"GeneDx"[submitter] AND "KRT4"[gene] - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 66516	NM_002272.4(KRT4):c.*269A>G	KRT4	Single nucleotide variant (3 prime UTR variant)	White sponge nevus 1 +1 more	GBenign
Select item 309670	NM_002272.4(KRT4):c.1381+15C>T	KRT4	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 309671	NM_002272.4(KRT4):c.1346+15A>G	KRT4	Single nucleotide variant (intron variant)	White sponge nevus 1 +1 more	GBenign
Select item 1246289	NM_002272.4(KRT4):c.1126-32G>A	KRT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 309677	NM_002272.4(KRT4):c.1020G>C (p.Ser340=)	KRT4	Single nucleotide variant (synonymous variant)	White sponge nevus 1 +1 more	GBenign
Select item 1290336	NM_002272.4(KRT4):c.999+90A>G	KRT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1264187	NM_002272.4(KRT4):c.835-225C>T	KRT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1275627	NM_002272.4(KRT4):c.739-214A>G	KRT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1247167	NM_002272.4(KRT4):c.738+213T>C	KRT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1179600	NM_002272.4(KRT4):c.738+16T>G	KRT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 309687	NM_002272.4(KRT4):c.678-14G>A	KRT4	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1231227	NM_002272.4(KRT4):c.678-157A>G	KRT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1251178	NM_002272.4(KRT4):c.677+104G>A	KRT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 309695	NM_002272.4(KRT4):c.467A>G (p.Gln156Arg)	KRT4 (Q156R)	Single nucleotide variant (missense variant)	White sponge nevus 1 +1 more	GBenign
Select item 1267686	NM_002272.4(KRT4):c.463-278C>T	KRT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1287977	NM_002272.4(KRT4):c.462+60G>A	KRT4	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 768551	NM_002272.4(KRT4):c.259_260insCCGGCGGCTTCGGAGCTGGTTTCGGCACTGGTGGCTTTGGTG (p.Gly86_Gly87insAlaGlyGlyPheGlyAlaGlyPheGlyThrGlyGlyPheGly)	KRT4	Insertion (inframe_insertion)	not specified +1 more	GBenign/Likely benign
Select item 309709	NM_002272.4(KRT4):c.215C>T (p.Ala72Val)	KRT4 (A72V)	Single nucleotide variant (missense variant)	White sponge nevus 1 +1 more	GBenign