List of variants in gene HNF1A reported as likely pathogenic for carcinoma

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 12

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HGVS	dbSNP	gnomAD frequency
NM_000545.8(HNF1A):c.1720A>G (p.Ser574Gly)	rs1169305	0.98610
NM_000545.8(HNF1A):c.827C>G (p.Ala276Gly)	rs137853245	0.00003
NM_000545.8(HNF1A):c.1556C>T (p.Pro519Leu)	rs749673816	0.00001
NM_000545.8(HNF1A):c.-64_-55delinsGC
NM_000545.8(HNF1A):c.1136C>A (p.Pro379His)	rs371717826
NM_000545.8(HNF1A):c.1310-2A>G	rs2135847311
NM_000545.8(HNF1A):c.1555_1556dup (p.Gln520fs)
NM_000545.8(HNF1A):c.1575_1576delinsA (p.Asp526fs)
NM_000545.8(HNF1A):c.1715del (p.Pro572fs)
NM_000545.8(HNF1A):c.1720delinsGGCATCCAGCACCG (p.Ser574fs)
NM_000545.8(HNF1A):c.3G>A (p.Met1Ile)
NM_000545.8(HNF1A):c.818AAG[2] (p.Glu275del)	rs1288094664

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