FAM228B[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 12

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3092362	NM_001145710.2(FAM228B):c.43C>A (p.Pro15Thr)	FAM228B (P15T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2220056	NM_001145710.2(FAM228B):c.75G>T (p.Glu25Asp)	FAM228B (E25D)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3092360	NM_001145710.2(FAM228B):c.219G>C (p.Lys73Asn)	FAM228B (K73N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3277408	NM_001145710.2(FAM228B):c.292T>C (p.Ser98Pro)	FAM228B (S98P)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2303424	NM_001145710.2(FAM228B):c.317G>A (p.Arg106Lys)	FAM228B (R106K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3092361	NM_001145710.2(FAM228B):c.374T>C (p.Ile125Thr)	FAM228B (I125T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2348949	NM_001145710.2(FAM228B):c.410A>G (p.Tyr137Cys)	FAM228B (Y137C)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2513203	NM_001145710.2(FAM228B):c.495T>G (p.Asp165Glu)	FAM228B (D165E +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2298398	NM_001145710.2(FAM228B):c.499G>A (p.Glu167Lys)	FAM228B (E167K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3277407	NM_001145710.2(FAM228B):c.653G>A (p.Arg218Lys)	FAM228B (R218K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2206655	NM_001145710.2(FAM228B):c.667G>A (p.Glu223Lys)	FAM228B (E86K +1 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 1184857	NM_001145710.2(FAM228B):c.907del (p.Gln303fs)	FAM228B (Q166fs +1 more)	Deletion (frameshift variant +1 more)	Essential tremor	GUncertain significance