ClinVar Miner

List of variants in gene RAB11B reported as benign for not provided

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Gene type:
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Total variants: 43
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HGVS dbSNP gnomAD frequency
NM_004218.4(RAB11B):c.511+125T>G rs8107834 0.95822
NM_004218.4(RAB11B):c.236+141G>A rs12979252 0.95799
NM_004218.4(RAB11B):c.430+72T>C rs2913968 0.28295
NM_004218.4(RAB11B):c.237-178G>A rs11670119 0.28172
NM_004218.4(RAB11B):c.237-179G>C rs11670118 0.28168
NM_004218.4(RAB11B):c.511+152T>C rs2913967 0.27606
NM_004218.4(RAB11B):c.552C>T (p.Arg184=) rs2230876 0.27283
NM_004218.4(RAB11B):c.41-94G>A rs2913970 0.25188
NM_004218.4(RAB11B):c.*43C>T rs2241588 0.14199
NM_004218.4(RAB11B):c.40+6G>T rs10426087 0.03103
NC_000019.10:g.8390114T>G rs77960487 0.01853
NM_004218.4(RAB11B):c.512-146C>T rs6603065 0.01674
NM_004218.4(RAB11B):c.258C>T (p.Gly86=) rs2230875 0.01671
NM_004218.4(RAB11B):c.12G>A (p.Arg4=) rs2913976 0.00577
NM_004218.4(RAB11B):c.357C>A (p.Ile119=) rs34741553 0.00463
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 0.00043
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.616G>A (p.Gly206Arg) rs142408908 0.00029
NM_004218.4(RAB11B):c.573G>A (p.Pro191=) rs201470573 0.00025
NM_004218.4(RAB11B):c.41-7C>T rs199798403 0.00019
NM_004218.4(RAB11B):c.41-6G>A rs201361496 0.00006
NM_004218.4(RAB11B):c.512-8C>T rs764322641 0.00006
NM_004218.4(RAB11B):c.553G>A (p.Ala185Thr) rs202233072 0.00006
NM_004218.4(RAB11B):c.525C>T (p.Ile175=) rs199957705 0.00004
NM_004218.4(RAB11B):c.40+7C>T rs565286209 0.00003
NM_004218.4(RAB11B):c.634C>A (p.Leu212Met) rs747256929 0.00003
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.87G>A (p.Ser29=) rs200833450 0.00001
NM_004218.4(RAB11B):c.11G>A (p.Arg4Gln) rs920560749
NM_004218.4(RAB11B):c.236+7G>C
NM_004218.4(RAB11B):c.237-20_237-8del
NM_004218.4(RAB11B):c.279C>T (p.Ile93=)
NM_004218.4(RAB11B):c.511+5_511+10del
NM_004218.4(RAB11B):c.511+6C>G
NM_004218.4(RAB11B):c.511+92_511+105dup rs59585874
NM_004218.4(RAB11B):c.625C>T (p.Pro209Ser)
NM_004218.4(RAB11B):c.629A>G (p.Asn210Ser)
NM_004218.4(RAB11B):c.63C>T (p.Gly21=)
NM_004218.4(RAB11B):c.93C>T (p.Phe31=)

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