List of variants in gene BBS10 reported as likely benign by PreventionGenetics, part of Exact Sciences

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 41

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HGVS	dbSNP	gnomAD frequency
NM_024685.4(BBS10):c.424G>A (p.Asp142Asn)	rs142863601	0.00738
NM_024685.4(BBS10):c.1631A>G (p.Asn544Ser)	rs34737974	0.00618
NM_024685.4(BBS10):c.1736A>G (p.Lys579Arg)	rs141521925	0.00159
NM_024685.4(BBS10):c.1245T>C (p.His415=)	rs147241753	0.00130
NM_024685.4(BBS10):c.1436C>A (p.Ala479Glu)	rs138434761	0.00058
NM_024685.4(BBS10):c.1276A>G (p.Lys426Glu)	rs149596527	0.00040
NM_024685.4(BBS10):c.957T>C (p.Val319=)	rs139645096	0.00039
NM_024685.4(BBS10):c.474G>T (p.Ser158=)	rs375436323	0.00032
NM_024685.4(BBS10):c.1923C>T (p.Pro641=)	rs201449351	0.00015
NM_024685.4(BBS10):c.1050A>G (p.Pro350=)	rs370953693	0.00014
NM_024685.4(BBS10):c.372T>A (p.Ser124=)	rs143366878	0.00014
NM_024685.4(BBS10):c.102G>T (p.Arg34=)	rs376601112	0.00013
NM_024685.4(BBS10):c.1590A>C (p.Arg530Ser)	rs146812823	0.00010
NM_024685.4(BBS10):c.1333C>A (p.Leu445Ile)	rs199878555	0.00009
NM_024685.4(BBS10):c.1265G>A (p.Arg422Gln)	rs138961848	0.00008
NM_024685.4(BBS10):c.1629C>T (p.Asn543=)	rs145124702	0.00008
NM_024685.4(BBS10):c.429T>C (p.Gly143=)	rs146587757	0.00006
NM_024685.4(BBS10):c.440A>G (p.Gln147Arg)	rs140585012	0.00006
NM_024685.4(BBS10):c.42G>A (p.Ala14=)	rs373458861	0.00005
NM_024685.4(BBS10):c.1548A>T (p.Thr516=)	rs771662934	0.00004
NM_024685.4(BBS10):c.163C>T (p.Leu55=)	rs887761680	0.00004
NM_024685.4(BBS10):c.1075C>G (p.Gln359Glu)	rs767572725	0.00003
NM_024685.4(BBS10):c.1041T>C (p.Gly347=)	rs747390360	0.00002
NM_024685.4(BBS10):c.1215T>G (p.Gly405=)	rs751592378	0.00002
NM_024685.4(BBS10):c.1437A>G (p.Ala479=)	rs201701959	0.00002
NM_024685.4(BBS10):c.1572A>G (p.Thr524=)	rs1271927802	0.00002
NM_024685.4(BBS10):c.637T>C (p.Leu213=)	rs367795705	0.00002
NM_024685.4(BBS10):c.63G>A (p.Leu21=)	rs779366264	0.00002
NM_024685.4(BBS10):c.1134C>T (p.Ser378=)	rs764371181	0.00001
NM_024685.4(BBS10):c.1866T>C (p.His622=)	rs1167846126	0.00001
NM_024685.4(BBS10):c.197+5C>T	rs754503828	0.00001
NM_024685.4(BBS10):c.1975A>T (p.Ile659Leu)	rs771355732	0.00001
NM_024685.4(BBS10):c.2142T>G (p.Val714=)	rs1463359253	0.00001
NM_024685.4(BBS10):c.393G>A (p.Gln131=)	rs369066076	0.00001
NM_024685.4(BBS10):c.483A>G (p.Lys161=)	rs748732850	0.00001
NM_024685.4(BBS10):c.630A>T (p.Val210=)	rs759791957	0.00001
NM_024685.4(BBS10):c.1074G>A (p.Ser358=)	rs551803123
NM_024685.4(BBS10):c.1677C>T (p.Tyr559=)	rs375413604
NM_024685.4(BBS10):c.1684T>C (p.Leu562=)	rs111773727
NM_024685.4(BBS10):c.1989T>C (p.His663=)
NM_024685.4(BBS10):c.687T>A (p.Pro229=)

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