List of variants in gene TDRD7 reported as likely benign for cataract

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 17

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HGVS	dbSNP	gnomAD frequency
NM_014290.3(TDRD7):c.1800T>C (p.Cys600=)	rs12552100	0.00769
NM_014290.3(TDRD7):c.1341C>T (p.Thr447=)	rs143511562	0.00035
NM_014290.3(TDRD7):c.2079+7C>T	rs201253435	0.00035
NM_014290.3(TDRD7):c.444C>T (p.Asn148=)	rs144510531	0.00033
NM_014290.3(TDRD7):c.622A>G (p.Thr208Ala)	rs139706467	0.00029
NM_014290.3(TDRD7):c.391A>G (p.Asn131Asp)	rs200841827	0.00009
NM_014290.3(TDRD7):c.1032A>G (p.Lys344=)	rs111320552	0.00002
NM_014290.3(TDRD7):c.2223T>C (p.Thr741=)	rs374967438	0.00001
NM_014290.3(TDRD7):c.2955A>G (p.Gly985=)	rs201216195	0.00001
NM_014290.3(TDRD7):c.1857G>A (p.Leu619=)
NM_014290.3(TDRD7):c.2025T>A (p.Gly675=)	rs1828958858
NM_014290.3(TDRD7):c.2338A>G (p.Ile780Val)
NM_014290.3(TDRD7):c.2412+8A>G
NM_014290.3(TDRD7):c.2841A>G (p.Leu947=)
NM_014290.3(TDRD7):c.2915+11G>A
NM_014290.3(TDRD7):c.624T>C (p.Thr208=)
NM_014290.3(TDRD7):c.825A>G (p.Gln275=)

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