| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.44388443T>A | CA359699348 | FGF10 | c.240A>T (p.Arg80Ser) | |
| 5 | g.44388443T>C | CA444400475 | FGF10 | c.240A>G (p.Arg80=) | gnomAD v4 |
| 5 | g.44388443T>G | CA118872 | FGF10 | c.240A>C (p.Arg80Ser) | ClinVar dbSNP |
| 5 | g.44388443T= | CA1543090831 | FGF10 | c.240A= (p.Arg80=) | |
| 5 | g.44388444C>A | CA359699349 | FGF10 | c.239G>T (p.Arg80Ile) | COSMIC |
| 5 | g.44388444C>G | CA359699350 | FGF10 | c.239G>C (p.Arg80Thr) | |
| 5 | g.44388444C>T | CA359699351 | FGF10 | c.239G>A (p.Arg80Lys) | |
| 5 | g.44388445T>A | CA359699353 | FGF10 | c.238A>T (p.Arg80Ter) | |
| 5 | g.44388445T>C | CA359699354 | FGF10 | c.238A>G (p.Arg80Gly) | COSMIC |
| 5 | g.44388445T>G | CA444400476 | FGF10 | c.238A>C (p.Arg80=) | COSMIC |
| 5 | g.44388446C>A | CA359699359 | FGF10 | c.237G>T (p.Trp79Cys) | |
| 5 | g.44388446C>G | CA359699361 | FGF10 | c.237G>C (p.Trp79Cys) | |
| 5 | g.44388446C>T | CA359699363 | FGF10 | c.237G>A (p.Trp79Ter) | |
| 5 | g.44388447C>A | CA359699370 | FGF10 | c.236G>T (p.Trp79Leu) | |
| 5 | g.44388447C>G | CA359699367 | FGF10 | c.236G>C (p.Trp79Ser) | |
| 5 | g.44388447C>T | CA359699365 | FGF10 | c.236G>A (p.Trp79Ter) | |
| 5 | g.44388448A>C | CA359699372 | FGF10 | c.235T>G (p.Trp79Gly) | COSMIC |
| 5 | g.44388448A>G | CA359699374 | FGF10 | c.235T>C (p.Trp79Arg) | |
| 5 | g.44388448A>T | CA359699376 | FGF10 | c.235T>A (p.Trp79Arg) | |
| 5 | g.44388449G>A | CA444400477 | FGF10 | c.234C>T (p.Arg78=) | |
| 5 | g.44388449G>C | CA444400478 | FGF10 | c.234C>G (p.Arg78=) | |
| 5 | g.44388449G>T | CA444400479 | FGF10 | c.234C>A (p.Arg78=) | dbSNP |
| 5 | g.44388449dup | CA2695204457 | FGF10 | c.234dup (p.Trp79LeufsTer15) | |
| 5 | g.44388450C>A | CA359699377 | FGF10 | c.233G>T (p.Arg78Leu) | dbSNP |
| 5 | g.44388450C= | CA1543090839 | FGF10 | c.233G= (p.Arg78=) | |
| 5 | g.44388450C>G | CA359699378 | FGF10 | c.233G>C (p.Arg78Pro) | |
| 5 | g.44388450C>T | CA359699380 | FGF10 | c.233G>A (p.Arg78His) | dbSNP |
| 5 | g.44388450_44388451delinsCG | CA1543090840 | FGF10 | c.232_233delinsCG (p.Arg78=) | |
| 5 | g.44388451G>A | CA359699383 | FGF10 | c.232C>T (p.Arg78Cys) | |
| 5 | g.44388451G>C | CA359699385 | FGF10 | c.232C>G (p.Arg78Gly) | |
| 5 | g.44388451G>T | CA359699387 | FGF10 | c.232C>A (p.Arg78Ser) | |
| 5 | g.44388452del | CA658822464 | FGF10 | c.232del (p.Arg78AlafsTer?) | ClinVar dbSNP |
| 5 | g.44388452G>A | CA444400480 | FGF10 | c.231C>T (p.Val77=) | dbSNP |
| 5 | g.44388452G>C | CA444400481 | FGF10 | c.231C>G (p.Val77=) | |
| 5 | g.44388452G= | CA1543090845 | FGF10 | c.231C= (p.Val77=) | |
| 5 | g.44388452G>T | CA444400482 | FGF10 | c.231C>A (p.Val77=) | |
| 5 | g.44388453A>C | CA359699388 | FGF10 | c.230T>G (p.Val77Gly) | |
| 5 | g.44388453A>G | CA359699389 | FGF10 | c.230T>C (p.Val77Ala) | |
| 5 | g.44388453A>T | CA359699392 | FGF10 | c.230T>A (p.Val77Asp) | |
| 5 | g.44388454C>A | CA359699398 | FGF10 | c.229G>T (p.Val77Phe) | |
| 5 | g.44388454C>G | CA359699396 | FGF10 | c.229G>C (p.Val77Leu) | |
| 5 | g.44388454C>T | CA359699394 | FGF10 | c.229G>A (p.Val77Ile) | |
| 5 | g.44388455A= | CA1543090847 | FGF10 | c.228T= (p.Asp76=) | |
| 5 | g.44388455A>C | CA359699400 | FGF10 | c.228T>G (p.Asp76Glu) | |
| 5 | g.44388455A>G | CA444400483 | FGF10 | c.228T>C (p.Asp76=) | gnomAD v4 |
| 5 | g.44388455A>T | CA3258549 | FGF10 | c.228T>A (p.Asp76Glu) | dbSNP ExAC gnomAD v3 gnomAD v4 |
| 5 | g.44388456T>A | CA359699404 | FGF10 | c.227A>T (p.Asp76Val) | |
| 5 | g.44388456T>C | CA359699406 | FGF10 | c.227A>G (p.Asp76Gly) | |
| 5 | g.44388456T>G | CA359699405 | FGF10 | c.227A>C (p.Asp76Ala) | |
| 5 | g.44388457C>A | CA359699407 | FGF10 | c.226G>T (p.Asp76Tyr) | gnomAD v4 |