Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.78304839C>A | CA373872298 | PSAT1 | c.296C>A (p.Ala99Asp) | |
9 | g.78304839C= | CA1857665727 | PSAT1 | c.296C= (p.Ala99=) | |
9 | g.78304839C>G | CA373872304 | PSAT1 | c.296C>G (p.Ala99Gly) | |
9 | g.78304839C>T | CA170850 | PSAT1 | c.296C>T (p.Ala99Val) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.78304839_78304840delinsCT | CA1857665726 | PSAT1 | c.296_297delinsCT (p.Ala99=) | |
9 | g.78304839_78304840delinsTG | CA16042652 | PSAT1 | c.296_297delinsTG (p.Ala99Val) | ClinVar dbSNP |
9 | g.78304841_78304844del | CA2690397189 | PSAT1 | c.298_301del (p.Asp100MetfsTer3) | gnomAD v4 |
9 | g.78304840T>A | CA465542955 | PSAT1 | c.297T>A (p.Ala99=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.78304840T>C | CA465542956 | PSAT1 | c.297T>C (p.Ala99=) | gnomAD v4 |
9 | g.78304840T>G | CA5095575 | PSAT1 | c.297T>G (p.Ala99=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
9 | g.78304840T= | CA1857665728 | PSAT1 | c.297T= (p.Ala99=) | |
9 | g.78304841G>A | CA373872307 | PSAT1 | c.298G>A (p.Asp100Asn) | |
9 | g.78304841G>C | CA373872309 | PSAT1 | c.298G>C (p.Asp100His) | |
9 | g.78304841G>T | CA373872311 | PSAT1 | c.298G>T (p.Asp100Tyr) | |
9 | g.78304842A= | CA1857665729 | PSAT1 | c.299A= (p.Asp100=) | |
9 | g.78304842A>C | CA114739 | PSAT1 | c.299A>C (p.Asp100Ala) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
9 | g.78304842A>G | CA373872313 | PSAT1 | c.299A>G (p.Asp100Gly) | |
9 | g.78304842A>T | CA373872314 | PSAT1 | c.299A>T (p.Asp100Val) | |
9 | g.78304843C>A | CA373872316 | PSAT1 | c.300C>A (p.Asp100Glu) | |
9 | g.78304843C>G | CA373872318 | PSAT1 | c.300C>G (p.Asp100Glu) | |
9 | g.78304843C>T | CA465542957 | PSAT1 | c.300C>T (p.Asp100=) | |
9 | g.78304844T>A | CA373872320 | PSAT1 | c.301T>A (p.Tyr101Asn) | |
9 | g.78304844T>C | CA373872321 | PSAT1 | c.301T>C (p.Tyr101His) | dbSNP |
9 | g.78304844T>G | CA373872323 | PSAT1 | c.301T>G (p.Tyr101Asp) | |
9 | g.78304844T= | CA1857665730 | PSAT1 | c.301T= (p.Tyr101=) | |
9 | g.78304845A>C | CA373872328 | PSAT1 | c.302A>C (p.Tyr101Ser) | |
9 | g.78304845A>G | CA373872326 | PSAT1 | c.302A>G (p.Tyr101Cys) | gnomAD v4 |
9 | g.78304845A>T | CA373872325 | PSAT1 | c.302A>T (p.Tyr101Phe) | |
9 | g.78304846T>A | CA373872330 | PSAT1 | c.303T>A (p.Tyr101Ter) | |
9 | g.78304846T>C | CA465542958 | PSAT1 | c.303T>C (p.Tyr101=) | dbSNP |
9 | g.78304846T>G | CA373872332 | PSAT1 | c.303T>G (p.Tyr101Ter) | |
9 | g.78304846T= | CA1857665731 | PSAT1 | c.303T= (p.Tyr101=) | |
9 | g.78304847G>A | CA373872334 | PSAT1 | c.304G>A (p.Val102Met) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.78304847G>C | CA373872335 | PSAT1 | c.304G>C (p.Val102Leu) | |
9 | g.78304847G= | CA1857665732 | PSAT1 | c.304G= (p.Val102=) | |
9 | g.78304847G>T | CA373872337 | PSAT1 | c.304G>T (p.Val102Leu) | |
9 | g.78304848T>A | CA373872339 | PSAT1 | c.305T>A (p.Val102Glu) | |
9 | g.78304848T>C | CA373872340 | PSAT1 | c.305T>C (p.Val102Ala) | |
9 | g.78304848T>G | CA373872343 | PSAT1 | c.305T>G (p.Val102Gly) | |
9 | g.78304849G>A | CA465542960 | PSAT1 | c.306G>A (p.Val102=) | |
9 | g.78304849G>C | CA465542961 | PSAT1 | c.306G>C (p.Val102=) | |
9 | g.78304849G>T | CA465542959 | PSAT1 | c.306G>T (p.Val102=) | COSMIC |
9 | g.78304850G>A | CA5095577 | PSAT1 | c.307G>A (p.Val103Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
9 | g.78304850G>C | CA5095576 | PSAT1 | c.307G>C (p.Val103Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.78304850G= | CA1857665733 | PSAT1 | c.307G= (p.Val103=) | |
9 | g.78304850G>T | CA373872346 | PSAT1 | c.307G>T (p.Val103Leu) | ClinVar dbSNP |
9 | g.78304851T>A | CA373872347 | PSAT1 | c.308T>A (p.Val103Glu) | |
9 | g.78304851T>C | CA373872349 | PSAT1 | c.308T>C (p.Val103Ala) | |
9 | g.78304851T>G | CA373872350 | PSAT1 | c.308T>G (p.Val103Gly) | |
9 | g.78304852G>A | CA465542964 | PSAT1 | c.309G>A (p.Val103=) | gnomAD v4 |