"GeneDx"[submitter] AND "KRT13"[gene] - ClinVar - NCBI

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Items: 18

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 58696	GRCh38/hg38 17q12-21.31(chr17:39199873-45629579)x3	LOC130060786, LOC130060787 +633 more	Copy number gain	See cases	GPathogenic
Select item 1278895	NC_000017.11:g.41500927G>C	KRT13	Single nucleotide variant	not provided	GBenign
Select item 323070	NM_153490.3(KRT13):c.*171G>T	KRT13	Single nucleotide variant (3 prime UTR variant)	White sponge nevus 2 +1 more	GBenign
Select item 323071	NM_153490.3(KRT13):c.*170C>T	KRT13	Single nucleotide variant (3 prime UTR variant)	White sponge nevus 2 +1 more	GBenign
Select item 1251738	NM_153490.3(KRT13):c.1244+27G>A	KRT13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1178644	NM_153490.3(KRT13):c.898-27A>G	KRT13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 323084	NM_153490.3(KRT13):c.897+6C>T	KRT13	Single nucleotide variant (intron variant)	White sponge nevus 2 +1 more	GBenign
Select item 323092	NM_153490.3(KRT13):c.736-7C>G	KRT13	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 323094	NM_153490.3(KRT13):c.735+6C>T	KRT13	Single nucleotide variant (intron variant)	not provided +1 more	GBenign
Select item 1179611	NM_153490.3(KRT13):c.579-29A>G	KRT13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 323096	NM_153490.3(KRT13):c.560C>T (p.Ala187Val)	KRT13 (A187V)	Single nucleotide variant (missense variant)	not provided +1 more	GBenign
Select item 1290052	NM_153490.3(KRT13):c.496-28A>G	KRT13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1249331	NM_153490.3(KRT13):c.496-266G>C	KRT13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1248237	NM_153490.3(KRT13):c.495+33A>T	KRT13	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 323101	NM_153490.3(KRT13):c.437C>G (p.Ala146Gly)	KRT13 (A146G)	Single nucleotide variant (missense variant)	White sponge nevus 2 +1 more	GBenign
Select item 323106	NM_153490.3(KRT13):c.204C>A (p.Gly68=)	KRT13	Single nucleotide variant (synonymous variant)	White sponge nevus 2 +1 more	GBenign
Select item 1278680	NC_000017.11:g.41505767G>A	KRT13	Single nucleotide variant	not provided	GBenign
Select item 1290185	NC_000017.11:g.41505917C>T	KRT13	Single nucleotide variant	not provided	GBenign