Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
1 | g.112913930_112913931del | CA2504103734 | SLC16A1 | c.1466_1467del (p.Thr489ArgfsTer17) | |
1 | g.112913928G>A | CA341826710 | SLC16A1 | c.1466C>T (p.Thr489Ile) | dbSNP gnomAD v2 gnomAD v4 |
1 | g.112913928G>C | CA341826711 | SLC16A1 | c.1466C>G (p.Thr489Arg) | |
1 | g.112913928G= | CA1189548318 | SLC16A1 | c.1466C= (p.Thr489=) | |
1 | g.112913928G>T | CA341826712 | SLC16A1 | c.1466C>A (p.Thr489Lys) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
1 | g.112913929T>A | CA341826713 | SLC16A1 | c.1465A>T (p.Thr489Ser) | |
1 | g.112913929T>C | CA341826715 | SLC16A1 | c.1465A>G (p.Thr489Ala) | gnomAD v4 |
1 | g.112913929T>G | CA341826714 | SLC16A1 | c.1465A>C (p.Thr489Pro) | |
1 | g.112913930G>A | CA419708012 | SLC16A1 | c.1464C>T (p.Asp488=) | gnomAD v4 |
1 | g.112913930G>C | CA341826716 | SLC16A1 | c.1464C>G (p.Asp488Glu) | |
1 | g.112913930G>T | CA341826717 | SLC16A1 | c.1464C>A (p.Asp488Glu) | |
1 | g.112913931T>A | CA341826718 | SLC16A1 | c.1463A>T (p.Asp488Val) | |
1 | g.112913931T>C | CA341826719 | SLC16A1 | c.1463A>G (p.Asp488Gly) | gnomAD v4 |
1 | g.112913931T>G | CA341826720 | SLC16A1 | c.1463A>C (p.Asp488Ala) | |
1 | g.112913932C>A | CA341826721 | SLC16A1 | c.1462G>T (p.Asp488Tyr) | |
1 | g.112913932C>G | CA341826722 | SLC16A1 | c.1462G>C (p.Asp488His) | |
1 | g.112913932C>T | CA341826723 | SLC16A1 | c.1462G>A (p.Asp488Asn) | |
1 | g.112913933T>A | CA341826724 | SLC16A1 | c.1461A>T (p.Lys487Asn) | |
1 | g.112913933T>C | CA419708013 | SLC16A1 | c.1461A>G (p.Lys487=) | dbSNP gnomAD v4 |
1 | g.112913933T>G | CA341826725 | SLC16A1 | c.1461A>C (p.Lys487Asn) | |
1 | g.112913933T= | CA1189548319 | SLC16A1 | c.1461A= (p.Lys487=) | |
1 | g.112913934T>A | CA341826728 | SLC16A1 | c.1460A>T (p.Lys487Ile) | |
1 | g.112913934T>C | CA341826727 | SLC16A1 | c.1460A>G (p.Lys487Arg) | |
1 | g.112913934T>G | CA341826726 | SLC16A1 | c.1460A>C (p.Lys487Thr) | |
1 | g.112913935T>A | CA341826731 | SLC16A1 | c.1459A>T (p.Lys487Ter) | |
1 | g.112913935T>C | CA341826729 | SLC16A1 | c.1459A>G (p.Lys487Glu) | |
1 | g.112913935T>G | CA341826730 | SLC16A1 | c.1459A>C (p.Lys487Gln) | |
1 | g.112913936C>A | CA341826732 | SLC16A1 | c.1458G>T (p.Gln486His) | |
1 | g.112913936C>G | CA341826733 | SLC16A1 | c.1458G>C (p.Gln486His) | |
1 | g.112913936C>T | CA419708015 | SLC16A1 | c.1458G>A (p.Gln486=) | |
1 | g.112913937T>A | CA341826734 | SLC16A1 | c.1457A>T (p.Gln486Leu) | |
1 | g.112913937T>C | CA341826735 | SLC16A1 | c.1457A>G (p.Gln486Arg) | gnomAD v4 |
1 | g.112913937T>G | CA341826736 | SLC16A1 | c.1457A>C (p.Gln486Pro) | |
1 | g.112913937dup | CA1005896138 | SLC16A1 | c.1457dup (p.Lys487GlufsTer20) | gnomAD v3 gnomAD v4 |
1 | g.112913938G>A | CA341826737 | SLC16A1 | c.1456C>T (p.Gln486Ter) | gnomAD v4 |
1 | g.112913938G>C | CA341826738 | SLC16A1 | c.1456C>G (p.Gln486Glu) | |
1 | g.112913938G>T | CA341826739 | SLC16A1 | c.1456C>A (p.Gln486Lys) | |
1 | g.112913939G>A | CA419708016 | SLC16A1 | c.1455C>T (p.Asp485=) | |
1 | g.112913939G>C | CA341826740 | SLC16A1 | c.1455C>G (p.Asp485Glu) | |
1 | g.112913939G>T | CA341826741 | SLC16A1 | c.1455C>A (p.Asp485Glu) | |
1 | g.112913940T>A | CA341826744 | SLC16A1 | c.1454A>T (p.Asp485Val) | |
1 | g.112913940T>C | CA341826743 | SLC16A1 | c.1454A>G (p.Asp485Gly) | |
1 | g.112913940T>G | CA341826742 | SLC16A1 | c.1454A>C (p.Asp485Ala) | |
1 | g.112913941C>A | CA341826745 | SLC16A1 | c.1453G>T (p.Asp485Tyr) | ClinVar |
1 | g.112913941C>G | CA341826746 | SLC16A1 | c.1453G>C (p.Asp485His) | |
1 | g.112913941C>T | CA341826747 | SLC16A1 | c.1453G>A (p.Asp485Asn) | ClinVar gnomAD v4 |
1 | g.112913942C>A | CA419708017 | SLC16A1 | c.1452G>T (p.Pro484=) | |
1 | g.112913942C= | CA1140474901 | SLC16A1 | c.1452G= (p.Pro484=) | |
1 | g.112913942C>G | CA419708018 | SLC16A1 | c.1452G>C (p.Pro484=) | |
1 | g.112913942C>T | CA1011240 | SLC16A1 | c.1452G>A (p.Pro484=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |