List of variants in gene TRIP4 studied for hereditary skeletal muscle disorder

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: 8

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HGVS	dbSNP	gnomAD frequency
NM_016213.5(TRIP4):c.1044-25G>A	rs2046356	0.74036
NM_016213.5(TRIP4):c.981C>T (p.Thr327=)	rs115922345	0.00975
NM_016213.5(TRIP4):c.950G>A (p.Arg317Gln)	rs200549601	0.00006
NM_016213.5(TRIP4):c.1465C>T (p.Arg489Cys)	rs764341782	0.00003
NM_016213.5(TRIP4):c.1065del (p.Ile356fs)	rs1891833492
NM_016213.5(TRIP4):c.1199del (p.Gln400fs)
NM_016213.5(TRIP4):c.135dup (p.Arg46fs)
NM_016213.5(TRIP4):c.55_56insCT (p.Gln19fs)

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