Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
3 | g.13854777C>A | CA351623391 | WNT7A | c.325G>T (p.Ala109Ser) c.124G>T (p.Ala42Ser) | |
3 | g.13854777C= | CA1346837666 | WNT7A | c.325G= (p.Ala109=) c.124G= (p.Ala42=) | |
3 | g.13854777C>G | CA351623392 | WNT7A | c.325G>C (p.Ala109Pro) c.124G>C (p.Ala42Pro) | |
3 | g.13854777C>T | CA119262 | WNT7A | c.325G>A (p.Ala109Thr) c.124G>A (p.Ala42Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
3 | g.13854778G>A | CA2266477 | WNT7A | c.324C>T (p.Tyr108=) c.123C>T (p.Tyr41=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
3 | g.13854778G>C | CA351623393 | WNT7A | c.324C>G (p.Tyr108Ter) c.123C>G (p.Tyr41Ter) | |
3 | g.13854778G= | CA1346837673 | WNT7A | c.324C= (p.Tyr108=) c.123C= (p.Tyr41=) | |
3 | g.13854778G>T | CA351623394 | WNT7A | c.324C>A (p.Tyr108Ter) c.123C>A (p.Tyr41Ter) | gnomAD v4 |
3 | g.13854779T>A | CA351623395 | WNT7A | c.323A>T (p.Tyr108Phe) c.122A>T (p.Tyr41Phe) | |
3 | g.13854779T>C | CA351623396 | WNT7A | c.323A>G (p.Tyr108Cys) c.122A>G (p.Tyr41Cys) | |
3 | g.13854779T>G | CA351623397 | WNT7A | c.323A>C (p.Tyr108Ser) c.122A>C (p.Tyr41Ser) | dbSNP |
3 | g.13854779T= | CA1346837676 | WNT7A | c.323A= (p.Tyr108=) c.122A= (p.Tyr41=) | |
3 | g.13854780A>C | CA351623398 | WNT7A | c.322T>G (p.Tyr108Asp) c.121T>G (p.Tyr41Asp) | |
3 | g.13854780A>G | CA351623399 | WNT7A | c.322T>C (p.Tyr108His) c.121T>C (p.Tyr41His) | |
3 | g.13854780A>T | CA351623400 | WNT7A | c.322T>A (p.Tyr108Asn) c.121T>A (p.Tyr41Asn) | |
3 | g.13854781G>A | CA2266478 | WNT7A | c.321C>T (p.Thr107=) c.120C>T (p.Thr40=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.13854781G>C | CA432695621 | WNT7A | c.321C>G (p.Thr107=) c.120C>G (p.Thr40=) | |
3 | g.13854781G= | CA1346837680 | WNT7A | c.321C= (p.Thr107=) c.120C= (p.Thr40=) | |
3 | g.13854781G>T | CA432695622 | WNT7A | c.321C>A (p.Thr107=) c.120C>A (p.Thr40=) | |
3 | g.13854782G>A | CA2266479 | WNT7A | c.320C>T (p.Thr107Ile) c.119C>T (p.Thr40Ile) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.13854782G>C | CA351623401 | WNT7A | c.320C>G (p.Thr107Ser) c.119C>G (p.Thr40Ser) | |
3 | g.13854782G= | CA1346837687 | WNT7A | c.320C= (p.Thr107=) c.119C= (p.Thr40=) | |
3 | g.13854782G>T | CA2266480 | WNT7A | c.320C>A (p.Thr107Asn) c.119C>A (p.Thr40Asn) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.13854783T>A | CA351623404 | WNT7A | c.319A>T (p.Thr107Ser) c.118A>T (p.Thr40Ser) | |
3 | g.13854783T>C | CA351623402 | WNT7A | c.319A>G (p.Thr107Ala) c.118A>G (p.Thr40Ala) | |
