| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 9 | g.136673693_136673721del | CA2692653662 | AGPAT2 | c.*37_*65del (n.*37_*65del) | gnomAD v4 |
| 9 | g.136673709C>A | CA2692653691 | AGPAT2 | c.*43G>T (n.*43G>T) n.808G>T | gnomAD v4 |
| 9 | g.136673710T>C | CA2692653692 | AGPAT2 | c.*42A>G (n.*42A>G) n.807A>G | gnomAD v4 |
| 9 | g.136673711dup | CA375576028 | AGPAT2 | c.*42dup (n.*42dup) n.807dup | dbSNP |
| 9 | g.136673711T>C | CA2692653693 | AGPAT2 | c.*41A>G (n.*41A>G) n.806A>G | gnomAD v4 |
| 9 | g.136673712C>A | CA2692653694 | AGPAT2 | c.*40G>T (n.*40G>T) n.805G>T | gnomAD v4 |
| 9 | g.136673712C>T | CA5342789 | AGPAT2 | c.*40G>A (n.*40G>A) n.805G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.136673713C>A | CA2692653695 | AGPAT2 | c.*39G>T (n.*39G>T) n.804G>T | gnomAD v4 |
| 9 | g.136673713C>G | CA2720766642 | AGPAT2 | c.*39G>C (n.*39G>C) n.804G>C | dbSNP |
| 9 | g.136673713C>T | CA5342790 | AGPAT2 | c.*39G>A (n.*39G>A) n.804G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136673714A>C | CA5342791 | AGPAT2 | c.*38T>G (n.*38T>G) n.803T>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.136673714A>G | CA2692653696 | AGPAT2 | c.*38T>C (n.*38T>C) n.803T>C | gnomAD v4 |
| 9 | g.136673715C>A | CA2692653697 | AGPAT2 | c.*37G>T (n.*37G>T) n.802G>T | gnomAD v4 |
| 9 | g.136673716C>A | CA2692653698 | AGPAT2 | c.*36G>T (n.*36G>T) n.801G>T | gnomAD v4 |
| 9 | g.136673716C>T | CA1130032996 | AGPAT2 | c.*36G>A (n.*36G>A) n.801G>A | dbSNP gnomAD v3 gnomAD v4 |
| 9 | g.136673717T>C | CA2692653699 | AGPAT2 | c.*35A>G (n.*35A>G) n.800A>G | gnomAD v4 |
| 9 | g.136673718G>A | CA5342793 | AGPAT2 | c.*34C>T (n.*34C>T) n.799C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.136673718G>C | CA5342792 | AGPAT2 | c.*34C>G (n.*34C>G) n.799C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136673718G>T | CA653636012 | AGPAT2 | c.*34C>A (n.*34C>A) n.799C>A | gnomAD v4 COSMIC |
| 9 | g.136673719C>A | CA2692653700 | AGPAT2 | c.*33G>T (n.*33G>T) n.798G>T | gnomAD v4 |
| 9 | g.136673719C>T | CA861080421 | AGPAT2 | c.*33G>A (n.*33G>A) n.798G>A | dbSNP gnomAD v4 |
| 9 | g.136673721del | CA2692653701 | AGPAT2 | c.*33del (n.*33del) n.798del | gnomAD v4 |
| 9 | g.136673720C>A | CA2692653702 | AGPAT2 | c.*32G>T (n.*32G>T) n.797G>T | gnomAD v4 |
| 9 | g.136673720C>T | CA2579519872 | AGPAT2 | c.*32G>A (n.*32G>A) n.797G>A | gnomAD v4 |
| 9 | g.136673721C>A | CA2692653703 | AGPAT2 | c.*31G>T (n.*31G>T) n.796G>T | gnomAD v4 |
| 9 | g.136673721C>T | CA5342794 | AGPAT2 | c.*31G>A (n.*31G>A) n.796G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136673722T>C | CA2692653704 | AGPAT2 | c.*30A>G (n.*30A>G) n.795A>G | gnomAD v4 |
