Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
14 | g.49621879C>A | CA389619543 | MGAT2 | c.611C>A (p.Ala204Asp) | |
14 | g.49621879C= | CA2135804724 | MGAT2 | c.611C= (p.Ala204=) | |
14 | g.49621879C>G | CA389619545 | MGAT2 | c.611C>G (p.Ala204Gly) | gnomAD v4 |
14 | g.49621879C>T | CA389619547 | MGAT2 | c.611C>T (p.Ala204Val) | dbSNP gnomAD v2 gnomAD v4 |
14 | g.49621880C>A | CA486350331 | MGAT2 | c.612C>A (p.Ala204=) | COSMIC |
14 | g.49621880C= | CA2135804725 | MGAT2 | c.612C= (p.Ala204=) | |
14 | g.49621880C>G | CA486350332 | MGAT2 | c.612C>G (p.Ala204=) | |
14 | g.49621880C>T | CA260660733 | MGAT2 | c.612C>T (p.Ala204=) | dbSNP gnomAD v4 |
14 | g.49621881G>A | CA389619552 | MGAT2 | c.613G>A (p.Ala205Thr) | gnomAD v4 |
14 | g.49621881G>C | CA389619550 | MGAT2 | c.613G>C (p.Ala205Pro) | gnomAD v4 |
14 | g.49621881G>T | CA389619548 | MGAT2 | c.613G>T (p.Ala205Ser) | |
14 | g.49621882C>A | CA389619554 | MGAT2 | c.614C>A (p.Ala205Asp) | |
14 | g.49621882C>G | CA389619556 | MGAT2 | c.614C>G (p.Ala205Gly) | |
14 | g.49621882C>T | CA389619557 | MGAT2 | c.614C>T (p.Ala205Val) | |
14 | g.49621883T>A | CA486350336 | MGAT2 | c.615T>A (p.Ala205=) | |
14 | g.49621883T>C | CA486350338 | MGAT2 | c.615T>C (p.Ala205=) | gnomAD v4 |
14 | g.49621883T>G | CA486350339 | MGAT2 | c.615T>G (p.Ala205=) | |
14 | g.49621884T>A | CA389619559 | MGAT2 | c.616T>A (p.Leu206Met) | |
14 | g.49621884T>C | CA486350340 | MGAT2 | c.616T>C (p.Leu206=) | dbSNP |
14 | g.49621884T>G | CA260660736 | MGAT2 | c.616T>G (p.Leu206Val) | dbSNP gnomAD v4 |
14 | g.49621884T= | CA2135804726 | MGAT2 | c.616T= (p.Leu206=) | |
14 | g.49621885T>A | CA389619561 | MGAT2 | c.617T>A (p.Leu206Ter) | |
14 | g.49621885T>C | CA389619562 | MGAT2 | c.617T>C (p.Leu206Ser) | |
14 | g.49621885T>G | CA389619564 | MGAT2 | c.617T>G (p.Leu206Trp) | |
14 | g.49621886G>A | CA486350344 | MGAT2 | c.618G>A (p.Leu206=) | COSMIC |
14 | g.49621886G>C | CA389619565 | MGAT2 | c.618G>C (p.Leu206Phe) | |
14 | g.49621886G>T | CA389619567 | MGAT2 | c.618G>T (p.Leu206Phe) | |
14 | g.49621887A>C | CA389619568 | MGAT2 | c.619A>C (p.Lys207Gln) | |
14 | g.49621887A>G | CA389619569 | MGAT2 | c.619A>G (p.Lys207Glu) | |
14 | g.49621887A>T | CA389619570 | MGAT2 | c.619A>T (p.Lys207Ter) | |
14 | g.49621888A>C | CA389619574 | MGAT2 | c.620A>C (p.Lys207Thr) | |
14 | g.49621888A>G | CA389619571 | MGAT2 | c.620A>G (p.Lys207Arg) | |
14 | g.49621888A>T | CA389619572 | MGAT2 | c.620A>T (p.Lys207Ile) | |
14 | g.49621889A= | CA2135804727 | MGAT2 | c.621A= (p.Lys207=) | |
14 | g.49621889A>C | CA389619575 | MGAT2 | c.621A>C (p.Lys207Asn) | |
14 | g.49621889A>G | CA486350345 | MGAT2 | c.621A>G (p.Lys207=) | dbSNP |
14 | g.49621889A>T | CA389619577 | MGAT2 | c.621A>T (p.Lys207Asn) | |
14 | g.49621890T>A | CA389619578 | MGAT2 | c.622T>A (p.Leu208Met) | |
14 | g.49621890T>C | CA7172583 | MGAT2 | c.622T>C (p.Leu208=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
14 | g.49621890T>G | CA389619581 | MGAT2 | c.622T>G (p.Leu208Val) | |
14 | g.49621890T= | CA2135804728 | MGAT2 | c.622T= (p.Leu208=) | |
14 | g.49621891T>A | CA389619582 | MGAT2 | c.623T>A (p.Leu208Ter) | |
14 | g.49621891T>C | CA389619584 | MGAT2 | c.623T>C (p.Leu208Ser) | |
14 | g.49621891T>G | CA389619585 | MGAT2 | c.623T>G (p.Leu208Trp) | |
14 | g.49621891_49621893delinsTGG | CA2135804729 | MGAT2 | c.623_625delinsTGG (p.Leu208=) | |
14 | g.49621892G>A | CA486350348 | MGAT2 | c.624G>A (p.Leu208=) | |
14 | g.49621892G>C | CA389619586 | MGAT2 | c.624G>C (p.Leu208Phe) | |
14 | g.49621892G>T | CA389619588 | MGAT2 | c.624G>T (p.Leu208Phe) | |
14 | g.49621894_49621895del | CA706480752 | MGAT2 | c.626_627del (p.Gly209ValfsTer5) | dbSNP gnomAD v3 gnomAD v4 |
14 | g.49621893G>A | CA389619589 | MGAT2 | c.625G>A (p.Gly209Arg) | gnomAD v4 |