List of variants in gene TGFB3 reported as likely pathogenic for not provided

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_003239.5(TGFB3):c.1034C>G (p.Ser345Ter)	rs1060502827
NM_003239.5(TGFB3):c.1080G>A (p.Thr360=)	rs1555360212
NM_003239.5(TGFB3):c.1195G>T (p.Glu399Ter)	rs1555360027
NM_003239.5(TGFB3):c.442C>T (p.Arg148Ter)	rs1057523647
NM_003239.5(TGFB3):c.514C>T (p.Gln172Ter)	rs1594787989
NM_003239.5(TGFB3):c.755-1G>C	rs1566679646
NM_003239.5(TGFB3):c.826C>T (p.Pro276Ser)	rs1057522944
NM_003239.5(TGFB3):c.886_893dup (p.Lys298fs)	rs1555360368
NM_003239.5(TGFB3):c.898C>T (p.Arg300Trp)	rs796051885
NM_003239.5(TGFB3):c.926+2T>A	rs2140238043
NM_003239.5(TGFB3):c.952C>T (p.Arg318Cys)	rs2140236263
NM_003239.5(TGFB3):c.996G>T (p.Trp332Cys)	rs2140236210

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