ClinVar Miner

List of variants in gene combination FOXE3, LINC01389 reported as likely benign for congenital primary aphakia

Included ClinVar conditions (4):
Minimum submission review status: Collection method:
Minimum conflict level:
Gene type:
ClinVar version:
Total variants: 87
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HGVS dbSNP gnomAD frequency
NM_012186.3(FOXE3):c.426C>T (p.Gly142=) rs1370214494 0.00025
NM_012186.3(FOXE3):c.405G>A (p.Glu135=) rs574859994 0.00021
NM_012186.3(FOXE3):c.240C>T (p.Ile80=) rs146608794 0.00020
NM_012186.3(FOXE3):c.466G>A (p.Asp156Asn) rs202086896 0.00020
NM_012186.3(FOXE3):c.828C>G (p.Pro276=) rs887265865 0.00019
NM_012186.3(FOXE3):c.849T>C (p.Ala283=) rs911846788 0.00016
NM_012186.3(FOXE3):c.51T>C (p.Pro17=) rs548368038 0.00014
NM_012186.3(FOXE3):c.882C>G (p.Ala294=) rs946810051 0.00007
NM_012186.3(FOXE3):c.192G>A (p.Arg64=) rs757496166 0.00006
NM_012186.3(FOXE3):c.813G>A (p.Leu271=) rs1003802007 0.00006
NM_012186.3(FOXE3):c.537G>C (p.Ala179=) rs544902810 0.00004
NM_012186.3(FOXE3):c.585C>G (p.Pro195=) rs890514968 0.00004
NM_012186.3(FOXE3):c.837C>T (p.Gly279=) rs752441939 0.00004
NM_012186.3(FOXE3):c.132G>A (p.Ala44=) rs1417103494 0.00003
NM_012186.3(FOXE3):c.282G>A (p.Leu94=) rs762854169 0.00003
NM_012186.3(FOXE3):c.378C>T (p.Asn126=) rs556872254 0.00003
NM_012186.3(FOXE3):c.492C>T (p.Arg164=) rs747963189 0.00003
NM_012186.3(FOXE3):c.777G>A (p.Pro259=) rs1045485277 0.00003
NM_012186.3(FOXE3):c.543G>T (p.Gly181=) rs765016567 0.00002
NM_012186.3(FOXE3):c.570C>T (p.Pro190=) rs1182253342 0.00002
NM_012186.3(FOXE3):c.876G>A (p.Pro292=) rs1646890706 0.00002
NM_012186.3(FOXE3):c.114G>A (p.Gly38=) rs1305763469 0.00001
NM_012186.3(FOXE3):c.171C>A (p.Pro57=) rs1303056091 0.00001
NM_012186.3(FOXE3):c.183G>C (p.Arg61=) rs1646883402 0.00001
NM_012186.3(FOXE3):c.258C>T (p.His86=) rs1225853707 0.00001
NM_012186.3(FOXE3):c.324C>T (p.Tyr108=) rs370268389 0.00001
NM_012186.3(FOXE3):c.411C>A (p.Gly137=) rs536267128 0.00001
NM_012186.3(FOXE3):c.420C>T (p.Gly140=) rs1352061807 0.00001
NM_012186.3(FOXE3):c.447C>G (p.Pro149=) rs1344716602 0.00001
NM_012186.3(FOXE3):c.489C>T (p.Arg163=) rs754808758 0.00001
NM_012186.3(FOXE3):c.579C>G (p.Pro193=) rs1174698590 0.00001
NM_012186.3(FOXE3):c.624G>C (p.Pro208=) rs1400982636 0.00001
NM_012186.3(FOXE3):c.711G>T (p.Pro237=) rs1177501502 0.00001
NM_012186.3(FOXE3):c.741C>T (p.Ala247=) rs1369565616 0.00001
NM_012186.3(FOXE3):c.804C>T (p.Arg268=) rs1332275509 0.00001
