ClinVar Miner

List of variants in gene PDGFRB reported as benign for connective tissue neoplasm

Included ClinVar conditions (122):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 42
Download table as spreadsheet
HGVS dbSNP
NM_002609.4(PDGFRB):c.102C>T (p.Val34=) rs17708515
NM_002609.4(PDGFRB):c.1033C>T (p.Pro345Ser) rs2229558
NM_002609.4(PDGFRB):c.1083C>T (p.Ser361=)
NM_002609.4(PDGFRB):c.1108C>T (p.Arg370Cys) rs200684708
NM_002609.4(PDGFRB):c.1119G>A (p.Ser373=) rs200225593
NM_002609.4(PDGFRB):c.1149G>C (p.Leu383=) rs2228439
NM_002609.4(PDGFRB):c.1223C>G (p.Ser408Cys) rs200203294
NM_002609.4(PDGFRB):c.12G>A (p.Pro4=) rs138641101
NM_002609.4(PDGFRB):c.1376G>A (p.Arg459His) rs149274963
NM_002609.4(PDGFRB):c.1391C>T (p.Thr464Met) rs74943037
NM_002609.4(PDGFRB):c.1393C>T (p.Leu465=) rs116171826
NM_002609.4(PDGFRB):c.1437C>T (p.Asn479=) rs371550567
NM_002609.4(PDGFRB):c.1453G>A (p.Glu485Lys) rs41287110
NM_002609.4(PDGFRB):c.1505G>A (p.Arg502Gln) rs148974733
NM_002609.4(PDGFRB):c.1539T>C (p.Ala513=) rs150562879
NM_002609.4(PDGFRB):c.1579+10C>T rs571420039
NM_002609.4(PDGFRB):c.1761G>A (p.Leu587=) rs56078873
NM_002609.4(PDGFRB):c.1854G>A (p.Thr618=) rs56072663
NM_002609.4(PDGFRB):c.1872T>C (p.His624=) rs141371542
NM_002609.4(PDGFRB):c.2053C>T (p.Arg685Cys)
NM_002609.4(PDGFRB):c.2164G>T (p.Val722Phe) rs142689325
NM_002609.4(PDGFRB):c.2463C>T (p.Asn821=) rs78336563
NM_002609.4(PDGFRB):c.2502C>T (p.Ile834=) rs143375423
NM_002609.4(PDGFRB):c.2523G>A (p.Lys841=) rs41287108
NM_002609.4(PDGFRB):c.2601A>G (p.Leu867=) rs246395
NM_002609.4(PDGFRB):c.2616G>A (p.Pro872=) rs148709288
NM_002609.4(PDGFRB):c.2844G>A (p.Arg948=) rs55647240
NM_002609.4(PDGFRB):c.2889C>T (p.Gly963=) rs139623802
NM_002609.4(PDGFRB):c.3030T>G (p.Thr1010=)
NM_002609.4(PDGFRB):c.3090C>T (p.Pro1030=) rs2228440
NM_002609.4(PDGFRB):c.3119G>T (p.Gly1040Val) rs149417689
NM_002609.4(PDGFRB):c.3137+4A>G rs246391
NM_002609.4(PDGFRB):c.3252A>G (p.Pro1084=) rs246388
NM_002609.4(PDGFRB):c.3270G>A (p.Pro1090=) rs183852315
NM_002609.4(PDGFRB):c.3287C>T (p.Ala1096Val) rs114435947
NM_002609.4(PDGFRB):c.365-4G>T rs139448702
NM_002609.4(PDGFRB):c.486G>A (p.Glu162=)
NM_002609.4(PDGFRB):c.590G>A (p.Arg197Lys) rs116642123
NM_002609.4(PDGFRB):c.714C>T (p.Ile238=) rs41287114
NM_002609.4(PDGFRB):c.85A>T (p.Ile29Phe) rs17110944
NM_002609.4(PDGFRB):c.945C>T (p.Tyr315=) rs56069016
NM_002609.4(PDGFRB):c.946G>A (p.Val316Met) rs41287112

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.