List of variants in gene PRIMA1 reported as uncertain significance by Ambry Genetics

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: 17

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HGVS	dbSNP	gnomAD frequency
NM_178013.4(PRIMA1):c.295G>A (p.Val99Ile)	rs200260569	0.00007
NM_178013.4(PRIMA1):c.163C>T (p.Arg55Trp)	rs146599561	0.00004
NM_178013.4(PRIMA1):c.176C>T (p.Pro59Leu)	rs550883370	0.00003
NM_178013.4(PRIMA1):c.442G>A (p.Val148Met)	rs140016687	0.00003
NM_178013.4(PRIMA1):c.290T>C (p.Ile97Thr)	rs763426300	0.00002
NM_178013.4(PRIMA1):c.332T>C (p.Val111Ala)	rs145843133	0.00002
NM_178013.4(PRIMA1):c.236A>G (p.Asn79Ser)	rs1000407112	0.00001
NM_178013.4(PRIMA1):c.426C>G (p.Ser142Arg)	rs370561739	0.00001
NM_178013.4(PRIMA1):c.104G>A (p.Gly35Asp)
NM_178013.4(PRIMA1):c.148C>T (p.His50Tyr)
NM_178013.4(PRIMA1):c.25C>T (p.Arg9Cys)	rs2503468406
NM_178013.4(PRIMA1):c.328C>T (p.Leu110Phe)
NM_178013.4(PRIMA1):c.41G>T (p.Trp14Leu)	rs2503468282
NM_178013.4(PRIMA1):c.440A>G (p.Asp147Gly)	rs2076037415
NM_178013.4(PRIMA1):c.44C>T (p.Ser15Phe)
NM_178013.4(PRIMA1):c.5T>C (p.Leu2Pro)
NM_178013.4(PRIMA1):c.77T>C (p.Leu26Pro)

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