Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.119677634T>A | CA383281841 | NECTIN1 | c.654A>T (p.Glu218Asp) n.628A>T | |
11 | g.119677634T>C | CA477263686 | NECTIN1 | c.654A>G (p.Glu218=) n.628A>G | |
11 | g.119677634T>G | CA383281842 | NECTIN1 | c.654A>C (p.Glu218Asp) n.628A>C | |
11 | g.119677635T>A | CA383281843 | NECTIN1 | c.653A>T (p.Glu218Val) n.627A>T | |
11 | g.119677635T>C | CA383281844 | NECTIN1 | c.653A>G (p.Glu218Gly) n.627A>G | |
11 | g.119677635T>G | CA383281845 | NECTIN1 | c.653A>C (p.Glu218Ala) n.627A>C | dbSNP gnomAD v2 gnomAD v4 |
11 | g.119677635T= | CA2004078776 | NECTIN1 | c.653A= (p.Glu218=) n.627A= | |
11 | g.119677636C>A | CA383281846 | NECTIN1 | c.652G>T (p.Glu218Ter) n.626G>T | |
11 | g.119677636C= | CA2004078787 | NECTIN1 | c.652G= (p.Glu218=) n.626G= | |
11 | g.119677636C>G | CA383281847 | NECTIN1 | c.652G>C (p.Glu218Gln) n.626G>C | |
11 | g.119677636C>T | CA6322036 | NECTIN1 | c.652G>A (p.Glu218Lys) n.626G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.119677637C>A | CA383281848 | NECTIN1 | c.651G>T (p.Arg217Ser) n.625G>T | |
11 | g.119677637C>G | CA383281849 | NECTIN1 | c.651G>C (p.Arg217Ser) n.625G>C | |
11 | g.119677637C>T | CA477263695 | NECTIN1 | c.651G>A (p.Arg217=) n.625G>A | |
11 | g.119677638C>A | CA383281850 | NECTIN1 | c.650G>T (p.Arg217Met) n.624G>T | |
11 | g.119677638C= | CA2004078793 | NECTIN1 | c.650G= (p.Arg217=) n.624G= | |
11 | g.119677638C>G | CA383281851 | NECTIN1 | c.650G>C (p.Arg217Thr) n.624G>C | dbSNP gnomAD v2 gnomAD v4 |
11 | g.119677638C>T | CA383281852 | NECTIN1 | c.650G>A (p.Arg217Lys) n.624G>A | |
11 | g.119677639del | CA645584366 | NECTIN1 | c.649del (p.Arg217GlyfsTer?) n.623del | COSMIC COSMIC COSMIC |
11 | g.119677639T>A | CA383281853 | NECTIN1 | c.649A>T (p.Arg217Trp) n.623A>T | |
11 | g.119677639T>C | CA383281854 | NECTIN1 | c.649A>G (p.Arg217Gly) n.623A>G | |
11 | g.119677639T>G | CA477263700 | NECTIN1 | c.649A>C (p.Arg217=) n.623A>C | |
11 | g.119677640G>A | CA477263703 | NECTIN1 | c.648C>T (p.Ser216=) n.622C>T | dbSNP gnomAD v4 |
11 | g.119677640G>C | CA383281856 | NECTIN1 | c.648C>G (p.Ser216Arg) n.622C>G | |
11 | g.119677640G= | CA2004078796 | NECTIN1 | c.648C= (p.Ser216=) n.622C= | |
11 | g.119677640G>T | CA383281855 | NECTIN1 | c.648C>A (p.Ser216Arg) n.622C>A | gnomAD v4 |
11 | g.119677641C>A | CA383281857 | NECTIN1 | c.647G>T (p.Ser216Ile) n.621G>T | |
11 | g.119677641C>G | CA383281858 | NECTIN1 | c.647G>C (p.Ser216Thr) n.621G>C | gnomAD v4 |
11 | g.119677641C>T | CA383281859 | NECTIN1 | c.647G>A (p.Ser216Asn) n.621G>A | |
11 | g.119677642T>A | CA383281860 | NECTIN1 | c.646A>T (p.Ser216Cys) n.620A>T | |
11 | g.119677642T>C | CA6322037 | NECTIN1 | c.646A>G (p.Ser216Gly) n.620A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
11 | g.119677642T>G | CA383281861 | NECTIN1 | c.646A>C (p.Ser216Arg) n.620A>C | gnomAD v4 |
11 | g.119677642T= | CA2004078803 | NECTIN1 | c.646A= (p.Ser216=) n.620A= | |
11 | g.119677643G>A | CA477263709 | NECTIN1 | c.645C>T (p.Pro215=) n.619C>T | dbSNP |
11 | g.119677643G>C | CA477263710 | NECTIN1 | c.645C>G (p.Pro215=) n.619C>G | |
11 | g.119677643G= | CA2004078815 | NECTIN1 | c.645C= (p.Pro215=) n.619C= | |
11 | g.119677643G>T | CA6322038 | NECTIN1 | c.645C>A (p.Pro215=) n.619C>A | dbSNP ExAC gnomAD v4 |
11 | g.119677644G>A | CA229370245 | NECTIN1 | c.644C>T (p.Pro215Leu) n.618C>T | dbSNP gnomAD v4 |
11 | g.119677644G>C | CA383281862 | NECTIN1 | c.644C>G (p.Pro215Arg) n.618C>G | |
11 | g.119677644G= | CA2004078822 | NECTIN1 | c.644C= (p.Pro215=) n.618C= | |
11 | g.119677644G>T | CA383281863 | NECTIN1 | c.644C>A (p.Pro215His) n.618C>A | |
11 | g.119677645G>A | CA383281864 | NECTIN1 | c.643C>T (p.Pro215Ser) n.617C>T | |
11 | g.119677645G>C | CA383281865 | NECTIN1 | c.643C>G (p.Pro215Ala) n.617C>G | |
11 | g.119677645G>T | CA383281866 | NECTIN1 | c.643C>A (p.Pro215Thr) n.617C>A | |
11 | g.119677646C>A | CA477263716 | NECTIN1 | c.642G>T (p.Val214=) n.616G>T | |
11 | g.119677646C>G | CA477263718 | NECTIN1 | c.642G>C (p.Val214=) n.616G>C | |
11 | g.119677646C>T | CA477263720 | NECTIN1 | c.642G>A (p.Val214=) n.616G>A | |
11 | g.119677647A= | CA2004078826 | NECTIN1 | c.641T= (p.Val214=) n.615T= | |
11 | g.119677647A>C | CA383281868 | NECTIN1 | c.641T>G (p.Val214Gly) n.615T>G | dbSNP |
11 | g.119677647A>G | CA383281869 | NECTIN1 | c.641T>C (p.Val214Ala) n.615T>C | dbSNP |