ClinVar Miner

List of variants in gene combination ATIC, FN1 reported as likely benign for not provided

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Total variants: 66
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HGVS dbSNP gnomAD frequency
NM_212482.4(FN1):c.7019-180_7019-179insT rs1191367459 0.01711
NM_212482.4(FN1):c.6854-179C>T rs144249483 0.01488
NM_212482.4(FN1):c.7144+195A>G rs16853839 0.01329
NM_212482.4(FN1):c.7018+223A>G rs147432901 0.01317
NM_212482.4(FN1):c.*130C>T rs141470685 0.01073
NM_212482.4(FN1):c.7362+62C>G rs114497844 0.01054
NM_212482.4(FN1):c.6854-314G>A rs72942040 0.00786
NM_212482.4(FN1):c.7019-181_7019-180insT rs200312347 0.00649
NM_212482.4(FN1):c.7019-150A>G rs112179130 0.00557
NM_212482.4(FN1):c.7251+78del rs144845461 0.00556
NM_212482.4(FN1):c.7363-44C>T rs113068773 0.00556
NM_212482.4(FN1):c.7018+314T>C rs112861030 0.00548
NM_212482.4(FN1):c.7019-303C>T rs112504284 0.00548
NM_212482.4(FN1):c.7144+197A>C rs112163563 0.00548
NM_212482.4(FN1):c.7144+202del rs112600151 0.00548
NM_212482.4(FN1):c.7363-30A>G rs116671379 0.00444
NM_212482.4(FN1):c.6923T>C (p.Val2308Ala) rs545761792 0.00120
NM_212482.4(FN1):c.7274G>A (p.Arg2425His) rs148505961 0.00048
NM_212482.4(FN1):c.7295G>C (p.Ser2432Thr) rs147460086 0.00041
NM_212482.4(FN1):c.7116C>T (p.Asn2372=) rs568449322 0.00006
NM_212482.4(FN1):c.7018+17T>C rs750467436 0.00004
NM_212482.4(FN1):c.7020A>G (p.Arg2340=) rs750707274 0.00002
NM_212482.4(FN1):c.6915T>C (p.His2305=) rs773443086 0.00001
NM_212482.4(FN1):c.7018+14T>C rs766654059 0.00001
NM_212482.4(FN1):c.7131C>T (p.Phe2377=) rs768302524 0.00001
NM_212482.4(FN1):c.7209T>C (p.Tyr2403=) rs541854686 0.00001
NM_212482.4(FN1):c.6854-4A>G
NM_212482.4(FN1):c.6854-61_6854-59del rs142073662
NM_212482.4(FN1):c.6879G>A (p.Thr2293=)
NM_212482.4(FN1):c.6882T>C (p.Asp2294=)
NM_212482.4(FN1):c.6888G>A (p.Ser2296=)
NM_212482.4(FN1):c.6921C>T (p.Ala2307=) rs372228808
NM_212482.4(FN1):c.7019-180_7019-177del rs10577918
NM_212482.4(FN1):c.7019-4A>G
NM_212482.4(FN1):c.7019-5dup
NM_212482.4(FN1):c.7019-7C>T
NM_212482.4(FN1):c.7038T>G (p.Gly2346=)
NM_212482.4(FN1):c.7041G>C (p.Val2347=)
NM_212482.4(FN1):c.7071T>A (p.Arg2357=)
NM_212482.4(FN1):c.7077A>T (p.Gly2359=)
NM_212482.4(FN1):c.7119A>G (p.Gly2373=)
NM_212482.4(FN1):c.7134G>A (p.Lys2378=)
NM_212482.4(FN1):c.7144+12C>T rs10498037
NM_212482.4(FN1):c.7145-14G>C
NM_212482.4(FN1):c.7145-19G>C
NM_212482.4(FN1):c.7212C>T (p.Leu2404=)
NM_212482.4(FN1):c.7251+7C>G rs2106137681
NM_212482.4(FN1):c.7252-10A>C
NM_212482.4(FN1):c.7252-10A>T
NM_212482.4(FN1):c.7252-13T>C
NM_212482.4(FN1):c.7252-14C>G
NM_212482.4(FN1):c.7252-15C>T
NM_212482.4(FN1):c.7252-8TC[2]
NM_212482.4(FN1):c.7299C>T (p.Pro2433=)
NM_212482.4(FN1):c.7308T>C (p.Thr2436=)
NM_212482.4(FN1):c.7335T>C (p.Ser2445=)
NM_212482.4(FN1):c.7346A>G (p.His2449Arg)
NM_212482.4(FN1):c.7362+107del rs55953250
NM_212482.4(FN1):c.7362+20A>G
NM_212482.4(FN1):c.7362+8C>G
NM_212482.4(FN1):c.7362+97_7362+98dup rs55953250
NM_212482.4(FN1):c.7362+9A>G
NM_212482.4(FN1):c.7363-12C>T
NM_212482.4(FN1):c.7363-72dup rs35258787
NM_212482.4(FN1):c.7386C>T (p.Cys2462=)
NM_212482.4(FN1):c.7427G>A (p.Arg2476Gln)

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