Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
2 | g.85545747A= | CA1266819759 | GGCX | c.*4187T= (n.*4187T=) | |
2 | g.85545747A>G | CA894034201 | GGCX | c.*4187T>C (n.*4187T>C) | dbSNP |
2 | g.85545747_85545748delinsAT | CA1266819760 | GGCX | c.*4186_*4187delinsAT (n.*4186_*4187delinsAT) | |
2 | g.85545748del | CA1266819762 | GGCX | c.*4186del (n.*4186del) | dbSNP |
2 | g.85545748T>C | CA1266819764 | GGCX | c.*4186A>G (n.*4186A>G) | dbSNP |
2 | g.85545748T= | CA1266819763 | GGCX | c.*4186A= (n.*4186A=) | |
2 | g.85545749G>A | CA51728618 | GGCX | c.*4185C>T (n.*4185C>T) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.85545749G= | CA1266819765 | GGCX | c.*4185C= (n.*4185C=) | |
2 | g.85545749_85545753delinsGTCTA | CA1266819766 | GGCX | c.*4181_*4185delinsTAGAC (n.*4181_*4185delinsTAGAC) | |
2 | g.85545750T>C | CA1266819768 | GGCX | c.*4184A>G (n.*4184A>G) | dbSNP |
2 | g.85545750T= | CA1266819769 | GGCX | c.*4184A= (n.*4184A=) | |
2 | g.85545754_85545757del | CA894034203 | GGCX | c.*4181_*4184del (n.*4181_*4184del) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.85545753A= | CA1266819774 | GGCX | c.*4181T= (n.*4181T=) | |
2 | g.85545753A>C | CA1266819775 | GGCX | c.*4181T>G (n.*4181T>G) | dbSNP |
2 | g.85545753A>G | CA51728621 | GGCX | c.*4181T>C (n.*4181T>C) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.85545754T>G | CA1266819778 | GGCX | c.*4180A>C (n.*4180A>C) | dbSNP |
2 | g.85545754T= | CA1266819777 | GGCX | c.*4180A= (n.*4180A=) | |
2 | g.85545755C= | CA1266819779 | GGCX | c.*4179G= (n.*4179G=) | |
2 | g.85545755C>T | CA51728625 | GGCX | c.*4179G>A (n.*4179G>A) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.85545756T>C | CA534171559 | GGCX | c.*4178A>G (n.*4178A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.85545756T= | CA1266819782 | GGCX | c.*4178A= (n.*4178A=) | |
2 | g.85545759dup | CA1266819785 | GGCX | c.*4177dup (n.*4177dup) | dbSNP |
2 | g.85545759A>G | CA2750761359 | GGCX | c.*4175T>C (n.*4175T>C) | |
2 | g.85545760G= | CA1266819786 | GGCX | c.*4174C= (n.*4174C=) | |
2 | g.85545760G>T | CA51728631 | GGCX | c.*4174C>A (n.*4174C>A) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.85545762C>A | CA894034210 | GGCX | c.*4172G>T (n.*4172G>T) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.85545762C= | CA1266819787 | GGCX | c.*4172G= (n.*4172G=) | |
2 | g.85545763C>A | CA1266819789 | GGCX | c.*4171G>T (n.*4171G>T) | dbSNP |
2 | g.85545763C= | CA1266819788 | GGCX | c.*4171G= (n.*4171G=) | |
2 | g.85545766G= | CA1266819791 | GGCX | c.*4168C= (n.*4168C=) | |
2 | g.85545766G>T | CA51728637 | GGCX | c.*4168C>A (n.*4168C>A) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.85545773A= | CA1266819793 | GGCX | c.*4161T= (n.*4161T=) | |
2 | g.85545773A>G | CA534171561 | GGCX | c.*4161T>C (n.*4161T>C) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.85545774A= | CA1266819794 | GGCX | c.*4160T= (n.*4160T=) | |
2 | g.85545774A>G | CA1033077609 | GGCX | c.*4160T>C (n.*4160T>C) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.85545776C= | CA1266819795 | GGCX | c.*4158G= (n.*4158G=) | |
2 | g.85545776C>T | CA51728644 | GGCX | c.*4158G>A (n.*4158G>A) | dbSNP |
2 | g.85545777C= | CA1266819797 | GGCX | c.*4157G= (n.*4157G=) | |
2 | g.85545777C>T | CA51728662 | GGCX | c.*4157G>A (n.*4157G>A) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.85545778T>A | CA2699813139 | GGCX | c.*4156A>T (n.*4156A>T) | dbSNP |
2 | g.85545778T>C | CA2659852265 | GGCX | c.*4156A>G (n.*4156A>G) | gnomAD v4 |
2 | g.85545779A= | CA1266819798 | GGCX | c.*4155T= (n.*4155T=) | |
2 | g.85545779A>G | CA894034217 | GGCX | c.*4155T>C (n.*4155T>C) | dbSNP gnomAD v3 gnomAD v4 |
2 | g.85545781T>C | CA51728667 | GGCX | c.*4153A>G (n.*4153A>G) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
2 | g.85545781T= | CA1266819801 | GGCX | c.*4153A= (n.*4153A=) | |
2 | g.85545781_85545782delinsTA | CA1266819800 | GGCX | c.*4152_*4153delinsTA (n.*4152_*4153delinsTA) | |
2 | g.85545783del | CA1266819804 | GGCX | c.*4152del (n.*4152del) | dbSNP |
2 | g.85545785_85545786delinsCT | CA1266819805 | GGCX | c.*4148_*4149delinsAG (n.*4148_*4149delinsAG) | |
2 | g.85545786del | CA1266819807 | GGCX | c.*4148del (n.*4148del) | dbSNP |
2 | g.85545786T>C | CA1266819809 | GGCX | c.*4148A>G (n.*4148A>G) | dbSNP |