NM_012186.3(FOXE3):c.819G>A (p.Ala273=) rs1035152511 0.00001
NM_012186.3(FOXE3):c.930C>T (p.Gly310=) rs963646314 0.00001
NM_012186.3(FOXE3):c.105C>T (p.Ala35=) rs1646882637
NM_012186.3(FOXE3):c.115C>A (p.Arg39=)
NM_012186.3(FOXE3):c.138T>C (p.Ala46=) rs1031196506
NM_012186.3(FOXE3):c.144C>G (p.Arg48=) rs1646883029
NM_012186.3(FOXE3):c.150G>A (p.Glu50=)
NM_012186.3(FOXE3):c.165C>G (p.Pro55=)
NM_012186.3(FOXE3):c.177G>C (p.Pro59=)
NM_012186.3(FOXE3):c.180G>A (p.Gly60=)
NM_012186.3(FOXE3):c.285C>G (p.Ala95=)
NM_012186.3(FOXE3):c.306C>T (p.Thr102=)
NM_012186.3(FOXE3):c.309A>G (p.Glu103=) rs2124042422
NM_012186.3(FOXE3):c.315T>C (p.Phe105=) rs2124042461
NM_012186.3(FOXE3):c.327C>A (p.Arg109=) rs2124042503
NM_012186.3(FOXE3):c.348G>A (p.Gln116=) rs774479548
NM_012186.3(FOXE3):c.408G>A (p.Pro136=)
NM_012186.3(FOXE3):c.408G>C (p.Pro136=) rs780736595
NM_012186.3(FOXE3):c.438G>A (p.Thr146=)
NM_012186.3(FOXE3):c.453C>G (p.Ala151=)
NM_012186.3(FOXE3):c.519C>A (p.Pro173=) rs577539007
NM_012186.3(FOXE3):c.519C>T (p.Pro173=)
NM_012186.3(FOXE3):c.534G>A (p.Ala178=)
NM_012186.3(FOXE3):c.552C>T (p.Leu184=)
NM_012186.3(FOXE3):c.55C>T (p.Leu19=)
NM_012186.3(FOXE3):c.576G>A (p.Ala192=) rs2124043529
NM_012186.3(FOXE3):c.636G>T (p.Pro212=) rs1289906223
NM_012186.3(FOXE3):c.666G>A (p.Leu222=) rs959738363
NM_012186.3(FOXE3):c.669G>T (p.Val223=)
NM_012186.3(FOXE3):c.681G>A (p.Pro227=)
NM_012186.3(FOXE3):c.696G>C (p.Leu232=)
NM_012186.3(FOXE3):c.6G>C (p.Ala2=) rs928328635
NM_012186.3(FOXE3):c.6G>T (p.Ala2=)
NM_012186.3(FOXE3):c.705C>G (p.Pro235=)
NM_012186.3(FOXE3):c.729C>T (p.Pro243=)
NM_012186.3(FOXE3):c.756C>G (p.Pro252=)
NM_012186.3(FOXE3):c.75G>C (p.Ser25=) rs1327386935
NM_012186.3(FOXE3):c.75G>T (p.Ser25=)
NM_012186.3(FOXE3):c.774C>T (p.Ser258=)
NM_012186.3(FOXE3):c.780A>G (p.Pro260=)
NM_012186.3(FOXE3):c.789G>A (p.Ser263=) rs1252974267
NM_012186.3(FOXE3):c.798C>G (p.Pro266=)
NM_012186.3(FOXE3):c.801C>T (p.Asp267=)
NM_012186.3(FOXE3):c.831C>A (p.Gly277=) rs527783871
NM_012186.3(FOXE3):c.834C>T (p.Pro278=) rs886042525
NM_012186.3(FOXE3):c.84G>A (p.Pro28=) rs2124041428
NM_012186.3(FOXE3):c.855C>T (p.Pro285=)
NM_012186.3(FOXE3):c.861G>A (p.Leu287=) rs1570406069
NM_012186.3(FOXE3):c.927G>A (p.Pro309=) rs1338427430
NM_012186.3(FOXE3):c.942G>T (p.Gly314=) rs1295698690
NM_012186.3(FOXE3):c.943C>T (p.Leu315=) rs1473311737
NM_012186.3(FOXE3):c.96C>T (p.Leu32=)

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