Related gene-specific medical variations for Gene (Select 80312) - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2690229	NM_030625.3(TET1):c.5716G>A (p.Glu1906Lys)	TET1 (E1075K +8 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 2428722	NM_030625.3(TET1):c.3974T>A (p.Val1325Asp)	TET1 (V1325D +2 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 687206	GRCh37/hg19 10q21.3(chr10:70290828-70428321)x3	TET1	Copy number gain	not provided	GUncertain significance

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