Related gene-specific medical variations for Gene (Select 23170) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3329986	NM_015140.4(TTLL12):c.47G>A (p.Ser16Asn)	LOC130067635, TTLL12 (S16N)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184570	NM_015140.4(TTLL12):c.95C>T (p.Ala32Val)	LOC130067634, TTLL12 (A32V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2467042	NM_015140.4(TTLL12):c.14G>A (p.Arg5Gln)	LOC130067635, TTLL12 (R5Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2410021	NM_015140.4(TTLL12):c.172C>G (p.His58Asp)	LOC130067634, TTLL12 (H58D)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2361124	NM_015140.4(TTLL12):c.10G>C (p.Glu4Gln)	LOC130067635, TTLL12 (E4Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2272701	NM_015140.4(TTLL12):c.28C>G (p.Arg10Gly)	LOC130067635, TTLL12 (R10G)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

ClinVar