List of variants in gene HNF1B, LOC126862549 studied for nonpapillary renal cell carcinoma

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Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000458.4(HNF1B):c.660T>C (p.Asp220=)	rs779375959	0.00008
NM_000458.4(HNF1B):c.723G>A (p.Ala241=)	rs768490293	0.00004
NM_000458.4(HNF1B):c.592A>C (p.Ser198Arg)	rs1321074352	0.00001
NM_000458.4(HNF1B):c.578T>C (p.Met193Thr)	rs760079000
NM_000458.4(HNF1B):c.634C>T (p.Gln212Ter)	rs2147553451
NM_000458.4(HNF1B):c.657C>T (p.Ser219=)	rs148713761
NM_000458.4(HNF1B):c.754C>T (p.Arg252Trp)	rs748416956
NM_000458.4(HNF1B):c.809+1G>A

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