CDRT15[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 16

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2366758	NM_001007530.3(CDRT15):c.487C>T (p.Leu163Phe)	CDRT15 (L97F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2558830	NM_001007530.3(CDRT15):c.422A>G (p.Glu141Gly)	CDRT15 (E141G +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141716	NM_001007530.3(CDRT15):c.419C>T (p.Pro140Leu)	CDRT15 (P74L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2296201	NM_001007530.3(CDRT15):c.338C>A (p.Pro113His)	CDRT15 (P47H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2478914	NM_001007530.3(CDRT15):c.305C>T (p.Ala102Val)	CDRT15 (A102V +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3141715	NM_001007530.3(CDRT15):c.274T>C (p.Cys92Arg)	CDRT15 (C26R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326639	NM_001007530.3(CDRT15):c.271C>G (p.Pro91Ala)	CDRT15 (P25A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3265606	NM_001007530.3(CDRT15):c.259C>T (p.Leu87Phe)	CDRT15 (L87F)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2455416	NM_001007530.3(CDRT15):c.245T>C (p.Ile82Thr)	CDRT15 (I82T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2482856	NM_001007530.3(CDRT15):c.199G>A (p.Gly67Arg)	CDRT15 (G67R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3265609	NM_001007530.3(CDRT15):c.172G>A (p.Gly58Ser)	CDRT15 (G58S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2225679	NM_001007530.3(CDRT15):c.113C>T (p.Ser38Leu)	CDRT15 (S38L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3141717	NM_001007530.3(CDRT15):c.56G>A (p.Ser19Asn)	CDRT15 (S19N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3265607	NM_001007530.3(CDRT15):c.49G>A (p.Gly17Arg)	CDRT15 (G17R)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3265608	NM_001007530.3(CDRT15):c.43A>G (p.Arg15Gly)	CDRT15 (R15G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3141713	NM_001007530.3(CDRT15):c.19C>T (p.Pro7Ser)	CDRT15 (P7S)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance