ClinVar Miner

List of variants in gene CCN6 reported as likely benign for not provided

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Gene type:
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Total variants: 95
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HGVS dbSNP gnomAD frequency
NM_198239.2(CCN6):c.48+229G>A rs76664940 0.00741
NM_198239.2(CCN6):c.310G>C (p.Val104Leu) rs78266262 0.00251
NM_198239.2(CCN6):c.77C>T (p.Pro26Leu) rs149609367 0.00210
NM_198239.2(CCN6):c.91C>A (p.Pro31Thr) rs145590972 0.00175
NM_198239.2(CCN6):c.148T>C (p.Trp50Arg) rs35914692 0.00061
NM_198239.2(CCN6):c.589+27C>T rs200472841 0.00047
NM_198239.2(CCN6):c.248G>A (p.Gly83Glu) rs147337485 0.00039
NM_198239.2(CCN6):c.219A>T (p.Gly73=) rs139375158 0.00032
NM_198239.2(CCN6):c.19T>C (p.Ser7Pro) rs34322868 0.00026
NM_198239.2(CCN6):c.130C>T (p.Arg44Cys) rs137881483 0.00022
NM_198239.2(CCN6):c.131G>A (p.Arg44His) rs782703789 0.00011
NM_198239.2(CCN6):c.48+13C>T rs375836805 0.00002
NM_198239.2(CCN6):c.33T>C (p.Leu11=) rs782215592 0.00001
NM_198239.2(CCN6):c.590-19T>C rs1776755983 0.00001
NM_198239.2(CCN6):c.594T>C (p.Tyr198=) rs564402147 0.00001
NM_198239.2(CCN6):c.783+12A>G rs782683729 0.00001
NM_198239.2(CCN6):c.783+14A>G rs781966767 0.00001
NM_198239.2(CCN6):c.784-9T>C rs782261016 0.00001
NM_198239.2(CCN6):c.1008G>A (p.Val336=)
NM_198239.2(CCN6):c.1062G>A (p.Leu354=)
NM_198239.2(CCN6):c.111A>G (p.Glu37=)
NM_198239.2(CCN6):c.114G>A (p.Val38=)
NM_198239.2(CCN6):c.117A>G (p.Ser39=)
NM_198239.2(CCN6):c.147C>T (p.His49=)
NM_198239.2(CCN6):c.156C>T (p.Cys52=)
NM_198239.2(CCN6):c.15C>A (p.Leu5=)
NM_198239.2(CCN6):c.15C>T (p.Leu5=)
NM_198239.2(CCN6):c.165T>C (p.Pro55=)
NM_198239.2(CCN6):c.195G>A (p.Val65=)
NM_198239.2(CCN6):c.195G>T (p.Val65=)
NM_198239.2(CCN6):c.210T>C (p.Asp70=)
NM_198239.2(CCN6):c.213C>A (p.Gly71=)
NM_198239.2(CCN6):c.246A>G (p.Pro82=)
NM_198239.2(CCN6):c.270C>T (p.Asp90=)
NM_198239.2(CCN6):c.28C>T (p.Leu10=)
NM_198239.2(CCN6):c.309A>G (p.Ser103=)
NM_198239.2(CCN6):c.346+16T>C
NM_198239.2(CCN6):c.346+17G>A
NM_198239.2(CCN6):c.346+8TCT[2]
NM_198239.2(CCN6):c.347-10C>T rs1583581459
NM_198239.2(CCN6):c.347-15C>G
NM_198239.2(CCN6):c.347-16T>C
NM_198239.2(CCN6):c.347-4T>C
NM_198239.2(CCN6):c.357T>A (p.Ala119=)
NM_198239.2(CCN6):c.378G>A (p.Gln126=)
NM_198239.2(CCN6):c.381A>G (p.Val127=)
NM_198239.2(CCN6):c.453A>G (p.Gly151=)
NM_198239.2(CCN6):c.48+10C>G
NM_198239.2(CCN6):c.48+17G>A
NM_198239.2(CCN6):c.48+7C>T
NM_198239.2(CCN6):c.48+8C>T
NM_198239.2(CCN6):c.49-13T>G
NM_198239.2(CCN6):c.49-14A>G
NM_198239.2(CCN6):c.49-19C>A
NM_198239.2(CCN6):c.49-763G>A
NM_198239.2(CCN6):c.49-763G>C
NM_198239.2(CCN6):c.49-7A>G
NM_198239.2(CCN6):c.49-9C>A
NM_198239.2(CCN6):c.516G>A (p.Lys172=)
NM_198239.2(CCN6):c.531A>G (p.Ser177=)
NM_198239.2(CCN6):c.546A>G (p.Glu182=)
NM_198239.2(CCN6):c.582A>G (p.Thr194=)
NM_198239.2(CCN6):c.589+19A>G
NM_198239.2(CCN6):c.589+20T>C
NM_198239.2(CCN6):c.589+7A>G
NM_198239.2(CCN6):c.590-11C>T
NM_198239.2(CCN6):c.590-6T>C
NM_198239.2(CCN6):c.590-9T>C
NM_198239.2(CCN6):c.666A>G (p.Thr222=)
NM_198239.2(CCN6):c.732A>G (p.Lys244=)
NM_198239.2(CCN6):c.738G>A (p.Leu246=)
NM_198239.2(CCN6):c.756C>T (p.Cys252=)
NM_198239.2(CCN6):c.75A>G (p.Gly25=)
NM_198239.2(CCN6):c.777A>G (p.Thr259=)
NM_198239.2(CCN6):c.783+22_783+26del
NM_198239.2(CCN6):c.784-10A>G
NM_198239.2(CCN6):c.784-19A>C
NM_198239.2(CCN6):c.784-19A>G
NM_198239.2(CCN6):c.784-20C>T
NM_198239.2(CCN6):c.784-6T>G
NM_198239.2(CCN6):c.789C>G (p.Pro263=)
NM_198239.2(CCN6):c.789C>T (p.Pro263=)
NM_198239.2(CCN6):c.804C>T (p.Cys268=)
NM_198239.2(CCN6):c.84T>C (p.Asp28=)
NM_198239.2(CCN6):c.867G>A (p.Gln289=)
NM_198239.2(CCN6):c.906G>A (p.Lys302=)
NM_198239.2(CCN6):c.90A>G (p.Thr30=)
NM_198239.2(CCN6):c.912C>T (p.Cys304=)
NM_198239.2(CCN6):c.921T>C (p.Pro307=)
NM_198239.2(CCN6):c.927G>A (p.Lys309=)
NM_198239.2(CCN6):c.930T>C (p.Ser310=)
NM_198239.2(CCN6):c.93T>C (p.Pro31=)
NM_198239.2(CCN6):c.963T>C (p.Asn321=)
NM_198239.2(CCN6):c.990G>C (p.Leu330=)
NM_198239.2(CCN6):c.999A>G (p.Thr333=)

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