ClinVar (all) for Orgtrack (Select 508222) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1210148	NM_031276.3(TEX11):c.812del (p.Lys271fs)	TEX11 (K271fs +1 more)	Deletion (frameshift variant)	Non-obstructive azoospermia	GPathogenic
Select item 1210147	NM_031276.3(TEX11):c.253del (p.Val85fs)	TEX11 (V100fs +1 more)	Deletion (frameshift variant)	Non-obstructive azoospermia	GPathogenic
Select item 1210146	NM_031276.3(TEX11):c.1208dup (p.Asn403fs)	TEX11 (N403fs +1 more)	Duplication (frameshift variant)	Non-obstructive azoospermia	GPathogenic
Select item 1210145	NM_031276.3(TEX11):c.1006G>T (p.Glu336Ter)	TEX11 (E336* +1 more)	Single nucleotide variant (nonsense)	Non-obstructive azoospermia	GPathogenic
Select item 1210144	NM_031276.3(TEX11):c.2568G>T (p.Trp856Cys)	TEX11 (W856C +1 more)	Single nucleotide variant (missense variant)	Non-obstructive azoospermia	GPathogenic
Select item 1210143	NM_031276.3(TEX11):c.1381-1G>A	TEX11	Single nucleotide variant (splice acceptor variant)	Non-obstructive azoospermia	GPathogenic
Select item 1210142	NM_031276.3(TEX11):c.1751+2T>G	TEX11	Single nucleotide variant (splice donor variant)	Non-obstructive azoospermia	GPathogenic

ClinVar