List of variants in gene TPM3 reported as not provided

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_152263.4(TPM3):c.855-1G>A	rs113605263	0.00002
NM_152263.4(TPM3):c.857A>C (p.Ter286Ser)	rs199474720	0.00001
NM_152263.4(TPM3):c.11C>T (p.Ala4Val)	rs199474711
NM_152263.4(TPM3):c.244-5T>C	rs199474712
NM_152263.4(TPM3):c.26T>G (p.Met9Arg)	rs80358247
NM_152263.4(TPM3):c.272G>C (p.Arg91Pro)	rs199474713
NM_152263.4(TPM3):c.298C>A (p.Leu100Met)	rs121964853
NM_152263.4(TPM3):c.466G>A (p.Ala156Thr)	rs199474714
NM_152263.4(TPM3):c.502C>G (p.Arg168Gly)	rs121964854
NM_152263.4(TPM3):c.502C>T (p.Arg168Cys)	rs121964854
NM_152263.4(TPM3):c.503G>A (p.Arg168His)	rs121964852
NM_152263.4(TPM3):c.505A>G (p.Lys169Glu)	rs199474715
NM_152263.4(TPM3):c.521A>C (p.Glu174Ala)	rs199474716
NM_152263.4(TPM3):c.721G>A (p.Glu241Lys)	rs199474717
NM_152263.4(TPM3):c.733A>G (p.Arg245Gly)	rs199474718
NM_152263.4(TPM3):c.855del (p.Ter286AsnextTer?)	rs199474719
NM_152263.4(TPM3):c.94C>T (p.Gln32Ter)	rs80358248

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