| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.50319641A>C | CA352906995 | HYAL2 | c.849T>G (p.His283Gln) n.984T>G | |
| 3 | g.50319641A>G | CA433690693 | HYAL2 | c.849T>C (p.His283=) n.984T>C | |
| 3 | g.50319641A>T | CA352906997 | HYAL2 | c.849T>A (p.His283Gln) n.984T>A | |
| 3 | g.50319642T>A | CA352907007 | HYAL2 | c.848A>T (p.His283Leu) n.983A>T | |
| 3 | g.50319642T>C | CA352907003 | HYAL2 | c.848A>G (p.His283Arg) n.983A>G | dbSNP gnomAD v3 gnomAD v4 |
| 3 | g.50319642T>G | CA352907000 | HYAL2 | c.848A>C (p.His283Pro) n.983A>C | dbSNP |
| 3 | g.50319642T= | CA1363891748 | HYAL2 | c.848A= (p.His283=) n.983A= | |
| 3 | g.50319643G>A | CA352907012 | HYAL2 | c.847C>T (p.His283Tyr) n.982C>T | |
| 3 | g.50319643G>C | CA352907016 | HYAL2 | c.847C>G (p.His283Asp) n.982C>G | |
| 3 | g.50319643G>T | CA352907018 | HYAL2 | c.847C>A (p.His283Asn) n.982C>A | |
| 3 | g.50319644G>A | CA433690703 | HYAL2 | c.846C>T (p.His282=) n.981C>T | |
| 3 | g.50319644G>C | CA352907020 | HYAL2 | c.846C>G (p.His282Gln) n.981C>G | |
| 3 | g.50319644G>T | CA352907022 | HYAL2 | c.846C>A (p.His282Gln) n.981C>A | |
| 3 | g.50319645T>A | CA352907026 | HYAL2 | c.845A>T (p.His282Leu) n.980A>T | gnomAD v4 |
| 3 | g.50319645T>C | CA352907027 | HYAL2 | c.845A>G (p.His282Arg) n.980A>G | gnomAD v4 |
| 3 | g.50319645T>G | CA352907028 | HYAL2 | c.845A>C (p.His282Pro) n.980A>C | dbSNP |
| 3 | g.50319645T= | CA1363891749 | HYAL2 | c.845A= (p.His282=) n.980A= | |
| 3 | g.50319646G>A | CA2416222 | HYAL2 | c.844C>T (p.His282Tyr) n.979C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 3 | g.50319646G>C | CA352907030 | HYAL2 | c.844C>G (p.His282Asp) n.979C>G | |
| 3 | g.50319646G= | CA1363891750 | HYAL2 | c.844C= (p.His282=) n.979C= | |
| 3 | g.50319646G>T | CA352907032 | HYAL2 | c.844C>A (p.His282Asn) n.979C>A | |
| 3 | g.50319647G>A | CA433690717 | HYAL2 | c.843C>T (p.Thr281=) n.978C>T | |
| 3 | g.50319647G>C | CA433690721 | HYAL2 | c.843C>G (p.Thr281=) n.978C>G | |
| 3 | g.50319647G= | CA1363891751 | HYAL2 | c.843C= (p.Thr281=) n.978C= | |
| 3 | g.50319647G>T | CA433690723 | HYAL2 | c.843C>A (p.Thr281=) n.978C>A | dbSNP |
| 3 | g.50319648G>A | CA352907039 | HYAL2 | c.842C>T (p.Thr281Ile) n.977C>T | gnomAD v4 |
| 3 | g.50319648G>C | CA352907037 | HYAL2 | c.842C>G (p.Thr281Ser) n.977C>G | gnomAD v4 |
| 3 | g.50319648G>T | CA352907034 | HYAL2 | c.842C>A (p.Thr281Asn) n.977C>A | |
| 3 | g.50319649T>A | CA352907041 | HYAL2 | c.841A>T (p.Thr281Ser) n.976A>T | |
| 3 | g.50319649T>C | CA352907044 | HYAL2 | c.841A>G (p.Thr281Ala) n.976A>G | |
| 3 | g.50319649T>G | CA352907048 | HYAL2 | c.841A>C (p.Thr281Pro) n.976A>C | dbSNP |
| 3 | g.50319649T= | CA1363891752 | HYAL2 | c.841A= (p.Thr281=) n.976A= | |
| 3 | g.50319650G>A | CA433690731 | HYAL2 | c.840C>T (p.Arg280=) n.975C>T | |
| 3 | g.50319650G>C | CA433690732 | HYAL2 | c.840C>G (p.Arg280=) n.975C>G | |
| 3 | g.50319650G>T | CA433690733 | HYAL2 | c.840C>A (p.Arg280=) n.975C>A | |
| 3 | g.50319651C>A | CA352907053 | HYAL2 | c.839G>T (p.Arg280Leu) n.974G>T | gnomAD v4 |
| 3 | g.50319651C= | CA1363891753 | HYAL2 | c.839G= (p.Arg280=) n.974G= | |
| 3 | g.50319651C>G | CA2416224 | HYAL2 | c.839G>C (p.Arg280Pro) n.974G>C | dbSNP ExAC gnomAD v4 |
| 3 | g.50319651C>T | CA2416223 | HYAL2 | c.839G>A (p.Arg280His) n.974G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.50319652G>A | CA2416225 | HYAL2 | c.838C>T (p.Arg280Cys) n.973C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.50319652G>C | CA352907059 | HYAL2 | c.838C>G (p.Arg280Gly) n.973C>G | dbSNP |
| 3 | g.50319652G= | CA1363891754 | HYAL2 | c.838C= (p.Arg280=) n.973C= | |
| 3 | g.50319652G>T | CA352907062 | HYAL2 | c.838C>A (p.Arg280Ser) n.973C>A | |
| 3 | g.50319653A>C | CA433690747 | HYAL2 | c.837T>G (p.Ala279=) n.972T>G | |
| 3 | g.50319653A>G | CA433690748 | HYAL2 | c.837T>C (p.Ala279=) n.972T>C | gnomAD v4 |
| 3 | g.50319653A>T | CA433690749 | HYAL2 | c.837T>A (p.Ala279=) n.972T>A | |
| 3 | g.50319654G>A | CA352907066 | HYAL2 | c.836C>T (p.Ala279Val) n.971C>T | |
| 3 | g.50319654G>C | CA352907068 | HYAL2 | c.836C>G (p.Ala279Gly) n.971C>G | gnomAD v4 |
| 3 | g.50319654G>T | CA352907072 | HYAL2 | c.836C>A (p.Ala279Asp) n.971C>A | |
| 3 | g.50319655C>A | CA352907078 | HYAL2 | c.835G>T (p.Ala279Ser) n.970G>T |