List of variants in gene RAB11B reported as benign by Labcorp Genetics (formerly Invitae), Labcorp

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: 32

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HGVS	dbSNP	gnomAD frequency
NM_004218.4(RAB11B):c.552C>T (p.Arg184=)	rs2230876	0.27692
NM_004218.4(RAB11B):c.40+6G>T	rs10426087	0.03103
NM_004218.4(RAB11B):c.258C>T (p.Gly86=)	rs2230875	0.01671
NM_004218.4(RAB11B):c.12G>A (p.Arg4=)	rs2913976	0.00547
NM_004218.4(RAB11B):c.357C>A (p.Ile119=)	rs34741553	0.00423
NM_004218.4(RAB11B):c.511+7G>A	rs189423671	0.00203
NM_004218.4(RAB11B):c.431-8T>C	rs201481532	0.00184
NM_004218.4(RAB11B):c.430+10C>T	rs369849901	0.00039
NM_004218.4(RAB11B):c.40+7C>T	rs565286209	0.00038
NM_004218.4(RAB11B):c.40+13G>T	rs200386569	0.00034
NM_004218.4(RAB11B):c.564C>T (p.Asp188=)	rs113471546	0.00031
NM_004218.4(RAB11B):c.41-7C>T	rs199798403	0.00029
NM_004218.4(RAB11B):c.616G>A (p.Gly206Arg)	rs142408908	0.00028
NM_004218.4(RAB11B):c.573G>A (p.Pro191=)	rs201470573	0.00025
NM_004218.4(RAB11B):c.553G>A (p.Ala185Thr)	rs202233072	0.00011
NM_004218.4(RAB11B):c.87G>A (p.Ser29=)	rs200833450	0.00009
NM_004218.4(RAB11B):c.41-6G>A	rs201361496	0.00008
NM_004218.4(RAB11B):c.512-8C>T	rs764322641	0.00006
NM_004218.4(RAB11B):c.525C>T (p.Ile175=)	rs199957705	0.00004
NM_004218.4(RAB11B):c.63C>T (p.Gly21=)	rs778638576	0.00004
NM_004218.4(RAB11B):c.625C>T (p.Pro209Ser)	rs564037425	0.00003
NM_004218.4(RAB11B):c.93C>T (p.Phe31=)	rs141259254	0.00003
NM_004218.4(RAB11B):c.279C>T (p.Ile93=)	rs746281382	0.00002
NM_004218.4(RAB11B):c.634C>A (p.Leu212Met)	rs747256929	0.00002
NM_004218.4(RAB11B):c.236+7G>C	rs777955946	0.00001
NM_004218.4(RAB11B):c.511+6C>T	rs369982611	0.00001
NM_004218.4(RAB11B):c.550C>T (p.Arg184Cys)	rs1299045693	0.00001
NM_004218.4(RAB11B):c.11G>A (p.Arg4Gln)	rs920560749
NM_004218.4(RAB11B):c.237-20_237-8del	rs2512747348
NM_004218.4(RAB11B):c.511+5_511+10del	rs749841821
NM_004218.4(RAB11B):c.511+6C>G	rs369982611
NM_004218.4(RAB11B):c.629A>G (p.Asn210Ser)	rs2512749151

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