| 9 | g.136673723C>A | CA2692653706 | AGPAT2 | c.*29G>T (n.*29G>T) n.794G>T | gnomAD v4 |
| 9 | g.136673726del | CA2692653705 | AGPAT2 | c.*29del (n.*29del) n.794del | gnomAD v4 |
| 9 | g.136673724C>A | CA2692653707 | AGPAT2 | c.*28G>T (n.*28G>T) n.793G>T | gnomAD v4 |
| 9 | g.136673724C>T | CA2692653708 | AGPAT2 | c.*28G>A (n.*28G>A) n.793G>A | gnomAD v4 |
| 9 | g.136673724_136673727del | CA918577849 | AGPAT2 | c.*25_*28del (n.*25_*28del) n.790_793del | dbSNP gnomAD v4 |
| 9 | g.136673725C>A | CA2692653709 | AGPAT2 | c.*27G>T (n.*27G>T) n.792G>T | gnomAD v4 |
| 9 | g.136673725C>G | CA2692653710 | AGPAT2 | c.*27G>C (n.*27G>C) n.792G>C | gnomAD v4 |
| 9 | g.136673725C>T | CA2692653711 | AGPAT2 | c.*27G>A (n.*27G>A) n.792G>A | gnomAD v4 |
| 9 | g.136673726C>A | CA2692653712 | AGPAT2 | c.*26G>T (n.*26G>T) n.791G>T | gnomAD v4 |
| 9 | g.136673726C>G | CA2692653713 | AGPAT2 | c.*26G>C (n.*26G>C) n.791G>C | dbSNP gnomAD v4 |
| 9 | g.136673726C>T | CA2579519873 | AGPAT2 | c.*26G>A (n.*26G>A) n.791G>A | gnomAD v4 |
| 9 | g.136673728G>A | CA2692653714 | AGPAT2 | c.*24C>T (n.*24C>T) n.789C>T | gnomAD v4 |
| 9 | g.136673728G>T | CA2692653715 | AGPAT2 | c.*24C>A (n.*24C>A) n.789C>A | gnomAD v4 |
| 9 | g.136673729G>A | CA2692653716 | AGPAT2 | c.*23C>T (n.*23C>T) n.788C>T | gnomAD v4 |
| 9 | g.136673729G>C | CA591183509 | AGPAT2 | c.*23C>G (n.*23C>G) n.788C>G | dbSNP gnomAD v2 |
| 9 | g.136673729G>T | CA201623469 | AGPAT2 | c.*23C>A (n.*23C>A) n.788C>A | dbSNP |
| 9 | g.136673730T>A | CA2692653717 | AGPAT2 | c.*22A>T (n.*22A>T) n.787A>T | gnomAD v4 |
| 9 | g.136673730T>C | CA2692653718 | AGPAT2 | c.*22A>G (n.*22A>G) n.787A>G | gnomAD v4 |
| 9 | g.136673731C>A | CA2692653719 | AGPAT2 | c.*21G>T (n.*21G>T) n.786G>T | gnomAD v4 |
| 9 | g.136673731C>G | CA5342795 | AGPAT2 | c.*21G>C (n.*21G>C) n.786G>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136673732A>G | CA2692653720 | AGPAT2 | c.*20T>C (n.*20T>C) n.785T>C | gnomAD v4 |
| 9 | g.136673733T>A | CA2692653721 | AGPAT2 | c.*19A>T (n.*19A>T) n.784A>T | gnomAD v4 |
| 9 | g.136673734G>T | CA2692653723 | AGPAT2 | c.*18C>A (n.*18C>A) n.783C>A | gnomAD v4 |
| 9 | g.136673734_136673735insGG | CA2692653722 | AGPAT2 | c.*18_*19insCC (n.*18_*19insCC) n.783_784insCC | gnomAD v4 |
| 9 | g.136673735C>A | CA5342797 | AGPAT2 | c.*17G>T (n.*17G>T) n.782G>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.136673735C>G | CA591183512 | AGPAT2 | c.*17G>C (n.*17G>C) n.782G>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136673735C>T | CA5342796 | AGPAT2 | c.*17G>A (n.*17G>A) n.782G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.136673735_136673736insA | CA2692653725 | AGPAT2 | c.*16_*17insT (n.*16_*17insT) n.781_782insT | gnomAD v4 |
