Tbcb Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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32 records found for search term Tbcb

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
156094147	CV2382267	single nucleotide variant	NM_001281.3(TBCB):c.26C>T (p.Pro9Leu)	not specified [RCV004228208]	uncertain significance	19	36115586	36115586	Human		name
401720614	CV2673399	single nucleotide variant	NM_001281.3(TBCB):c.16G>A (p.Val6Met)	not specified [RCV004288375]	uncertain significance	19	36115576	36115576	Human		name
405791076	CV3335332	single nucleotide variant	NM_001281.3(TBCB):c.50G>A (p.Ser17Asn)	not specified [RCV004474094]	uncertain significance	19	36115610	36115610	Human		name
597761811	CV3619166	single nucleotide variant	NM_001281.3(TBCB):c.75G>C (p.Glu25Asp)	not specified [RCV004869502]	uncertain significance	19	36115635	36115635	Human		name
155975706	CV2231435	single nucleotide variant	NM_001281.3(TBCB):c.269A>G (p.His90Arg)	not specified [RCV004096514]	uncertain significance	19	36120720	36120720	Human		name
156093700	CV2252886	single nucleotide variant	NM_001281.3(TBCB):c.194G>A (p.Ser65Asn)	not specified [RCV004120719]	uncertain significance	19	36116120	36116120	Human		name
401889788	CV2754996	single nucleotide variant	NM_001281.3(TBCB):c.281G>A (p.Arg94His)	not specified [RCV004335153]	uncertain significance	19	36120732	36120732	Human		name
407512600	CV3485662	single nucleotide variant	NM_001281.3(TBCB):c.241G>A (p.Asp81Asn)	not specified [RCV004673487]	uncertain significance	19	36116167	36116167	Human		name
598196870	CV3912938	single nucleotide variant	NM_001281.3(TBCB):c.100A>G (p.Ile34Val)	not specified [RCV005289497]	uncertain significance	19	36115660	36115660	Human		name
598196877	CV3912939	single nucleotide variant	NM_001281.3(TBCB):c.251G>T (p.Arg84Leu)	not specified [RCV005289498]	uncertain significance	19	36116177	36116177	Human		name
156313669	CV2196533	single nucleotide variant	NM_001281.3(TBCB):c.598C>T (p.Pro200Ser)	not specified [RCV004073822]	uncertain significance	19	36125501	36125501	Human		name
156289047	CV2229857	single nucleotide variant	NM_001281.3(TBCB):c.308G>C (p.Arg103Pro)	not specified [RCV004105421]	uncertain significance	19	36120759	36120759	Human		name
156128710	CV2238476	single nucleotide variant	NM_001281.3(TBCB):c.632A>G (p.Lys211Arg)	not specified [RCV004113528]	uncertain significance	19	36125679	36125679	Human		name
156083282	CV2249190	single nucleotide variant	NM_001281.3(TBCB):c.589T>A (p.Tyr197Asn)	not specified [RCV004118237]	uncertain significance	19	36125492	36125492	Human		name
156277443	CV2277031	single nucleotide variant	NM_001281.3(TBCB):c.361G>T (p.Val121Phe)	not specified [RCV004140351]	uncertain significance	19	36121532	36121532	Human		name
329387043	CV2436229	single nucleotide variant	NM_001281.3(TBCB):c.481G>T (p.Val161Leu)	not specified [RCV004251647]	uncertain significance	19	36121652	36121652	Human		name
329353727	CV2439604	single nucleotide variant	NM_001281.3(TBCB):c.718G>A (p.Gly240Arg)	not specified [RCV004255622]	uncertain significance	19	36125765	36125765	Human		name
329401270	CV2442271	single nucleotide variant	NM_001281.3(TBCB):c.634C>T (p.Arg212Cys)	not specified [RCV004264753]	uncertain significance	19	36125681	36125681	Human		name
329397803	CV2456384	single nucleotide variant	NM_001281.3(TBCB):c.391G>C (p.Gly131Arg)	not specified [RCV004275545]	uncertain significance	19	36121562	36121562	Human		name
401866845	CV2759024	single nucleotide variant	NM_001281.3(TBCB):c.627T>A (p.Asn209Lys)	not specified [RCV004342331]	uncertain significance	19	36125674	36125674	Human		name
405791073	CV3335331	single nucleotide variant	NM_001281.3(TBCB):c.326T>C (p.Ile109Thr)	not specified [RCV004474093]	uncertain significance	19	36120777	36120777	Human		name
405791079	CV3335333	single nucleotide variant	NM_001281.3(TBCB):c.520C>G (p.Pro174Ala)	not specified [RCV004474095]	uncertain significance	19	36121691	36121691	Human		name
405791082	CV3335334	single nucleotide variant	NM_001281.3(TBCB):c.565C>A (p.Pro189Thr)	not specified [RCV004474096]	uncertain significance	19	36125468	36125468	Human		name
405791086	CV3335335	single nucleotide variant	NM_001281.3(TBCB):c.586C>T (p.Arg196Cys)	not specified [RCV004474097]	uncertain significance	19	36125489	36125489	Human		name
405791087	CV3335336	single nucleotide variant	NM_001281.3(TBCB):c.689C>T (p.Thr230Met)	not specified [RCV004474098]	uncertain significance	19	36125736	36125736	Human		name
407530676	CV3485661	single nucleotide variant	NM_001281.3(TBCB):c.368C>G (p.Ser123Cys)	not specified [RCV004682029]	uncertain significance	19	36121539	36121539	Human		name
597761800	CV3619164	single nucleotide variant	NM_001281.3(TBCB):c.695G>A (p.Gly232Glu)	not specified [RCV004869500]	uncertain significance	19	36125742	36125742	Human		name
597761806	CV3619165	single nucleotide variant	NM_001281.3(TBCB):c.563A>G (p.Lys188Arg)	not specified [RCV004869501]	uncertain significance	19	36125466	36125466	Human		name
597761816	CV3619167	single nucleotide variant	NM_001281.3(TBCB):c.407A>G (p.Glu136Gly)	not specified [RCV004869503]	uncertain significance	19	36121578	36121578	Human		name
597761823	CV3619168	single nucleotide variant	NM_001281.3(TBCB):c.653C>G (p.Ala218Gly)	not specified [RCV004869504]	uncertain significance	19	36125700	36125700	Human		name
598196858	CV3912936	single nucleotide variant	NM_001281.3(TBCB):c.512G>A (p.Gly171Glu)	not specified [RCV005289495]	uncertain significance	19	36121683	36121683	Human		name
598196864	CV3912937	single nucleotide variant	NM_001281.3(TBCB):c.540G>C (p.Met180Ile)	not specified [RCV005289496]	uncertain significance	19	36121711	36121711	Human		name

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