"GeneDx"[submitter] AND "KRT74"[gene] - ClinVar

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Search results

Items: 44

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1247065	NM_175053.4(KRT74):c.1507A>G (p.Thr503Ala)	KRT74 (T503A)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1243772	NM_175053.4(KRT74):c.1391-201G>T	KRT74	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1265618	NM_175053.4(KRT74):c.1391-202T>C	KRT74	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1242399	NM_175053.4(KRT74):c.1390+226G>C	KRT74	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1273296	NM_175053.4(KRT74):c.1390+138T>A	KRT74	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1238205	NM_175053.4(KRT74):c.1390+125G>A	KRT74	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1295082	NM_175053.4(KRT74):c.1356-233C>T	KRT74	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1174188	NM_175053.4(KRT74):c.1135-346G>T	KRT74	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1264948	NM_175053.4(KRT74):c.1009-11T>C	KRT74	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1289575	NM_175053.4(KRT74):c.1009-118A>G	KRT74	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1251323	NM_175053.4(KRT74):c.1009-175_1009-174insC	KRT74	Insertion (intron variant)	not provided	GBenign
Select item 1270768	NM_175053.4(KRT74):c.1008+262G>T	KRT74	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1263892	NM_175053.4(KRT74):c.1008+110G>T	KRT74	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1279153	NM_175053.4(KRT74):c.1008+51G>T	KRT74	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1239349	NM_175053.4(KRT74):c.1008+43C>T	KRT74	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1231679	NM_175053.4(KRT74):c.1008+36T>C	KRT74	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1250491	NM_175053.4(KRT74):c.844-89T>C	KRT74	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1221182	NM_175053.4(KRT74):c.844-101C>T	KRT74	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1282120	NM_175053.4(KRT74):c.843+219G>A	KRT74	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1282581	NM_175053.4(KRT74):c.843+209A>C	KRT74	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1275494	NM_175053.4(KRT74):c.843+165G>A	KRT74	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1281160	NM_175053.4(KRT74):c.843+162T>C	KRT74	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1257637	NM_175053.4(KRT74):c.748-210T>C	KRT74	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1277029	NM_175053.4(KRT74):c.747+6A>G	KRT74	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1267618	NM_175053.4(KRT74):c.714G>A (p.Thr238=)	KRT74	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1279978	NM_175053.4(KRT74):c.693A>G (p.Glu231=)	KRT74	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1290299	NM_175053.4(KRT74):c.687-89A>C	KRT74	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1286437	NM_175053.4(KRT74):c.687-175A>G	KRT74	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1229937	NM_175053.4(KRT74):c.687-203T>A	KRT74	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1279070	NM_175053.4(KRT74):c.686+190G>A	KRT74	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1222253	NM_175053.4(KRT74):c.686+100A>T	KRT74, LOC132090115	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1237606	NM_175053.4(KRT74):c.686+92del	KRT74, LOC132090115	Deletion (intron variant)	not provided	GBenign
Select item 1234778	NM_175053.4(KRT74):c.674A>T (p.Asp225Val)	KRT74 (D225V)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1286421	NM_175053.4(KRT74):c.533T>A (p.Leu178Gln)	KRT74 (L178Q)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1289755	NM_175053.4(KRT74):c.495C>G (p.Asn165Lys)	KRT74 (N165K)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1242117	NM_175053.4(KRT74):c.486G>A (p.Glu162=)	KRT74	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1269321	NM_175053.4(KRT74):c.472-61G>T	KRT74	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1226994	NM_175053.4(KRT74):c.471+192T>C	KRT74	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1222134	NM_175053.4(KRT74):c.471+94T>C	KRT74	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1254234	NM_175053.4(KRT74):c.471+11T>C	KRT74	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 1289735	NM_175053.4(KRT74):c.445G>A (p.Asp149Asn)	KRT74 (D149N)	Single nucleotide variant (missense variant)	not provided	GBenign
Select item 1224684	NM_175053.4(KRT74):c.288T>C (p.Ser96=)	KRT74	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1227906	NM_175053.4(KRT74):c.126C>T (p.Gly42=)	KRT74	Single nucleotide variant (synonymous variant)	not provided	GBenign
Select item 1225607	NC_000012.12:g.52574076A>G	KRT74	Single nucleotide variant	not provided	GBenign

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Items: 44