| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 4 | g.67753919G>A | CA439930588 | GNRHR | c.417C>T (p.Arg139=) | dbSNP gnomAD v4 |
| 4 | g.67753919G>C | CA439930590 | GNRHR | c.417C>G (p.Arg139=) | |
| 4 | g.67753919G= | CA1465420606 | GNRHR | c.417C= (p.Arg139=) | |
| 4 | g.67753919G>T | CA439930592 | GNRHR | c.417C>A (p.Arg139=) | |
| 4 | g.67753920C>A | CA357054555 | GNRHR | c.416G>T (p.Arg139Leu) | ClinVar |
| 4 | g.67753920C= | CA1465420612 | GNRHR | c.416G= (p.Arg139=) | |
| 4 | g.67753920C>G | CA357054557 | GNRHR | c.416G>C (p.Arg139Pro) | gnomAD v4 |
| 4 | g.67753920C>T | CA249862 | GNRHR | c.416G>A (p.Arg139His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 4 | g.67753921G>A | CA357054559 | GNRHR | c.415C>T (p.Arg139Cys) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
| 4 | g.67753921G>C | CA357054560 | GNRHR | c.415C>G (p.Arg139Gly) | |
| 4 | g.67753921G= | CA1465420618 | GNRHR | c.415C= (p.Arg139=) | |
| 4 | g.67753921G>T | CA357054561 | GNRHR | c.415C>A (p.Arg139Ser) | COSMIC |
| 4 | g.67753922G>A | CA439930601 | GNRHR | c.414C>T (p.Asp138=) | |
| 4 | g.67753922G>C | CA357054563 | GNRHR | c.414C>G (p.Asp138Glu) | |
| 4 | g.67753922G>T | CA357054565 | GNRHR | c.414C>A (p.Asp138Glu) | |
| 4 | g.67753923T>A | CA357054567 | GNRHR | c.413A>T (p.Asp138Val) | gnomAD v4 |
| 4 | g.67753923T>C | CA16618053 | GNRHR | c.413A>G (p.Asp138Gly) | ClinVar dbSNP |
| 4 | g.67753923T>G | CA357054568 | GNRHR | c.413A>C (p.Asp138Ala) | |
| 4 | g.67753923T= | CA1465420623 | GNRHR | c.413A= (p.Asp138=) | |
| 4 | g.67753924C>A | CA357054569 | GNRHR | c.412G>T (p.Asp138Tyr) | |
| 4 | g.67753924C>G | CA357054570 | GNRHR | c.412G>C (p.Asp138His) | |
| 4 | g.67753924C>T | CA357054572 | GNRHR | c.412G>A (p.Asp138Asn) | |
| 4 | g.67753925C>A | CA439930617 | GNRHR | c.411G>T (p.Leu137=) | |
| 4 | g.67753925C>G | CA439930618 | GNRHR | c.411G>C (p.Leu137=) | |
| 4 | g.67753925C>T | CA439930620 | GNRHR | c.411G>A (p.Leu137=) | dbSNP |
| 4 | g.67753926A= | CA1465420628 | GNRHR | c.410T= (p.Leu137=) | |
| 4 | g.67753926A>C | CA357054573 | GNRHR | c.410T>G (p.Leu137Arg) | |
| 4 | g.67753926A>G | CA357054575 | GNRHR | c.410T>C (p.Leu137Pro) | dbSNP gnomAD v4 |
| 4 | g.67753926A>T | CA357054576 | GNRHR | c.410T>A (p.Leu137Gln) | |
| 4 | g.67753927G>A | CA439930625 | GNRHR | c.409C>T (p.Leu137=) | dbSNP |
| 4 | g.67753927G>C | CA357054578 | GNRHR | c.409C>G (p.Leu137Val) | |
| 4 | g.67753927G= | CA1465420630 | GNRHR | c.409C= (p.Leu137=) | |
| 4 | g.67753927G>T | CA357054579 | GNRHR | c.409C>A (p.Leu137Met) | |
| 4 | g.67753928G>A | CA98671975 | GNRHR | c.408C>T (p.Ser136=) | dbSNP gnomAD v4 |
| 4 | g.67753928G>C | CA357054581 | GNRHR | c.408C>G (p.Ser136Arg) | gnomAD v4 |
| 4 | g.67753928G= | CA1465420636 | GNRHR | c.408C= (p.Ser136=) | |
| 4 | g.67753928G>T | CA357054582 | GNRHR | c.408C>A (p.Ser136Arg) | |
| 4 | g.67753929C>A | CA357054583 | GNRHR | c.407G>T (p.Ser136Ile) | gnomAD v4 |
| 4 | g.67753929C>G | CA357054586 | GNRHR | c.407G>C (p.Ser136Thr) | |
| 4 | g.67753929C>T | CA357054585 | GNRHR | c.407G>A (p.Ser136Asn) | |
| 4 | g.67753930T>A | CA357054588 | GNRHR | c.406A>T (p.Ser136Cys) | |
| 4 | g.67753930T>C | CA357054591 | GNRHR | c.406A>G (p.Ser136Gly) | |
| 4 | g.67753930T>G | CA357054589 | GNRHR | c.406A>C (p.Ser136Arg) | |
| 4 | g.67753931G>A | CA439930645 | GNRHR | c.405C>T (p.Ile135=) | |
| 4 | g.67753931G>C | CA357054592 | GNRHR | c.405C>G (p.Ile135Met) | |
| 4 | g.67753931G>T | CA439930648 | GNRHR | c.405C>A (p.Ile135=) | |
| 4 | g.67753932A= | CA1465420640 | GNRHR | c.404T= (p.Ile135=) | |
| 4 | g.67753932A>C | CA357054594 | GNRHR | c.404T>G (p.Ile135Ser) | |
| 4 | g.67753932A>G | CA357054595 | GNRHR | c.404T>C (p.Ile135Thr) | dbSNP |
| 4 | g.67753932A>T | CA357054597 | GNRHR | c.404T>A (p.Ile135Asn) | dbSNP gnomAD v2 gnomAD v4 |