Mbd3 Variant Search Result - Rat Genome Database

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25 records found for search term Mbd3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15106932	CV786102	single nucleotide variant	NM_001281453.2(MBD3):c.24C>T (p.Cys8=)	not provided [RCV000976723]	likely benign	19	1592608	1592608	Human		name
15173428	CV727993	single nucleotide variant	NM_001281453.2(MBD3):c.276G>A (p.Lys92=)	not provided [RCV000884021]	benign	19	1584672	1584672	Human		name
15103775	CV727992	single nucleotide variant	NM_001281453.2(MBD3):c.591G>A (p.Ser197=)	not provided [RCV000892747]	likely benign	19	1581178	1581178	Human		name
8628223	CV83367	single nucleotide variant	NM_001281453.1(MBD3):c.677G>A (p.Arg226Lys)	Malignant melanoma [RCV000063447]	not provided	19	1581092	1581092	Human		name
401928422	CV2815315	single nucleotide variant	NM_144614.4(MBD3L2):c.387A>G (p.Arg129=)	not provided [RCV003406811]	likely benign	19	7051382	7051382	Human		name
617149228	CV4021552	single nucleotide variant	NM_001164425.4(MBD3L3):c.91C>A (p.Arg31=)	not provided [RCV005425521]	likely benign	19	7056858	7056858	Human		name
401874676	CV2759315	single nucleotide variant	NM_001393532.1(MBD3L1):c.61G>C (p.Gly21Arg)	not specified [RCV004335899]	uncertain significance	19	8842739	8842739	Human		name
407472826	CV3457064	single nucleotide variant	NM_001393532.1(MBD3L1):c.76A>G (p.Ile26Val)	not specified [RCV004637727]	uncertain significance	19	8842754	8842754	Human		name
598199687	CV3981784	single nucleotide variant	NM_001393532.1(MBD3L1):c.29G>A (p.Arg10His)	not specified [RCV005375733]	uncertain significance	19	8842707	8842707	Human		name
156085755	CV2205681	single nucleotide variant	NM_001393532.1(MBD3L1):c.251C>T (p.Ser84Leu)	not specified [RCV004075746]	likely benign	19	8842929	8842929	Human		name
156311556	CV2260197	single nucleotide variant	NM_001393532.1(MBD3L1):c.107A>C (p.Lys36Thr)	not specified [RCV004120974]	uncertain significance	19	8842785	8842785	Human		name
329376331	CV2425075	single nucleotide variant	NM_001393532.1(MBD3L1):c.214C>A (p.Gln72Lys)	not specified [RCV004248971]	uncertain significance	19	8842892	8842892	Human		name
401721736	CV2710135	single nucleotide variant	NM_001393532.1(MBD3L1):c.187C>G (p.Gln63Glu)	not specified [RCV004315186]	uncertain significance	19	8842865	8842865	Human		name
405659627	CV3278168	single nucleotide variant	NM_001393532.1(MBD3L1):c.119C>T (p.Thr40Met)	not specified [RCV004416843]	uncertain significance	19	8842797	8842797	Human		name
597637850	CV3694463	single nucleotide variant	NM_001393532.1(MBD3L1):c.166G>C (p.Glu56Gln)	not specified [RCV004941048]	uncertain significance	19	8842844	8842844	Human		name
597637855	CV3694464	single nucleotide variant	NM_001393532.1(MBD3L1):c.257C>T (p.Thr86Ile)	not specified [RCV004941049]	uncertain significance	19	8842935	8842935	Human		name
598177605	CV3981782	single nucleotide variant	NM_001393532.1(MBD3L1):c.163T>A (p.Trp55Arg)	not specified [RCV005371625]	uncertain significance	19	8842841	8842841	Human		name
156063689	CV2331029	single nucleotide variant	NM_001393532.1(MBD3L1):c.580C>T (p.Arg194Cys)	not specified [RCV004188067]	uncertain significance	19	8843258	8843258	Human		name
156075322	CV2331729	single nucleotide variant	NM_001393532.1(MBD3L1):c.571C>A (p.Pro191Thr)	not specified [RCV004184355]	uncertain significance	19	8843249	8843249	Human		name
405659630	CV3278169	single nucleotide variant	NM_001393532.1(MBD3L1):c.317T>C (p.Leu106Pro)	not specified [RCV004416844]	likely benign	19	8842995	8842995	Human		name
405659638	CV3278171	single nucleotide variant	NM_001393532.1(MBD3L1):c.482T>C (p.Val161Ala)	not specified [RCV004416846]	uncertain significance	19	8843160	8843160	Human		name
597637845	CV3694462	single nucleotide variant	NM_001393532.1(MBD3L1):c.502C>T (p.Leu168Phe)	not specified [RCV004941047]	uncertain significance	19	8843180	8843180	Human		name
598177598	CV3981780	single nucleotide variant	NM_001393532.1(MBD3L1):c.515T>G (p.Leu172Arg)	not specified [RCV005371624]	uncertain significance	19	8843193	8843193	Human		name
598199680	CV3981781	single nucleotide variant	NM_001393532.1(MBD3L1):c.524A>G (p.Asp175Gly)	not specified [RCV005375732]	uncertain significance	19	8843202	8843202	Human		name
598177612	CV3981783	single nucleotide variant	NM_001393532.1(MBD3L1):c.424C>G (p.Leu142Val)	not specified [RCV005371626]	uncertain significance	19	8843102	8843102	Human		name

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