_001862.3(COX5B):c.34C>G (p.Leu12Val)	not specified [RCV004177577]	uncertain significance	2	97646120	97646120	Human		name
329372412	CV2424083	single nucleotide variant	NM_001862.3(COX5B):c.29G>A (p.Gly10Glu)	not specified [RCV004247989]	uncertain significance	2	97646115	97646115	Human		name
401749725	CV2694726	single nucleotide variant	NM_001862.3(COX5B):c.93G>T (p.Met31Ile)	not specified [RCV004298816]	uncertain significance	2	97646179	97646179	Human		name
598234846	CV3945073	single nucleotide variant	NM_001862.3(COX5B):c.85C>T (p.Arg29Cys)	not specified [RCV005320142]	uncertain significance	2	97646171	97646171	Human		name
598234886	CV3945078	single nucleotide variant	NM_001862.3(COX5B):c.28G>A (p.Gly10Arg)	not specified [RCV005320147]	uncertain significance	2	97646114	97646114	Human		name
597649876	CV3654317	single nucleotide variant	NM_001862.3(COX5B):c.113C>G (p.Pro38Arg)	not specified [RCV004910395]	uncertain significance	2	97647076	97647076	Human		name
598234853	CV3945074	single nucleotide variant	NM_001862.3(COX5B):c.161C>T (p.Ala54Val)	not specified [RCV005320143]	uncertain significance	2	97647124	97647124	Human		name
598234879	CV3945077	single nucleotide variant	NM_001862.3(COX5B):c.101G>A (p.Gly34Glu)	not specified [RCV005320146]	uncertain significance	2	97646187	97646187	Human		name
401743527	CV2696811	single nucleotide variant	NM_001862.3(COX5B):c.301G>A (p.Val101Ile)	not specified [RCV004290780]	likely benign	2	97648019	97648019	Human		name
401771525	CV2722859	single nucleotide variant	NM_001862.3(COX5B):c.335G>A (p.Arg112Gln)	not specified [RCV004325271]	uncertain significance	2	97648053	97648053	Human		name
405685647	CV3235756	single nucleotide variant	NM_001862.3(COX5B):c.325G>A (p.Glu109Lys)	not specified [RCV004372270]	uncertain significance	2	97648043	97648043	Human		name