Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.81729637C>A | CA367870785 | HGF | c.1008G>T (p.Glu336Asp) c.993G>T (p.Glu331Asp) | |
7 | g.81729637C= | CA1720888246 | HGF | c.1008G= (p.Glu336=) c.993G= (p.Glu331=) | |
7 | g.81729637C>G | CA367870786 | HGF | c.1008G>C (p.Glu336Asp) c.993G>C (p.Glu331Asp) | |
7 | g.81729637C>T | CA132813 | HGF | c.1008G>A (p.Glu336=) c.993G>A (p.Glu331=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.81729638T>A | CA367870787 | HGF | c.1007A>T (p.Glu336Val) c.992A>T (p.Glu331Val) | |
7 | g.81729638T>C | CA367870789 | HGF | c.1007A>G (p.Glu336Gly) c.992A>G (p.Glu331Gly) | |
7 | g.81729638T>G | CA367870788 | HGF | c.1007A>C (p.Glu336Ala) c.992A>C (p.Glu331Ala) | |
7 | g.81729639C>A | CA367870790 | HGF | c.1006G>T (p.Glu336Ter) c.991G>T (p.Glu331Ter) | |
7 | g.81729639C= | CA1720888247 | HGF | c.1006G= (p.Glu336=) c.991G= (p.Glu331=) | |
7 | g.81729639C>G | CA367870791 | HGF | c.1006G>C (p.Glu336Gln) c.991G>C (p.Glu331Gln) | |
7 | g.81729639C>T | CA4317011 | HGF | c.1006G>A (p.Glu336Lys) c.991G>A (p.Glu331Lys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.81729640G>A | CA4317012 | HGF | c.1005C>T (p.His335=) c.990C>T (p.His330=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.81729640G>C | CA367870792 | HGF | c.1005C>G (p.His335Gln) c.990C>G (p.His330Gln) | |
7 | g.81729640G= | CA1720888248 | HGF | c.1005C= (p.His335=) c.990C= (p.His330=) | |
7 | g.81729640G>T | CA367870793 | HGF | c.1005C>A (p.His335Gln) c.990C>A (p.His330Gln) | dbSNP gnomAD v2 gnomAD v4 |
7 | g.81729641T>A | CA367870794 | HGF | c.1004A>T (p.His335Leu) c.989A>T (p.His330Leu) | |
7 | g.81729641T>C | CA367870795 | HGF | c.1004A>G (p.His335Arg) c.989A>G (p.His330Arg) | |
7 | g.81729641T>G | CA367870796 | HGF | c.1004A>C (p.His335Pro) c.989A>C (p.His330Pro) | |
7 | g.81729642G>A | CA367870797 | HGF | c.1003C>T (p.His335Tyr) c.988C>T (p.His330Tyr) | dbSNP |
7 | g.81729642G>C | CA367870798 | HGF | c.1003C>G (p.His335Asp) c.988C>G (p.His330Asp) | |
7 | g.81729642G= | CA1720888249 | HGF | c.1003C= (p.His335=) c.988C= (p.His330=) | |
7 | g.81729642G>T | CA367870799 | HGF | c.1003C>A (p.His335Asn) c.988C>A (p.His330Asn) | |
7 | g.81729643A>C | CA456129148 | HGF | c.1002T>G (p.Pro334=) c.987T>G (p.Pro329=) | |
7 | g.81729643A>G | CA456129150 | HGF | c.1002T>C (p.Pro334=) c.987T>C (p.Pro329=) | |
7 | g.81729643A>T | CA456129149 | HGF | c.1002T>A (p.Pro334=) c.987T>A (p.Pro329=) | |
7 | g.81729644G>A | CA367870801 | HGF | c.1001C>T (p.Pro334Leu) c.986C>T (p.Pro329Leu) | dbSNP |
7 | g.81729644G>C | CA367870802 | HGF | c.1001C>G (p.Pro334Arg) c.986C>G (p.Pro329Arg) | |
7 | g.81729644G>T | CA367870800 | HGF | c.1001C>A (p.Pro334His) c.986C>A (p.Pro329His) | |
7 | g.81729645G>A | CA367870805 | HGF | c.1000C>T (p.Pro334Ser) c.985C>T (p.Pro329Ser) | dbSNP |
7 | g.81729645G>C | CA367870803 | HGF | c.1000C>G (p.Pro334Ala) c.985C>G (p.Pro329Ala) | |
7 | g.81729645G= | CA1720888250 | HGF | c.1000C= (p.Pro334=) c.985C= (p.Pro329=) | |
7 | g.81729645G>T | CA367870804 | HGF | c.1000C>A (p.Pro334Thr) c.985C>A (p.Pro329Thr) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.81729646A= | CA1720888251 | HGF | c.999T= (p.Tyr333=) c.984T= (p.Tyr328=) | |
7 | g.81729646A>C | CA367870806 | HGF | c.999T>G (p.Tyr333Ter) c.984T>G (p.Tyr328Ter) | |
7 | g.81729646A>G | CA4317013 | HGF | c.999T>C (p.Tyr333=) c.984T>C (p.Tyr328=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.81729646A>T | CA367870807 | HGF | c.999T>A (p.Tyr333Ter) c.984T>A (p.Tyr328Ter) | |
7 | g.81729647T>A | CA367870808 | HGF | c.998A>T (p.Tyr333Phe) c.983A>T (p.Tyr328Phe) | dbSNP gnomAD v3 gnomAD v4 |
7 | g.81729647T>C | CA367870809 | HGF | c.998A>G (p.Tyr333Cys) c.983A>G (p.Tyr328Cys) | dbSNP |
7 | g.81729647T>G | CA367870810 | HGF | c.998A>C (p.Tyr333Ser) c.983A>C (p.Tyr328Ser) | |
7 | g.81729647T= | CA1720888252 | HGF | c.998A= (p.Tyr333=) c.983A= (p.Tyr328=) | |
7 | g.81729648A>C | CA367870811 | HGF | c.997T>G (p.Tyr333Asp) c.982T>G (p.Tyr328Asp) | |
7 | g.81729648A>G | CA367870812 | HGF | c.997T>C (p.Tyr333His) c.982T>C (p.Tyr328His) | COSMIC |
7 | g.81729648A>T | CA367870813 | HGF | c.997T>A (p.Tyr333Asn) c.982T>A (p.Tyr328Asn) | |
7 | g.81729649C>A | CA367870814 | HGF | c.996G>T (p.Gln332His) c.981G>T (p.Gln327His) | |
7 | g.81729649C= | CA1720888253 | HGF | c.996G= (p.Gln332=) c.981G= (p.Gln327=) | |
7 | g.81729649C>G | CA367870815 | HGF | c.996G>C (p.Gln332His) c.981G>C (p.Gln327His) | |
7 | g.81729649C>T | CA161089691 | HGF | c.996G>A (p.Gln332=) c.981G>A (p.Gln327=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.81729650T>A | CA367870818 | HGF | c.995A>T (p.Gln332Leu) c.980A>T (p.Gln327Leu) | dbSNP |
7 | g.81729650T>C | CA367870817 | HGF | c.995A>G (p.Gln332Arg) c.980A>G (p.Gln327Arg) | gnomAD v4 COSMIC |
7 | g.81729650T>G | CA367870816 | HGF | c.995A>C (p.Gln332Pro) c.980A>C (p.Gln327Pro) | gnomAD v4 |