Related gene-specific medical variations for Gene (Select 56155) - ClinVar

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3176294	NM_031272.5(TEX14):c.547G>A (p.Val183Met)	LOC130061306, TEX14 (V183M)	Single nucleotide variant (missense variant)	not specified	GLikely benign
Select item 2441771	NM_031272.5(TEX14):c.3652A>T (p.Arg1218Ter)	TEX14 (R1218* +2 more)	Single nucleotide variant (nonsense)	Spermatogenic failure 23	GLikely pathogenic
Select item 1809267	GRCh37/hg19 17q22(chr17:56654007-56712517)x1	TEX14	Copy number loss	not provided	GUncertain significance
Select item 1340303	GRCh37/hg19 17q22(chr17:56654008-56711888)x1	TEX14	Copy number loss	not provided	GLikely benign
Select item 815941	GRCh37/hg19 17q22(chr17:56629526-56680615)x1	TEX14	Copy number loss	not provided	GUncertain significance
Select item 685922	GRCh37/hg19 17q22(chr17:56721367-56766202)x1	TEX14	Copy number loss	not provided	GPathogenic
Select item 564456	GRCh37/hg19 17q22(chr17:56654006-56712517)x1	TEX14	Copy number loss	not provided	GLikely benign
Select item 161852	NM_031272.5(TEX14):c.3172-1908C>T	TEX14 (S1088L +1 more)	Single nucleotide variant (missense variant +1 more)	Malignant tumor of prostate	GUncertain significance

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