List of variants in gene VHL studied for clear cell renal carcinoma

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 30

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HGVS	dbSNP	gnomAD frequency
NM_000551.3(VHL):c.-73C>T	rs1034934219	0.00031
NM_000551.3(VHL):c.-207C>T	rs886057698	0.00006
NM_000551.4(VHL):c.28G>A (p.Glu10Lys)	rs1057519261	0.00006
NM_000551.4(VHL):c.167C>G (p.Ala56Gly)	rs752980085	0.00004
NM_000551.4(VHL):c.267C>A (p.Leu89=)	rs755794553	0.00002
NM_000551.4(VHL):c.31G>C (p.Ala11Pro)	rs1236604706	0.00002
NM_000551.4(VHL):c.323G>A (p.Arg108His)	rs367594943	0.00002
NM_000551.4(VHL):c.172C>T (p.Arg58Trp)	rs757781272	0.00001
NM_000551.4(VHL):c.205C>G (p.Arg69Gly)	rs1428175816	0.00001
NM_000551.4(VHL):c.275A>T (p.Asp92Val)	rs749091984	0.00001
NM_000551.4(VHL):c.298A>G (p.Thr100Ala)	rs745901803	0.00001
NM_000551.4(VHL):c.40G>C (p.Gly14Arg)	rs1060503559	0.00001
NM_000551.4(VHL):c.95A>G (p.Glu32Gly)	rs786203104	0.00001
NM_000551.4(VHL):c.-10C>T	rs1192379474
NM_000551.4(VHL):c.-9_5dup (p.Ala5fs)	rs730882038
NM_000551.4(VHL):c.116G>T (p.Gly39Val)	rs368473853
NM_000551.4(VHL):c.125A>C (p.Glu42Ala)	rs1064796244
NM_000551.4(VHL):c.130G>C (p.Gly44Arg)	rs1575921446
NM_000551.4(VHL):c.154G>T (p.Glu52Ter)	rs373068386
NM_000551.4(VHL):c.167C>T (p.Ala56Val)	rs752980085
NM_000551.4(VHL):c.181C>G (p.Pro61Ala)	rs113612866
NM_000551.4(VHL):c.221T>C (p.Val74Ala)	rs5030803
NM_000551.4(VHL):c.235C>G (p.Arg79Gly)	rs200885420
NM_000551.4(VHL):c.251T>C (p.Val84Ala)	rs1264207864
NM_000551.4(VHL):c.319C>G (p.Arg107Gly)	rs397516440
NM_000551.4(VHL):c.36G>C (p.Glu12Asp)	rs973493604
NM_000551.4(VHL):c.3G>A (p.Met1Ile)	rs578091032
NM_000551.4(VHL):c.3G>T (p.Met1Ile)	rs578091032
NM_000551.4(VHL):c.70G>T (p.Gly24Cys)	rs1438223626
NM_000551.4(VHL):c.88G>C (p.Gly30Arg)	rs913104799

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