S100A16[gene] and "single gene"[properties] - ClinVar - NCBI

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Items: 9

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2375810	NM_080388.3(S100A16):c.287A>G (p.Glu96Gly)	S100A16 (E96G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2252181	NM_080388.3(S100A16):c.284A>G (p.His95Arg)	S100A16 (H95R)	Single nucleotide variant (missense variant +1 more)	not specified	GLikely benign
Select item 3157394	NM_080388.3(S100A16):c.281T>A (p.Ile94Asn)	S100A16 (I94N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3157393	NM_080388.3(S100A16):c.218G>A (p.Arg73His)	S100A16 (R73H)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2222068	NM_080388.3(S100A16):c.195C>A (p.Asn65Lys)	S100A16 (N65K)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2381874	NM_080388.3(S100A16):c.183G>C (p.Lys61Asn)	S100A16 (K61N)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3157392	NM_080388.3(S100A16):c.167G>T (p.Arg56Leu)	S100A16 (R56L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3157391	NM_080388.3(S100A16):c.166C>T (p.Arg56Trp)	S100A16 (R56W)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3157390	NM_080388.3(S100A16):c.116G>T (p.Arg39Leu)	S100A16 (R39L)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance