Related gene-specific medical variations for Gene (Select 170690) - ClinVar - NCBI

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Items: 10

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3266921	NM_139056.4(ADAMTS16):c.457T>A (p.Ser153Thr)	ADAMTS16, LOC126807300 (S153T)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3266859	NM_139056.4(ADAMTS16):c.299G>A (p.Arg100Gln)	ADAMTS16, LOC126807300 (R100Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 3147619	NM_139056.4(ADAMTS16):c.331G>T (p.Asp111Tyr)	ADAMTS16, LOC126807300 (D111Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2559641	NM_139056.4(ADAMTS16):c.238A>G (p.Met80Val)	ADAMTS16, LOC126807300 (M80V)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2353076	NM_139056.4(ADAMTS16):c.254G>A (p.Arg85Gln)	ADAMTS16, LOC126807300 (R85Q)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2349405	NM_139056.4(ADAMTS16):c.284A>G (p.Glu95Gly)	ADAMTS16, LOC126807300 (E95G)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 2321171	NM_139056.4(ADAMTS16):c.460C>T (p.His154Tyr)	ADAMTS16, LOC126807300 (H154Y)	Single nucleotide variant (missense variant +1 more)	not specified	GUncertain significance
Select item 979668	GRCh37/hg19 5p15.32(chr5:4798963-5166195)x3	ADAMTS16	Copy number gain	not provided	GUncertain significance
Select item 685725	GRCh37/hg19 5p15.33-15.32(chr5:4162339-5309811)x3	ADAMTS16	Copy number gain	not provided	GUncertain significance
Select item 563030	GRCh37/hg19 5p15.32(chr5:4766315-5313790)x3	ADAMTS16	Copy number gain	not provided	GLikely benign