Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.47733844A= | CA2262805822 | TBX21 | c.390A= (p.Gly130=) n.420A= | |
17 | g.47733844A>C | CA500652785 | TBX21 | c.390A>C (p.Gly130=) n.420A>C | dbSNP gnomAD v3 gnomAD v4 |
17 | g.47733844A>G | CA8626259 | TBX21 | c.390A>G (p.Gly130=) n.420A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.47733844A>T | CA8626260 | TBX21 | c.390A>T (p.Gly130=) n.420A>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.47733845C>A | CA400059292 | TBX21 | c.391C>A (p.Leu131Met) n.421C>A | |
17 | g.47733845C= | CA2262805823 | TBX21 | c.391C= (p.Leu131=) n.421C= | |
17 | g.47733845C>G | CA400059297 | TBX21 | c.391C>G (p.Leu131Val) n.421C>G | |
17 | g.47733845C>T | CA500652789 | TBX21 | c.391C>T (p.Leu131=) n.421C>T | dbSNP gnomAD v4 |
17 | g.47733846T>A | CA400059309 | TBX21 | c.392T>A (p.Leu131Gln) n.422T>A | |
17 | g.47733846T>C | CA400059301 | TBX21 | c.392T>C (p.Leu131Pro) n.422T>C | gnomAD v4 |
17 | g.47733846T>G | CA400059304 | TBX21 | c.392T>G (p.Leu131Arg) n.422T>G | gnomAD v4 |
17 | g.47733847G>A | CA500652795 | TBX21 | c.393G>A (p.Leu131=) n.423G>A | |
17 | g.47733847G>C | CA500652792 | TBX21 | c.393G>C (p.Leu131=) n.423G>C | gnomAD v4 |
17 | g.47733847G>T | CA500652794 | TBX21 | c.393G>T (p.Leu131=) n.423G>T | |
17 | g.47733848G>A | CA400059319 | TBX21 | c.394G>A (p.Glu132Lys) n.424G>A | |
17 | g.47733848G>C | CA400059321 | TBX21 | c.394G>C (p.Glu132Gln) n.424G>C | |
17 | g.47733848G>T | CA400059323 | TBX21 | c.394G>T (p.Glu132Ter) n.424G>T | |
17 | g.47733849A>C | CA400059332 | TBX21 | c.395A>C (p.Glu132Ala) n.425A>C | |
17 | g.47733849A>G | CA400059333 | TBX21 | c.395A>G (p.Glu132Gly) n.425A>G | |
17 | g.47733849A>T | CA400059337 | TBX21 | c.395A>T (p.Glu132Val) n.425A>T | |
17 | g.47733850G>A | CA500652808 | TBX21 | c.396G>A (p.Glu132=) n.426G>A | dbSNP gnomAD v2 gnomAD v4 |
17 | g.47733850G>C | CA400059342 | TBX21 | c.396G>C (p.Glu132Asp) n.426G>C | |
17 | g.47733850G= | CA2262805824 | TBX21 | c.396G= (p.Glu132=) n.426G= | |
17 | g.47733850G>T | CA400059339 | TBX21 | c.396G>T (p.Glu132Asp) n.426G>T | |
17 | g.47733851G>A | CA400059348 | TBX21 | c.397G>A (p.Val133Met) n.427G>A | dbSNP gnomAD v4 |
17 | g.47733851G>C | CA400059352 | TBX21 | c.397G>C (p.Val133Leu) n.427G>C | |
17 | g.47733851G= | CA2262805825 | TBX21 | c.397G= (p.Val133=) n.427G= | |
17 | g.47733851G>T | CA400059355 | TBX21 | c.397G>T (p.Val133Leu) n.427G>T | gnomAD v4 |
17 | g.47733852T>A | CA400059359 | TBX21 | c.398T>A (p.Val133Glu) n.428T>A | |
17 | g.47733852T>C | CA400059362 | TBX21 | c.398T>C (p.Val133Ala) n.428T>C | |
17 | g.47733852T>G | CA400059366 | TBX21 | c.398T>G (p.Val133Gly) n.428T>G | dbSNP gnomAD v4 |
17 | g.47733852T= | CA2262805826 | TBX21 | c.398T= (p.Val133=) n.428T= | |
17 | g.47733853G>A | CA500652442 | TBX21 | c.399G>A (p.Val133=) n.429G>A | |
17 | g.47733853G>C | CA500652444 | TBX21 | c.399G>C (p.Val133=) n.429G>C | |
17 | g.47733853G>T | CA500652445 | TBX21 | c.399G>T (p.Val133=) n.429G>T | gnomAD v4 |
17 | g.47733854T>A | CA400059375 | TBX21 | c.400T>A (p.Ser134Thr) n.430T>A | |
17 | g.47733854T>C | CA400059368 | TBX21 | c.400T>C (p.Ser134Pro) n.430T>C | |
17 | g.47733854T>G | CA400059373 | TBX21 | c.400T>G (p.Ser134Ala) n.430T>G | |
17 | g.47733855C>A | CA400059378 | TBX21 | c.401C>A (p.Ser134Ter) n.431C>A | |
17 | g.47733855C>G | CA400059380 | TBX21 | c.401C>G (p.Ser134Trp) n.431C>G | |
17 | g.47733855C>T | CA400059382 | TBX21 | c.401C>T (p.Ser134Leu) n.431C>T | gnomAD v4 |
17 | g.47733856G>A | CA500652446 | TBX21 | c.402G>A (p.Ser134=) n.432G>A | gnomAD v4 |
17 | g.47733856G>C | CA500652447 | TBX21 | c.402G>C (p.Ser134=) n.432G>C | |
17 | g.47733856G>T | CA500652448 | TBX21 | c.402G>T (p.Ser134=) n.432G>T | gnomAD v4 |
17 | g.47733857G>A | CA400059383 | TBX21 | c.403G>A (p.Gly135Arg) n.433G>A | gnomAD v4 |
17 | g.47733857G>C | CA400059385 | TBX21 | c.403G>C (p.Gly135Arg) n.433G>C | gnomAD v4 |
17 | g.47733857G>T | CA400059386 | TBX21 | c.403G>T (p.Gly135Trp) n.433G>T | |
17 | g.47733858G>A | CA400059392 | TBX21 | c.404G>A (p.Gly135Glu) n.434G>A | |
17 | g.47733858G>C | CA400059395 | TBX21 | c.404G>C (p.Gly135Ala) n.434G>C | |
17 | g.47733858G>T | CA400059397 | TBX21 | c.404G>T (p.Gly135Val) n.434G>T |