ClinVar Miner

List of variants in gene VPS33B reported by PreventionGenetics, part of Exact Sciences

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 52
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_018668.5(VPS33B):c.1540G>A (p.Gly514Ser) rs11073964 0.58143
NM_018668.5(VPS33B):c.1105+9C>T rs3826033 0.13431
NM_018668.5(VPS33B):c.151C>A (p.Arg51=) rs11542638 0.09422
NM_018668.5(VPS33B):c.1656A>T (p.Thr552=) rs16945153 0.05737
NM_018668.5(VPS33B):c.1405+36G>A rs116787959 0.03351
NM_018668.5(VPS33B):c.648C>T (p.Gly216=) rs59648701 0.01941
NM_018668.5(VPS33B):c.597C>T (p.Cys199=) rs60198611 0.01658
NM_018668.5(VPS33B):c.-8C>T rs11542639 0.01125
NM_018668.5(VPS33B):c.1671A>G (p.Glu557=) rs148071246 0.00686
NM_018668.5(VPS33B):c.1658-36G>A rs115092755 0.00531
NM_018668.5(VPS33B):c.1392C>T (p.Thr464=) rs142845101 0.00362
NM_018668.5(VPS33B):c.1166G>A (p.Arg389Gln) rs145070485 0.00158
NM_018668.5(VPS33B):c.852+13G>A rs188518961 0.00130
NM_018668.5(VPS33B):c.357G>A (p.Lys119=) rs146758743 0.00120
NM_018668.5(VPS33B):c.944G>A (p.Arg315Gln) rs145303578 0.00116
NM_018668.5(VPS33B):c.1148T>C (p.Ile383Thr) rs149121639 0.00114
NM_018668.5(VPS33B):c.1274G>A (p.Ser425Asn) rs139709507 0.00094
NM_018668.5(VPS33B):c.1714T>G (p.Phe572Val) rs145092724 0.00079
NM_018668.5(VPS33B):c.1362C>T (p.Ala454=) rs142964161 0.00049
NM_018668.5(VPS33B):c.1207T>C (p.Leu403=) rs139655526 0.00039
NM_018668.5(VPS33B):c.1351A>G (p.Thr451Ala) rs148809175 0.00024
NM_018668.5(VPS33B):c.1658-7C>T rs375376103 0.00023
NM_018668.5(VPS33B):c.240-9C>T rs781107857 0.00023
NM_018668.5(VPS33B):c.1171-6A>G rs370691219 0.00013
NM_018668.5(VPS33B):c.637G>A (p.Glu213Lys) rs951699405 0.00013
NM_018668.5(VPS33B):c.1105+10G>A rs370555380 0.00010
NM_018668.5(VPS33B):c.177+5T>A rs747146575 0.00008
NM_018668.5(VPS33B):c.1749C>T (p.Ala583=) rs201436915 0.00005
NM_018668.5(VPS33B):c.277C>T (p.Arg93Ter) rs368124813 0.00005
NM_018668.5(VPS33B):c.1170+5G>A rs201431055 0.00004
NM_018668.5(VPS33B):c.1193G>A (p.Arg398His) rs762843831 0.00004
NM_018668.5(VPS33B):c.1014C>T (p.His338=) rs765002211 0.00002
NM_018668.5(VPS33B):c.1225+5G>C rs398122407 0.00002
NM_018668.5(VPS33B):c.1454G>A (p.Arg485His) rs141601851 0.00001
NM_018668.5(VPS33B):c.456G>T (p.Leu152=) rs997425993 0.00001
NM_018668.5(VPS33B):c.1015C>T (p.Arg339Cys)
NM_018668.5(VPS33B):c.1307A>G (p.Asn436Ser)
NM_018668.5(VPS33B):c.1384C>T (p.Leu462=)
NM_018668.5(VPS33B):c.1463_1464delinsA (p.Ser488fs)
NM_018668.5(VPS33B):c.1575T>A (p.Ile525=)
NM_018668.5(VPS33B):c.1623_1641del (p.Arg542fs)
NM_018668.5(VPS33B):c.1816G>A (p.Ala606Thr)
NM_018668.5(VPS33B):c.183C>T (p.His61=)
NM_018668.5(VPS33B):c.240-13_240-12del rs111274092
NM_018668.5(VPS33B):c.30T>G (p.Pro10=)
NM_018668.5(VPS33B):c.326G>A (p.Arg109His)
NM_018668.5(VPS33B):c.366G>A (p.Ala122=)
NM_018668.5(VPS33B):c.457C>T (p.Leu153=)
NM_018668.5(VPS33B):c.499-17T>C
NM_018668.5(VPS33B):c.825G>A (p.Leu275=)
NM_018668.5(VPS33B):c.852+9G>A
NM_018668.5(VPS33B):c.894T>C (p.Phe298=)

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.