3 | g.13854783T>G | CA351623403 | WNT7A | c.319A>C (p.Thr107Pro) c.118A>C (p.Thr40Pro) | dbSNP |
3 | g.13854783T= | CA1346837690 | WNT7A | c.319A= (p.Thr107=) c.118A= (p.Thr40=) | |
3 | g.13854784G>A | CA2266481 | WNT7A | c.318C>T (p.Phe106=) c.117C>T (p.Phe39=) | dbSNP ExAC gnomAD v2 |
3 | g.13854784G>C | CA351623405 | WNT7A | c.318C>G (p.Phe106Leu) c.117C>G (p.Phe39Leu) | |
3 | g.13854784G= | CA1346837694 | WNT7A | c.318C= (p.Phe106=) c.117C= (p.Phe39=) | |
3 | g.13854784G>T | CA351623406 | WNT7A | c.318C>A (p.Phe106Leu) c.117C>A (p.Phe39Leu) | gnomAD v4 |
3 | g.13854785A= | CA1346837698 | WNT7A | c.317T= (p.Phe106=) c.116T= (p.Phe39=) | |
3 | g.13854785A>C | CA351623407 | WNT7A | c.317T>G (p.Phe106Cys) c.116T>G (p.Phe39Cys) | |
3 | g.13854785A>G | CA351623408 | WNT7A | c.317T>C (p.Phe106Ser) c.116T>C (p.Phe39Ser) | dbSNP |
3 | g.13854785A>T | CA351623409 | WNT7A | c.317T>A (p.Phe106Tyr) c.116T>A (p.Phe39Tyr) | |
3 | g.13854785_13854786del | CA2577516057 | WNT7A | c.316_317del (p.Phe106HisfsTer?) c.115_116del (p.Phe39HisfsTer?) | |
3 | g.13854786A>C | CA351623410 | WNT7A | c.316T>G (p.Phe106Val) c.115T>G (p.Phe39Val) | gnomAD v4 |
3 | g.13854786A>G | CA351623411 | WNT7A | c.316T>C (p.Phe106Leu) c.115T>C (p.Phe39Leu) | |
3 | g.13854786A>T | CA351623412 | WNT7A | c.316T>A (p.Phe106Ile) c.115T>A (p.Phe39Ile) | |
3 | g.13854787C>A | CA432695623 | WNT7A | c.315G>T (p.Ala105=) c.114G>T (p.Ala38=) | gnomAD v4 |
3 | g.13854787C= | CA1346837701 | WNT7A | c.315G= (p.Ala105=) c.114G= (p.Ala38=) | |
3 | g.13854787C>G | CA432695624 | WNT7A | c.315G>C (p.Ala105=) c.114G>C (p.Ala38=) | |
3 | g.13854787C>T | CA2266482 | WNT7A | c.315G>A (p.Ala105=) c.114G>A (p.Ala38=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
3 | g.13854788G>A | CA2266483 | WNT7A | c.314C>T (p.Ala105Val) c.113C>T (p.Ala38Val) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
3 | g.13854788G>C | CA351623413 | WNT7A | c.314C>G (p.Ala105Gly) c.113C>G (p.Ala38Gly) | gnomAD v4 |
3 | g.13854788G= | CA1346837704 | WNT7A | c.314C= (p.Ala105=) c.113C= (p.Ala38=) | |
3 | g.13854788G>T | CA351623414 | WNT7A | c.314C>A (p.Ala105Glu) c.113C>A (p.Ala38Glu) | COSMIC |
3 | g.13854789C>A | CA351623415 | WNT7A | c.313G>T (p.Ala105Ser) c.112G>T (p.Ala38Ser) | |
3 | g.13854789C>G | CA351623416 | WNT7A | c.313G>C (p.Ala105Pro) c.112G>C (p.Ala38Pro) | |
3 | g.13854789C>T | CA351623417 | WNT7A | c.313G>A (p.Ala105Thr) c.112G>A (p.Ala38Thr) |