Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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) | |
16 | g.74636475T>C | CA8169257 | RFWD3 | c.1297A>G (p.Lys433Glu) c.463A>G (p.Lys155Glu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
16 | g.74636475T>G | CA396761890 | RFWD3 | c.1297A>C (p.Lys433Gln) c.463A>C (p.Lys155Gln) | dbSNP gnomAD v2 |
16 | g.74636475T= | CA2232905960 | RFWD3 | c.1297A= (p.Lys433=) c.463A= (p.Lys155=) | |
16 | g.74636476G>A | CA496542797 | RFWD3 | c.1296C>T (p.His432=) c.462C>T (p.His154=) | |
16 | g.74636476G>C | CA396761893 | RFWD3 | c.1296C>G (p.His432Gln) c.462C>G (p.His154Gln) | dbSNP gnomAD v2 gnomAD v4 |
16 | g.74636476G= | CA2232905961 | RFWD3 | c.1296C= (p.His432=) c.462C= (p.His154=) | |
16 | g.74636476G>T | CA396761894 | RFWD3 | c.1296C>A (p.His432Gln) c.462C>A (p.His154Gln) | |
16 | g.74636477T>A | CA396761896 | RFWD3 | c.1295A>T (p.His432Leu) c.461A>T (p.His154Leu) | |
16 | g.74636477T>C | CA396761898 | RFWD3 | c.1295A>G (p.His432Arg) c.461A>G (p.His154Arg) | |
16 | g.74636477T>G | CA396761900 | RFWD3 | c.1295A>C (p.His432Pro) c.461A>C (p.His154Pro) | |
16 | g.74636478G>A | CA283745857 | RFWD3 | c.1294C>T (p.His432Tyr) c.460C>T (p.His154Tyr) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
16 | g.74636478G>C | CA396761906 | RFWD3 | c.1294C>G (p.His432Asp) c.460C>G (p.His154Asp) | |
16 | g.74636478G= | CA2232905962 | RFWD3 | c.1294C= (p.His432=) c.460C= (p.His154=) | |
16 | g.74636478G>T | CA396761903 | RFWD3 | c.1294C>A (p.His432Asn) c.460C>A (p.His154Asn) | |
16 | g.74636479C>A | CA396761908 | RFWD3 | c.1293G>T (p.Gln431His) c.459G>T (p.Gln153His) | |
16 | g.74636479C= | CA2232905963 | RFWD3 | c.1293G= (p.Gln431=) c.459G= (p.Gln153=) | |
16 | g.74636479C>G | CA396761909 | RFWD3 | c.1293G>C (p.Gln431His) c.459G>C (p.Gln153His) | |
16 | g.74636479C>T | CA496542815 | RFWD3 | c.1293G>A (p.Gln431=) c.459G>A (p.Gln153=) | dbSNP gnomAD v3 gnomAD v4 COSMIC |
16 | g.74636480T>A | CA396761910 | RFWD3 | c.1292A>T (p.Gln431Leu) c.458A>T (p.Gln153Leu) | |
16 | g.74636480T>C | CA396761912 | RFWD3 | c.1292A>G (p.Gln431Arg) c.458A>G (p.Gln153Arg) |