List of variants in gene TRIP12 reported as likely pathogenic for not provided

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

Total variants: 11

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HGVS	dbSNP	gnomAD frequency
NM_001348323.3(TRIP12):c.1373dup (p.Leu459fs)	rs2052640598
NM_001348323.3(TRIP12):c.1819C>T (p.Gln607Ter)
NM_001348323.3(TRIP12):c.2996A>T (p.Glu999Val)	rs2154270375
NM_001348323.3(TRIP12):c.3208C>T (p.Arg1070Ter)	rs1575161164
NM_001348323.3(TRIP12):c.4290del (p.Pro1429_Tyr1430insTer)
NM_001348323.3(TRIP12):c.4302_4303del (p.Tyr1435fs)	rs2154259932
NM_001348323.3(TRIP12):c.4695+5G>A	rs1575023205
NM_001348323.3(TRIP12):c.4903C>T (p.Arg1635Ter)	rs1574994308
NM_001348323.3(TRIP12):c.4936G>A (p.Glu1646Lys)
NM_001348323.3(TRIP12):c.6032T>G (p.Leu2011Trp)	rs2154220561
NM_001348323.3(TRIP12):c.6181C>T (p.Gln2061Ter)	rs2032190831

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