List of variants in gene TGM1 reported as benign by Natera, Inc.

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: 23

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HGVS	dbSNP	gnomAD frequency
NM_000359.3(TGM1):c.726G>A (p.Glu242=)	rs35755034	0.04892
NM_000359.3(TGM1):c.366G>A (p.Ser122=)	rs17102410	0.03062
NM_000359.3(TGM1):c.1552G>A (p.Val518Met)	rs35312232	0.01146
NM_000359.3(TGM1):c.54G>A (p.Gln18=)	rs41295336	0.00761
NM_000359.3(TGM1):c.2264C>T (p.Ser755Leu)	rs35926651	0.00599
NM_000359.3(TGM1):c.285C>T (p.Ser95=)	rs2228336	0.00581
NM_000359.3(TGM1):c.1559A>G (p.Glu520Gly)	rs142404759	0.00555
NM_000359.3(TGM1):c.365C>T (p.Ser122Leu)	rs141486741	0.00492
NM_000359.3(TGM1):c.1645+5C>A	rs187575724	0.00468
NM_000359.3(TGM1):c.168G>A (p.Ala56=)	rs79251149	0.00439
NM_000359.3(TGM1):c.125C>A (p.Ser42Tyr)	rs41295338	0.00428
NM_000359.3(TGM1):c.1113C>T (p.Ser371=)	rs61747601	0.00421
NM_000359.3(TGM1):c.1819C>T (p.Arg607Cys)	rs2229464	0.00382
NM_000359.3(TGM1):c.2405A>T (p.Asp802Val)	rs2228337	0.00273
NM_000359.3(TGM1):c.394G>A (p.Asp132Asn)	rs2229462	0.00244
NM_000359.3(TGM1):c.429C>T (p.Arg143=)	rs144989372	0.00239
NM_000359.3(TGM1):c.1298+9G>A	rs201015655	0.00140
NM_000359.3(TGM1):c.432G>A (p.Gly144=)	rs141559048	0.00102
NM_000359.3(TGM1):c.2258G>A (p.Arg753His)	rs202020907	0.00029
NM_000359.3(TGM1):c.319+8C>T	rs41295342	0.00021
NM_000359.3(TGM1):c.550C>T (p.Pro184Ser)	rs200517023	0.00006
NM_000359.3(TGM1):c.66G>A (p.Thr22=)	rs756448718	0.00006
NM_000359.3(TGM1):c.1146C>A (p.Gly382=)	rs1126432

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