KRT86[gene] and "single gene"[properties] - ClinVar

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Items: 32

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1267877	NM_001320198.2(KRT86):c.-4-67C>T	KRT86	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1248361	NM_001320198.2(KRT86):c.54C>T (p.Cys18=)	KRT86	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1219942	NM_001320198.2(KRT86):c.60C>G (p.Pro20=)	KRT86	Single nucleotide variant (synonymous variant)	not provided	GBenign/Likely benign
Select item 1229890	NM_001320198.2(KRT86):c.87C>T (p.Ala29=)	KRT86	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 66547	NM_001320198.2(KRT86):c.197G>A (p.Arg66His)	KRT86 (R66H)	Single nucleotide variant (missense variant)	not provided	GLikely benign
Select item 66549	NM_001320198.2(KRT86):c.348G>A (p.Arg116=)	KRT86	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1186158	NM_001320198.2(KRT86):c.370-9G>A	KRT86	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 66550	NM_001320198.2(KRT86):c.416A>C (p.Gln139Pro)	KRT86 (Q139P)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1252633	NM_001320198.2(KRT86):c.578+178G>C	KRT86	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1271070	NM_001320198.2(KRT86):c.579-93T>C	KRT86	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1228047	NM_001320198.2(KRT86):c.579-89C>T	KRT86	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1227864	NM_001320198.2(KRT86):c.579-86G>C	KRT86	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1283930	NM_001320198.2(KRT86):c.636G>A (p.Lys212=)	KRT86	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1224561	NM_001320198.2(KRT86):c.684T>C (p.Asn228=)	KRT86	Single nucleotide variant (synonymous variant)	Beaded hair +1 more	GBenign/Likely benign
Select item 1268982	NM_001320198.2(KRT86):c.873T>C (p.Ala291=)	KRT86	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1249366	NM_001320198.2(KRT86):c.900+25G>T	KRT86	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1204798	NM_001320198.2(KRT86):c.901-28A>G	KRT86	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 768544	NM_001320198.2(KRT86):c.979C>T (p.Arg327Cys)	KRT86 (R327C)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1252238	NM_001320198.2(KRT86):c.1002T>C (p.Ala334=)	KRT86	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1266646	NM_001320198.2(KRT86):c.1027-116G>A	KRT86	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1207369	NM_001320198.2(KRT86):c.1027-15C>T	KRT86	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1193794	NM_001320198.2(KRT86):c.1044T>C (p.Ala348=)	KRT86	Single nucleotide variant (synonymous variant)	not provided	GLikely benign
Select item 768545	NM_001320198.2(KRT86):c.1053T>C (p.Ala351=)	KRT86	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 768546	NM_001320198.2(KRT86):c.1102T>C (p.Leu368=)	KRT86	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 1224621	NM_001320198.2(KRT86):c.1247+36C>A	KRT86	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1215565	NM_001320198.2(KRT86):c.1248-152C>T	KRT86	Single nucleotide variant (intron variant)	not provided	GLikely benign
Select item 1284069	NM_001320198.2(KRT86):c.*94A>G	KRT86	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1179347	NM_001320198.2(KRT86):c.*127C>T	KRT86	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1264242	NM_001320198.2(KRT86):c.*264G>A	KRT86	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign
Select item 1269078	NM_001320198.2(KRT86):c.*279dup	KRT86	Duplication (3 prime UTR variant)	not provided	GBenign
Select item 1237101	NM_001320198.2(KRT86):c.278_279dup	KRT86	Duplication (3 prime UTR variant)	not provided	GBenign
Select item 1260744	NM_001320198.2(KRT86):c.*287A>G	KRT86	Single nucleotide variant (3 prime UTR variant)	not provided	GBenign

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Items: 32