List of variants reported as likely pathogenic for kidney cancer by Fulgent Genetics, Fulgent Genetics

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Total variants: 19

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HGVS	dbSNP	gnomAD frequency
NM_000059.4(BRCA2):c.7878G>C (p.Trp2626Cys)	rs80359013	0.00001
NM_000545.8(HNF1A):c.1556C>T (p.Pro519Leu)	rs749673816	0.00001
NM_144997.7(FLCN):c.779+1G>T	rs758175953	0.00001
NM_000059.4(BRCA2):c.15del (p.Glu7fs)	rs1064795072
NM_000059.4(BRCA2):c.1889del (p.Thr630fs)	rs80359315
NM_000059.4(BRCA2):c.574_575del (p.Met192fs)	rs80359533
NM_000458.4(HNF1B):c.1130_1131del (p.Ser377fs)	rs2147473703
NM_000458.4(HNF1B):c.634C>T (p.Gln212Ter)	rs2147553451
NM_000458.4(HNF1B):c.865A>G (p.Asn289Asp)
NM_000545.8(HNF1A):c.1136C>A (p.Pro379His)	rs371717826
NM_000545.8(HNF1A):c.1310-2A>G	rs2135847311
NM_000545.8(HNF1A):c.818AAG[2] (p.Glu275del)	rs1288094664
NM_000546.6(TP53):c.722C>T (p.Ser241Phe)	rs28934573
NM_000546.6(TP53):c.799C>T (p.Arg267Trp)	rs55832599
NM_000551.4(VHL):c.319C>G (p.Arg107Gly)	rs397516440
NM_000612.6(IGF2):c.100G>T (p.Gly34Cys)	rs1858937359
NM_144997.7(FLCN):c.1357_1363del (p.Gly453fs)	rs1131690841
NM_144997.7(FLCN):c.1657T>C (p.Trp553Arg)	rs1131690833
NM_144997.7(FLCN):c.189del (p.Ala64fs)	rs876660611

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