List of variants in gene TPP1 reported as benign for not specified

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: 26

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HGVS	dbSNP	gnomAD frequency
NM_000391.4(TPP1):c.1542A>T (p.Gly514=)	rs1128396	0.19057
NM_000391.4(TPP1):c.441A>G (p.Glu147=)	rs2555170	0.04313
NM_000391.4(TPP1):c.381-10dup	rs146315473	0.02726
NM_000391.4(TPP1):c.1266+5G>A	rs1800753	0.01932
NM_000391.4(TPP1):c.1044C>T (p.Ala348=)	rs35706972	0.00982
NM_000391.4(TPP1):c.1494C>T (p.Pro498=)	rs117942457	0.00902
NM_000391.4(TPP1):c.299A>G (p.Gln100Arg)	rs1800746	0.00889
NM_000391.4(TPP1):c.1117C>G (p.Gln373Glu)	rs112812685	0.00817
NM_000391.4(TPP1):c.185C>T (p.Ser62Leu)	rs2734715	0.00549
NM_000391.4(TPP1):c.1253G>A (p.Arg418Gln)	rs138744051	0.00456
NM_000391.4(TPP1):c.42C>A (p.Ile14=)	rs35903915	0.00419
NM_000391.4(TPP1):c.1396G>A (p.Val466Met)	rs78970155	0.00339
NM_000391.4(TPP1):c.840G>C (p.Leu280=)	rs140349036	0.00257
NM_000391.4(TPP1):c.293C>T (p.Thr98Met)	rs140726254	0.00209
NM_000391.4(TPP1):c.1497T>C (p.Pro499=)	rs142672910	0.00170
NM_000391.3(TPP1):c.-40T>C	rs200184958	0.00053
NM_000391.4(TPP1):c.513G>T (p.Gly171=)	rs145224171	0.00039
NM_000391.4(TPP1):c.688-18C>T	rs376868997	0.00038
NM_000391.4(TPP1):c.1383G>A (p.Val461=)	rs202190396	0.00007
NM_000391.4(TPP1):c.1125C>T (p.Arg375=)	rs587780972	0.00005
NM_000391.4(TPP1):c.228C>T (p.Tyr76=)	rs373318861	0.00004
NM_000391.4(TPP1):c.435T>C (p.Pro145=)	rs188822344	0.00001
NM_000391.4(TPP1):c.1002C>T (p.Ser334=)	rs796053432
NM_000391.4(TPP1):c.1426-10A>G	rs200965587
NM_000391.4(TPP1):c.887-6del	rs35039601
NM_000391.4(TPP1):c.887-8_887-6del	rs35039601

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