ClinVar Miner

List of variants in gene FGD4 reported as uncertain significance by Ambry Genetics

Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 75
Download table as spreadsheet
HGVS dbSNP gnomAD frequency
NM_001370298.3(FGD4):c.2560G>A (p.Val854Met) rs61753359 0.00131
NM_001370298.3(FGD4):c.1973A>G (p.Asp658Gly) rs141237776 0.00015
NM_001370298.3(FGD4):c.2506A>G (p.Met836Val) rs140220443 0.00013
NM_001370298.3(FGD4):c.1759A>G (p.Met587Val) rs201186597 0.00012
NM_001370298.3(FGD4):c.506C>T (p.Ser169Leu) rs143251785 0.00011
NM_001370298.3(FGD4):c.2123C>A (p.Pro708His) rs145071617 0.00010
NM_001370298.3(FGD4):c.1508T>C (p.Leu503Ser) rs555510533 0.00009
NM_001370298.3(FGD4):c.461C>G (p.Pro154Arg) rs371407163 0.00008
NM_001370298.3(FGD4):c.1078A>C (p.Asn360His) rs761788290 0.00006
NM_001370298.3(FGD4):c.792A>G (p.Ile264Met) rs774466701 0.00006
NM_001370298.3(FGD4):c.808G>A (p.Asp270Asn) rs113416502 0.00006
NM_001370298.3(FGD4):c.980T>A (p.Leu327Gln) rs144980336 0.00006
NM_001370298.3(FGD4):c.469G>A (p.Val157Ile) rs755068251 0.00005
NM_001370298.3(FGD4):c.1586G>A (p.Ser529Asn) rs781528826 0.00004
NM_001370298.3(FGD4):c.2518G>A (p.Ala840Thr) rs145630882 0.00004
NM_001370298.3(FGD4):c.472T>C (p.Ser158Pro) rs989660324 0.00004
NM_001370298.3(FGD4):c.1220C>A (p.Pro407Gln) rs781381508 0.00003
NM_001370298.3(FGD4):c.1975G>A (p.Ala659Thr) rs750531320 0.00003
NM_001370298.3(FGD4):c.2289A>C (p.Glu763Asp) rs907657345 0.00003
NM_001370298.3(FGD4):c.2455-5T>G rs749267223 0.00003
NM_001370298.3(FGD4):c.2512A>G (p.Arg838Gly) rs756201273 0.00003
NM_001370298.3(FGD4):c.2644G>C (p.Gly882Arg) rs775920519 0.00003
NM_001370298.3(FGD4):c.1536T>G (p.Asp512Glu) rs778471949 0.00002
NM_001370298.3(FGD4):c.2404G>A (p.Val802Met) rs768786804 0.00002
NM_001370298.3(FGD4):c.809A>G (p.Asp270Gly) rs759415605 0.00002
NM_001370298.3(FGD4):c.1102-5T>A rs1459339879 0.00001
NM_001370298.3(FGD4):c.1158G>A (p.Met386Ile) rs1335886616 0.00001
NM_001370298.3(FGD4):c.1348G>A (p.Val450Ile) rs768392772 0.00001
NM_001370298.3(FGD4):c.1502G>C (p.Arg501Thr) rs755934741 0.00001
NM_001370298.3(FGD4):c.1588G>A (p.Ala530Thr) rs746426982 0.00001
NM_001370298.3(FGD4):c.1936A>G (p.Lys646Glu) rs1217036684 0.00001
NM_001370298.3(FGD4):c.2030T>C (p.Ile677Thr) rs760696455 0.00001
NM_001370298.3(FGD4):c.2132C>T (p.Ala711Val) rs1341534652 0.00001
NM_001370298.3(FGD4):c.2263A>G (p.Ile755Val) rs764635514 0.00001
NM_001370298.3(FGD4):c.2450C>T (p.Pro817Leu) rs751271158 0.00001
NM_001370298.3(FGD4):c.2458G>A (p.Val820Ile) rs374917482 0.00001
NM_001370298.3(FGD4):c.2509C>A (p.Pro837Thr) rs756057996 0.00001
