"Ambry Genetics"[submitter] AND "CHRNA6"[gene] - ClinVar - NCBI

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Items: 15

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2487044	NM_004198.3(CHRNA6):c.1368G>T (p.Trp456Cys)	CHRNA6 (W456C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2370628	NM_004198.3(CHRNA6):c.1277C>G (p.Ser426Trp)	CHRNA6 (S426W +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462644	NM_004198.3(CHRNA6):c.1244C>T (p.Pro415Leu)	CHRNA6 (P415L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3267174	NM_004198.3(CHRNA6):c.1186T>C (p.Phe396Leu)	CHRNA6 (F381L +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2332430	NM_004198.3(CHRNA6):c.1025A>G (p.Lys342Arg)	CHRNA6 (K342R +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2596970	NM_004198.3(CHRNA6):c.1006A>G (p.Thr336Ala)	CHRNA6 (T321A +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2350027	NM_004198.3(CHRNA6):c.997A>G (p.Thr333Ala)	CHRNA6 (T333A +1 more)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2328861	NM_004198.3(CHRNA6):c.992C>T (p.Thr331Ile)	CHRNA6 (T316I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2205930	NM_004198.3(CHRNA6):c.989G>A (p.Arg330His)	CHRNA6 (R315H +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3144633	NM_004198.3(CHRNA6):c.923T>A (p.Leu308Gln)	CHRNA6 (L293Q +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2278969	NM_004198.3(CHRNA6):c.887C>T (p.Thr296Ile)	CHRNA6 (T296I +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3144632	NM_004198.3(CHRNA6):c.884C>T (p.Ser295Phe)	CHRNA6 (S280F +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3144631	NM_004198.3(CHRNA6):c.286C>T (p.Arg96Cys)	CHRNA6 (R81C +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2520900	NM_004198.3(CHRNA6):c.128C>T (p.Ser43Phe)	CHRNA6 (S43F)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2463042	NM_004198.3(CHRNA6):c.49T>C (p.Trp17Arg)	CHRNA6 (W17R)	Single nucleotide variant (missense variant)	not specified	GUncertain significance