Cd69 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 Cd69

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RGD ID	Symbol	Variant Type	Name	Trait	Clinical Significance	Chr	Start	Stop	Species	Annotations	Match
8582508	CV117058	single nucleotide variant	NM_001781.2(CD69):c.*324G>A	Lung cancer [RCV000097579]	uncertain significance	12	9753157	9753157	Human		name
156222768	CV2343984	single nucleotide variant	NM_001781.2(CD69):c.38C>T (p.Ser13Phe)	not specified [RCV004195601]	uncertain significance	12	9760783	9760783	Human		name
156078905	CV2351146	single nucleotide variant	NM_001781.2(CD69):c.95G>A (p.Arg32His)	not specified [RCV004214001]	likely benign	12	9756389	9756389	Human		name
156051307	CV2367730	single nucleotide variant	NM_001781.2(CD69):c.66T>G (p.Asn22Lys)	not specified [RCV004213691]	uncertain significance	12	9756418	9756418	Human		name
15164631	CV702558	single nucleotide variant	NM_001781.2(CD69):c.531A>G (p.Lys177=)	not provided [RCV000948392]	benign	12	9753550	9753550	Human		name
597738846	CV3648482	single nucleotide variant	NM_001781.2(CD69):c.232T>C (p.Ser78Pro)	not specified [RCV004890204]	uncertain significance	12	9755217	9755217	Human		name
598207709	CV3950821	single nucleotide variant	NM_001781.2(CD69):c.116T>A (p.Val39Asp)	not specified [RCV005315332]	uncertain significance	12	9756368	9756368	Human		name
155924975	CV2248913	single nucleotide variant	NM_001781.2(CD69):c.356C>T (p.Thr119Ile)	not specified [RCV004115919]	uncertain significance	12	9755093	9755093	Human		name
156115819	CV2349332	single nucleotide variant	NM_001781.2(CD69):c.451C>T (p.His151Tyr)	not specified [RCV004199275]	uncertain significance	12	9754627	9754627	Human		name
598207697	CV3950819	single nucleotide variant	NM_001781.2(CD69):c.427G>A (p.Val143Ile)	not specified [RCV005315330]	likely benign	12	9754651	9754651	Human		name
598207703	CV3950820	single nucleotide variant	NM_001781.2(CD69):c.511G>A (p.Asp171Asn)	not specified [RCV005315331]	uncertain significance	12	9753570	9753570	Human		name