Chr Mutation (hg38) CAid Gene Transcript Linkouts
7g.1234209A>TCA12553356UNCXn.450+514A>T (p.=)
c.450+514A>T (p.=)
dbSNP gnomAD
7g.1234210A>GCA832638608UNCXn.450+515A>G (p.=)
c.450+515A>G (p.=)
7g.1234215A>CCA1097509775UNCXn.450+520A>C (p.=)
c.450+520A>C (p.=)
7g.1234216C>GCA832638611UNCXn.450+521C>G (p.=)
c.450+521C>G (p.=)
7g.1234216C>TCA152421793UNCXn.450+521C>T (p.=)
c.450+521C>T (p.=)
dbSNP
7g.1234223G>ACA572109234UNCXn.450+528G>A (p.=)
c.450+528G>A (p.=)
gnomAD
7g.1234224G>ACA832638613UNCXn.450+529G>A (p.=)
c.450+529G>A (p.=)
7g.1234227G>ACA1097509780UNCXn.450+532G>A (p.=)
c.450+532G>A (p.=)
7g.1234234C>TCA651259755UNCXn.450+539C>T (p.=)
c.450+539C>T (p.=)
COSMIC
7g.1234240C>GCA832638614UNCXn.450+545C>G (p.=)
c.450+545C>G (p.=)
7g.1234248G>CCA1097509785UNCXn.450+553G>C (p.=)
c.450+553G>C (p.=)
7g.1234250delCA152421794UNCXn.450+555del (p.=)
c.450+555del (p.=)
dbSNP gnomAD
7g.1234267G>CCA152421796UNCXn.450+572G>C (p.=)
c.450+572G>C (p.=)
dbSNP
7g.1234271dupCA832638623UNCXn.450+576dup (p.=)
c.450+576dup (p.=)
dbSNP
7g.1234278delCA152421802UNCXn.450+583del (p.=)
c.450+583del (p.=)
dbSNP
7g.1234274A>GCA832638626UNCXn.450+579A>G (p.=)
c.450+579A>G (p.=)
7g.1234278A>GCA152421809UNCXn.450+583A>G (p.=)
c.450+583A>G (p.=)
dbSNP gnomAD
7g.1234278A>TCA152421812UNCXn.450+583A>T (p.=)
c.450+583A>T (p.=)
dbSNP gnomAD
7g.1234279G>ACA1097509794UNCXn.450+584G>A (p.=)
c.450+584G>A (p.=)
7g.1234280G>CCA1097509801UNCXn.450+585G>C (p.=)
c.450+585G>C (p.=)
7g.1234283T>ACA572109236UNCXn.450+588T>A (p.=)
c.450+588T>A (p.=)
gnomAD
7g.1234285T>CCA572109237UNCXn.450+590T>C (p.=)
c.450+590T>C (p.=)
gnomAD
7g.1234286G>CCA152421815UNCXn.450+591G>C (p.=)
c.450+591G>C (p.=)
dbSNP
7g.1234296T>CCA152421820UNCXn.450+601T>C (p.=)
c.450+601T>C (p.=)
dbSNP
7g.1234297A>GCA572109239UNCXn.450+602A>G (p.=)
c.450+602A>G (p.=)
gnomAD
7g.1234302C>TCA152421826UNCXn.450+607C>T (p.=)
c.450+607C>T (p.=)
dbSNP gnomAD

Number of alleles fetched