List of variants in gene TMPRSS3 reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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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: 21

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HGVS	dbSNP	gnomAD frequency
NM_001256317.3(TMPRSS3):c.1042G>A (p.Asp348Asn)	rs111033261	0.00071
NM_001256317.3(TMPRSS3):c.347T>C (p.Val116Ala)	rs201007237	0.00051
NM_001256317.3(TMPRSS3):c.1272C>T (p.Cys424=)	rs56178910	0.00039
NM_001256317.3(TMPRSS3):c.279C>T (p.Asp93=)	rs145824109	0.00022
NM_001256317.3(TMPRSS3):c.789C>T (p.Tyr263=)	rs147181936	0.00014
NM_001256317.3(TMPRSS3):c.239G>A (p.Arg80His)	rs146159479	0.00013
NM_001256317.3(TMPRSS3):c.300C>T (p.Asp100=)	rs146621712	0.00009
NM_001256317.3(TMPRSS3):c.1020G>A (p.Thr340=)	rs374149338	0.00008
NM_001256317.3(TMPRSS3):c.1155C>T (p.Cys385=)	rs746293388	0.00008
NM_001256317.3(TMPRSS3):c.975G>T (p.Leu325=)	rs397517379	0.00007
NM_001256317.3(TMPRSS3):c.1053C>T (p.Asp351=)	rs397517369	0.00006
NM_001256317.3(TMPRSS3):c.993C>T (p.Asn331=)	rs397517380	0.00005
NM_001256317.3(TMPRSS3):c.309C>T (p.Asp103=)	rs111033502	0.00004
NM_001256317.3(TMPRSS3):c.783C>T (p.Asp261=)	rs397517378	0.00004
NM_001256317.3(TMPRSS3):c.1191+11G>A	rs727505305	0.00003
NM_001256317.3(TMPRSS3):c.333T>C (p.Gly111=)	rs397517375
NM_001256317.3(TMPRSS3):c.446+9A>G	rs367594676
NM_001256317.3(TMPRSS3):c.497G>A (p.Arg166Gln)	rs150397427
NM_001256317.3(TMPRSS3):c.497G>T (p.Arg166Leu)	rs150397427
NM_001256317.3(TMPRSS3):c.918C>T (p.Ala306=)	rs749538864
NM_001256317.3(TMPRSS3):c.953-9T>C	rs1555853318

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