List of variants in gene TPP1 reported as uncertain significance by Mayo Clinic Laboratories, Mayo Clinic

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_000391.4(TPP1):c.542C>T (p.Ser181Phe)	rs139059149	0.00093
NM_000391.4(TPP1):c.1307T>C (p.Leu436Pro)	rs150039898	0.00029
NM_000391.4(TPP1):c.7C>A (p.Leu3Ile)	rs142163063	0.00022
NM_000391.4(TPP1):c.947C>A (p.Ala316Asp)	rs149463616	0.00007
NM_000391.4(TPP1):c.313G>T (p.Ala105Ser)	rs368435226	0.00006
NM_000391.4(TPP1):c.1225G>A (p.Gly409Ser)	rs1429220241	0.00001
NM_000391.4(TPP1):c.209A>G (p.Asp70Gly)	rs775780584	0.00001
NM_000391.4(TPP1):c.556C>T (p.Pro186Ser)	rs1855598679	0.00001
NM_000391.4(TPP1):c.68C>G (p.Pro23Arg)	rs2134598745
NM_000391.4(TPP1):c.86G>A (p.Arg29Lys)	rs1378365512

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