List of variants in gene TPM2 reported as likely benign by PreventionGenetics, part of Exact Sciences

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_003289.4(TPM2):c.493-43G>C	rs181404400	0.00156
NM_003289.4(TPM2):c.18G>A (p.Lys6=)	rs144658309	0.00015
NM_003289.4(TPM2):c.-10C>A	rs372751531	0.00006
NM_003289.4(TPM2):c.357G>A (p.Ala119=)	rs376028030	0.00006
NM_003289.4(TPM2):c.374+9G>C	rs200730708	0.00004
NM_003289.4(TPM2):c.114+10G>A	rs1416639797
NM_003289.4(TPM2):c.278A>G (p.Gln93Arg)	rs199476151
NM_003289.4(TPM2):c.300C>T (p.Asp100=)	rs532190742
NM_003289.4(TPM2):c.375-37G>A	rs145455780
NM_003289.4(TPM2):c.493-11_493-8del	rs528068364
NM_003289.4(TPM2):c.563+175C>T
NM_003289.4(TPM2):c.773-5_773-3dup	rs35401252
NM_003289.4(TPM2):c.773-9_773-8insCG

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