List of variants in gene TRIP11 reported by SIB Swiss Institute of Bioinformatics

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_004239.4(TRIP11):c.3962T>A (p.Leu1321Ter)	rs745372938	0.00016
NM_004239.4(TRIP11):c.1228G>T (p.Asp410Tyr)	rs1566863801
NM_004239.4(TRIP11):c.3478C>T (p.Gln1160Ter)	rs1595387492
NM_004239.4(TRIP11):c.3671G>A (p.Trp1224Ter)	rs776935608
NM_004239.4(TRIP11):c.4127C>A (p.Ser1376Ter)	rs1045076800
NM_004239.4(TRIP11):c.4534C>T (p.Gln1512Ter)	rs780625551
NM_004239.4(TRIP11):c.5416A>G (p.Met1806Val)	rs1566843321
NM_004239.4(TRIP11):c.586C>T (p.Gln196Ter)	rs149079426
NM_004239.4(TRIP11):c.790C>T (p.Arg264Ter)	rs267607138

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