Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.136676051_136677087del | CA277954 | AGPAT2 | c.366_588+534del c.366_492+910del n.294_516+534del | ClinVar |
9 | g.136676957_136676960del | CA16043673 | AGPAT2 | c.492+4_492+7del (n.492+4_492+7del) n.420+4_420+7del | ClinVar dbSNP gnomAD v2 gnomAD v4 |
9 | g.136676960C>A | CA375581657 | AGPAT2 | c.492+1G>T (n.492+1G>T) n.420+1G>T | gnomAD v4 |
9 | g.136676960C>G | CA375581661 | AGPAT2 | c.492+1G>C (n.492+1G>C) n.420+1G>C | gnomAD v4 |
9 | g.136676960C>T | CA16042196 | AGPAT2 | c.492+1G>A (n.492+1G>A) n.420+1G>A | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136676962_136676978del | CA2692654878 | AGPAT2 | c.477_492+1del n.405_420+1del | gnomAD v4 |
9 | g.136676961G>A | CA201629785 | AGPAT2 | c.492C>T (p.Asn164=) n.420C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136676961G>C | CA201629794 | AGPAT2 | c.492C>G (p.Asn164Lys) n.420C>G | dbSNP gnomAD v4 |
9 | g.136676961G>T | CA375581678 | AGPAT2 | c.492C>A (p.Asn164Lys) n.420C>A | |
9 | g.136676962T>A | CA375581682 | AGPAT2 | c.491A>T (p.Asn164Ile) n.419A>T | gnomAD v4 |
9 | g.136676962T>C | CA375581686 | AGPAT2 | c.491A>G (p.Asn164Ser) n.419A>G | |
9 | g.136676962T>G | CA375581683 | AGPAT2 | c.491A>C (p.Asn164Thr) n.419A>C | gnomAD v4 |
9 | g.136676963T>A | CA375581690 | AGPAT2 | c.490A>T (p.Asn164Tyr) n.418A>T | |
9 | g.136676963T>C | CA375581692 | AGPAT2 | c.490A>G (p.Asn164Asp) n.418A>G | |
9 | g.136676963T>G | CA375581694 | AGPAT2 | c.490A>C (p.Asn164His) n.418A>C | |
9 | g.136676964C>A | CA375581699 | AGPAT2 | c.489G>T (p.Glu163Asp) n.417G>T | |
9 | g.136676964C>G | CA375581700 | AGPAT2 | c.489G>C (p.Glu163Asp) n.417G>C | |
9 | g.136676964C>T | CA467739418 | AGPAT2 | c.489G>A (p.Glu163=) n.417G>A | |
9 | g.136676965T>A | CA375581701 | AGPAT2 | c.488A>T (p.Glu163Val) n.416A>T | |
9 | g.136676965T>C | CA375581702 | AGPAT2 | c.488A>G (p.Glu163Gly) n.416A>G | |
9 | g.136676965T>G | CA375581705 | AGPAT2 | c.488A>C (p.Glu163Ala) n.416A>C | |
9 | g.136676966C>A | CA375581709 | AGPAT2 | c.487G>T (p.Glu163Ter) n.415G>T | |
9 | g.136676966C>G | CA375581719 | AGPAT2 | c.487G>C (p.Glu163Gln) n.415G>C | gnomAD v4 |
9 | g.136676966C>T | CA201629800 | AGPAT2 | c.487G>A (p.Glu163Lys) n.415G>A | dbSNP gnomAD v3 gnomAD v4 |
9 | g.136676968del | CA5342989 | AGPAT2 | c.487del (p.Glu163ArgfsTer?) n.415del | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.136676967C>A | CA375581728 | AGPAT2 | c.486G>T (p.Arg162Ser) n.414G>T | |
9 | g.136676967C>G | CA375581735 | AGPAT2 | c.486G>C (p.Arg162Ser) n.414G>C | |
9 | g.136676967C>T | CA467739430 | AGPAT2 | c.486G>A (p.Arg162=) n.414G>A | |
9 | g.136676968C>A | CA375581738 | AGPAT2 | c.485G>T (p.Arg162Met) n.413G>T | |
9 | g.136676968C>G | CA5342990 | AGPAT2 | c.485G>C (p.Arg162Thr) n.413G>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136676968C>T | CA375581739 | AGPAT2 | c.485G>A (p.Arg162Lys) n.413G>A | gnomAD v4 |
9 | g.136676969T>A | CA375581741 | AGPAT2 | c.484A>T (p.Arg162Trp) n.412A>T | |
9 | g.136676969T>C | CA375581749 | AGPAT2 | c.484A>G (p.Arg162Gly) n.412A>G | |
9 | g.136676969T>G | CA467739447 | AGPAT2 | c.484A>C (p.Arg162=) n.412A>C | |
9 | g.136676970G>A | CA5342991 | AGPAT2 | c.483C>T (p.Val161=) n.411C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136676970G>C | CA467739453 | AGPAT2 | c.483C>G (p.Val161=) n.411C>G | |
9 | g.136676970G>T | CA467739455 | AGPAT2 | c.483C>A (p.Val161=) n.411C>A | dbSNP gnomAD v2 gnomAD v4 |
9 | g.136676971A>C | CA375581756 | AGPAT2 | c.482T>G (p.Val161Gly) n.410T>G | dbSNP gnomAD v3 gnomAD v4 |
9 | g.136676971A>G | CA375581758 | AGPAT2 | c.482T>C (p.Val161Ala) n.410T>C | |
9 | g.136676971A>T | CA375581760 | AGPAT2 | c.482T>A (p.Val161Asp) n.410T>A | |
9 | g.136676972C>A | CA375581763 | AGPAT2 | c.481G>T (p.Val161Phe) n.409G>T | |
9 | g.136676972C>G | CA375581769 | AGPAT2 | c.481G>C (p.Val161Leu) n.409G>C | |
9 | g.136676972C>T | CA375581774 | AGPAT2 | c.481G>A (p.Val161Ile) n.409G>A | |
9 | g.136676973C>A | CA375581779 | AGPAT2 | c.480G>T (p.Met160Ile) n.408G>T | |
9 | g.136676973C>G | CA375581782 | AGPAT2 | c.480G>C (p.Met160Ile) n.408G>C | |
9 | g.136676973C>T | CA5342992 | AGPAT2 | c.480G>A (p.Met160Ile) n.408G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.136676974A>C | CA375581800 | AGPAT2 | c.479T>G (p.Met160Arg) n.407T>G | |
9 | g.136676974A>G | CA375581791 | AGPAT2 | c.479T>C (p.Met160Thr) n.407T>C | dbSNP gnomAD v3 gnomAD v4 |
9 | g.136676974A>T | CA375581799 | AGPAT2 | c.479T>A (p.Met160Lys) n.407T>A | |
9 | g.136676975T>A | CA375581801 | AGPAT2 | c.478A>T (p.Met160Leu) n.406A>T |