ClinVar Miner

List of variants in gene ANKS6 reported as likely benign by Fulgent Genetics, Fulgent Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 29
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HGVS dbSNP gnomAD frequency
NM_173551.5(ANKS6):c.862+20G>A rs115965425 0.00695
NM_173551.5(ANKS6):c.603C>T (p.His201=) rs137870160 0.00264
NM_173551.5(ANKS6):c.615C>T (p.Ala205=) rs145249233 0.00139
NM_173551.5(ANKS6):c.1008G>A (p.Thr336=) rs373872443 0.00113
NM_173551.5(ANKS6):c.1533A>C (p.Ala511=) rs200743968 0.00109
NM_173551.5(ANKS6):c.1782C>T (p.Ala594=) rs78732864 0.00077
NM_173551.5(ANKS6):c.2409G>A (p.Ala803=) rs373756771 0.00065
NM_173551.5(ANKS6):c.975C>T (p.Asp325=) rs76803608 0.00055
NM_173551.5(ANKS6):c.1617+12G>A rs199751679 0.00053
NM_173551.5(ANKS6):c.1458T>C (p.Pro486=) rs201904871 0.00048
NM_173551.5(ANKS6):c.2343C>T (p.Ile781=) rs146161090 0.00045
NM_173551.5(ANKS6):c.537A>G (p.Gln179=) rs200417280 0.00044
NM_173551.5(ANKS6):c.609C>T (p.His203=) rs372936113 0.00042
NM_173551.5(ANKS6):c.1219+18A>T rs372791631 0.00036
NM_173551.5(ANKS6):c.2143-15T>C rs376048873 0.00035
NM_173551.5(ANKS6):c.498C>T (p.Ala166=) rs374209515 0.00031
NM_173551.5(ANKS6):c.1731G>A (p.Thr577=) rs201821907 0.00021
NM_173551.5(ANKS6):c.908-16C>T rs375604399 0.00021
NM_173551.5(ANKS6):c.2142+14G>T rs545751955 0.00014
NM_173551.5(ANKS6):c.1134T>C (p.Tyr378=) rs200656157 0.00010
NM_173551.5(ANKS6):c.354G>A (p.Ala118=) rs980440912 0.00009
NM_173551.5(ANKS6):c.1185G>A (p.Thr395=) rs146980948 0.00008
NM_173551.5(ANKS6):c.1125T>C (p.Ile375=) rs200355078 0.00003
NM_173551.5(ANKS6):c.1989T>C (p.Asn663=) rs756110261 0.00003
NM_173551.5(ANKS6):c.2395-7T>C rs775510768 0.00003
NM_173551.5(ANKS6):c.2487G>A (p.Ala829=) rs758679399 0.00001
NM_173551.5(ANKS6):c.2265G>A (p.Ser755=) rs566372073
NM_173551.5(ANKS6):c.2327-19dup rs575021016
NM_173551.5(ANKS6):c.907+8C>G rs775680028

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