ClinVar for MedGen (Select 374322) - ClinVar

VariationLocation		Gene(s)	Protein change	Condition(s)	Clinical significance (Last reviewed)	Review status
Select item 1923811.	NM_031276.3(TEX11):c.405C>T (p.Ala135=) GRCh37: ChrX:70073098 GRCh38: ChrX:70853248	TEX11		not provided	Benign/Likely benign (Apr 1, 2023)	criteria provided, multiple submitters, no conflicts
Select item 1923802.	NM_031276.3(TEX11):c.2047G>A (p.Ala683Thr) GRCh37: ChrX:69825271 GRCh38: ChrX:70605421	TEX11	A698T, A683T	not specified, not provided	Conflicting interpretations of pathogenicity (May 4, 2022)	criteria provided, conflicting interpretations
Select item 1923793.	NM_031276.3(TEX11):c.466A>G (p.Met156Val) GRCh37: ChrX:70072943 GRCh38: ChrX:70853093	TEX11	M171V, M156V	not specified, not provided	Conflicting interpretations of pathogenicity (May 4, 2022)	criteria provided, conflicting interpretations
Select item 1923784.	NC_000023.10:g.69954448_70045530del GRCh37: ChrX:69954448-70045530	TEX11		Spermatogenic failure, X-linked, 2	Pathogenic (May 28, 2015)	no assertion criteria provided

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