List of variants in gene combination LOC126860075, POR reported by Illumina Laboratory Services, Illumina

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: 10

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HGVS	dbSNP	gnomAD frequency
NM_001395413.1(POR):c.975C>T (p.Ala325=)	rs72557941	0.00136
NM_001395413.1(POR):c.889G>A (p.Glu297Lys)	rs11540674	0.00044
NM_001395413.1(POR):c.991G>A (p.Val331Ile)	rs562241770	0.00031
NM_001395413.1(POR):c.888C>T (p.Thr296=)	rs180683888	0.00005
NM_001395413.1(POR):c.938+10G>A	rs781980999	0.00004
NM_001395413.1(POR):c.990C>T (p.Leu330=)	rs376830846	0.00004
NM_001395413.1(POR):c.1033G>A (p.Val345Ile)	rs373128937	0.00002
NM_001395413.1(POR):c.938+3A>G	rs782232516	0.00001
NM_001395413.1(POR):c.938G>C (p.Arg313Thr)	rs782572970	0.00001
NM_001395413.1(POR):c.939-14A>C	rs886062441

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