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.136676962_136676978del | CA2692654878 | AGPAT2 | c.477_492+1del n.405_420+1del | gnomAD v4 |
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 | |
9 | g.136676975T>C | CA5342993 | AGPAT2 | c.478A>G (p.Met160Val) n.406A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136676975T>G | CA375581803 | AGPAT2 | c.478A>C (p.Met160Leu) n.406A>C | |
9 | g.136676976G>A | CA467739476 | AGPAT2 | c.477C>T (p.Arg159=) n.405C>T | |
9 | g.136676976G>C | CA467739478 | AGPAT2 | c.477C>G (p.Arg159=) n.405C>G | |
9 | g.136676976G>T | CA467739475 | AGPAT2 | c.477C>A (p.Arg159=) n.405C>A | dbSNP gnomAD v3 gnomAD v4 |
9 | g.136676977C>A | CA5342995 | AGPAT2 | c.476G>T (p.Arg159Leu) n.404G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136676977C>G | CA375581807 | AGPAT2 | c.476G>C (p.Arg159Pro) n.404G>C | COSMIC |
9 | g.136676977C>T | CA5342994 | AGPAT2 | c.476G>A (p.Arg159His) n.404G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136676978G>A | CA207355 | AGPAT2 | c.475C>T (p.Arg159Cys) n.403C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
9 | g.136676978G>C | CA375581810 | AGPAT2 | c.475C>G (p.Arg159Gly) n.403C>G | |
9 | g.136676978G>T | CA375581813 | AGPAT2 | c.475C>A (p.Arg159Ser) n.403C>A | gnomAD v4 |
9 | g.136676979C>A | CA375581819 | AGPAT2 | c.474G>T (p.Glu158Asp) n.402G>T | |
9 | g.136676979C>G | CA375581821 | AGPAT2 | c.474G>C (p.Glu158Asp) n.402G>C | |
9 | g.136676979C>T | CA467739489 | AGPAT2 | c.474G>A (p.Glu158=) n.402G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136676980T>A | CA375581827 | AGPAT2 | c.473A>T (p.Glu158Val) n.401A>T | |
9 | g.136676980T>C | CA375581831 | AGPAT2 | c.473A>G (p.Glu158Gly) n.401A>G | dbSNP |
9 | g.136676980T>G | CA375581824 | AGPAT2 | c.473A>C (p.Glu158Ala) n.401A>C | |
9 | g.136676983_136676991del | CA2497275544 | AGPAT2 | c.465_473del (p.Asp155_Gly157del) n.393_401del | dbSNP gnomAD v4 |
9 | g.136676981C>A | CA375581833 | AGPAT2 | c.472G>T (p.Glu158Ter) n.400G>T | |
9 | g.136676981C>G | CA375581836 | AGPAT2 | c.472G>C (p.Glu158Gln) n.400G>C | |
9 | g.136676981C>T | CA375581839 | AGPAT2 | c.472G>A (p.Glu158Lys) n.400G>A | dbSNP gnomAD v3 gnomAD v4 |
9 | g.136676982G>A | CA5342996 | AGPAT2 | c.471C>T (p.Gly157=) n.399C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136676982G>C | CA467739492 | AGPAT2 | c.471C>G (p.Gly157=) n.399C>G | gnomAD v4 |
9 | g.136676982G>T | CA467739494 | AGPAT2 | c.471C>A (p.Gly157=) n.399C>A | |
9 | g.136676983C>A | CA375581842 | AGPAT2 | c.470G>T (p.Gly157Val) n.398G>T | |
9 | g.136676983C>G | CA375581845 | AGPAT2 | c.470G>C (p.Gly157Ala) n.398G>C | |
9 | g.136676983C>T | CA375581849 | AGPAT2 | c.470G>A (p.Gly157Asp) n.398G>A | |
9 | g.136676984C>A | CA201629850 | AGPAT2 | c.469G>T (p.Gly157Cys) n.397G>T | dbSNP gnomAD v2 gnomAD v4 |
9 | g.136676984C>G | CA375581853 | AGPAT2 | c.469G>C (p.Gly157Arg) n.397G>C | |
9 | g.136676984C>T | CA375581854 | AGPAT2 | c.469G>A (p.Gly157Ser) n.397G>A | |
9 | g.136676985C>A | CA467739508 | AGPAT2 | c.468G>T (p.Leu156=) n.396G>T | |
9 | g.136676985C>G | CA467739510 | AGPAT2 | c.468G>C (p.Leu156=) n.396G>C |