Ccl17 Variant Search Result - Rat Genome Database

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Variants search result for Homo sapiens
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12 records found for search term Ccl17

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
15199423	CV726707	single nucleotide variant	NM_002987.3(CCL17):c.84T>C (p.Asn28=)	not provided [RCV000890630]	benign	16	57415094	57415094	Human		name
156330725	CV2210689	single nucleotide variant	NM_002987.3(CCL17):c.92G>A (p.Arg31Gln)	not specified [RCV004083830]	uncertain significance	16	57415102	57415102	Human		name
405739923	CV3292452	single nucleotide variant	NM_002987.3(CCL17):c.46G>A (p.Ala16Thr)	not specified [RCV004430541]	uncertain significance	16	57413978	57413978	Human		name
407491480	CV3428548	single nucleotide variant	NM_002987.3(CCL17):c.77G>T (p.Gly26Val)	not specified [RCV004604756]	uncertain significance	16	57415087	57415087	Human		name
407491485	CV3428549	single nucleotide variant	NM_002987.3(CCL17):c.28G>T (p.Val10Phe)	not specified [RCV004604757]	uncertain significance	16	57413960	57413960	Human		name
598192748	CV3939674	single nucleotide variant	NM_002987.3(CCL17):c.74G>A (p.Arg25Gln)	not specified [RCV005312839]	uncertain significance	16	57415084	57415084	Human		name
156345767	CV2356360	single nucleotide variant	NM_002987.3(CCL17):c.205G>A (p.Gly69Ser)	not specified [RCV004206163]	uncertain significance	16	57415781	57415781	Human		name
156072179	CV2365367	single nucleotide variant	NM_002987.3(CCL17):c.119G>A (p.Gly40Glu)	not specified [RCV004209451]	uncertain significance	16	57415129	57415129	Human		name
401861539	CV2779845	single nucleotide variant	NM_002987.3(CCL17):c.121G>A (p.Ala41Thr)	not specified [RCV004353465]	uncertain significance	16	57415131	57415131	Human		name
407491490	CV3428550	single nucleotide variant	NM_002987.3(CCL17):c.182C>T (p.Ala61Val)	not specified [RCV004604758]	uncertain significance	16	57415192	57415192	Human		name
597765710	CV3641529	single nucleotide variant	NM_002987.3(CCL17):c.126T>G (p.Ile42Met)	not specified [RCV004895936]	uncertain significance	16	57415136	57415136	Human		name
598192755	CV3939675	single nucleotide variant	NM_002987.3(CCL17):c.187G>A (p.Val63Ile)	not specified [RCV005312840]	uncertain significance	16	57415197	57415197	Human		name