FAM107A[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 17

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3091623	NM_001076778.3(FAM107A):c.417C>G (p.Ser139Arg)	FAM107A (S170R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3091622	NM_001076778.3(FAM107A):c.416G>T (p.Ser139Ile)	FAM107A (S170I +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2241262	NM_001076778.3(FAM107A):c.415A>G (p.Ser139Gly)	FAM107A (S139G +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2398403	NM_001076778.3(FAM107A):c.413C>A (p.Thr138Asn)	FAM107A (T169N +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2489871	NM_001076778.3(FAM107A):c.365C>G (p.Pro122Arg)	FAM107A (P153R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2214226	NM_001076778.3(FAM107A):c.362C>T (p.Ala121Val)	FAM107A (A149V +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2210524	NM_001076778.3(FAM107A):c.307C>T (p.Arg103Trp)	FAM107A (R103W +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2274527	NM_001076778.3(FAM107A):c.272G>A (p.Arg91Gln)	FAM107A (R119Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2325157	NM_001076778.3(FAM107A):c.209T>A (p.Val70Asp)	FAM107A (V101D +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2340663	NM_001076778.3(FAM107A):c.146G>A (p.Arg49Gln)	FAM107A (R49Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3091621	NM_001076778.3(FAM107A):c.125G>A (p.Arg42Gln)	FAM107A (R42Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2326642	NM_001076778.3(FAM107A):c.121T>C (p.Ser41Pro)	FAM107A (S41P +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2277443	NM_001076778.3(FAM107A):c.67G>C (p.Glu23Gln)	FAM107A (E23Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 751950	NM_001076778.3(FAM107A):c.60A>G (p.Glu20=)	FAM107A	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 3091624	NM_001076778.3(FAM107A):c.47T>G (p.Met16Arg)	FAM107A (M16R +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2374132	NM_001076778.3(FAM107A):c.35T>C (p.Ile12Thr)	FAM107A (I12T +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2594473	NM_001076778.3(FAM107A):c.26G>A (p.Arg9Gln)	FAM107A (R37Q +2 more)	Single nucleotide variant (missense variant)	not specified	GUncertain significance