Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
7 | g.81752150C>A | CA367874762 | HGF | c.595G>T (p.Glu199Ter) c.580G>T (p.Glu194Ter) n.608G>T | dbSNP |
7 | g.81752150C>G | CA367874763 | HGF | c.595G>C (p.Glu199Gln) c.580G>C (p.Glu194Gln) n.608G>C | dbSNP |
7 | g.81752150C>T | CA367874764 | HGF | c.595G>A (p.Glu199Lys) c.580G>A (p.Glu194Lys) n.608G>A | dbSNP gnomAD v4 COSMIC |
7 | g.81752151G>A | CA4317166 | HGF | c.594C>T (p.Tyr198=) c.579C>T (p.Tyr193=) n.607C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.81752151G>C | CA367874765 | HGF | c.594C>G (p.Tyr198Ter) c.579C>G (p.Tyr193Ter) n.607C>G | dbSNP |
7 | g.81752151G= | CA1720885400 | HGF | c.594C= (p.Tyr198=) c.579C= (p.Tyr193=) n.607C= | |
7 | g.81752151G>T | CA367874766 | HGF | c.594C>A (p.Tyr198Ter) c.579C>A (p.Tyr193Ter) n.607C>A | |
7 | g.81752152T>A | CA367874767 | HGF | c.593A>T (p.Tyr198Phe) c.578A>T (p.Tyr193Phe) n.606A>T | dbSNP |
7 | g.81752152T>C | CA367874768 | HGF | c.593A>G (p.Tyr198Cys) c.578A>G (p.Tyr193Cys) n.606A>G | |
7 | g.81752152T>G | CA367874769 | HGF | c.593A>C (p.Tyr198Ser) c.578A>C (p.Tyr193Ser) n.606A>C | |
7 | g.81752153A>C | CA367874772 | HGF | c.592T>G (p.Tyr198Asp) c.577T>G (p.Tyr193Asp) n.605T>G | |
7 | g.81752153A>G | CA367874771 | HGF | c.592T>C (p.Tyr198His) c.577T>C (p.Tyr193His) n.605T>C | |
7 | g.81752153A>T | CA367874770 | HGF | c.592T>A (p.Tyr198Asn) c.577T>A (p.Tyr193Asn) n.605T>A | dbSNP |
7 | g.81752154G>A | CA456129437 | HGF | c.591C>T (p.Arg197=) c.576C>T (p.Arg192=) n.604C>T | |
7 | g.81752154G>C | CA456129438 | HGF | c.591C>G (p.Arg197=) c.576C>G (p.Arg192=) n.604C>G | dbSNP |
7 | g.81752154G>T | CA456129439 | HGF | c.591C>A (p.Arg197=) c.576C>A (p.Arg192=) n.604C>A | |
7 | g.81752155C>A | CA367874773 | HGF | c.590G>T (p.Arg197Leu) c.575G>T (p.Arg192Leu) n.603G>T | dbSNP |
7 | g.81752155C= | CA1720885401 | HGF | c.590G= (p.Arg197=) c.575G= (p.Arg192=) n.603G= | |
7 | g.81752155C>G | CA367874774 | HGF | c.590G>C (p.Arg197Pro) c.575G>C (p.Arg192Pro) n.603G>C | dbSNP |
7 | g.81752155C>T | CA4317167 | HGF | c.590G>A (p.Arg197His) c.575G>A (p.Arg192His) n.603G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
7 | g.81752156G>A | CA4317168 | HGF | c.589C>T (p.Arg197Cys) c.574C>T (p.Arg192Cys) n.602C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
7 | g.81752156G>C | CA367874775 | HGF | c.589C>G (p.Arg197Gly) c.574C>G (p.Arg192Gly) n.602C>G | dbSNP |
7 | g.81752156G= | CA1720885402 | HGF | c.589C= (p.Arg197=) c.574C= (p.Arg192=) n.602C= | |
7 | g.81752156G>T | CA367874776 | HGF | c.589C>A (p.Arg197Ser) c.574C>A (p.Arg192Ser) n.602C>A | |
