List of variants in gene combination LOC107303340, VHL reported by Urologic Oncology Branch, National Institutes of Health

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
NC_000003.12:g.10139220_10148953del
NC_000003.12:g.10139708_10142406del
NC_000003.12:g.10139761_10142459del
NC_000003.12:g.10140648_10148414del
NC_000003.12:g.10140738_10142535del
NC_000003.12:g.10141523_10142610del
NC_000003.12:g.10148440_10158273del
NC_000003.12:g.10148566_10158401del
NC_000003.12:g.10148615_10158450del
NM_000551.4(VHL):c.340+1019_463+450del
NM_000551.4(VHL):c.340+1543_464-1191del
NM_000551.4(VHL):c.340+1580_464-1477del
NM_000551.4(VHL):c.340+221_464-1411del
NM_000551.4(VHL):c.340+283_463+499del
NM_000551.4(VHL):c.340+307_464-1191del
NM_000551.4(VHL):c.340+365_464-909del
NM_000551.4(VHL):c.340+428_464-1203del
NM_000551.4(VHL):c.340+444_464-1187del
NM_000551.4(VHL):c.340+994_*2333del
NM_000551.4(VHL):c.341-1382_*3401del
NM_000551.4(VHL):c.341-1406_*3377del
NM_000551.4(VHL):c.341-1583_464-1477del
NM_000551.4(VHL):c.341-1857_464-1328del
NM_000551.4(VHL):c.341-279_464-614del
NM_000551.4(VHL):c.341-49_*2815del
NM_000551.4(VHL):c.341-929_*3191del
NM_000551.4(VHL):c.341-951_464-1018del
NM_000551.4(VHL):c.463+1008_*2803del
NM_000551.4(VHL):c.463+439_*991del
NM_000551.4(VHL):c.464-1226_*2771del

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