Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
16 | g.74636460A= | CA2232905956 | RFWD3 | c.1312T= (p.Phe438=) c.478T= (p.Phe160=) | |
16 | g.74636460A>C | CA396761816 | RFWD3 | c.1312T>G (p.Phe438Val) c.478T>G (p.Phe160Val) | |
16 | g.74636460A>G | CA8169253 | RFWD3 | c.1312T>C (p.Phe438Leu) c.478T>C (p.Phe160Leu) | dbSNP ExAC gnomAD v2 gnomAD v4 |
16 | g.74636460A>T | CA396761815 | RFWD3 | c.1312T>A (p.Phe438Ile) c.478T>A (p.Phe160Ile) | |
16 | g.74636461G>A | CA496542744 | RFWD3 | c.1311C>T (p.His437=) c.477C>T (p.His159=) | dbSNP gnomAD v3 gnomAD v4 |
16 | g.74636461G>C | CA396761818 | RFWD3 | c.1311C>G (p.His437Gln) c.477C>G (p.His159Gln) | |
16 | g.74636461G= | CA2232905957 | RFWD3 | c.1311C= (p.His437=) c.477C= (p.His159=) | |
16 | g.74636461G>T | CA396761820 | RFWD3 | c.1311C>A (p.His437Gln) c.477C>A (p.His159Gln) | |
16 | g.74636462T>A | CA396761823 | RFWD3 | c.1310A>T (p.His437Leu) c.476A>T (p.His159Leu) | |
16 | g.74636462T>C | CA396761825 | RFWD3 | c.1310A>G (p.His437Arg) c.476A>G (p.His159Arg) | |
16 | g.74636462T>G | CA396761826 | RFWD3 | c.1310A>C (p.His437Pro) c.476A>C (p.His159Pro) | |
16 | g.74636463G>A | CA396761828 | RFWD3 | c.1309C>T (p.His437Tyr) c.475C>T (p.His159Tyr) | |
16 | g.74636463G>C | CA396761830 | RFWD3 | c.1309C>G (p.His437Asp) c.475C>G (p.His159Asp) | gnomAD v4 |
16 | g.74636463G>T | CA396761831 | RFWD3 | c.1309C>A (p.His437Asn) c.475C>A (p.His159Asn) | |
16 | g.74636464G>A | CA496542751 | RFWD3 | c.1308C>T (p.Tyr436=) c.474C>T (p.Tyr158=) | |
16 | g.74636464G>C | CA396761833 | RFWD3 | c.1308C>G (p.Tyr436Ter) c.474C>G (p.Tyr158Ter) | |
16 | g.74636464G>T | CA396761835 | RFWD3 | c.1308C>A (p.Tyr436Ter) c.474C>A (p.Tyr158Ter) | gnomAD v4 |
16 | g.74636465T>A | CA396761837 | RFWD3 | c.1307A>T (p.Tyr436Phe) c.473A>T (p.Tyr158Phe) | |
16 | g.74636465T>C | CA396761839 | RFWD3 | c.1307A>G (p.Tyr436Cys) c.473A>G (p.Tyr158Cys) | gnomAD v4 |
16 | g.74636465T>G | CA396761841 | RFWD3 | c.1307A>C (p.Tyr436Ser) c.473A>C (p.Tyr158Ser) | |
16 | g.74636466A>C | CA396761847 | RFWD3 | c.1306T>G (p.Tyr436Asp) c.472T>G (p.Tyr158Asp) | |
16 | g.74636466A>G | CA396761845 | RFWD3 | c.1306T>C (p.Tyr436His) c.472T>C (p.Tyr158His) | |
16 | g.74636466A>T | CA396761843 | RFWD3 | c.1306T>A (p.Tyr436Asn) c.472T>A (p.Tyr158Asn) | |
16 | g.74636467C>A | CA396761851 | RFWD3 | c.1305G>T (p.Lys435Asn) c.471G>T (p.Lys157Asn) | |
16 | g.74636467C>G | CA396761849 | RFWD3 | c.1305G>C (p.Lys435Asn) c.471G>C (p.Lys157Asn) | |
