Dmc1 Variant Search Result - Rat Genome Database

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24 records found for search term Dmc1

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
401770268	CV2715108	single nucleotide variant	NM_007068.4(DMC1):c.56C>A (p.Ser19Tyr)	not specified [RCV004322689]	uncertain significance	22	38567623	38567623	Human		name
155912220	CV2308699	single nucleotide variant	NM_007068.4(DMC1):c.208G>A (p.Val70Ile)	not specified [RCV004169029]	uncertain significance	22	38566625	38566625	Human		name
405670116	CV3240632	single nucleotide variant	NM_007068.4(DMC1):c.222A>T (p.Lys74Asn)	not specified [RCV004368493]	uncertain significance	22	38566611	38566611	Human		name
597801774	CV3658993	single nucleotide variant	NM_007068.4(DMC1):c.131G>A (p.Gly44Glu)	not specified [RCV004906380]	uncertain significance	22	38566702	38566702	Human		name
597848963	CV3762277	single nucleotide variant	NM_007068.4(DMC1):c.164C>T (p.Thr55Ile)	Non-obstructive azoospermia [RCV005087697]	likely pathogenic	22	38566669	38566669	Human	2	name
14351044	CV590633	single nucleotide variant	NM_007068.4(DMC1):c.106G>A (p.Asp36Asn)	not provided [RCV000735974]	uncertain significance	22	38566727	38566727	Human		name
151236186	CV1319631	single nucleotide variant	NM_007068.4(DMC1):c.364A>G (p.Thr122Ala)	Azoospermia [RCV001797567]	pathogenic	22	38555372	38555372	Human	2	name
151236187	CV1319632	single nucleotide variant	NM_007068.4(DMC1):c.860C>A (p.Pro287His)	Azoospermia [RCV001797568]	pathogenic	22	38521701	38521701	Human	2	name
156125338	CV2237564	single nucleotide variant	NM_007068.4(DMC1):c.747G>A (p.Met249Ile)	not specified [RCV004106504]	uncertain significance	22	38538323	38538323	Human		name
156284216	CV2291889	single nucleotide variant	NM_007068.4(DMC1):c.527G>A (p.Arg176His)	not specified [RCV004158411]	uncertain significance	22	38539380	38539380	Human		name
156163816	CV2376188	single nucleotide variant	NM_007068.4(DMC1):c.539A>G (p.Asp180Gly)	not specified [RCV004220414]	uncertain significance	22	38539368	38539368	Human		name
156156488	CV2388867	single nucleotide variant	NM_007068.4(DMC1):c.730C>A (p.Gln244Lys)	not specified [RCV004239708]	uncertain significance	22	38538340	38538340	Human		name
401874905	CV2781354	single nucleotide variant	NM_007068.4(DMC1):c.851C>T (p.Pro284Leu)	not specified [RCV004352363]	uncertain significance	22	38521710	38521710	Human		name
405670121	CV3240633	single nucleotide variant	NM_007068.4(DMC1):c.301A>G (p.Ile101Val)	not specified [RCV004368494]	uncertain significance	22	38562312	38562312	Human		name
405670125	CV3240634	single nucleotide variant	NM_007068.4(DMC1):c.679G>A (p.Ala227Thr)	not specified [RCV004368495]	uncertain significance	22	38538391	38538391	Human		name
405670130	CV3240635	single nucleotide variant	NM_007068.4(DMC1):c.707G>T (p.Arg236Leu)	not specified [RCV004368496]	uncertain significance	22	38538363	38538363	Human		name
597848966	CV3762278	single nucleotide variant	NM_007068.4(DMC1):c.490A>G (p.Thr164Ala)	Non-obstructive azoospermia [RCV005087698]	likely pathogenic	22	38549929	38549929	Human	2	name
597848969	CV3762279	single nucleotide variant	NM_007068.4(DMC1):c.581A>G (p.Tyr194Cys)	Non-obstructive azoospermia [RCV005087699]	likely pathogenic	22	38539326	38539326	Human	2	name
597848971	CV3762280	single nucleotide variant	NM_007068.4(DMC1):c.479A>G (p.Asp160Gly)	Cryptozoospermia [RCV005087700]	uncertain significance	22	38549940	38549940	Human	2	name
598184876	CV3960343	single nucleotide variant	NM_007068.4(DMC1):c.985G>A (p.Ala329Thr)	not specified [RCV005333753]	uncertain significance	22	38520058	38520058	Human		name
598184884	CV3960344	single nucleotide variant	NM_007068.4(DMC1):c.310G>A (p.Gly104Arg)	not specified [RCV005333754]	uncertain significance	22	38562303	38562303	Human		name
598184890	CV3960345	single nucleotide variant	NM_007068.4(DMC1):c.526C>T (p.Arg176Cys)	not specified [RCV005333755]	uncertain significance	22	38539381	38539381	Human		name
598184895	CV3960346	single nucleotide variant	NM_007068.4(DMC1):c.476T>C (p.Ile159Thr)	not specified [RCV005333756]	uncertain significance	22	38549943	38549943	Human		name
40816154	CV967238	single nucleotide variant	NM_007068.4(DMC1):c.598A>G (p.Met200Val)	Premature ovarian failure [RCV001258296]\|not provided [RCV004714211]	benign	22	38538601	38538601	Human	2	name

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