| 9 | g.136673736C>A | CA2692653724 | AGPAT2 | c.*16G>T (n.*16G>T) n.781G>T | gnomAD v4 |
| 9 | g.136673736C>T | CA2786279652 | AGPAT2 | c.*16G>A (n.*16G>A) n.781G>A | |
| 9 | g.136673737C>A | CA2579519874 | AGPAT2 | c.*15G>T (n.*15G>T) n.780G>T | gnomAD v4 |
| 9 | g.136673738T>A | CA1130033008 | AGPAT2 | c.*14A>T (n.*14A>T) n.779A>T | dbSNP gnomAD v3 gnomAD v4 |
| 9 | g.136673738_136673743del | CA2497275505 | AGPAT2 | c.*9_*14del (n.*9_*14del) n.774_779del | dbSNP |
| 9 | g.136673739G>A | CA2692653726 | AGPAT2 | c.*13C>T (n.*13C>T) n.778C>T | gnomAD v4 |
| 9 | g.136673739G>T | CA2692653727 | AGPAT2 | c.*13C>A (n.*13C>A) n.778C>A | gnomAD v4 |
| 9 | g.136673740C>A | CA2692653729 | AGPAT2 | c.*12G>T (n.*12G>T) n.777G>T | gnomAD v4 |
| 9 | g.136673740C>T | CA2692653728 | AGPAT2 | c.*12G>A (n.*12G>A) n.777G>A | gnomAD v4 |
| 9 | g.136673740_136673741del | CA1130033011 | AGPAT2 | c.*11_*12del (n.*11_*12del) n.776_777del | dbSNP gnomAD v3 gnomAD v4 |
| 9 | g.136673741del | CA5342798 | AGPAT2 | c.*12del (n.*12del) n.777del | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136673741C>A | CA2692653730 | AGPAT2 | c.*11G>T (n.*11G>T) n.776G>T | gnomAD v4 |
| 9 | g.136673741C>G | CA2692653731 | AGPAT2 | c.*11G>C (n.*11G>C) n.776G>C | gnomAD v4 |
| 9 | g.136673741C>T | CA5342799 | AGPAT2 | c.*11G>A (n.*11G>A) n.776G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136673742G>A | CA5342800 | AGPAT2 | c.*10C>T (n.*10C>T) n.775C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136673743T>C | CA1130033030 | AGPAT2 | c.*9A>G (n.*9A>G) n.774A>G | dbSNP gnomAD v3 gnomAD v4 |
| 9 | g.136673743_136673746del | CA1130033021 | AGPAT2 | c.*6_*9del (n.*6_*9del) n.771_774del | dbSNP gnomAD v3 gnomAD v4 |
| 9 | g.136673744G>A | CA2692653732 | AGPAT2 | c.*8C>T (n.*8C>T) n.773C>T | dbSNP gnomAD v4 |
| 9 | g.136673744G>T | CA2692653733 | AGPAT2 | c.*8C>A (n.*8C>A) n.773C>A | gnomAD v4 |
| 9 | g.136673745G>A | CA2692653735 | AGPAT2 | c.*7C>T (n.*7C>T) n.772C>T | gnomAD v4 |
| 9 | g.136673745G>T | CA2692653734 | AGPAT2 | c.*7C>A (n.*7C>A) n.772C>A | gnomAD v4 |
| 9 | g.136673746T>C | CA2692653736 | AGPAT2 | c.*6A>G (n.*6A>G) n.771A>G | gnomAD v4 |
| 9 | g.136673746T>G | CA2720854538 | AGPAT2 | c.*6A>C (n.*6A>C) n.771A>C | dbSNP |
| 9 | g.136673747C>A | CA2692653737 | AGPAT2 | c.*5G>T (n.*5G>T) n.770G>T | dbSNP gnomAD v4 |
| 9 | g.136673747C>G | CA591183518 | AGPAT2 | c.*5G>C (n.*5G>C) n.770G>C | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.136673753_136673760del | CA2692653738 | AGPAT2 | c.835_*5del (n.[c.835_*5del;Ter279ThrextTer?]) c.739_*5del (n.[c.739_*5del;Ter247ThrextTer?]) n.763_770del | gnomAD v4 |
