ClinVar for MedGen (Select 1684744) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 805961	NM_031956.4(TTC29):c.977+1G>T	TTC29	Single nucleotide variant (splice donor variant)	Spermatogenic failure 42	GPathogenic
Select item 805960	NM_031956.4(TTC29):c.412_425del (p.Asp138fs)	TTC29 (D164fs +1 more)	Deletion (frameshift variant +1 more)	Spermatogenic failure 42	GPathogenic
Select item 805959	NM_031956.4(TTC29):c.1107C>G (p.Tyr369Ter)	TTC29 (Y369* +1 more)	Single nucleotide variant (nonsense +1 more)	Spermatogenic failure 42	GPathogenic
Select item 805958	NM_031956.4(TTC29):c.750C>A (p.Tyr250Ter)	TTC29 (Y250* +1 more)	Single nucleotide variant (nonsense +1 more)	Spermatogenic failure 42	GPathogenic
Select item 805957	NM_031956.4(TTC29):c.330_334del (p.Glu111fs)	TTC29 (E137fs +1 more)	Deletion (frameshift variant +1 more)	Spermatogenic failure 42	GPathogenic
Select item 805956	NM_031956.4(TTC29):c.*334G>A	TTC29	Single nucleotide variant (3 prime UTR variant +1 more)	Spermatogenic failure 42	GPathogenic

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