ClinVar Miner

List of variants in gene VHL reported as likely benign for adrenal gland disease

Included ClinVar conditions (122):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 48
Download table as spreadsheet
HGVS dbSNP
NM_000551.3(VHL):c.-77C>T rs3087462
NM_000551.3(VHL):c.105C>G (p.Ala35=) rs1310829877
NM_000551.3(VHL):c.108G>A (p.Glu36=) rs1553619344
NM_000551.3(VHL):c.114C>T (p.Ser38=) rs417164
NM_000551.3(VHL):c.119C>T (p.Pro40Leu) rs200343185
NM_000551.3(VHL):c.129C>T (p.Ser43=) rs864622645
NM_000551.3(VHL):c.12G>A (p.Arg4=) rs1553619274
NM_000551.3(VHL):c.134C>G (p.Pro45Arg) rs199583685
NM_000551.3(VHL):c.135G>A (p.Pro45=) rs773519476
NM_000551.3(VHL):c.150C>A (p.Ala50=) rs61751580
NM_000551.3(VHL):c.159G>A (p.Glu53=) rs1553619385
NM_000551.3(VHL):c.168C>G (p.Ala56=) rs864622714
NM_000551.3(VHL):c.168C>T (p.Ala56=) rs864622714
NM_000551.3(VHL):c.172C>A (p.Arg58=) rs757781272
NM_000551.3(VHL):c.183C>G (p.Pro61=) rs63650860
NM_000551.3(VHL):c.192C>T (p.Arg64=) rs1012545817
NM_000551.3(VHL):c.195G>C (p.Ser65=) rs1553619409
NM_000551.3(VHL):c.213C>T (p.Pro71=) rs201663073
NM_000551.3(VHL):c.216C>T (p.Ser72=) rs774557051
NM_000551.3(VHL):c.225C>T (p.Ile75=) rs768104793
NM_000551.3(VHL):c.240T>C (p.Ser80=) rs1553619424
NM_000551.3(VHL):c.241C>T (p.Pro81Ser) rs104893829
NM_000551.3(VHL):c.246C>T (p.Arg82=) rs587780993
NM_000551.3(VHL):c.249C>G (p.Val83=) rs1271292937
NM_000551.3(VHL):c.255G>T (p.Leu85=) rs876658508
NM_000551.3(VHL):c.258C>G (p.Pro86=) rs781063331
NM_000551.3(VHL):c.271T>G (p.Phe91Val)
NM_000551.3(VHL):c.27C>T (p.Asp9=) rs1017141110
NM_000551.3(VHL):c.291C>G (p.Pro97=) rs1805159
NM_000551.3(VHL):c.291C>T (p.Pro97=) rs1805159
NM_000551.3(VHL):c.297A>C (p.Pro99=) rs774753107
NM_000551.3(VHL):c.315G>C (p.Thr105=) rs769102979
NM_000551.3(VHL):c.324C>T (p.Arg108=) rs878854124
NM_000551.3(VHL):c.327C>T (p.Ile109=) rs863224371
NM_000551.3(VHL):c.333C>T (p.Ser111=) rs765978945
NM_000551.3(VHL):c.340+5G>C rs61758376
NM_000551.3(VHL):c.340+7G>C rs869025635
NM_000551.3(VHL):c.340+8C>T
NM_000551.3(VHL):c.45G>A (p.Ala15=) rs563813895
NM_000551.3(VHL):c.48G>A (p.Glu16=) rs1057522140
NM_000551.3(VHL):c.54A>C (p.Ala18=) rs1305687580
NM_000551.3(VHL):c.57C>A (p.Gly19=) rs1453582828
NM_000551.3(VHL):c.60C>G (p.Val20=) rs1553619311
NM_000551.3(VHL):c.6C>G (p.Pro2=) rs1014417508
NM_000551.3(VHL):c.72C>A (p.Gly24=) rs1375079282
NM_000551.3(VHL):c.74C>T (p.Pro25Leu) rs35460768
NM_000551.3(VHL):c.75T>C (p.Pro25=) rs1553619317
NM_000551.3(VHL):c.99G>C (p.Ser33=) rs912159589

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.