List of variants in gene TNNT2 reported as benign for not specified

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: 44

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HGVS	dbSNP	gnomAD frequency
NM_001276345.2(TNNT2):c.601-32A>C	rs1104859	0.73965
NM_001276345.2(TNNT2):c.348C>T (p.Ile116=)	rs3729547	0.69444
NM_001276345.2(TNNT2):c.811-122C>G	rs45509695	0.22049
NM_001276345.2(TNNT2):c.811-33C>T	rs2275863	0.22049
NM_001276345.2(TNNT2):c.237G>A (p.Ser79=)	rs3729845	0.08311
NM_001276345.2(TNNT2):c.788A>G (p.Lys263Arg)	rs3730238	0.05965
NM_001276345.2(TNNT2):c.610-90G>A	rs11810834	0.03251
NM_001276345.2(TNNT2):c.163+12G>A	rs45580032	0.01441
NM_001276345.2(TNNT2):c.851+22C>T	rs45495692	0.01327
NM_001276345.2(TNNT2):c.42-20G>A	rs45561443	0.01192
NM_001276345.2(TNNT2):c.294+7G>A	rs45490292	0.01066
NM_001276345.2(TNNT2):c.68-8A>G	rs115805892	0.00864
NM_001276345.2(TNNT2):c.610-81C>T	rs28730745	0.00831
NM_001276345.2(TNNT2):c.474G>C (p.Arg158=)	rs35914325	0.00788
NM_001276345.2(TNNT2):c.200-29C>G	rs45449197	0.00690
NM_001276345.2(TNNT2):c.52+48G>A	rs45582534	0.00432
NM_001276345.2(TNNT2):c.68-3del	rs200153031	0.00133
NM_001276345.2(TNNT2):c.68-5C>T	rs540630390	0.00133
NM_000364.3(TNNT2):c.113C>T (p.Ala38Val)	rs200754249	0.00046
NM_001276345.2(TNNT2):c.200-11A>G	rs368658464	0.00021
NM_001276345.2(TNNT2):c.852-19C>T	rs759855940	0.00011
NM_001276345.2(TNNT2):c.295-19C>T	rs587780969	0.00009
NM_001276345.2(TNNT2):c.837C>T (p.Asn279=)	rs376923877	0.00009
NM_001276345.2(TNNT2):c.52+7G>A	rs374443596	0.00007
NM_001276345.2(TNNT2):c.114G>A (p.Ala38=)	rs200283086	0.00006
NM_001276345.2(TNNT2):c.489+18C>T	rs377743847	0.00006
NM_001276345.2(TNNT2):c.601-8C>T	rs397516475	0.00006
NM_001276345.2(TNNT2):c.52+13G>A	rs376820377	0.00004
NM_001276345.2(TNNT2):c.435C>T (p.Ala145=)	rs375675827	0.00003
NM_001276345.2(TNNT2):c.282A>G (p.Arg94=)	rs397516453	0.00002
NM_001276345.2(TNNT2):c.63T>G (p.Val21=)	rs397516477	0.00002
NM_001276345.2(TNNT2):c.720-6G>A	rs113471285	0.00002
NM_001276345.2(TNNT2):c.144C>T (p.Thr48=)	rs746492909	0.00001
NM_001276345.2(TNNT2):c.200-4C>G	rs397516448	0.00001
NM_001276345.2(TNNT2):c.450C>T (p.Ile150=)	rs200604266	0.00001
NM_001276345.2(TNNT2):c.522C>T (p.Asn174=)	rs483352833	0.00001
NM_001001430.3(TNNT2):c.68-1623_68-1621delinsTT	rs397516362
NM_001276345.2(TNNT2):c.164-50G>A	rs3729843
NM_001276345.2(TNNT2):c.270C>T (p.Pro90=)	rs140245123
NM_001276345.2(TNNT2):c.412-6_412-4del	rs397516462
NM_001276345.2(TNNT2):c.53-11_53-7del	rs45533739
NM_001276345.2(TNNT2):c.68-3C>T	rs587780970
NM_001276345.2(TNNT2):c.719+13A>C	rs563883763
NM_001276345.2(TNNT2):c.777C>T (p.Asp259=)	rs2102228925

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