NM_001370298.3(FGD4):c.2523C>A (p.Asp841Glu) rs751777807 0.00001
NM_001370298.3(FGD4):c.2608A>G (p.Lys870Glu) rs746459196 0.00001
NM_001370298.3(FGD4):c.2645G>T (p.Gly882Val) rs1951104872 0.00001
NM_001370298.3(FGD4):c.499_501dup (p.Gly167_Ser168insGly) rs1223446306 0.00001
NM_001370298.3(FGD4):c.638G>A (p.Gly213Glu) rs61754560 0.00001
NM_001370298.3(FGD4):c.721G>A (p.Glu241Lys) rs752621629 0.00001
NM_001370298.3(FGD4):c.790A>G (p.Ile264Val) rs768685900 0.00001
NM_001370298.3(FGD4):c.904C>G (p.Leu302Val) rs376977755 0.00001
NM_001370298.3(FGD4):c.1042G>A (p.Ala348Thr)
NM_001370298.3(FGD4):c.1102G>T (p.Val368Leu)
NM_001370298.3(FGD4):c.1118T>C (p.Leu373Pro) rs1948408106
NM_001370298.3(FGD4):c.1390G>C (p.Val464Leu)
NM_001370298.3(FGD4):c.1795G>A (p.Gly599Ser) rs2540750559
NM_001370298.3(FGD4):c.1943A>G (p.Glu648Gly) rs2540776088
NM_001370298.3(FGD4):c.1952A>G (p.Lys651Arg) rs2540776132
NM_001370298.3(FGD4):c.2047A>C (p.Thr683Pro) rs2540785921
NM_001370298.3(FGD4):c.2091T>A (p.Asn697Lys)
NM_001370298.3(FGD4):c.2122C>G (p.Pro708Ala) rs144693221
NM_001370298.3(FGD4):c.2159G>A (p.Arg720Gln) rs1950123802
NM_001370298.3(FGD4):c.2194G>A (p.Asp732Asn) rs1950615426
NM_001370298.3(FGD4):c.2281A>C (p.Ser761Arg)
NM_001370298.3(FGD4):c.2313+5G>C rs777362500
NM_001370298.3(FGD4):c.2339A>G (p.Asn780Ser) rs2540855976
NM_001370298.3(FGD4):c.2386T>C (p.Trp796Arg) rs1950990735
NM_001370298.3(FGD4):c.2421C>A (p.Asp807Glu)
NM_001370298.3(FGD4):c.2477T>G (p.Ile826Ser) rs2540868022
NM_001370298.3(FGD4):c.2492_2493del (p.Tyr831fs) rs2540868121
NM_001370298.3(FGD4):c.2564A>G (p.His855Arg)
NM_001370298.3(FGD4):c.2602T>C (p.Trp868Arg) rs980987965
NM_001370298.3(FGD4):c.2690C>T (p.Pro897Leu)
NM_001370298.3(FGD4):c.434C>T (p.Ser145Phe) rs2540515478
NM_001370298.3(FGD4):c.500G>A (p.Gly167Asp) rs2540516069
NM_001370298.3(FGD4):c.544G>A (p.Val182Met)
NM_001370298.3(FGD4):c.698C>G (p.Ala233Gly) rs754778284
NM_001370298.3(FGD4):c.719_733del (p.Glu240_Ala244del) rs1314855895
NM_001370298.3(FGD4):c.899C>G (p.Pro300Arg) rs2540548466
NM_001370298.3(FGD4):c.908C>G (p.Pro303Arg) rs145496133
NM_001370298.3(FGD4):c.970C>A (p.Pro324Thr)

The information on this website is not intended for direct diagnostic use or medical decision-making without review by a genetics professional. Individuals should not change their health behavior solely on the basis of information contained on this website. Neither the University of Utah nor the National Institutes of Health independently verfies the submitted information. If you have questions about the information contained on this website, please see a health care professional.