| 9 | g.136673748T>A | CA1130033034 | AGPAT2 | c.*4A>T (n.*4A>T) n.769A>T | dbSNP gnomAD v3 gnomAD v4 |
| 9 | g.136673748T>C | CA2692653739 | AGPAT2 | c.*4A>G (n.*4A>G) n.769A>G | gnomAD v4 |
| 9 | g.136673748T>G | CA591183523 | AGPAT2 | c.*4A>C (n.*4A>C) n.769A>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136673749G>A | CA1130033049 | AGPAT2 | c.*3C>T (n.*3C>T) n.768C>T | dbSNP gnomAD v3 gnomAD v4 |
| 9 | g.136673749G>T | CA2692653740 | AGPAT2 | c.*3C>A (n.*3C>A) n.768C>A | dbSNP gnomAD v4 |
| 9 | g.136673750G>A | CA2692653742 | AGPAT2 | c.*2C>T (n.*2C>T) n.767C>T | gnomAD v4 |
| 9 | g.136673750G>C | CA2692653741 | AGPAT2 | c.*2C>G (n.*2C>G) n.767C>G | dbSNP gnomAD v4 |
| 9 | g.136673751G>A | CA2692653744 | AGPAT2 | c.*1C>T (n.*1C>T) n.766C>T | dbSNP gnomAD v4 |
| 9 | g.136673751G>T | CA2692653743 | AGPAT2 | c.*1C>A (n.*1C>A) n.766C>A | gnomAD v4 |
| 9 | g.136673752C>A | CA375576040 | AGPAT2 | c.837G>T (p.Ter279Tyr) c.741G>T (p.Ter247Tyr) n.765G>T | gnomAD v4 |
| 9 | g.136673752C>G | CA375576042 | AGPAT2 | c.837G>C (p.Ter279Tyr) c.741G>C (p.Ter247Tyr) n.765G>C | |
| 9 | g.136673752C>T | CA467736139 | AGPAT2 | c.837G>A (p.Ter279=) c.741G>A (p.Ter247=) n.765G>A | gnomAD v4 |
| 9 | g.136673753T>A | CA375576044 | AGPAT2 | c.836A>T (p.Ter279Leu) c.740A>T (p.Ter247Leu) n.764A>T | gnomAD v4 |
| 9 | g.136673753T>C | CA375576046 | AGPAT2 | c.836A>G (p.Ter279Trp) c.740A>G (p.Ter247Trp) n.764A>G | |
| 9 | g.136673753T>G | CA375576048 | AGPAT2 | c.836A>C (p.Ter279Ser) c.740A>C (p.Ter247Ser) n.764A>C | |
| 9 | g.136673754A>C | CA375576050 | AGPAT2 | c.835T>G (p.Ter279Glu) c.739T>G (p.Ter247Glu) n.763T>G | |
| 9 | g.136673754A>G | CA375576052 | AGPAT2 | c.835T>C (p.Ter279Gln) c.739T>C (p.Ter247Gln) n.763T>C | ClinVar dbSNP gnomAD v4 |
| 9 | g.136673754A>T | CA375576054 | AGPAT2 | c.835T>A (p.Ter279Lys) c.739T>A (p.Ter247Lys) n.763T>A | |
| 9 | g.136673754_136673761dup | CA2692653745 | AGPAT2 | c.828_835dup (p.Ter279TrpextTer11) c.732_739dup (p.Ter247TrpextTer11) n.756_763dup | gnomAD v4 |
| 9 | g.136673755C>A | CA375576056 | AGPAT2 | c.834G>T (p.Gln278His) c.738G>T (p.Gln246His) n.762G>T | |
| 9 | g.136673755C>G | CA375576058 | AGPAT2 | c.834G>C (p.Gln278His) c.738G>C (p.Gln246His) n.762G>C | |
| 9 | g.136673755C>T | CA467736156 | AGPAT2 | c.834G>A (p.Gln278=) c.738G>A (p.Gln246=) n.762G>A | gnomAD v4 |
| 9 | g.136673756T>A | CA375576061 | AGPAT2 | c.833A>T (p.Gln278Leu) c.737A>T (p.Gln246Leu) n.761A>T | |
