List of variants in gene TBX5 reported as benign for not provided

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: 37

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HGVS	dbSNP	gnomAD frequency
NM_181486.4(TBX5):c.*1101A>G	rs6489956	0.80110
NM_181486.4(TBX5):c.983-146A>C	rs2113433	0.79600
NM_181486.4(TBX5):c.243-324C>T	rs1946299	0.72041
NM_181486.4(TBX5):c.-38-255T>C	rs2113436	0.68487
NM_181486.4(TBX5):c.663+186A>G	rs2236018	0.58134
NM_181486.4(TBX5):c.663+36G>T	rs2236017	0.54802
NM_000192.3(TBX5):c.-39+113A>G	rs1248046	0.31120
NM_181486.4(TBX5):c.755+94C>A	rs2277377	0.25733
NM_181486.4(TBX5):c.983-292A>G	rs73201491	0.18971
NM_181486.4(TBX5):c.*77A>G	rs28730761	0.07861
NM_181486.4(TBX5):c.148-206A>C	rs76448968	0.04732
NM_181486.4(TBX5):c.309C>T (p.Leu103=)	rs28730763	0.04319
NM_181486.4(TBX5):c.664-161T>C	rs16944184	0.03898
NM_181486.4(TBX5):c.243-284T>C	rs79492814	0.02260
NM_181486.4(TBX5):c.148-19T>A	rs80026530	0.01865
NM_181486.4(TBX5):c.1281C>T (p.Ser427=)	rs6489957	0.01766
NM_181486.4(TBX5):c.*40A>G	rs10850326	0.01186
NM_181486.4(TBX5):c.982+16C>T	rs28730762	0.00694
NM_181486.4(TBX5):c.663+34C>T	rs114389588	0.00446
NM_181486.4(TBX5):c.787G>A (p.Val263Met)	rs147405081	0.00423
NM_181486.4(TBX5):c.331G>T (p.Asp111Tyr)	rs77357563	0.00382
NM_181486.4(TBX5):c.1234G>A (p.Val412Ile)	rs114124210	0.00301
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.827G>A (p.Ser276Asn)	rs147977741	0.00049
NM_181486.4(TBX5):c.786C>T (p.Thr262=)	rs375955080	0.00006
NM_181486.4(TBX5):c.*97G>A	rs883079
NM_181486.4(TBX5):c.141C>T (p.Thr47=)	rs564730479
NM_181486.4(TBX5):c.244C>A (p.Arg82=)	rs1871673360
NM_181486.4(TBX5):c.362+84dup	rs55980450
NM_181486.4(TBX5):c.362+98del	rs55980450
NM_181486.4(TBX5):c.664-287_664-286dup	rs35970834
NM_181486.4(TBX5):c.664-287dup	rs35970834
NM_181486.4(TBX5):c.982+320_982+321dup	rs56315440
NM_181486.4(TBX5):c.982+320dup	rs56315440
NM_181486.4(TBX5):c.982+329_982+335del	rs56315440
NM_181486.4(TBX5):c.982+335del	rs56315440

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