Related gene-specific medical variations for Gene (Select 51807) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2036635	NM_018943.3(TUBA8):c.3+15G>T	LOC130066945, TUBA8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1916347	NM_018943.3(TUBA8):c.-2_3+5del	LOC130066945, TUBA8	Deletion (splice donor variant +2 more)	not provided	GUncertain significance
Select item 1650004	NM_018943.3(TUBA8):c.3+17C>G	LOC130066945, TUBA8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1350951	NM_018943.3(TUBA8):c.3+2T>G	LOC130066945, TUBA8	Single nucleotide variant (splice donor variant +1 more)	not provided	GUncertain significance
Select item 1198662	NM_018943.3(TUBA8):c.3+48G>A	LOC130066945, TUBA8	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 809315	NM_018943.3(TUBA8):c.818C>T (p.Ala273Val)	TUBA8 (A207V +1 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 384315	NM_018943.3(TUBA8):c.-7G>C	LOC130066945, TUBA8	Single nucleotide variant (5 prime UTR variant +1 more)	TUBA8-related condition +1 more	GLikely benign

ClinVar