Dtwd1 Variant Search Result - Rat Genome Database

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20 records found for search term Dtwd1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597683003	CV3673835	single nucleotide variant	NM_001144955.2(DTWD1):c.91G>T (p.Ala31Ser)	not specified [RCV004914537]	uncertain significance	15	49625258	49625258	Human		name
155928078	CV2218543	single nucleotide variant	NM_001144955.2(DTWD1):c.182G>A (p.Cys61Tyr)	not specified [RCV004090818]	uncertain significance	15	49625349	49625349	Human		name
156036582	CV2303761	single nucleotide variant	NM_001144955.2(DTWD1):c.184G>A (p.Gly62Ser)	not specified [RCV004163611]	uncertain significance	15	49625351	49625351	Human		name
329388917	CV2448497	single nucleotide variant	NM_001144955.2(DTWD1):c.254C>T (p.Pro85Leu)	not specified [RCV004259184]	uncertain significance	15	49625421	49625421	Human		name
405733256	CV3244942	single nucleotide variant	NM_001144955.2(DTWD1):c.119G>A (p.Cys40Tyr)	not specified [RCV004379485]	uncertain significance	15	49625286	49625286	Human		name
407489895	CV3431009	single nucleotide variant	NM_001144955.2(DTWD1):c.286A>G (p.Ile96Val)	not specified [RCV004620053]	uncertain significance	15	49632180	49632180	Human		name
597682981	CV3673833	single nucleotide variant	NM_001144955.2(DTWD1):c.185G>T (p.Gly62Val)	not specified [RCV004914535]	uncertain significance	15	49625352	49625352	Human		name
598189582	CV3957388	single nucleotide variant	NM_001144955.2(DTWD1):c.232A>C (p.Asn78His)	not specified [RCV005334575]	uncertain significance	15	49625399	49625399	Human		name
401735811	CV2692205	single nucleotide variant	NM_001144955.2(DTWD1):c.613A>G (p.Ile205Val)	not specified [RCV004301901]	uncertain significance	15	49634740	49634740	Human		name
401773400	CV2716553	single nucleotide variant	NM_001144955.2(DTWD1):c.496G>A (p.Gly166Ser)	not specified [RCV004327629]	uncertain significance	15	49634623	49634623	Human		name
405733264	CV3244943	single nucleotide variant	NM_001144955.2(DTWD1):c.311G>A (p.Gly104Asp)	not specified [RCV004379486]	uncertain significance	15	49632205	49632205	Human		name
405733273	CV3244944	single nucleotide variant	NM_001144955.2(DTWD1):c.701C>T (p.Thr234Ile)	not specified [RCV004379487]	uncertain significance	15	49643364	49643364	Human		name
407489883	CV3431007	single nucleotide variant	NM_001144955.2(DTWD1):c.713G>A (p.Arg238His)	not specified [RCV004620051]	uncertain significance	15	49643376	49643376	Human		name
407489888	CV3431008	single nucleotide variant	NM_001144955.2(DTWD1):c.823G>A (p.Asp275Asn)	not specified [RCV004620052]	uncertain significance	15	49643486	49643486	Human		name
407489900	CV3431010	single nucleotide variant	NM_001144955.2(DTWD1):c.581G>T (p.Cys194Phe)	not specified [RCV004620054]	uncertain significance	15	49634708	49634708	Human		name
597682991	CV3673831	single nucleotide variant	NM_001144955.2(DTWD1):c.532C>T (p.Arg178Cys)	not specified [RCV004914534]	uncertain significance	15	49634659	49634659	Human		name
597735034	CV3673832	single nucleotide variant	NM_001144955.2(DTWD1):c.430C>T (p.Pro144Ser)	not specified [RCV004920389]	uncertain significance	15	49634557	49634557	Human		name
597683836	CV3673834	single nucleotide variant	NM_001144955.2(DTWD1):c.673T>A (p.Leu225Ile)	not specified [RCV004914536]	uncertain significance	15	49643336	49643336	Human		name
598189594	CV3957390	single nucleotide variant	NM_001144955.2(DTWD1):c.346C>A (p.Pro116Thr)	not specified [RCV005334577]	uncertain significance	15	49632240	49632240	Human		name
598189600	CV3957391	single nucleotide variant	NM_001144955.2(DTWD1):c.587G>T (p.Gly196Val)	not specified [RCV005334578]	uncertain significance	15	49634714	49634714	Human		name

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Gene Annotator (Functional Annotation)	Gene Annotator (Annotation Distribution)	Variant Visualizer (Genomic Variants)

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