Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
5 | g.44305155A= | CA1543079689 | FGF10 | c.467T= (p.Ile156=) | |
5 | g.44305155A>C | CA118869 | FGF10 | c.467T>G (p.Ile156Arg) | ClinVar dbSNP |
5 | g.44305155A>G | CA359697833 | FGF10 | c.467T>C (p.Ile156Thr) | |
5 | g.44305155A>T | CA359697834 | FGF10 | c.467T>A (p.Ile156Lys) | |
5 | g.44305156T>A | CA359697835 | FGF10 | c.466A>T (p.Ile156Leu) | |
5 | g.44305156T>C | CA359697837 | FGF10 | c.466A>G (p.Ile156Val) | |
5 | g.44305156T>G | CA359697836 | FGF10 | c.466A>C (p.Ile156Leu) | |
5 | g.44305157C>A | CA359697838 | FGF10 | c.465G>T (p.Arg155Ser) | |
5 | g.44305157C= | CA1543079693 | FGF10 | c.465G= (p.Arg155=) | |
5 | g.44305157C>G | CA359697839 | FGF10 | c.465G>C (p.Arg155Ser) | |
5 | g.44305157C>T | CA3258488 | FGF10 | c.465G>A (p.Arg155=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
5 | g.44305158C>A | CA359697840 | FGF10 | c.464G>T (p.Arg155Met) | dbSNP |
5 | g.44305158C= | CA1543079698 | FGF10 | c.464G= (p.Arg155=) | |
5 | g.44305158C>G | CA359697842 | FGF10 | c.464G>C (p.Arg155Thr) | |
5 | g.44305158C>T | CA359697841 | FGF10 | c.464G>A (p.Arg155Lys) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
5 | g.44305159T>A | CA359697843 | FGF10 | c.463A>T (p.Arg155Trp) | |
5 | g.44305159T>C | CA359697844 | FGF10 | c.463A>G (p.Arg155Gly) | |
5 | g.44305159T>G | CA444230960 | FGF10 | c.463A>C (p.Arg155=) | |
5 | g.44305160C>A | CA359697845 | FGF10 | c.462G>T (p.Glu154Asp) | |
5 | g.44305160C= | CA1543079701 | FGF10 | c.462G= (p.Glu154=) | |
5 | g.44305160C>G | CA359697846 | FGF10 | c.462G>C (p.Glu154Asp) | |
5 | g.44305160C>T | CA444230961 | FGF10 | c.462G>A (p.Glu154=) | dbSNP gnomAD v2 gnomAD v4 |
5 | g.44305161T>A | CA359697847 | FGF10 | c.461A>T (p.Glu154Val) | |
5 | g.44305161T>C | CA359697848 | FGF10 | c.461A>G (p.Glu154Gly) | |
5 | g.44305161T>G | CA359697849 | FGF10 | c.461A>C (p.Glu154Ala) | |
5 | g.44305162C>A | CA359697850 | FGF10 | c.460G>T (p.Glu154Ter) | |
5 | g.44305162C>G | CA359697851 | FGF10 | c.460G>C (p.Glu154Gln) | |
5 | g.44305162C>T | CA359697852 | FGF10 | c.460G>A (p.Glu154Lys) | |
5 | g.44305163C>A | CA359697854 | FGF10 | c.459G>T (p.Lys153Asn) | |
5 | g.44305163C>G | CA359697853 | FGF10 | c.459G>C (p.Lys153Asn) | |
5 | g.44305163C>T | CA444230962 | FGF10 | c.459G>A (p.Lys153=) | |
5 | g.44305164T>A | CA359697855 | FGF10 | c.458A>T (p.Lys153Met) | |
5 | g.44305164T>C | CA359697856 | FGF10 | c.458A>G (p.Lys153Arg) | |
5 | g.44305164T>G | CA359697857 | FGF10 | c.458A>C (p.Lys153Thr) | |
5 | g.44305165T>A | CA359697858 | FGF10 | c.457A>T (p.Lys153Ter) | |
5 | g.44305165T>C | CA359697859 | FGF10 | c.457A>G (p.Lys153Glu) | |
5 | g.44305165T>G | CA359697860 | FGF10 | c.457A>C (p.Lys153Gln) | |
5 | g.44305166C>A | CA444230963 | FGF10 | c.456G>T (p.Leu152=) | |
5 | g.44305166C>G | CA444230964 | FGF10 | c.456G>C (p.Leu152=) | |
5 | g.44305166C>T | CA444230965 | FGF10 | c.456G>A (p.Leu152=) | |
5 | g.44305167A>C | CA359697861 | FGF10 | c.455T>G (p.Leu152Arg) | |
5 | g.44305167A>G | CA359697862 | FGF10 | c.455T>C (p.Leu152Pro) | |
5 | g.44305167A>T | CA359697863 | FGF10 | c.455T>A (p.Leu152Gln) | |
5 | g.44305168G>A | CA444230966 | FGF10 | c.454C>T (p.Leu152=) | dbSNP |
5 | g.44305168G>C | CA359697864 | FGF10 | c.454C>G (p.Leu152Val) | |
5 | g.44305168G= | CA1543079703 | FGF10 | c.454C= (p.Leu152=) | |
5 | g.44305168G>T | CA359697865 | FGF10 | c.454C>A (p.Leu152Met) | |
5 | g.44305169C>A | CA359697866 | FGF10 | c.453G>T (p.Lys151Asn) | |
5 | g.44305169C= | CA1543079707 | FGF10 | c.453G= (p.Lys151=) | |
5 | g.44305169C>G | CA359697867 | FGF10 | c.453G>C (p.Lys151Asn) | ClinVar |