| 9 | g.136673756T>C | CA375576062 | AGPAT2 | c.833A>G (p.Gln278Arg) c.737A>G (p.Gln246Arg) n.761A>G | gnomAD v4 |
| 9 | g.136673756T>G | CA375576064 | AGPAT2 | c.833A>C (p.Gln278Pro) c.737A>C (p.Gln246Pro) n.761A>C | |
| 9 | g.136673756_136673759dup | CA2692653746 | AGPAT2 | c.830_833dup (p.Gln278HisfsTer?) c.734_737dup (p.Gln246HisfsTer?) n.758_761dup | gnomAD v4 |
| 9 | g.136673757G>A | CA375576066 | AGPAT2 | c.832C>T (p.Gln278Ter) c.736C>T (p.Gln246Ter) n.760C>T | |
| 9 | g.136673757G>C | CA375576067 | AGPAT2 | c.832C>G (p.Gln278Glu) c.736C>G (p.Gln246Glu) n.760C>G | |
| 9 | g.136673757G>T | CA375576065 | AGPAT2 | c.832C>A (p.Gln278Lys) c.736C>A (p.Gln246Lys) n.760C>A | gnomAD v4 |
| 9 | g.136673758G>A | CA467736167 | AGPAT2 | c.831C>T (p.Ala277=) c.735C>T (p.Ala245=) n.759C>T | gnomAD v4 |
| 9 | g.136673758G>C | CA467736169 | AGPAT2 | c.831C>G (p.Ala277=) c.735C>G (p.Ala245=) n.759C>G | |
| 9 | g.136673758G>T | CA467736171 | AGPAT2 | c.831C>A (p.Ala277=) c.735C>A (p.Ala245=) n.759C>A | |
| 9 | g.136673760_136673825del | CA5342801 | AGPAT2 | c.766_831del (p.Phe256_Ala277del) c.670_735del (p.Phe224_Ala245del) n.694_759del | ExAC gnomAD v2 gnomAD v4 |
| 9 | g.136673759G>A | CA375576069 | AGPAT2 | c.830C>T (p.Ala277Val) c.734C>T (p.Ala245Val) n.758C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136673759G>C | CA375576071 | AGPAT2 | c.830C>G (p.Ala277Gly) c.734C>G (p.Ala245Gly) n.758C>G | |
| 9 | g.136673759G>T | CA375576072 | AGPAT2 | c.830C>A (p.Ala277Asp) c.734C>A (p.Ala245Asp) n.758C>A | dbSNP gnomAD v3 gnomAD v4 |
| 9 | g.136673760C>A | CA375576075 | AGPAT2 | c.829G>T (p.Ala277Ser) c.733G>T (p.Ala245Ser) n.757G>T | gnomAD v4 |
| 9 | g.136673760C>G | CA375576077 | AGPAT2 | c.829G>C (p.Ala277Pro) c.733G>C (p.Ala245Pro) n.757G>C | |
| 9 | g.136673760C>T | CA375576078 | AGPAT2 | c.829G>A (p.Ala277Thr) c.733G>A (p.Ala245Thr) n.757G>A | |
| 9 | g.136673769_136673770insAGCCCGGCTGCAC | CA2579519875 | AGPAT2 | c.829_830insGCTGTGCAGCCGG (p.Ala277GlyfsTer?) c.733_734insGCTGTGCAGCCGG (p.Ala245GlyfsTer?) n.757_758insGCTGTGCAGCCGG | |
| 9 | g.136673761C>A | CA467736186 | AGPAT2 | c.828G>T (p.Pro276=) c.732G>T (p.Pro244=) n.756G>T | dbSNP gnomAD v4 COSMIC |
| 9 | g.136673761C>G | CA467736189 | AGPAT2 | c.828G>C (p.Pro276=) c.732G>C (p.Pro244=) n.756G>C | |
| 9 | g.136673761C>T | CA467736191 | AGPAT2 | c.828G>A (p.Pro276=) c.732G>A (p.Pro244=) n.756G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.136673762G>A | CA5342802 | AGPAT2 | c.827C>T (p.Pro276Leu) c.731C>T (p.Pro244Leu) n.755C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136673762G>C | CA375576080 | AGPAT2 | c.827C>G (p.Pro276Arg) c.731C>G (p.Pro244Arg) n.755C>G | |
