ClinVar Miner

List of variants in gene BUB1B reported as uncertain significance for colorectal cancer

Included ClinVar conditions (91):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 34
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001211.6(BUB1B):c.1001C>T (p.Pro334Leu) rs141953425 0.00063
NM_001211.6(BUB1B):c.805A>G (p.Asn269Asp) rs148159407 0.00041
NM_001211.6(BUB1B):c.1943C>T (p.Thr648Ile) rs148348158 0.00029
NM_001211.6(BUB1B):c.1227A>C (p.Glu409Asp) rs28989188 0.00027
NM_001211.6(BUB1B):c.2351C>T (p.Ala784Val) rs142705245 0.00013
NM_001211.6(BUB1B):c.1478C>T (p.Thr493Ile) rs146795655 0.00011
NM_001211.6(BUB1B):c.1630C>T (p.Pro544Ser) rs138332995 0.00011
NM_001211.6(BUB1B):c.464A>G (p.Tyr155Cys) rs764923350 0.00006
NM_001211.6(BUB1B):c.959A>G (p.Glu320Gly) rs771382233 0.00005
NM_001211.6(BUB1B):c.1150A>G (p.Ser384Gly) rs202114756 0.00004
NM_001211.6(BUB1B):c.1361A>G (p.Lys454Arg) rs373256667 0.00004
NM_001211.6(BUB1B):c.1382A>C (p.Gln461Pro) rs747886467 0.00004
NM_001211.6(BUB1B):c.542A>G (p.Gln181Arg) rs375798678 0.00004
NM_001211.6(BUB1B):c.440T>C (p.Ile147Thr) rs763623522 0.00003
NM_001211.6(BUB1B):c.484T>C (p.Tyr162His) rs77520855 0.00003
NM_001211.6(BUB1B):c.1875A>G (p.Ile625Met) rs541881263 0.00002
NM_001211.6(BUB1B):c.2530C>T (p.Leu844Phe) rs28989181 0.00002
NM_001211.6(BUB1B):c.1163C>T (p.Ala388Val) rs771602632 0.00001
NM_001211.6(BUB1B):c.1464A>T (p.Lys488Asn) rs368023159 0.00001
NM_001211.6(BUB1B):c.2271G>T (p.Lys757Asn) rs1007572176 0.00001
NM_001211.6(BUB1B):c.234G>T (p.Trp78Cys) rs760085736 0.00001
NM_001211.6(BUB1B):c.242A>G (p.Tyr81Cys) rs1212671249 0.00001
NM_001211.6(BUB1B):c.596G>A (p.Arg199Gln) rs779260067 0.00001
NM_001211.6(BUB1B):c.1168GAG[1] (p.Glu391del) rs778590557
NM_001211.6(BUB1B):c.1453G>A (p.Glu485Lys) rs770704003
NM_001211.6(BUB1B):c.1636G>A (p.Ala546Thr)
NM_001211.6(BUB1B):c.1784G>T (p.Gly595Val)
NM_001211.6(BUB1B):c.2051G>C (p.Gly684Ala)
NM_001211.6(BUB1B):c.2434A>G (p.Lys812Glu)
NM_001211.6(BUB1B):c.2450A>C (p.Glu817Ala)
NM_001211.6(BUB1B):c.418A>G (p.Ser140Gly)
NM_001211.6(BUB1B):c.458A>T (p.Gln153Leu) rs776363221
NM_001211.6(BUB1B):c.737G>A (p.Gly246Glu) rs1407334063
NM_001211.6(BUB1B):c.74G>A (p.Ser25Asn)

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.