| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 14 | g.49621979G>A | CA486349797 | MGAT2 | c.711G>A (p.Lys237=) | dbSNP gnomAD v4 |
| 14 | g.49621979G>C | CA249931 | MGAT2 | c.711G>C (p.Lys237Asn) | ClinVar dbSNP |
| 14 | g.49621979G= | CA2135804761 | MGAT2 | c.711G= (p.Lys237=) | |
| 14 | g.49621979G>T | CA389620059 | MGAT2 | c.711G>T (p.Lys237Asn) | |
| 14 | g.49621980C>A | CA7172592 | MGAT2 | c.712C>A (p.Leu238Met) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 14 | g.49621980C= | CA2135804762 | MGAT2 | c.712C= (p.Leu238=) | |
| 14 | g.49621980C>G | CA389620062 | MGAT2 | c.712C>G (p.Leu238Val) | |
| 14 | g.49621980C>T | CA486349800 | MGAT2 | c.712C>T (p.Leu238=) | |
| 14 | g.49621981T>A | CA389620073 | MGAT2 | c.713T>A (p.Leu238Gln) | |
| 14 | g.49621981T>C | CA389620071 | MGAT2 | c.713T>C (p.Leu238Pro) | gnomAD v4 |
| 14 | g.49621981T>G | CA389620068 | MGAT2 | c.713T>G (p.Leu238Arg) | |
| 14 | g.49621982G>A | CA7172593 | MGAT2 | c.714G>A (p.Leu238=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 14 | g.49621982G>C | CA486349804 | MGAT2 | c.714G>C (p.Leu238=) | |
| 14 | g.49621982G= | CA2135804763 | MGAT2 | c.714G= (p.Leu238=) | |
| 14 | g.49621982G>T | CA486349803 | MGAT2 | c.714G>T (p.Leu238=) | |
| 14 | g.49621983C>A | CA389620079 | MGAT2 | c.715C>A (p.His239Asn) | |
| 14 | g.49621983C= | CA2135804764 | MGAT2 | c.715C= (p.His239=) | |
| 14 | g.49621983C>G | CA389620088 | MGAT2 | c.715C>G (p.His239Asp) | |
| 14 | g.49621983C>T | CA389620090 | MGAT2 | c.715C>T (p.His239Tyr) | dbSNP |
| 14 | g.49621984A>C | CA389620093 | MGAT2 | c.716A>C (p.His239Pro) | |
| 14 | g.49621984A>G | CA389620094 | MGAT2 | c.716A>G (p.His239Arg) | |
| 14 | g.49621984A>T | CA389620096 | MGAT2 | c.716A>T (p.His239Leu) | |
| 14 | g.49621985T>A | CA389620097 | MGAT2 | c.717T>A (p.His239Gln) | |
| 14 | g.49621985T>C | CA486349807 | MGAT2 | c.717T>C (p.His239=) | |
| 14 | g.49621985T>G | CA389620099 | MGAT2 | c.717T>G (p.His239Gln) | |
| 14 | g.49621986T>A | CA389620102 | MGAT2 | c.718T>A (p.Phe240Ile) | |
| 14 | g.49621986T>C | CA389620105 | MGAT2 | c.718T>C (p.Phe240Leu) | |
| 14 | g.49621986T>G | CA389620108 | MGAT2 | c.718T>G (p.Phe240Val) | gnomAD v4 |
| 14 | g.49621987T>A | CA389620110 | MGAT2 | c.719T>A (p.Phe240Tyr) | |
| 14 | g.49621987T>C | CA389620116 | MGAT2 | c.719T>C (p.Phe240Ser) | |
| 14 | g.49621987T>G | CA389620109 | MGAT2 | c.719T>G (p.Phe240Cys) | |
| 14 | g.49621988T>A | CA389620119 | MGAT2 | c.720T>A (p.Phe240Leu) | |
| 14 | g.49621988T>C | CA486349811 | MGAT2 | c.720T>C (p.Phe240=) | |
| 14 | g.49621988T>G | CA389620124 | MGAT2 | c.720T>G (p.Phe240Leu) | |
| 14 | g.49621989G>A | CA389620126 | MGAT2 | c.721G>A (p.Val241Met) | |
| 14 | g.49621989G>C | CA389620127 | MGAT2 | c.721G>C (p.Val241Leu) | |
| 14 | g.49621989G= | CA2135804765 | MGAT2 | c.721G= (p.Val241=) | |
| 14 | g.49621989G>T | CA389620129 | MGAT2 | c.721G>T (p.Val241Leu) | dbSNP gnomAD v3 gnomAD v4 |
| 14 | g.49621990T>A | CA389620135 | MGAT2 | c.722T>A (p.Val241Glu) | |
| 14 | g.49621990T>C | CA260660767 | MGAT2 | c.722T>C (p.Val241Ala) | dbSNP |
| 14 | g.49621990T>G | CA389620133 | MGAT2 | c.722T>G (p.Val241Gly) | |
| 14 | g.49621990T= | CA2135804766 | MGAT2 | c.722T= (p.Val241=) | |
| 14 | g.49621991G>A | CA486349814 | MGAT2 | c.723G>A (p.Val241=) | dbSNP |
| 14 | g.49621991G>C | CA486349815 | MGAT2 | c.723G>C (p.Val241=) | |
| 14 | g.49621991G= | CA2135804767 | MGAT2 | c.723G= (p.Val241=) | |
| 14 | g.49621991G>T | CA486349816 | MGAT2 | c.723G>T (p.Val241=) | gnomAD v4 |
| 14 | g.49621992T>A | CA389620137 | MGAT2 | c.724T>A (p.Trp242Arg) | |
| 14 | g.49621992T>C | CA389620140 | MGAT2 | c.724T>C (p.Trp242Arg) | |
| 14 | g.49621992T>G | CA389620144 | MGAT2 | c.724T>G (p.Trp242Gly) | dbSNP |
| 14 | g.49621992T= | CA2135804768 | MGAT2 | c.724T= (p.Trp242=) |