| 9 | g.136673762G>T | CA375576082 | AGPAT2 | c.827C>A (p.Pro276Gln) c.731C>A (p.Pro244Gln) n.755C>A | gnomAD v4 |
| 9 | g.136673763G>A | CA375576086 | AGPAT2 | c.826C>T (p.Pro276Ser) c.730C>T (p.Pro244Ser) n.754C>T | gnomAD v4 |
| 9 | g.136673763G>C | CA375576087 | AGPAT2 | c.826C>G (p.Pro276Ala) c.730C>G (p.Pro244Ala) n.754C>G | gnomAD v4 |
| 9 | g.136673763G>T | CA375576090 | AGPAT2 | c.826C>A (p.Pro276Thr) c.730C>A (p.Pro244Thr) n.754C>A | gnomAD v4 |
| 9 | g.136673764_136673774dup | CA2579519876 | AGPAT2 | c.816_826dup (p.Pro276LeufsTer15) c.720_730dup (p.Pro244LeufsTer15) n.744_754dup | gnomAD v4 |
| 9 | g.136673764C>A | CA375576093 | AGPAT2 | c.825G>T (p.Gln275His) c.729G>T (p.Gln243His) n.753G>T | gnomAD v4 |
| 9 | g.136673764C>G | CA375576094 | AGPAT2 | c.825G>C (p.Gln275His) c.729G>C (p.Gln243His) n.753G>C | |
| 9 | g.136673764C>T | CA467736208 | AGPAT2 | c.825G>A (p.Gln275=) c.729G>A (p.Gln243=) n.753G>A | gnomAD v4 |
| 9 | g.136673765T>A | CA375576100 | AGPAT2 | c.824A>T (p.Gln275Leu) c.728A>T (p.Gln243Leu) n.752A>T | |
| 9 | g.136673765T>C | CA375576097 | AGPAT2 | c.824A>G (p.Gln275Arg) c.728A>G (p.Gln243Arg) n.752A>G | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.136673765T>G | CA375576098 | AGPAT2 | c.824A>C (p.Gln275Pro) c.728A>C (p.Gln243Pro) n.752A>C | dbSNP gnomAD v3 gnomAD v4 |
| 9 | g.136673766G>A | CA375576103 | AGPAT2 | c.823C>T (p.Gln275Ter) c.727C>T (p.Gln243Ter) n.751C>T | dbSNP gnomAD v3 gnomAD v4 |
| 9 | g.136673766G>C | CA375576104 | AGPAT2 | c.823C>G (p.Gln275Glu) c.727C>G (p.Gln243Glu) n.751C>G | |
| 9 | g.136673766G>T | CA375576105 | AGPAT2 | c.823C>A (p.Gln275Lys) c.727C>A (p.Gln243Lys) n.751C>A | gnomAD v4 |
| 9 | g.136673767C>A | CA467736227 | AGPAT2 | c.822G>T (p.Val274=) c.726G>T (p.Val242=) n.750G>T | gnomAD v4 |
| 9 | g.136673767C>G | CA467736220 | AGPAT2 | c.822G>C (p.Val274=) c.726G>C (p.Val242=) n.750G>C | |
| 9 | g.136673767C>T | CA467736224 | AGPAT2 | c.822G>A (p.Val274=) c.726G>A (p.Val242=) n.750G>A | gnomAD v4 |
| 9 | g.136673768A>C | CA375576108 | AGPAT2 | c.821T>G (p.Val274Gly) c.725T>G (p.Val242Gly) n.749T>G | |
| 9 | g.136673768A>G | CA375576110 | AGPAT2 | c.821T>C (p.Val274Ala) c.725T>C (p.Val242Ala) n.749T>C | gnomAD v4 |
| 9 | g.136673768A>T | CA375576111 | AGPAT2 | c.821T>A (p.Val274Glu) c.725T>A (p.Val242Glu) n.749T>A | |
| 9 | g.136673769C>A | CA375576114 | AGPAT2 | c.820G>T (p.Val274Leu) c.724G>T (p.Val242Leu) n.748G>T | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.136673769C>G | CA375576115 | AGPAT2 | c.820G>C (p.Val274Leu) c.724G>C (p.Val242Leu) n.748G>C | gnomAD v4 |
