Hddc3 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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11 records found for search term Hddc3

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597695935	CV3679172	single nucleotide variant	NM_001286451.2(HDDC3):c.76G>T (p.Asp26Tyr)	not specified [RCV004930965]	uncertain significance	15	90932465	90932465	Human		name
597695945	CV3679174	single nucleotide variant	NM_001286451.2(HDDC3):c.47C>T (p.Ala16Val)	not specified [RCV004930966]	uncertain significance	15	90932494	90932494	Human		name
598266498	CV3967769	single nucleotide variant	NM_001286451.2(HDDC3):c.59G>C (p.Arg20Pro)	not specified [RCV005349292]	uncertain significance	15	90932482	90932482	Human		name
598266503	CV3967770	single nucleotide variant	NM_001286451.2(HDDC3):c.31G>A (p.Ala11Thr)	not specified [RCV005349293]	uncertain significance	15	90932510	90932510	Human		name
407483329	CV3440265	single nucleotide variant	NM_001286451.2(HDDC3):c.290A>G (p.Lys97Arg)	not specified [RCV004627643]	uncertain significance	15	90931823	90931823	Human		name
329349904	CV2462821	single nucleotide variant	NM_001286451.2(HDDC3):c.332G>A (p.Ser111Asn)	not specified [RCV004278729]	uncertain significance	15	90931781	90931781	Human		name
401902361	CV2814498	single nucleotide variant	NM_001286451.2(HDDC3):c.414G>A (p.Trp138Ter)	not provided [RCV003390558]	likely benign	15	90931401	90931401	Human		name
405796304	CV3266541	single nucleotide variant	NM_001286451.2(HDDC3):c.392A>G (p.Asn131Ser)	not specified [RCV004401533]	uncertain significance	15	90931721	90931721	Human		name
405796307	CV3266542	single nucleotide variant	NM_001286451.2(HDDC3):c.394C>A (p.Arg132Ser)	not specified [RCV004401534]	uncertain significance	15	90931719	90931719	Human		name
597694013	CV3679171	single nucleotide variant	NM_001286451.2(HDDC3):c.340G>A (p.Gly114Arg)	not specified [RCV004917494]	uncertain significance	15	90931773	90931773	Human		name
597694025	CV3679173	single nucleotide variant	NM_001286451.2(HDDC3):c.403C>G (p.Pro135Ala)	not specified [RCV004917495]	uncertain significance	15	90931710	90931710	Human		name