List of variants in gene TAT reported as likely pathogenic by Myriad Genetics, 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: 7

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HGVS	dbSNP	gnomAD frequency
NM_000353.3(TAT):c.1015del (p.Tyr339fs)	rs2507662751
NM_000353.3(TAT):c.1037_1038del (p.Leu346fs)	rs2507662681
NM_000353.3(TAT):c.18_19del (p.Gln7fs)	rs2507673070
NM_000353.3(TAT):c.274_275del (p.Glu92fs)	rs2507672235
NM_000353.3(TAT):c.283C>T (p.Gln95Ter)	rs2507672211
NM_000353.3(TAT):c.313A>T (p.Lys105Ter)	rs2507672161
NM_000353.3(TAT):c.8dup (p.Tyr4fs)	rs2507673107

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