ClinVar Miner

List of variants in gene GIPC3 reported as likely benign by Laboratory for Molecular Medicine, Mass General Brigham Personalized Medicine

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Gene type:
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Total variants: 24
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HGVS dbSNP gnomAD frequency
NM_133261.3(GIPC3):c.132G>C (p.Ala44=) rs80060313 0.00180
NM_133261.3(GIPC3):c.207C>T (p.Phe69=) rs727504653 0.00059
NM_133261.3(GIPC3):c.319C>A (p.Arg107=) rs138707041 0.00032
NM_133261.3(GIPC3):c.20G>A (p.Arg7Gln) rs998073430 0.00031
NM_133261.3(GIPC3):c.440G>A (p.Arg147Gln) rs141293401 0.00031
NM_133261.3(GIPC3):c.626G>A (p.Cys209Tyr) rs374129877 0.00016
NM_133261.3(GIPC3):c.871G>A (p.Ala291Thr) rs199951984 0.00009
NM_133261.3(GIPC3):c.57G>T (p.Ala19=) rs754337950 0.00008
NM_133261.3(GIPC3):c.639G>A (p.Ala213=) rs371566042 0.00008
NM_133261.3(GIPC3):c.702A>G (p.Glu234=) rs748059362 0.00006
NM_133261.3(GIPC3):c.706-7C>T rs775627552 0.00006
NM_133261.3(GIPC3):c.213C>A (p.Ile71=) rs876657467 0.00004
NM_133261.3(GIPC3):c.915C>T (p.Gly305=) rs142749099 0.00003
NM_133261.3(GIPC3):c.192G>A (p.Lys64=) rs876657466 0.00001
NM_133261.3(GIPC3):c.315C>T (p.His105=) rs876657468 0.00001
NM_133261.3(GIPC3):c.75G>T (p.Ser25=) rs1321208549 0.00001
NM_133261.3(GIPC3):c.788-5C>T rs528822982 0.00001
NM_133261.3(GIPC3):c.381G>A (p.Thr127=) rs766652884
NM_133261.3(GIPC3):c.576G>A (p.Gln192=) rs727504632
NM_133261.3(GIPC3):c.66C>T (p.Pro22=) rs1269578352
NM_133261.3(GIPC3):c.69G>A (p.Ala23=) rs150473323
NM_133261.3(GIPC3):c.69G>C (p.Ala23=) rs150473323
NM_133261.3(GIPC3):c.787+5G>C rs876657816
NM_133261.3(GIPC3):c.821C>T (p.Ala274Val) rs149028750

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