Chr Mutation (hg38) CAid Gene Transcript Linkouts
5g.44305155A=CA1543079689FGF10c.467T= (p.Ile156=)
5g.44305155A>CCA118869FGF10c.467T>G (p.Ile156Arg)
ClinVar dbSNP
5g.44305155A>GCA359697833FGF10c.467T>C (p.Ile156Thr)
5g.44305155A>TCA359697834FGF10c.467T>A (p.Ile156Lys)
5g.44305156T>ACA359697835FGF10c.466A>T (p.Ile156Leu)
5g.44305156T>CCA359697837FGF10c.466A>G (p.Ile156Val)
5g.44305156T>GCA359697836FGF10c.466A>C (p.Ile156Leu)
5g.44305157C>ACA359697838FGF10c.465G>T (p.Arg155Ser)
5g.44305157C=CA1543079693FGF10c.465G= (p.Arg155=)
5g.44305157C>GCA359697839FGF10c.465G>C (p.Arg155Ser)
5g.44305157C>TCA3258488FGF10c.465G>A (p.Arg155=)
dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC
5g.44305158C>ACA359697840FGF10c.464G>T (p.Arg155Met)
dbSNP
5g.44305158C=CA1543079698FGF10c.464G= (p.Arg155=)
5g.44305158C>GCA359697842FGF10c.464G>C (p.Arg155Thr)
5g.44305158C>TCA359697841FGF10c.464G>A (p.Arg155Lys)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
5g.44305159T>ACA359697843FGF10c.463A>T (p.Arg155Trp)
5g.44305159T>CCA359697844FGF10c.463A>G (p.Arg155Gly)
5g.44305159T>GCA444230960FGF10c.463A>C (p.Arg155=)
5g.44305160C>ACA359697845FGF10c.462G>T (p.Glu154Asp)
5g.44305160C=CA1543079701FGF10c.462G= (p.Glu154=)
5g.44305160C>GCA359697846FGF10c.462G>C (p.Glu154Asp)
5g.44305160C>TCA444230961FGF10c.462G>A (p.Glu154=)
dbSNP gnomAD v2 gnomAD v4
5g.44305161T>ACA359697847FGF10c.461A>T (p.Glu154Val)
5g.44305161T>CCA359697848FGF10c.461A>G (p.Glu154Gly)
5g.44305161T>GCA359697849FGF10c.461A>C (p.Glu154Ala)
5g.44305162C>ACA359697850FGF10c.460G>T (p.Glu154Ter)
5g.44305162C>GCA359697851FGF10c.460G>C (p.Glu154Gln)
5g.44305162C>TCA359697852FGF10c.460G>A (p.Glu154Lys)
5g.44305163C>ACA359697854FGF10c.459G>T (p.Lys153Asn)
5g.44305163C>GCA359697853FGF10c.459G>C (p.Lys153Asn)
5g.44305163C>TCA444230962FGF10c.459G>A (p.Lys153=)
5g.44305164T>ACA359697855FGF10c.458A>T (p.Lys153Met)
5g.44305164T>CCA359697856FGF10c.458A>G (p.Lys153Arg)
5g.44305164T>GCA359697857FGF10c.458A>C (p.Lys153Thr)
5g.44305165T>ACA359697858FGF10c.457A>T (p.Lys153Ter)
5g.44305165T>CCA359697859FGF10c.457A>G (p.Lys153Glu)
5g.44305165T>GCA359697860FGF10c.457A>C (p.Lys153Gln)
5g.44305166C>ACA444230963FGF10c.456G>T (p.Leu152=)
5g.44305166C>GCA444230964FGF10c.456G>C (p.Leu152=)
5g.44305166C>TCA444230965FGF10c.456G>A (p.Leu152=)
5g.44305167A>CCA359697861FGF10c.455T>G (p.Leu152Arg)
5g.44305167A>GCA359697862FGF10c.455T>C (p.Leu152Pro)
5g.44305167A>TCA359697863FGF10c.455T>A (p.Leu152Gln)
5g.44305168G>ACA444230966FGF10c.454C>T (p.Leu152=)
dbSNP
5g.44305168G>CCA359697864FGF10c.454C>G (p.Leu152Val)
5g.44305168G=CA1543079703FGF10c.454C= (p.Leu152=)
5g.44305168G>TCA359697865FGF10c.454C>A (p.Leu152Met)
5g.44305169C>ACA359697866FGF10c.453G>T (p.Lys151Asn)
5g.44305169C=CA1543079707FGF10c.453G= (p.Lys151=)
5g.44305169C>GCA359697867FGF10c.453G>C (p.Lys151Asn)
ClinVar

Number of alleles fetched