Related gene-specific medical variations for Gene (Select 164118) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3329814	NM_001105669.4(TTC24):c.632G>A (p.Arg211Gln)	LOC129931634, TTC24 (R211Q)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184194	NM_001105669.4(TTC24):c.631C>T (p.Arg211Trp)	TTC24, LOC129931634 (R211W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 3184193	NM_001105669.4(TTC24):c.626G>A (p.Arg209Gln)	TTC24, LOC129931634 (R209Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2507848	NM_001105669.4(TTC24):c.571C>T (p.Arg191Trp)	LOC129931633, TTC24 (R191W)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2468416	NM_001105669.4(TTC24):c.514C>G (p.Leu172Val)	LOC129931633, TTC24 (L172V)	Single nucleotide variant (missense variant)	not specified	GUncertain significance
Select item 2284165	NM_001105669.4(TTC24):c.572G>A (p.Arg191Gln)	LOC129931633, TTC24 (R191Q)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2207972	NM_001105669.4(TTC24):c.496G>A (p.Ala166Thr)	LOC129931633, TTC24 (A166T)	Single nucleotide variant (missense variant)	not specified	GUncertain significance

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