Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
11 | g.47448079G>A | CA474430514 | RAPSN | c.264C>T (p.Asn88=) | |
11 | g.47448079G>C | CA380334837 | RAPSN | c.264C>G (p.Asn88Lys) | |
11 | g.47448079G= | CA1969378565 | RAPSN | c.264C= (p.Asn88=) | |
11 | g.47448079G>T | CA199511 | RAPSN | c.264C>A (p.Asn88Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
11 | g.47448080T>A | CA380334845 | RAPSN | c.263A>T (p.Asn88Ile) | |
11 | g.47448080T>C | CA380334850 | RAPSN | c.263A>G (p.Asn88Ser) | dbSNP |
11 | g.47448080T>G | CA380334851 | RAPSN | c.263A>C (p.Asn88Thr) | |
11 | g.47448080T= | CA1969378570 | RAPSN | c.263A= (p.Asn88=) | |
11 | g.47448081T>A | CA380334854 | RAPSN | c.262A>T (p.Asn88Tyr) | |
11 | g.47448081T>C | CA380334855 | RAPSN | c.262A>G (p.Asn88Asp) | |
11 | g.47448081T>G | CA380334857 | RAPSN | c.262A>C (p.Asn88His) | |
11 | g.47448082C>A | CA474430520 | RAPSN | c.261G>T (p.Leu87=) | |
11 | g.47448082C>G | CA474430519 | RAPSN | c.261G>C (p.Leu87=) | |
11 | g.47448082C>T | CA474430518 | RAPSN | c.261G>A (p.Leu87=) | |
11 | g.47448083A= | CA1969378574 | RAPSN | c.260T= (p.Leu87=) | |
11 | g.47448083A>C | CA380334862 | RAPSN | c.260T>G (p.Leu87Arg) | |
11 | g.47448083A>G | CA380334869 | RAPSN | c.260T>C (p.Leu87Pro) | dbSNP gnomAD v2 gnomAD v4 |
11 | g.47448083A>T | CA380334872 | RAPSN | c.260T>A (p.Leu87Gln) | |
11 | g.47448084G>A | CA5976772 | RAPSN | c.259C>T (p.Leu87=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.47448084G>C | CA380334874 | RAPSN | c.259C>G (p.Leu87Val) | gnomAD v4 |
11 | g.47448084G= | CA1969378576 | RAPSN | c.259C= (p.Leu87=) | |
11 | g.47448084G>T | CA380334875 | RAPSN | c.259C>A (p.Leu87Met) | |
11 | g.47448085G>A | CA474430522 | RAPSN | c.258C>T (p.Tyr86=) | ClinVar COSMIC |
11 | g.47448085G>C | CA380334876 | RAPSN | c.258C>G (p.Tyr86Ter) | |
11 | g.47448085G>T | CA380334877 | RAPSN | c.258C>A (p.Tyr86Ter) | |
11 | g.47448086T>A | CA380334881 | RAPSN | c.257A>T (p.Tyr86Phe) | |
11 | g.47448086T>C | CA380334883 | RAPSN | c.257A>G (p.Tyr86Cys) | |
11 | g.47448086T>G | CA380334887 | RAPSN | c.257A>C (p.Tyr86Ser) | |
11 | g.47448087A= | CA1969378583 | RAPSN | c.256T= (p.Tyr86=) | |
11 | g.47448087A>C | CA380334889 | RAPSN | c.256T>G (p.Tyr86Asp) | |
11 | g.47448087A>G | CA5976773 | RAPSN | c.256T>C (p.Tyr86His) | dbSNP ExAC gnomAD v2 gnomAD v4 |
11 | g.47448087A>T | CA380334898 | RAPSN | c.256T>A (p.Tyr86Asn) | |
11 | g.47448088G>A | CA474430524 | RAPSN | c.255C>T (p.Ser85=) | |
11 | g.47448088G>C | CA380334900 | RAPSN | c.255C>G (p.Ser85Arg) | |
11 | g.47448088G>T | CA380334904 | RAPSN | c.255C>A (p.Ser85Arg) | |
11 | g.47448089C>A | CA380334907 | RAPSN | c.254G>T (p.Ser85Ile) | |
11 | g.47448089C= | CA1969378588 | RAPSN | c.254G= (p.Ser85=) | |
11 | g.47448089C>G | CA380334909 | RAPSN | c.254G>C (p.Ser85Thr) | dbSNP |
11 | g.47448089C>T | CA380334916 | RAPSN | c.254G>A (p.Ser85Asn) | |
11 | g.47448090T>A | CA380334920 | RAPSN | c.253A>T (p.Ser85Cys) | |
11 | g.47448090T>C | CA380334922 | RAPSN | c.253A>G (p.Ser85Gly) | |
11 | g.47448090T>G | CA380334933 | RAPSN | c.253A>C (p.Ser85Arg) | |
11 | g.47448091C>A | CA380334935 | RAPSN | c.252G>T (p.Glu84Asp) | |
11 | g.47448091C>G | CA380334937 | RAPSN | c.252G>C (p.Glu84Asp) | |
11 | g.47448091C>T | CA474430526 | RAPSN | c.252G>A (p.Glu84=) | |
11 | g.47448092T>A | CA380334939 | RAPSN | c.251A>T (p.Glu84Val) | |
11 | g.47448092T>C | CA380334941 | RAPSN | c.251A>G (p.Glu84Gly) | |
11 | g.47448092T>G | CA380334945 | RAPSN | c.251A>C (p.Glu84Ala) | ClinVar dbSNP gnomAD v4 |
11 | g.47448093C>A | CA380334957 | RAPSN | c.250G>T (p.Glu84Ter) | |
11 | g.47448093C= | CA1969378591 | RAPSN | c.250G= (p.Glu84=) |