Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.50319754T>A | CA352909292 | HYAL2 | c.736A>T (p.Thr246Ser) n.871A>T | |
3 | g.50319754T>C | CA352909294 | HYAL2 | c.736A>G (p.Thr246Ala) n.871A>G | dbSNP gnomAD v2 gnomAD v4 |
3 | g.50319754T>G | CA352909297 | HYAL2 | c.736A>C (p.Thr246Pro) n.871A>C | |
3 | g.50319754T= | CA1363891853 | HYAL2 | c.736A= (p.Thr246=) n.871A= | |
3 | g.50319755G>A | CA433864290 | HYAL2 | c.735C>T (p.Ser245=) n.870C>T | |
3 | g.50319755G>C | CA352909300 | HYAL2 | c.735C>G (p.Ser245Arg) n.870C>G | |
3 | g.50319755G>T | CA352909303 | HYAL2 | c.735C>A (p.Ser245Arg) n.870C>A | |
3 | g.50319756C>A | CA352909305 | HYAL2 | c.734G>T (p.Ser245Ile) n.869G>T | |
3 | g.50319756C= | CA1363891855 | HYAL2 | c.734G= (p.Ser245=) n.869G= | |
3 | g.50319756C>G | CA352909308 | HYAL2 | c.734G>C (p.Ser245Thr) n.869G>C | |
3 | g.50319756C>T | CA2416248 | HYAL2 | c.734G>A (p.Ser245Asn) n.869G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.50319757T>A | CA352909311 | HYAL2 | c.733A>T (p.Ser245Cys) n.868A>T | |
3 | g.50319757T>C | CA352909313 | HYAL2 | c.733A>G (p.Ser245Gly) n.868A>G | |
3 | g.50319757T>G | CA352909316 | HYAL2 | c.733A>C (p.Ser245Arg) n.868A>C | |
3 | g.50319758C>A | CA352909319 | HYAL2 | c.732G>T (p.Glu244Asp) n.867G>T | |
3 | g.50319758C= | CA1363891857 | HYAL2 | c.732G= (p.Glu244=) n.867G= | |
3 | g.50319758C>G | CA74612591 | HYAL2 | c.732G>C (p.Glu244Asp) n.867G>C | dbSNP gnomAD v2 gnomAD v4 |
3 | g.50319758C>T | CA433864294 | HYAL2 | c.732G>A (p.Glu244=) n.867G>A | dbSNP gnomAD v2 gnomAD v4 |
3 | g.50319759T>A | CA352909324 | HYAL2 | c.731A>T (p.Glu244Val) n.866A>T | |
3 | g.50319759T>C | CA352909326 | HYAL2 | c.731A>G (p.Glu244Gly) n.866A>G | gnomAD v4 |
3 | g.50319759T>G | CA352909325 | HYAL2 | c.731A>C (p.Glu244Ala) n.866A>C | |
3 | g.50319760C>A | CA352909327 | HYAL2 | c.730G>T (p.Glu244Ter) n.865G>T | |
3 | g.50319760C>G | CA352909330 | HYAL2 | c.730G>C (p.Glu244Gln) n.865G>C | gnomAD v4 |
3 | g.50319760C>T | CA352909333 | HYAL2 | c.730G>A (p.Glu244Lys) n.865G>A | COSMIC |
3 | g.50319761A>C | CA433864297 | HYAL2 | c.729T>G (p.Ala243=) n.864T>G | |
3 | g.50319761A>G | CA433864298 | HYAL2 | c.729T>C (p.Ala243=) n.864T>C | |
3 | g.50319761A>T | CA433864299 | HYAL2 | c.729T>A (p.Ala243=) n.864T>A | |
3 | g.50319762G>A | CA352909335 | HYAL2 | c.728C>T (p.Ala243Val) n.863C>T | |
3 | g.50319762G>C | CA352909337 | HYAL2 | c.728C>G (p.Ala243Gly) n.863C>G | dbSNP gnomAD v3 gnomAD v4 |
3 | g.50319762G= | CA1363891859 | HYAL2 | c.728C= (p.Ala243=) n.863C= | |
3 | g.50319762G>T | CA352909340 | HYAL2 | c.728C>A (p.Ala243Asp) n.863C>A | |
3 | g.50319763C>A | CA352909342 | HYAL2 | c.727G>T (p.Ala243Ser) n.862G>T | |
3 | g.50319763C= | CA1363891861 | HYAL2 | c.727G= (p.Ala243=) n.862G= | |
3 | g.50319763C>G | CA352909345 | HYAL2 | c.727G>C (p.Ala243Pro) n.862G>C | |
3 | g.50319763C>T | CA352909346 | HYAL2 | c.727G>A (p.Ala243Thr) n.862G>A | dbSNP gnomAD v4 |
3 | g.50319764C>A | CA352909349 | HYAL2 | c.726G>T (p.Trp242Cys) n.861G>T | |
3 | g.50319764C= | CA1363891863 | HYAL2 | c.726G= (p.Trp242=) n.861G= | |
3 | g.50319764C>G | CA352909351 | HYAL2 | c.726G>C (p.Trp242Cys) n.861G>C | |
3 | g.50319764C>T | CA352909354 | HYAL2 | c.726G>A (p.Trp242Ter) n.861G>A | dbSNP gnomAD v3 gnomAD v4 |
3 | g.50319765C>A | CA352909364 | HYAL2 | c.725G>T (p.Trp242Leu) n.860G>T | |
3 | g.50319765C= | CA1363891865 | HYAL2 | c.725G= (p.Trp242=) n.860G= | |
3 | g.50319765C>G | CA352909361 | HYAL2 | c.725G>C (p.Trp242Ser) n.860G>C | |
3 | g.50319765C>T | CA352909358 | HYAL2 | c.725G>A (p.Trp242Ter) n.860G>A | dbSNP |
3 | g.50319766A>C | CA352909367 | HYAL2 | c.724T>G (p.Trp242Gly) n.859T>G | |
3 | g.50319766A>G | CA352909371 | HYAL2 | c.724T>C (p.Trp242Arg) n.859T>C | |
3 | g.50319766A>T | CA352909374 | HYAL2 | c.724T>A (p.Trp242Arg) n.859T>A | |
3 | g.50319767C>A | CA433864303 | HYAL2 | c.723G>T (p.Leu241=) n.858G>T | |
3 | g.50319767C>G | CA433864305 | HYAL2 | c.723G>C (p.Leu241=) n.858G>C | |
3 | g.50319767C>T | CA433864304 | HYAL2 | c.723G>A (p.Leu241=) n.858G>A | dbSNP gnomAD v4 |
3 | g.50319768A= | CA1363891867 | HYAL2 | c.722T= (p.Leu241=) n.857T= |