Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
4 | g.154580323_154590216del | CA915940499 | |||
4 | g.154585696C>A | CA358526697 | FGA | c.1733G>T (p.Ser578Ile) c.658G>T (p.Val220Phe) | |
4 | g.154585696C= | CA1504943153 | FGA | c.1733G= (p.Ser578=) c.658G= (p.Val220=) | |
4 | g.154585696C>G | CA358526700 | FGA | c.1733G>C (p.Ser578Thr) c.658G>C (p.Val220Leu) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
4 | g.154585696C>T | CA358526703 | FGA | c.1733G>A (p.Ser578Asn) c.658G>A (p.Val220Ile) | |
4 | g.154585697T>A | CA358526705 | FGA | c.1732A>T (p.Ser578Cys) c.657A>T (p.Gln219His) | |
4 | g.154585697T>C | CA358526710 | FGA | c.1732A>G (p.Ser578Gly) c.657A>G (p.Gln219=) | |
4 | g.154585697T>G | CA358526707 | FGA | c.1732A>C (p.Ser578Arg) c.657A>C (p.Gln219His) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.154585697T= | CA1504943154 | FGA | c.1732A= (p.Ser578=) c.657A= (p.Gln219=) | |
4 | g.154585698T>A | CA358526713 | FGA | c.1731A>T (p.Ser577=) c.656A>T (p.Gln219Leu) | |
4 | g.154585698T>C | CA358526715 | FGA | c.1731A>G (p.Ser577=) c.656A>G (p.Gln219Arg) | |
4 | g.154585698T>G | CA358526716 | FGA | c.1731A>C (p.Ser577=) c.656A>C (p.Gln219Pro) | |
4 | g.154585699G>A | CA358526719 | FGA | c.1730C>T (p.Ser577Leu) c.655C>T (p.Gln219Ter) | gnomAD v4 |
4 | g.154585699G>C | CA3115043 | FGA | c.1730C>G (p.Ser577Ter) c.655C>G (p.Gln219Glu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
4 | g.154585699G= | CA1504943155 | FGA | c.1730C= (p.Ser577=) c.655C= (p.Gln219=) | |
4 | g.154585699G>T | CA358526724 | FGA | c.1730C>A (p.Ser577Ter) c.655C>A (p.Gln219Lys) | |
4 | g.154585700A>C | CA358526727 | FGA | c.1729T>G (p.Ser577Ala) c.654T>G (p.Leu218=) | COSMIC COSMIC |
4 | g.154585700A>G | CA358526729 | FGA | c.1729T>C (p.Ser577Pro) c.654T>C (p.Leu218=) | COSMIC COSMIC |
4 | g.154585700A>T | CA358526732 | FGA | c.1729T>A (p.Ser577Thr) c.654T>A (p.Leu218=) | |
4 | g.154585701A= | CA1504943156 | FGA | c.1728T= (p.Ser576=) c.653T= (p.Leu218=) | |
4 | g.154585701A>C | CA358526738 | FGA | c.1728T>G (p.Ser576=) c.653T>G (p.Leu218Arg) | COSMIC COSMIC |
4 | g.154585701A>G | CA358526735 | FGA | c.1728T>C (p.Ser576=) c.653T>C (p.Leu218Pro) | dbSNP gnomAD v2 gnomAD v4 |
4 | g.154585701A>T | CA358526734 | FGA | c.1728T>A (p.Ser576=) c.653T>A (p.Leu218His) | |
4 | g.154585702G>A | CA358526740 | FGA | c.1727C>T (p.Ser576Phe) c.652C>T (p.Leu218Phe) | |
4 | g.154585702G>C | CA358526741 | FGA | c.1727C>G (p.Ser576Cys) c.652C>G (p.Leu218Val) | |
4 | g.154585702G>T | CA358526742 | FGA | c.1727C>A (p.Ser576Tyr) c.652C>A (p.Leu218Ile) | gnomAD v4 |
4 | g.154585703A= | CA1504943157 | FGA | c.1726T= (p.Ser576=) c.651T= (p.Asn217=) | |
4 | g.154585703A>C | CA358526743 | FGA | c.1726T>G (p.Ser576Ala) c.651T>G (p.Asn217Lys) | |
4 | g.154585703A>G | CA358526744 | FGA | c.1726T>C (p.Ser576Pro) c.651T>C (p.Asn217=) | dbSNP gnomAD v4 |
4 | g.154585703A>T | CA358526746 | FGA | c.1726T>A (p.Ser576Thr) c.651T>A (p.Asn217Lys) | dbSNP |
4 | g.154585704T>A | CA358526747 | FGA | c.1725A>T (p.Lys575Asn) c.650A>T (p.Asn217Ile) | |
4 | g.154585704T>C | CA358526749 | FGA | c.1725A>G (p.Lys575=) c.650A>G (p.Asn217Ser) | |
4 | g.154585704T>G | CA358526750 | FGA | c.1725A>C (p.Lys575Asn) c.650A>C (p.Asn217Thr) | |
4 | g.154585706del | CA2695204019 | FGA | c.1725del (p.Lys575AsnfsTer?) c.650del (p.Asn217IlefsTer10) | |
4 | g.154585705T>A | CA358526752 | FGA | c.1724A>T (p.Lys575Ile) c.649A>T (p.Asn217Tyr) | |
4 | g.154585705T>C | CA358526754 | FGA | c.1724A>G (p.Lys575Arg) c.649A>G (p.Asn217Asp) | |
4 | g.154585705T>G | CA358526755 | FGA | c.1724A>C (p.Lys575Thr) c.649A>C (p.Asn217His) | |
4 | g.154585706T>A | CA358526761 | FGA | c.1723A>T (p.Lys575Ter) c.648A>T (p.Val216=) | |
4 | g.154585706T>C | CA358526759 | FGA | c.1723A>G (p.Lys575Glu) c.648A>G (p.Val216=) | |
4 | g.154585706T>G | CA358526757 | FGA | c.1723A>C (p.Lys575Gln) c.648A>C (p.Val216=) | |
4 | g.154585707A= | CA1504943158 | FGA | c.1722T= (p.Gly574=) c.647T= (p.Val216=) | |
4 | g.154585707A>C | CA358526766 | FGA | c.1722T>G (p.Gly574=) c.647T>G (p.Val216Gly) | |
4 | g.154585707A>G | CA108760895 | FGA | c.1722T>C (p.Gly574=) c.647T>C (p.Val216Ala) | dbSNP gnomAD v3 gnomAD v4 |
4 | g.154585707A>T | CA358526769 | FGA | c.1722T>A (p.Gly574=) c.647T>A (p.Val216Glu) | |
4 | g.154585708C>A | CA358526771 | FGA | c.1721G>T (p.Gly574Val) c.646G>T (p.Val216Leu) | |
4 | g.154585708C>G | CA358526772 | FGA | c.1721G>C (p.Gly574Ala) c.646G>C (p.Val216Leu) | |
4 | g.154585708C>T | CA358526773 | FGA | c.1721G>A (p.Gly574Asp) c.646G>A (p.Val216Ile) | |
4 | g.154585708_154585709delinsAA | CA2695204020 | FGA | c.1720_1721delinsTT (p.Gly574Phe) c.645_646delinsTT (p.Leu215_Val216delinsPheLeu) | |
4 | g.154585709del | CA2672444877 | FGA | c.1721del (p.Gly574ValfsTer?) c.646del (p.Val216Ter) | gnomAD v4 |
4 | g.154585709C>A | CA358526774 | FGA | c.1720G>T (p.Gly574Cys) c.645G>T (p.Leu215Phe) |