List of variants in gene TPI1 reported by ARUP Laboratories, Molecular Genetics and Genomics, ARUP Laboratories

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 18

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HGVS	dbSNP	gnomAD frequency
NM_001159287.1(TPI1):c.69A>G (p.Arg23=)	rs1800200	0.09809
NM_001159287.1(TPI1):c.66G>A (p.Pro22=)	rs1800201	0.03488
NM_000365.6(TPI1):c.544-10C>G	rs115061797	0.02638
NM_000365.6(TPI1):c.631+13G>A	rs60115912	0.02344
NM_000365.6(TPI1):c.544-14G>A	rs72661109	0.01198
NM_000365.6(TPI1):c.600G>A (p.Ala200=)	rs61747602	0.00452
NM_001159287.1(TPI1):c.50T>G (p.Ile17Arg)	rs1800202	0.00329
NM_001159287.1(TPI1):c.31C>T (p.His11Tyr)	rs781949460	0.00200
NM_000365.6(TPI1):c.321T>C (p.Asp107=)	rs141972556	0.00104
NM_000365.6(TPI1):c.366C>T (p.Leu122=)	rs138131191	0.00081
NM_000365.6(TPI1):c.448G>T (p.Val150Phe)	rs150585849	0.00067
NM_000365.6(TPI1):c.116-12T>C	rs369077745	0.00019
NM_000365.6(TPI1):c.-11G>A	rs199634350	0.00010
NM_000365.6(TPI1):c.690C>T (p.Phe230=)	rs782267337	0.00004
NM_000365.6(TPI1):c.543+5C>G	rs782153322	0.00002
NM_000365.6(TPI1):c.-29C>G	rs181882616
NM_000365.6(TPI1):c.383T>C (p.Ile128Thr)	rs199881593
NM_000365.6(TPI1):c.457+7C>G

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