| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 10 | g.72007785_72007829del | CA2541830907 | CHST3 | c.754_798del (p.Cys252_Arg266del) | |
| 10 | g.72007803_72007883dup | CA2609582001 | CHST3 | c.772_852dup (p.Gln284_Pro285insThrLeuAlaAlaGluAlaCysArgArgLysGluHisMetAlaLeuLysAlaValArgIleArgGlnLeuGluPheLeuGln) | gnomAD v4 |
| 10 | g.72007807T>A | CA377146645 | CHST3 | c.776T>A (p.Leu259Gln) | |
| 10 | g.72007807T>C | CA253725 | CHST3 | c.776T>C (p.Leu259Pro) | ClinVar dbSNP |
| 10 | g.72007807T>G | CA377146643 | CHST3 | c.776T>G (p.Leu259Arg) | |
| 10 | g.72007807T= | CA1918976345 | CHST3 | c.776T= (p.Leu259=) | |
| 10 | g.72007808G>A | CA470283870 | CHST3 | c.777G>A (p.Leu259=) | ClinVar |
| 10 | g.72007808G>C | CA470283872 | CHST3 | c.777G>C (p.Leu259=) | |
| 10 | g.72007808G>T | CA470283874 | CHST3 | c.777G>T (p.Leu259=) | |
| 10 | g.72007809del | CA2609582012 | CHST3 | c.778del (p.Ala260ProfsTer?) | gnomAD v4 |
| 10 | g.72007809G>A | CA377146647 | CHST3 | c.778G>A (p.Ala260Thr) | |
| 10 | g.72007809G>C | CA377146649 | CHST3 | c.778G>C (p.Ala260Pro) | gnomAD v4 |
| 10 | g.72007809G>T | CA377146651 | CHST3 | c.778G>T (p.Ala260Ser) | |
| 10 | g.72007810C>A | CA377146654 | CHST3 | c.779C>A (p.Ala260Asp) | |
| 10 | g.72007810C= | CA1918976350 | CHST3 | c.779C= (p.Ala260=) | |
| 10 | g.72007810C>G | CA377146657 | CHST3 | c.779C>G (p.Ala260Gly) | |
| 10 | g.72007810C>T | CA377146659 | CHST3 | c.779C>T (p.Ala260Val) | dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.72007811C>A | CA470283878 | CHST3 | c.780C>A (p.Ala260=) | gnomAD v4 COSMIC |
| 10 | g.72007811C= | CA1918976353 | CHST3 | c.780C= (p.Ala260=) | |
| 10 | g.72007811C>G | CA470283880 | CHST3 | c.780C>G (p.Ala260=) | |
| 10 | g.72007811C>T | CA470283881 | CHST3 | c.780C>T (p.Ala260=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.72007812G>A | CA5548166 | CHST3 | c.781G>A (p.Ala261Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 10 | g.72007812G>C | CA377146664 | CHST3 | c.781G>C (p.Ala261Pro) | |
| 10 | g.72007812G= | CA1918976356 | CHST3 | c.781G= (p.Ala261=) | |
| 10 | g.72007812G>T | CA377146667 | CHST3 | c.781G>T (p.Ala261Ser) | dbSNP gnomAD v4 |
| 10 | g.72007812dup | CA645561183 | CHST3 | c.781dup (p.Ala261GlyfsTer?) | COSMIC |
| 10 | g.72007813C>A | CA377146671 | CHST3 | c.782C>A (p.Ala261Glu) | |
| 10 | g.72007813C>G | CA377146673 | CHST3 | c.782C>G (p.Ala261Gly) | |
| 10 | g.72007813C>T | CA377146675 | CHST3 | c.782C>T (p.Ala261Val) | |
| 10 | g.72007814A>C | CA470283885 | CHST3 | c.783A>C (p.Ala261=) | |
| 10 | g.72007814A>G | CA470283883 | CHST3 | c.783A>G (p.Ala261=) | |
| 10 | g.72007814A>T | CA470283884 | CHST3 | c.783A>T (p.Ala261=) | |
| 10 | g.72007815G>A | CA377146684 | CHST3 | c.784G>A (p.Glu262Lys) | dbSNP |
| 10 | g.72007815G>C | CA377146681 | CHST3 | c.784G>C (p.Glu262Gln) | |
| 10 | g.72007815G= | CA1918976360 | CHST3 | c.784G= (p.Glu262=) | |
| 10 | g.72007815G>T | CA377146679 | CHST3 | c.784G>T (p.Glu262Ter) | |
| 10 | g.72007816A>C | CA377146689 | CHST3 | c.785A>C (p.Glu262Ala) | |
| 10 | g.72007816A>G | CA377146691 | CHST3 | c.785A>G (p.Glu262Gly) | |
| 10 | g.72007816A>T | CA377146694 | CHST3 | c.785A>T (p.Glu262Val) | |
| 10 | g.72007817G>A | CA470283887 | CHST3 | c.786G>A (p.Glu262=) | dbSNP gnomAD v2 gnomAD v4 |
| 10 | g.72007817G>C | CA377146697 | CHST3 | c.786G>C (p.Glu262Asp) | |
| 10 | g.72007817G= | CA1918976363 | CHST3 | c.786G= (p.Glu262=) | |
| 10 | g.72007817G>T | CA377146699 | CHST3 | c.786G>T (p.Glu262Asp) | gnomAD v4 |
| 10 | g.72007818G>A | CA377146707 | CHST3 | c.787G>A (p.Ala263Thr) | gnomAD v4 |
| 10 | g.72007818G>C | CA5548167 | CHST3 | c.787G>C (p.Ala263Pro) | dbSNP ExAC |
| 10 | g.72007818G= | CA1918976367 | CHST3 | c.787G= (p.Ala263=) | |
| 10 | g.72007818G>T | CA377146703 | CHST3 | c.787G>T (p.Ala263Ser) | |
| 10 | g.72007819C>A | CA377146710 | CHST3 | c.788C>A (p.Ala263Asp) | |
| 10 | g.72007819C>G | CA377146712 | CHST3 | c.788C>G (p.Ala263Gly) | |
| 10 | g.72007819C>T | CA377146715 | CHST3 | c.788C>T (p.Ala263Val) |