16 | g.74636467C>T | CA496542766 | RFWD3 | c.1305G>A (p.Lys435=) c.471G>A (p.Lys157=) | |
16 | g.74636468T>A | CA396761854 | RFWD3 | c.1304A>T (p.Lys435Met) c.470A>T (p.Lys157Met) | |
16 | g.74636468T>C | CA8169255 | RFWD3 | c.1304A>G (p.Lys435Arg) c.470A>G (p.Lys157Arg) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.74636468T>G | CA8169254 | RFWD3 | c.1304A>C (p.Lys435Thr) c.470A>C (p.Lys157Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
16 | g.74636468T= | CA2232905958 | RFWD3 | c.1304A= (p.Lys435=) c.470A= (p.Lys157=) | |
16 | g.74636469T>A | CA396761856 | RFWD3 | c.1303A>T (p.Lys435Ter) c.469A>T (p.Lys157Ter) | gnomAD v4 |
16 | g.74636469T>C | CA396761858 | RFWD3 | c.1303A>G (p.Lys435Glu) c.469A>G (p.Lys157Glu) | |
16 | g.74636469T>G | CA396761860 | RFWD3 | c.1303A>C (p.Lys435Gln) c.469A>C (p.Lys157Gln) | |
16 | g.74636470G>A | CA496542775 | RFWD3 | c.1302C>T (p.His434=) c.468C>T (p.His156=) | |
16 | g.74636470G>C | CA8169256 | RFWD3 | c.1302C>G (p.His434Gln) c.468C>G (p.His156Gln) | dbSNP ExAC gnomAD v2 |
16 | g.74636470G= | CA2232905959 | RFWD3 | c.1302C= (p.His434=) c.468C= (p.His156=) | |
16 | g.74636470G>T | CA396761863 | RFWD3 | c.1302C>A (p.His434Gln) c.468C>A (p.His156Gln) | |
16 | g.74636471T>A | CA396761866 | RFWD3 | c.1301A>T (p.His434Leu) c.467A>T (p.His156Leu) | |
16 | g.74636471T>C | CA396761868 | RFWD3 | c.1301A>G (p.His434Arg) c.467A>G (p.His156Arg) | gnomAD v4 |
16 | g.74636471T>G | CA396761869 | RFWD3 | c.1301A>C (p.His434Pro) c.467A>C (p.His156Pro) | |
16 | g.74636472G>A | CA396761876 | RFWD3 | c.1300C>T (p.His434Tyr) c.466C>T (p.His156Tyr) | |
16 | g.74636472G>C | CA396761874 | RFWD3 | c.1300C>G (p.His434Asp) c.466C>G (p.His156Asp) | gnomAD v4 |
16 | g.74636472G>T | CA396761872 | RFWD3 | c.1300C>A (p.His434Asn) c.466C>A (p.His156Asn) | |
16 | g.74636473C>A | CA396761878 | RFWD3 | c.1299G>T (p.Lys433Asn) c.465G>T (p.Lys155Asn) | gnomAD v4 |
16 | g.74636473C>G | CA396761880 | RFWD3 | c.1299G>C (p.Lys433Asn) c.465G>C (p.Lys155Asn) | |
16 | g.74636473C>T | CA496542785 | RFWD3 | c.1299G>A (p.Lys433=) c.465G>A (p.Lys155=) | dbSNP |
16 | g.74636474T>A | CA396761882 | RFWD3 | c.1298A>T (p.Lys433Met) c.464A>T (p.Lys155Met) | |
16 | g.74636474T>C | CA396761884 | RFWD3 | c.1298A>G (p.Lys433Arg) c.464A>G (p.Lys155Arg) | |
16 | g.74636474T>G | CA396761886 | RFWD3 | c.1298A>C (p.Lys433Thr) c.464A>C (p.Lys155Thr) | |
16 | g.74636475T>A | CA396761887 | RFWD3 | c.1297A>T (p.Lys433Ter) c.463A>T (p.Lys155Ter) |