ClinVar Miner

List of variants studied for Bardet-Biedl syndrome 4 by Baylor Genetics

Included ClinVar conditions (1):
Minimum submission review status: Collection method:
Minimum conflict level:
ClinVar version:
Total variants: 55
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_033028.5(BBS4):c.712-1G>A rs377031435 0.00003
NM_033028.5(BBS4):c.1375C>T (p.Gln459Ter) rs914062190 0.00002
NM_033028.5(BBS4):c.1072_1073del (p.Lys358fs) rs2065896039 0.00001
NM_033028.5(BBS4):c.1091C>A (p.Ala364Glu) rs28938468 0.00001
NM_033028.5(BBS4):c.1103A>G (p.Asp368Gly) rs772548770 0.00001
NM_033028.5(BBS4):c.883C>T (p.Arg295Ter) rs775710800 0.00001
NM_033028.5(BBS4):c.101del (p.Lys34fs)
NM_033028.5(BBS4):c.1037-2A>G
NM_033028.5(BBS4):c.103C>T (p.Gln35Ter)
NM_033028.5(BBS4):c.10G>T (p.Glu4Ter)
NM_033028.5(BBS4):c.1106+1G>A
NM_033028.5(BBS4):c.1106+2T>C
NM_033028.5(BBS4):c.1106del (p.Lys369fs)
NM_033028.5(BBS4):c.1118T>A (p.Leu373Ter)
NM_033028.5(BBS4):c.1185T>A (p.Tyr395Ter)
NM_033028.5(BBS4):c.1202_1203dup (p.Val402fs)
NM_033028.5(BBS4):c.1248+1G>A
NM_033028.5(BBS4):c.1248+2T>C rs2151055229
NM_033028.5(BBS4):c.1248+2dup
NM_033028.5(BBS4):c.1264C>T (p.Gln422Ter)
NM_033028.5(BBS4):c.1294dup (p.Glu432fs)
NM_033028.5(BBS4):c.1308G>A (p.Trp436Ter)
NM_033028.5(BBS4):c.1318_1321del (p.Val440fs) rs1281334523
NM_033028.5(BBS4):c.1389dup (p.Ser464fs)
NM_033028.5(BBS4):c.1398del (p.Ala467fs)
NM_033028.5(BBS4):c.1450+2T>C
NM_033028.5(BBS4):c.150del (p.Cys51fs)
NM_033028.5(BBS4):c.157-2A>G rs113994192
NM_033028.5(BBS4):c.172C>T (p.Gln58Ter) rs886039802
NM_033028.5(BBS4):c.210_213del (p.Ile70fs) rs775928735
NM_033028.5(BBS4):c.220+1G>A
NM_033028.5(BBS4):c.24+1G>A rs759520211
NM_033028.5(BBS4):c.276_277del (p.Ala94fs)
NM_033028.5(BBS4):c.295C>T (p.Gln99Ter)
NM_033028.5(BBS4):c.31C>T (p.Gln11Ter)
NM_033028.5(BBS4):c.332+2_332+3insTT rs753360929
NM_033028.5(BBS4):c.333-2A>C
NM_033028.5(BBS4):c.341del (p.Leu114fs) rs750258633
NM_033028.5(BBS4):c.405G>A (p.Trp135Ter)
NM_033028.5(BBS4):c.406G>T (p.Glu136Ter)
NM_033028.5(BBS4):c.439T>A (p.Tyr147Asn) rs781691906
NM_033028.5(BBS4):c.511dup (p.Tyr171fs)
NM_033028.5(BBS4):c.514dup (p.Ile172fs)
NM_033028.5(BBS4):c.55C>T (p.Gln19Ter)
NM_033028.5(BBS4):c.584_585dup (p.Glu196fs)
NM_033028.5(BBS4):c.608_609del (p.Glu203fs)
NM_033028.5(BBS4):c.616dup (p.Thr206fs)
NM_033028.5(BBS4):c.638T>A (p.Leu213Ter) rs1060503692
NM_033028.5(BBS4):c.642+2T>G
NM_033028.5(BBS4):c.819del (p.Leu272_Trp273insTer)
NM_033028.5(BBS4):c.864+1G>A
NM_033028.5(BBS4):c.864+1G>C rs2151047618
NM_033028.5(BBS4):c.87del (p.Pro30fs)
NM_033028.5(BBS4):c.95T>A (p.Leu32Ter)
NM_033028.5(BBS4):c.960T>A (p.Tyr320Ter) rs770891152

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.