7 | g.81752157T>A | CA456129440 | HGF | c.588A>T (p.Val196=) c.573A>T (p.Val191=) n.601A>T | dbSNP |
7 | g.81752157T>C | CA456129441 | HGF | c.588A>G (p.Val196=) c.573A>G (p.Val191=) n.601A>G | dbSNP gnomAD v2 gnomAD v4 |
7 | g.81752157T>G | CA456129442 | HGF | c.588A>C (p.Val196=) c.573A>C (p.Val191=) n.601A>C | |
7 | g.81752157T= | CA1720885403 | HGF | c.588A= (p.Val196=) c.573A= (p.Val191=) n.601A= | |
7 | g.81752158A>C | CA367874777 | HGF | c.587T>G (p.Val196Gly) c.572T>G (p.Val191Gly) n.600T>G | dbSNP |
7 | g.81752158A>G | CA367874778 | HGF | c.587T>C (p.Val196Ala) c.572T>C (p.Val191Ala) n.600T>C | gnomAD v4 |
7 | g.81752158A>T | CA367874779 | HGF | c.587T>A (p.Val196Glu) c.572T>A (p.Val191Glu) n.600T>A | dbSNP |
7 | g.81752159C>A | CA367874780 | HGF | c.586G>T (p.Val196Leu) c.571G>T (p.Val191Leu) n.599G>T | |
7 | g.81752159C>G | CA367874781 | HGF | c.586G>C (p.Val196Leu) c.571G>C (p.Val191Leu) n.599G>C | dbSNP |
7 | g.81752159C>T | CA367874782 | HGF | c.586G>A (p.Val196Ile) c.571G>A (p.Val191Ile) n.599G>A | dbSNP |
7 | g.81752160C>A | CA367874783 | HGF | c.585G>T (p.Glu195Asp) c.570G>T (p.Glu190Asp) n.598G>T | dbSNP |
7 | g.81752160C>G | CA367874784 | HGF | c.585G>C (p.Glu195Asp) c.570G>C (p.Glu190Asp) n.598G>C | dbSNP |
7 | g.81752160C>T | CA456129443 | HGF | c.585G>A (p.Glu195=) c.570G>A (p.Glu190=) n.598G>A | dbSNP COSMIC |
7 | g.81752161T>A | CA367874786 | HGF | c.584A>T (p.Glu195Val) c.569A>T (p.Glu190Val) n.597A>T | dbSNP |
7 | g.81752161T>C | CA367874787 | HGF | c.584A>G (p.Glu195Gly) c.569A>G (p.Glu190Gly) n.597A>G | |
7 | g.81752161T>G | CA367874785 | HGF | c.584A>C (p.Glu195Ala) c.569A>C (p.Glu190Ala) n.597A>C | |
7 | g.81752162C>A | CA367874788 | HGF | c.583G>T (p.Glu195Ter) c.568G>T (p.Glu190Ter) n.596G>T | |
7 | g.81752162C>G | CA367874789 | HGF | c.583G>C (p.Glu195Gln) c.568G>C (p.Glu190Gln) n.596G>C | dbSNP |
7 | g.81752162C>T | CA367874790 | HGF | c.583G>A (p.Glu195Lys) c.568G>A (p.Glu190Lys) n.596G>A | dbSNP |
7 | g.81752163T>A | CA456129446 | HGF | c.582A>T (p.Pro194=) c.567A>T (p.Pro189=) n.595A>T | |
7 | g.81752163T>C | CA456129444 | HGF | c.582A>G (p.Pro194=) c.567A>G (p.Pro189=) n.595A>G | |
7 | g.81752163T>G | CA456129445 | HGF | c.582A>C (p.Pro194=) c.567A>C (p.Pro189=) n.595A>C | |
7 | g.81752164G>A | CA367874791 | HGF | c.581C>T (p.Pro194Leu) c.566C>T (p.Pro189Leu) n.594C>T | dbSNP gnomAD v2 gnomAD v4 |
7 | g.81752164G>C | CA367874792 | HGF | c.581C>G (p.Pro194Arg) c.566C>G (p.Pro189Arg) n.594C>G | dbSNP |
7 | g.81752164G= | CA1720885404 | HGF | c.581C= (p.Pro194=) c.566C= (p.Pro189=) n.594C= | |
7 | g.81752164G>T | CA367874793 | HGF | c.581C>A (p.Pro194Gln) c.566C>A (p.Pro189Gln) n.594C>A |