List of variants in gene TDRD7 reported as uncertain significance by CeGaT Center for Human Genetics Tuebingen

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_014290.3(TDRD7):c.2791C>T (p.Pro931Ser)	rs146083361	0.00033
NM_014290.3(TDRD7):c.622A>G (p.Thr208Ala)	rs139706467	0.00029
NM_014290.3(TDRD7):c.1305G>T (p.Leu435Phe)	rs186876252	0.00012
NM_014290.3(TDRD7):c.911A>G (p.Lys304Arg)	rs1466116523	0.00001
NM_014290.3(TDRD7):c.2093A>T (p.Glu698Val)	rs2490700064
NM_014290.3(TDRD7):c.2579C>T (p.Pro860Leu)	rs1384859480
NM_014290.3(TDRD7):c.419_427dup (p.Pro142_Leu143insSerAlaPro)	rs2490585220

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