Ccl20 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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8 records found for search term Ccl20

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
597765732	CV3641535	single nucleotide variant	NM_004591.3(CCL20):c.26T>C (p.Leu9Pro)	not specified [RCV004895942]	uncertain significance	2	227813937	227813937	Human		name
15185717	CV733244	single nucleotide variant	NM_004591.3(CCL20):c.222C>T (p.Cys74=)	not provided [RCV000908605]	benign	2	227816337	227816337	Human		name
156201071	CV2362998	single nucleotide variant	NM_004591.3(CCL20):c.152G>A (p.Arg51Gln)	not specified [RCV004211139]	likely benign	2	227815529	227815529	Human		name
329377636	CV2435984	single nucleotide variant	NM_004591.3(CCL20):c.182A>G (p.Asn61Ser)	not specified [RCV004255206]	uncertain significance	2	227815559	227815559	Human		name
405739966	CV3292458	single nucleotide variant	NM_004591.3(CCL20):c.260G>A (p.Arg87His)	not specified [RCV004430547]	likely benign	2	227816375	227816375	Human		name
597762011	CV3641537	single nucleotide variant	NM_004591.3(CCL20):c.116G>A (p.Arg39His)	not specified [RCV004895065]	likely benign	2	227815493	227815493	Human		name
598192760	CV3939677	single nucleotide variant	NM_004591.3(CCL20):c.259C>T (p.Arg87Cys)	not specified [RCV005312841]	uncertain significance	2	227816374	227816374	Human		name
598192765	CV3939678	single nucleotide variant	NM_004591.3(CCL20):c.170G>T (p.Gly57Val)	not specified [RCV005312842]	uncertain significance	2	227815547	227815547	Human		name