| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| X | g.116172342G>A | CA414337509 | AGTR2 | c.62G>A (p.Gly21Glu) n.530G>A | |
| X | g.116172342G>C | CA414337510 | AGTR2 | c.62G>C (p.Gly21Ala) n.530G>C | |
| X | g.116172342G= | CA2453331670 | AGTR2 | c.62G= (p.Gly21=) n.530G= | |
| X | g.116172342G>T | CA151691 | AGTR2 | c.62G>T (p.Gly21Val) n.530G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.116172343G>A | CA518449131 | AGTR2 | c.63G>A (p.Gly21=) n.531G>A | dbSNP |
| X | g.116172343G>C | CA518449130 | AGTR2 | c.63G>C (p.Gly21=) n.531G>C | dbSNP gnomAD v2 gnomAD v4 |
| X | g.116172343G= | CA2453331671 | AGTR2 | c.63G= (p.Gly21=) n.531G= | |
| X | g.116172343G>T | CA518449129 | AGTR2 | c.63G>T (p.Gly21=) n.531G>T | |
| X | g.116172344C>A | CA414337511 | AGTR2 | c.64C>A (p.Leu22Ile) n.532C>A | |
| X | g.116172344C>G | CA414337512 | AGTR2 | c.64C>G (p.Leu22Val) n.532C>G | |
| X | g.116172344C>T | CA414337513 | AGTR2 | c.64C>T (p.Leu22Phe) n.532C>T | |
| X | g.116172345T>A | CA414337516 | AGTR2 | c.65T>A (p.Leu22His) n.533T>A | |
| X | g.116172345T>C | CA414337515 | AGTR2 | c.65T>C (p.Leu22Pro) n.533T>C | dbSNP |
| X | g.116172345T>G | CA414337514 | AGTR2 | c.65T>G (p.Leu22Arg) n.533T>G | |
| X | g.116172345T= | CA2453331672 | AGTR2 | c.65T= (p.Leu22=) n.533T= | |
| X | g.116172346T>A | CA518449132 | AGTR2 | c.66T>A (p.Leu22=) n.534T>A | |
| X | g.116172346T>C | CA518449133 | AGTR2 | c.66T>C (p.Leu22=) n.534T>C | |
| X | g.116172346T>G | CA518449134 | AGTR2 | c.66T>G (p.Leu22=) n.534T>G | |
| X | g.116172347G>A | CA334723677 | AGTR2 | c.67G>A (p.Val23Met) n.535G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| X | g.116172347G>C | CA414337517 | AGTR2 | c.67G>C (p.Val23Leu) n.535G>C | |
| X | g.116172347G= | CA2453331673 | AGTR2 | c.67G= (p.Val23=) n.535G= | |
| X | g.116172347G>T | CA414337518 | AGTR2 | c.67G>T (p.Val23Leu) n.535G>T | |
| X | g.116172348T>A | CA414337519 | AGTR2 | c.68T>A (p.Val23Glu) n.536T>A | |
| X | g.116172348T>C | CA414337521 | AGTR2 | c.68T>C (p.Val23Ala) n.536T>C | |
| X | g.116172348T>G | CA414337522 | AGTR2 | c.68T>G (p.Val23Gly) n.536T>G | |
| X | g.116172349G>A | CA518449135 | AGTR2 | c.69G>A (p.Val23=) n.537G>A | |
| X | g.116172349G>C | CA518449136 | AGTR2 | c.69G>C (p.Val23=) n.537G>C | |
| X | g.116172349G>T | CA518449137 | AGTR2 | c.69G>T (p.Val23=) n.537G>T | |
| X | g.116172350A>C | CA414337525 | AGTR2 | c.70A>C (p.Asn24His) n.538A>C | |
| X | g.116172350A>G | CA414337523 | AGTR2 | c.70A>G (p.Asn24Asp) n.538A>G | |
| X | g.116172350A>T | CA414337524 | AGTR2 | c.70A>T (p.Asn24Tyr) n.538A>T | |
| X | g.116172351A>C | CA414337528 | AGTR2 | c.71A>C (p.Asn24Thr) n.539A>C | |
| X | g.116172351A>G | CA414337529 | AGTR2 | c.71A>G (p.Asn24Ser) n.539A>G | |
| X | g.116172351A>T | CA414337530 | AGTR2 | c.71A>T (p.Asn24Ile) n.539A>T | |
| X | g.116172352C>A | CA414337531 | AGTR2 | c.72C>A (p.Asn24Lys) n.540C>A | |
| X | g.116172352C>G | CA414337532 | AGTR2 | c.72C>G (p.Asn24Lys) n.540C>G | |
| X | g.116172352C>T | CA518449138 | AGTR2 | c.72C>T (p.Asn24=) n.540C>T | gnomAD v4 |
| X | g.116172353A>C | CA414337533 | AGTR2 | c.73A>C (p.Ile25Leu) n.541A>C | |
| X | g.116172353A>G | CA414337535 | AGTR2 | c.73A>G (p.Ile25Val) n.541A>G | |
| X | g.116172353A>T | CA414337534 | AGTR2 | c.73A>T (p.Ile25Phe) n.541A>T | |
| X | g.116172354T>A | CA414337536 | AGTR2 | c.74T>A (p.Ile25Asn) n.542T>A | gnomAD v4 |
| X | g.116172354T>C | CA414337537 | AGTR2 | c.74T>C (p.Ile25Thr) n.542T>C | |
| X | g.116172354T>G | CA414337538 | AGTR2 | c.74T>G (p.Ile25Ser) n.542T>G | |
| X | g.116172355C>A | CA518449139 | AGTR2 | c.75C>A (p.Ile25=) n.543C>A | |
| X | g.116172355C>G | CA414337539 | AGTR2 | c.75C>G (p.Ile25Met) n.543C>G | |
| X | g.116172355C>T | CA518449140 | AGTR2 | c.75C>T (p.Ile25=) n.543C>T | |
| X | g.116172356T>A | CA414337540 | AGTR2 | c.76T>A (p.Ser26Thr) n.544T>A | |
| X | g.116172356T>C | CA414337541 | AGTR2 | c.76T>C (p.Ser26Pro) n.544T>C | ClinVar |
| X | g.116172356T>G | CA414337542 | AGTR2 | c.76T>G (p.Ser26Ala) n.544T>G | |
| X | g.116172357C>A | CA414337543 | AGTR2 | c.77C>A (p.Ser26Tyr) n.545C>A |