| 9 | g.136673769C>T | CA5342803 | AGPAT2 | c.820G>A (p.Val274Met) c.724G>A (p.Val242Met) n.748G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136673770G>A | CA5342804 | AGPAT2 | c.819C>T (p.Gly273=) c.723C>T (p.Gly241=) n.747C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136673770G>C | CA467736241 | AGPAT2 | c.819C>G (p.Gly273=) c.723C>G (p.Gly241=) n.747C>G | |
| 9 | g.136673770G>T | CA467736240 | AGPAT2 | c.819C>A (p.Gly273=) c.723C>A (p.Gly241=) n.747C>A | gnomAD v4 |
| 9 | g.136673771_136673804del | CA2692653747 | AGPAT2 | c.786_819del (p.Pro263CysfsTer13) c.690_723del (p.Pro231CysfsTer13) n.714_747del | gnomAD v4 |
| 9 | g.136673771C>A | CA375576118 | AGPAT2 | c.818G>T (p.Gly273Val) c.722G>T (p.Gly241Val) n.746G>T | gnomAD v4 |
| 9 | g.136673771C>G | CA5342805 | AGPAT2 | c.818G>C (p.Gly273Ala) c.722G>C (p.Gly241Ala) n.746G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.136673771C>T | CA375576121 | AGPAT2 | c.818G>A (p.Gly273Asp) c.722G>A (p.Gly241Asp) n.746G>A | gnomAD v4 |
| 9 | g.136673772_136673779dup | CA2692653748 | AGPAT2 | c.811_818dup (p.Val274GlyfsTer16) c.715_722dup (p.Val242GlyfsTer16) n.739_746dup | gnomAD v4 |
| 9 | g.136673772C>A | CA375576124 | AGPAT2 | c.817G>T (p.Gly273Cys) c.721G>T (p.Gly241Cys) n.745G>T | |
| 9 | g.136673772C>G | CA375576127 | AGPAT2 | c.817G>C (p.Gly273Arg) c.721G>C (p.Gly241Arg) n.745G>C | |
| 9 | g.136673772C>T | CA375576125 | AGPAT2 | c.817G>A (p.Gly273Ser) c.721G>A (p.Gly241Ser) n.745G>A | dbSNP gnomAD v4 |
| 9 | g.136673773A>C | CA467736254 | AGPAT2 | c.816T>G (p.Ser272=) c.720T>G (p.Ser240=) n.744T>G | |
| 9 | g.136673773A>G | CA467736255 | AGPAT2 | c.816T>C (p.Ser272=) c.720T>C (p.Ser240=) n.744T>C | gnomAD v4 |
| 9 | g.136673773A>T | CA467736253 | AGPAT2 | c.816T>A (p.Ser272=) c.720T>A (p.Ser240=) n.744T>A | |
| 9 | g.136673774G>A | CA375576128 | AGPAT2 | c.815C>T (p.Ser272Phe) c.719C>T (p.Ser240Phe) n.743C>T | |
| 9 | g.136673774G>C | CA201623549 | AGPAT2 | c.815C>G (p.Ser272Cys) c.719C>G (p.Ser240Cys) n.743C>G | dbSNP gnomAD v4 |
| 9 | g.136673774G>T | CA375576131 | AGPAT2 | c.815C>A (p.Ser272Tyr) c.719C>A (p.Ser240Tyr) n.743C>A | gnomAD v4 |
| 9 | g.136673775A>C | CA375576134 | AGPAT2 | c.814T>G (p.Ser272Ala) c.718T>G (p.Ser240Ala) n.742T>G | |
| 9 | g.136673775A>G | CA375576136 | AGPAT2 | c.814T>C (p.Ser272Pro) c.718T>C (p.Ser240Pro) n.742T>C | gnomAD v4 |
| 9 | g.136673775A>T | CA375576137 | AGPAT2 | c.814T>A (p.Ser272Thr) c.718T>A (p.Ser240Thr) n.742T>A | |
| 9 | g.136673776C>A | CA5342806 | AGPAT2 | c.813G>T (p.Gly271=) c.717G>T (p.Gly239=) n.741G>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136673776C>G | CA467736906 | AGPAT2 | c.813G>C (p.Gly271=) c.717G>C (p.Gly239=) n.741G>C | |
