Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
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 | |
X | g.116172357C>G | CA414337544 | AGTR2 | c.77C>G (p.Ser26Cys) n.545C>G | |
X | g.116172357C>T | CA414337545 | AGTR2 | c.77C>T (p.Ser26Phe) n.545C>T | |
X | g.116172358T>A | CA518449141 | AGTR2 | c.78T>A (p.Ser26=) n.546T>A | |
X | g.116172358T>C | CA518449142 | AGTR2 | c.78T>C (p.Ser26=) n.546T>C | gnomAD v4 |
X | g.116172358T>G | CA518449143 | AGTR2 | c.78T>G (p.Ser26=) n.546T>G | |
X | g.116172359G>A | CA414337548 | AGTR2 | c.79G>A (p.Gly27Ser) n.547G>A | dbSNP gnomAD v2 |
X | g.116172359G>C | CA414337547 | AGTR2 | c.79G>C (p.Gly27Arg) n.547G>C | |
X | g.116172359G= | CA2453331674 | AGTR2 | c.79G= (p.Gly27=) n.547G= | |
X | g.116172359G>T | CA414337546 | AGTR2 | c.79G>T (p.Gly27Cys) n.547G>T | |
X | g.116172360G>A | CA414337549 | AGTR2 | c.80G>A (p.Gly27Asp) n.548G>A | |
X | g.116172360G>C | CA414337551 | AGTR2 | c.80G>C (p.Gly27Ala) n.548G>C | gnomAD v4 |
X | g.116172360G>T | CA414337550 | AGTR2 | c.80G>T (p.Gly27Val) n.548G>T | |
X | g.116172361C>A | CA518449144 | AGTR2 | c.81C>A (p.Gly27=) n.549C>A | |
X | g.116172361C>G | CA518449145 | AGTR2 | c.81C>G (p.Gly27=) n.549C>G | |
X | g.116172361C>T | CA518449146 | AGTR2 | c.81C>T (p.Gly27=) n.549C>T | |
X | g.116172364_116172366del | CA2556362418 | AGTR2 | c.84_86del (p.Asn29del) n.552_554del | |
X | g.116172362A>C | CA414337552 | AGTR2 | c.82A>C (p.Asn28His) n.550A>C | |
X | g.116172362A>G | CA414337554 | AGTR2 | c.82A>G (p.Asn28Asp) n.550A>G | |
X | g.116172362A>T | CA414337553 | AGTR2 | c.82A>T (p.Asn28Tyr) n.550A>T | |
X | g.116172363A= | CA2453331675 | AGTR2 | c.83A= (p.Asn28=) n.551A= | |
X | g.116172363A>C | CA414337555 | AGTR2 | c.83A>C (p.Asn28Thr) n.551A>C | |
X | g.116172363A>G | CA334723678 | AGTR2 | c.83A>G (p.Asn28Ser) n.551A>G | dbSNP |
X | g.116172363A>T | CA414337556 | AGTR2 | c.83A>T (p.Asn28Ile) n.551A>T | gnomAD v4 |
X | g.116172364C>A | CA414337557 | AGTR2 | c.84C>A (p.Asn28Lys) n.552C>A | |
X | g.116172364C>G | CA414337558 | AGTR2 | c.84C>G (p.Asn28Lys) n.552C>G | |
X | g.116172364C>T | CA518449147 | AGTR2 | c.84C>T (p.Asn28=) n.552C>T | |
X | g.116172365A>C | CA414337559 | AGTR2 | c.85A>C (p.Asn29His) n.553A>C | |
X | g.116172365A>G | CA414337560 | AGTR2 | c.85A>G (p.Asn29Asp) n.553A>G | |
X | g.116172365A>T | CA414337561 | AGTR2 | c.85A>T (p.Asn29Tyr) n.553A>T | |
X | g.116172365_116172367del | CA2694510859 | AGTR2 | c.85_87del (p.Asn29del) n.553_555del | gnomAD v4 |
X | g.116172366A= | CA2453331676 | AGTR2 | c.86A= (p.Asn29=) n.554A= | |
X | g.116172366A>C | CA414337562 | AGTR2 | c.86A>C (p.Asn29Thr) n.554A>C | |
X | g.116172366A>G | CA10497226 | AGTR2 | c.86A>G (p.Asn29Ser) n.554A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
X | g.116172366A>T | CA414337563 | AGTR2 | c.86A>T (p.Asn29Ile) n.554A>T | |
X | g.116172367T>A | CA414337564 | AGTR2 | c.87T>A (p.Asn29Lys) n.555T>A | |
X | g.116172367T>C | CA518449148 | AGTR2 | c.87T>C (p.Asn29=) n.555T>C | dbSNP gnomAD v4 |
X | g.116172367T>G | CA414337565 | AGTR2 | c.87T>G (p.Asn29Lys) n.555T>G | gnomAD v4 |
X | g.116172367T= | CA2453331677 | AGTR2 | c.87T= (p.Asn29=) n.555T= | |
X | g.116172368G>A | CA414337568 | AGTR2 | c.88G>A (p.Glu30Lys) n.556G>A | |
X | g.116172368G>C | CA414337567 | AGTR2 | c.88G>C (p.Glu30Gln) n.556G>C | |
X | g.116172368G>T | CA414337566 | AGTR2 | c.88G>T (p.Glu30Ter) n.556G>T | gnomAD v4 |
X | g.116172369A>C | CA414337569 | AGTR2 | c.89A>C (p.Glu30Ala) n.557A>C | |
X | g.116172369A>G | CA414337570 | AGTR2 | c.89A>G (p.Glu30Gly) n.557A>G |