EXOC6[gene] and "single gene"[properties] - ClinVar

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Items: 28

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2459641	NM_019053.6(EXOC6):c.18G>C (p.Glu6Asp)	EXOC6 (E6D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3091138	NM_019053.6(EXOC6):c.23T>C (p.Leu8Pro)	EXOC6 (L8P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3276805	NM_019053.6(EXOC6):c.31G>C (p.Val11Leu)	EXOC6 (V11L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3091135	NM_019053.6(EXOC6):c.158C>T (p.Ala53Val)	EXOC6 (A48V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2560258	NM_019053.6(EXOC6):c.167G>A (p.Arg56His)	EXOC6 (R72H +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2542362	NM_019053.6(EXOC6):c.267A>C (p.Lys89Asn)	EXOC6 (K89N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3276806	NM_019053.6(EXOC6):c.337G>A (p.Glu113Lys)	EXOC6 (E108K +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2533175	NM_019053.6(EXOC6):c.343A>G (p.Ile115Val)	EXOC6 (I115V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2208088	NM_019053.6(EXOC6):c.347T>C (p.Ile116Thr)	EXOC6 (I111T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2640680	NM_019053.6(EXOC6):c.387A>G (p.Val129=)	EXOC6	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2368134	NM_019053.6(EXOC6):c.390A>C (p.Glu130Asp)	EXOC6 (E125D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3091139	NM_019053.6(EXOC6):c.616A>G (p.Ser206Gly)	EXOC6 (S201G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2465044	NM_019053.6(EXOC6):c.652G>A (p.Ala218Thr)	EXOC6 (A234T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2230054	NM_019053.6(EXOC6):c.691T>C (p.Ser231Pro)	EXOC6 (S226P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214187	NM_019053.6(EXOC6):c.842T>A (p.Val281Asp)	EXOC6 (V281D +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3091141	NM_019053.6(EXOC6):c.863G>A (p.Arg288Gln)	EXOC6 (R288Q +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2541477	NM_019053.6(EXOC6):c.1105C>T (p.Leu369Phe)	EXOC6 (L369F +2 more)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3091133	NM_019053.6(EXOC6):c.1396C>G (p.Gln466Glu)	EXOC6 (Q461E +3 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3276804	NM_019053.6(EXOC6):c.1523G>A (p.Arg508Gln)	EXOC6 (R405Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2227655	NM_019053.6(EXOC6):c.1686A>C (p.Lys562Asn)	EXOC6 (K459N +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2292186	NM_019053.6(EXOC6):c.1688A>C (p.Tyr563Ser)	EXOC6 (Y460S +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3091136	NM_019053.6(EXOC6):c.1709A>T (p.Asn570Ile)	EXOC6 (N586I +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3276803	NM_019053.6(EXOC6):c.1717A>G (p.Asn573Asp)	EXOC6 (N470D +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3091137	NM_019053.6(EXOC6):c.1781G>A (p.Arg594Gln)	EXOC6 (R491Q +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2338463	NM_019053.6(EXOC6):c.2155A>G (p.Ile719Val)	EXOC6 (I714V +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2592980	NM_019053.6(EXOC6):c.2293A>G (p.Thr765Ala)	EXOC6 (T760A +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2462522	NM_019053.6(EXOC6):c.2338C>G (p.Arg780Gly)	EXOC6 (R677G +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2412000	NM_019053.6(EXOC6):c.2368G>A (p.Val790Met)	EXOC6 (V789M +4 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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Items: 28