List of variants in gene TPP1 reported as likely benign by Invitae

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Gene type:		Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 19

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HGVS	dbSNP
NM_000391.4(TPP1):c.1089C>T (p.Ala363=)	rs151068181
NM_000391.4(TPP1):c.1266+8T>C	rs752269166
NM_000391.4(TPP1):c.1426-10A>G	rs200965587
NM_000391.4(TPP1):c.1426-10A>T	rs200965587
NM_000391.4(TPP1):c.14C>A (p.Ala5Asp)	rs138976576
NM_000391.4(TPP1):c.1569T>C (p.His523=)	rs1029334403
NM_000391.4(TPP1):c.1593A>G (p.Val531=)	rs1554901473
NM_000391.4(TPP1):c.18-10G>T	rs778206032
NM_000391.4(TPP1):c.219T>C (p.Ser73=)	rs1456089848
NM_000391.4(TPP1):c.229+8T>C	rs1263525920
NM_000391.4(TPP1):c.297G>A (p.Val99=)	rs753066277
NM_000391.4(TPP1):c.318C>T (p.Ala106=)	rs774528021
NM_000391.4(TPP1):c.381-4C>G	rs529421892
NM_000391.4(TPP1):c.513G>T (p.Gly171=)	rs145224171
NM_000391.4(TPP1):c.542C>T (p.Ser181Phe)	rs139059149
NM_000391.4(TPP1):c.544C>T (p.Leu182=)	rs776858324
NM_000391.4(TPP1):c.669C>T (p.Asn223=)	rs1554901936
NM_000391.4(TPP1):c.688-4A>G	rs370683758
NM_000391.4(TPP1):c.69G>A (p.Pro23=)	rs141680923

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