Txnl4b Variant Search Result - Rat Genome Database

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13 records found for search term Txnl4b

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401882379	CV2793470	single nucleotide variant	NM_017853.3(TXNL4B):c.74T>C (p.Val25Ala)	not specified [RCV004362556]	uncertain significance	16	72090676	72090676	Human		name
407522308	CV3493164	single nucleotide variant	NM_017853.3(TXNL4B):c.80T>C (p.Val27Ala)	not specified [RCV004677629]	uncertain significance	16	72090670	72090670	Human		name
156075074	CV2365574	single nucleotide variant	NM_017853.3(TXNL4B):c.109G>A (p.Val37Ile)	not specified [RCV004211687]	uncertain significance	16	72090641	72090641	Human		name
329402765	CV2451342	single nucleotide variant	NM_017853.3(TXNL4B):c.109G>T (p.Val37Phe)	not specified [RCV004272032]	uncertain significance	16	72090641	72090641	Human		name
401782584	CV2697105	single nucleotide variant	NM_017853.3(TXNL4B):c.131T>C (p.Ile44Thr)	not specified [RCV004302104]	uncertain significance	16	72090619	72090619	Human		name
401720004	CV2729498	single nucleotide variant	NM_017853.3(TXNL4B):c.196A>G (p.Thr66Ala)	not specified [RCV004333584]	uncertain significance	16	72089075	72089075	Human		name
401861193	CV2769565	single nucleotide variant	NM_017853.3(TXNL4B):c.212A>G (p.Gln71Arg)	not specified [RCV004351214]	uncertain significance	16	72089059	72089059	Human		name
405813842	CV3344924	single nucleotide variant	NM_017853.3(TXNL4B):c.269T>A (p.Met90Lys)	not specified [RCV004484057]	uncertain significance	16	72089002	72089002	Human		name
407522311	CV3493165	single nucleotide variant	NM_017853.3(TXNL4B):c.268A>G (p.Met90Val)	not specified [RCV004677630]	uncertain significance	16	72089003	72089003	Human		name
597802769	CV3628934	single nucleotide variant	NM_017853.3(TXNL4B):c.194A>G (p.Gln65Arg)	not specified [RCV004881404]	uncertain significance	16	72089077	72089077	Human		name
156181332	CV2288165	single nucleotide variant	NM_017853.3(TXNL4B):c.313A>G (p.Ser105Gly)	not specified [RCV004149685]	uncertain significance	16	72086774	72086774	Human		name
156098515	CV2294557	single nucleotide variant	NM_017853.3(TXNL4B):c.332A>G (p.Asp111Gly)	not specified [RCV004161827]	uncertain significance	16	72086755	72086755	Human		name
597802766	CV3628933	single nucleotide variant	NM_017853.3(TXNL4B):c.367G>A (p.Ala123Thr)	not specified [RCV004881403]	uncertain significance	16	72086720	72086720	Human		name