Related gene-specific medical variations for Gene (Select 203068) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3359267	NM_178014.4(TUBB):c.281A>T (p.Gln94Leu)	TUBB (Q114L +3 more)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 3237496	NM_178014.4(TUBB):c.801G>T (p.Met267Ile)	TUBB (M195I +3 more)	Single nucleotide variant (missense variant +1 more)	Multiple benign circumferential skin creases on limbs 1 +1 more	GUncertain significance
Select item 1076997	NM_178014.4(TUBB):c.58-574C>A	TUBB (L29I)	Single nucleotide variant (missense variant +1 more)	Not Specified	Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant
Select item 1076996	NM_178014.4(TUBB):c.58-593_58-575del	TUBB (G23fs)	Deletion (frameshift variant +1 more)	Not Specified	Gno classification for the single variant Sno classification for the single variant Ono classification for the single variant
Select item 809889	NM_178014.4(TUBB):c.224_225del (p.Ser75fs)	TUBB (S75fs +3 more)	Microsatellite (frameshift variant +1 more)	not provided	GUncertain significance
Select item 376764	NM_178014.4(TUBB):c.533C>G (p.Thr178Ser)	TUBB (T178S +3 more)	Single nucleotide variant (missense variant +1 more)	not provided	GLikely pathogenic

ClinVar