"PreventionGenetics, part of Exact Sciences"[submitter] AND "KRT74"[ge - ClinVar - NCBI

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Items: 13

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 3058228	NM_175053.4(KRT74):c.1534G>A (p.Asp512Asn)	KRT74 (D512N)	Single nucleotide variant (missense variant)	KRT74-related disorder	GUncertain significance
Select item 712119	NM_175053.4(KRT74):c.1515G>T (p.Ala505=)	KRT74	Single nucleotide variant (synonymous variant)	KRT74-related disorder +1 more	GBenign/Likely benign
Select item 2047552	NM_175053.4(KRT74):c.1491C>T (p.Ser497=)	KRT74	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 3046321	NM_175053.4(KRT74):c.1470C>T (p.Gly490=)	KRT74	Single nucleotide variant (synonymous variant)	KRT74-related disorder	GLikely benign
Select item 729449	NM_175053.4(KRT74):c.1426C>T (p.Pro476Ser)	KRT74 (P476S)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 770985	NM_175053.4(KRT74):c.1258C>T (p.Arg420Trp)	KRT74 (R420W)	Single nucleotide variant (missense variant)	KRT74-related disorder +1 more	GLikely benign
Select item 3058034	NM_175053.4(KRT74):c.1179A>C (p.Gly393=)	KRT74	Single nucleotide variant (synonymous variant)	KRT74-related disorder	GLikely benign
Select item 2039430	NM_175053.4(KRT74):c.1141A>G (p.Ser381Gly)	KRT74 (S381G)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 96741	NM_175053.4(KRT74):c.821T>C (p.Phe274Ser)	KRT74 (F274S)	Single nucleotide variant (missense variant)	KRT74-related disorder +1 more	GBenign/Likely benign
Select item 3041164	NM_175053.4(KRT74):c.770T>A (p.Val257Asp)	KRT74 (V257D)	Single nucleotide variant (missense variant)	KRT74-related disorder	GLikely benign
Select item 729450	NM_175053.4(KRT74):c.748-2A>G	KRT74	Single nucleotide variant (splice acceptor variant)	not provided +1 more	GBenign/Likely benign
Select item 740841	NM_175053.4(KRT74):c.411C>T (p.Arg137=)	KRT74	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 789219	NM_175053.4(KRT74):c.298G>A (p.Gly100Arg)	KRT74 (G100R)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign