List of variants in gene KRT2 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: 14

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HGVS	dbSNP	gnomAD frequency
NM_000423.3(KRT2):c.1426G>A (p.Glu476Lys)	rs56829062
NM_000423.3(KRT2):c.1427A>T (p.Glu476Val)	rs60537449
NM_000423.3(KRT2):c.1435A>C (p.Thr479Pro)	rs137852630
NM_000423.3(KRT2):c.1448T>A (p.Leu483Gln)	rs61726456
NM_000423.3(KRT2):c.1451T>C (p.Leu484Pro)	rs61726451
NM_000423.3(KRT2):c.1459G>A (p.Glu487Lys)	rs137852629
NM_000423.3(KRT2):c.1461G>T (p.Glu487Asp)	rs137852628
NM_000423.3(KRT2):c.1462G>A (p.Glu488Lys)	rs61726452
NM_000423.3(KRT2):c.532G>A (p.Glu178Lys)	rs57728941
NM_000423.3(KRT2):c.542A>T (p.Gln181Leu)	rs57510142
NM_000423.3(KRT2):c.545T>A (p.Ile182Asn)	rs61622714
NM_000423.3(KRT2):c.556A>T (p.Asn186Tyr)	rs137852631
NM_000423.3(KRT2):c.558C>A (p.Asn186Lys)	rs137852632
NM_000423.3(KRT2):c.607A>G (p.Asn203Asp)	rs61726455

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