List of variants in gene TBX5 reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 16

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HGVS	dbSNP	gnomAD frequency
NM_181486.4(TBX5):c.982+16C>T	rs28730762	0.00694
NM_181486.4(TBX5):c.331G>T (p.Asp111Tyr)	rs77357563	0.00382
NM_181486.4(TBX5):c.836G>A (p.Arg279Gln)	rs115178276	0.00087
NM_181486.4(TBX5):c.316A>G (p.Ile106Val)	rs147710408	0.00086
NM_181486.4(TBX5):c.55G>T (p.Ala19Ser)	rs200461617	0.00054
NM_181486.4(TBX5):c.747A>G (p.Arg249=)	rs138552878	0.00051
NM_181486.4(TBX5):c.827G>A (p.Ser276Asn)	rs147977741	0.00049
NM_181486.4(TBX5):c.755+35A>G	rs199731693	0.00046
NM_181486.4(TBX5):c.354T>C (p.Asp118=)	rs151249768	0.00039
NM_181486.4(TBX5):c.865T>G (p.Ser289Ala)	rs543015692	0.00030
NM_181486.4(TBX5):c.948G>A (p.Glu316=)	rs767086503	0.00028
NM_181486.4(TBX5):c.600G>T (p.Ala200=)	rs139329918	0.00019
NM_181486.4(TBX5):c.1152G>A (p.Ala384=)	rs200073406	0.00009
NM_181486.4(TBX5):c.1545C>T (p.Ser515=)	rs186780790	0.00007
NM_181486.4(TBX5):c.1313G>A (p.Arg438Gln)	rs557758851	0.00001
NM_181486.4(TBX5):c.983-8C>T

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