List of variants in gene combination KRT81, KRT86 reported as not provided by Epithelial Biology; Institute of Medical Biology, Singapore

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: 13

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HGVS	dbSNP	gnomAD frequency
NM_002281.4(KRT81):c.735+4C>T	rs12812669	0.23428
NM_001320198.2(KRT86):c.348G>A (p.Arg116=)	rs58580222	0.13244
NM_001320198.2(KRT86):c.416A>C (p.Gln139Pro)	rs58717266	0.10399
NM_001320198.2(KRT86):c.197G>A (p.Arg66His)	rs57242951	0.00769
NM_001320198.2(KRT86):c.1204G>A (p.Glu402Lys)	rs60687604	0.00001
NM_002281.4(KRT81):c.1237G>A (p.Glu413Lys)	rs57419521	0.00001
NM_001320198.2(KRT86):c.1204G>C (p.Glu402Gln)	rs60687604
NM_001320198.2(KRT86):c.1237G>A (p.Glu413Lys)	rs121909129
NM_001320198.2(KRT86):c.1239G>T (p.Glu413Asp)	rs121909130
NM_001320198.2(KRT86):c.340A>C (p.Asn114His)	rs61091894
NM_001320198.2(KRT86):c.340A>G (p.Asn114Asp)	rs61091894
NM_001320198.2(KRT86):c.353C>A (p.Ala118Glu)	rs60612575
NM_002281.4(KRT81):c.1204G>A (p.Glu402Lys)	rs56821304

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