List of variants in gene C10orf55, LOC126860960, PLAU studied for hematologic 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: 19

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HGVS	dbSNP	gnomAD frequency
NM_002658.6(PLAU):c.681-7C>T	rs2227566	0.50640
NM_002658.6(PLAU):c.822C>T (p.Asn274=)	rs2227568	0.12381
NM_002658.6(PLAU):c.691A>C (p.Lys231Gln)	rs2227567	0.04766
NM_002658.6(PLAU):c.445C>T (p.His149Tyr)	rs117135013	0.00070
NM_002658.6(PLAU):c.453C>T (p.Cys151=)	rs374267816	0.00014
NM_002658.6(PLAU):c.581C>T (p.Ala194Val)	rs145865648	0.00011
NM_002658.6(PLAU):c.706A>G (p.Ile236Val)	rs150389556	0.00006
NM_002658.6(PLAU):c.308C>T (p.Thr103Met)	rs370278611	0.00004
NM_002658.6(PLAU):c.368+6G>C	rs186447765	0.00003
NM_002658.6(PLAU):c.602G>T (p.Arg201Leu)	rs549461157	0.00001
NM_002658.6(PLAU):c.316G>C (p.Ala106Pro)	rs886047206
NM_002658.6(PLAU):c.467dup (p.Pro157fs)	rs1435611170
NM_002658.6(PLAU):c.539T>C (p.Ile180Thr)
NM_002658.6(PLAU):c.548A>G (p.Glu183Gly)
NM_002658.6(PLAU):c.559A>G (p.Ile187Val)	rs528761202
NM_002658.6(PLAU):c.581C>A (p.Ala194Glu)	rs145865648
NM_002658.6(PLAU):c.735C>A (p.Asn245Lys)	rs1249124159
NM_002658.6(PLAU):c.750G>C (p.Gly250=)	rs886047207
NM_002658.6(PLAU):c.754A>T (p.Met252Leu)

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