Related gene-specific medical variations for Gene (Select 100128071) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3277410	NM_001167676.2(FAM229A):c.89C>A (p.Ala30Asp)	FAM229A, LOC129930041 (A30D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3092364	NM_001167676.2(FAM229A):c.34G>A (p.Ala12Thr)	FAM229A, LOC129930041 (A12T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2638609	NM_001167676.2(FAM229A):c.63A>C (p.Gly21=)	FAM229A, LOC129930041	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 2411059	NM_001167676.2(FAM229A):c.156G>C (p.Met52Ile)	FAM229A, LOC129930041 (M52I)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2347520	NM_001167676.2(FAM229A):c.227C>T (p.Ala76Val)	FAM229A, LOC129930041 (A76V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272962	NM_001167676.2(FAM229A):c.139C>T (p.Pro47Ser)	FAM229A, LOC129930041 (P47S)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2210998	NM_001167676.2(FAM229A):c.223G>A (p.Ala75Thr)	FAM229A, LOC129930041 (A75T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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