| 9 | g.136673776C>T | CA201626747 | AGPAT2 | c.813G>A (p.Gly271=) c.717G>A (p.Gly239=) n.741G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136673777C>A | CA375577056 | AGPAT2 | c.812G>T (p.Gly271Val) c.716G>T (p.Gly239Val) n.740G>T | gnomAD v4 |
| 9 | g.136673777C>G | CA375577058 | AGPAT2 | c.812G>C (p.Gly271Ala) c.716G>C (p.Gly239Ala) n.740G>C | |
| 9 | g.136673777C>T | CA375577060 | AGPAT2 | c.812G>A (p.Gly271Glu) c.716G>A (p.Gly239Glu) n.740G>A | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.136673778C>A | CA375577062 | AGPAT2 | c.811G>T (p.Gly271Trp) c.715G>T (p.Gly239Trp) n.739G>T | |
| 9 | g.136673778C>G | CA375577064 | AGPAT2 | c.811G>C (p.Gly271Arg) c.715G>C (p.Gly239Arg) n.739G>C | |
| 9 | g.136673778C>T | CA375577066 | AGPAT2 | c.811G>A (p.Gly271Arg) c.715G>A (p.Gly239Arg) n.739G>A | gnomAD v4 |
| 9 | g.136673779C>A | CA467736922 | AGPAT2 | c.810G>T (p.Ala270=) c.714G>T (p.Ala238=) n.738G>T | gnomAD v4 |
| 9 | g.136673779C>G | CA467736924 | AGPAT2 | c.810G>C (p.Ala270=) c.714G>C (p.Ala238=) n.738G>C | |
| 9 | g.136673779C>T | CA5342807 | AGPAT2 | c.810G>A (p.Ala270=) c.714G>A (p.Ala238=) n.738G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136673780G>A | CA5342808 | AGPAT2 | c.809C>T (p.Ala270Val) c.713C>T (p.Ala238Val) n.737C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136673780G>C | CA375577068 | AGPAT2 | c.809C>G (p.Ala270Gly) c.713C>G (p.Ala238Gly) n.737C>G | |
| 9 | g.136673780G>T | CA375577069 | AGPAT2 | c.809C>A (p.Ala270Glu) c.713C>A (p.Ala238Glu) n.737C>A | |
| 9 | g.136673781C>A | CA375577071 | AGPAT2 | c.808G>T (p.Ala270Ser) c.712G>T (p.Ala238Ser) n.736G>T | gnomAD v4 |
| 9 | g.136673781C>G | CA375577072 | AGPAT2 | c.808G>C (p.Ala270Pro) c.712G>C (p.Ala238Pro) n.736G>C | |
| 9 | g.136673781C>T | CA375577073 | AGPAT2 | c.808G>A (p.Ala270Thr) c.712G>A (p.Ala238Thr) n.736G>A | dbSNP gnomAD v4 |
| 9 | g.136673782A>C | CA467736942 | AGPAT2 | c.807T>G (p.Thr269=) c.711T>G (p.Thr237=) n.735T>G | |
| 9 | g.136673782A>G | CA467736944 | AGPAT2 | c.807T>C (p.Thr269=) c.711T>C (p.Thr237=) n.735T>C | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.136673782A>T | CA467736946 | AGPAT2 | c.807T>A (p.Thr269=) c.711T>A (p.Thr237=) n.735T>A | |
| 9 | g.136673783G>A | CA375577074 | AGPAT2 | c.806C>T (p.Thr269Ile) c.710C>T (p.Thr237Ile) n.734C>T | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.136673783G>C | CA375577076 | AGPAT2 | c.806C>G (p.Thr269Ser) c.710C>G (p.Thr237Ser) n.734C>G | |
| 9 | g.136673783G>T | CA375577077 | AGPAT2 | c.806C>A (p.Thr269Asn) c.710C>A (p.Thr237Asn) n.734C>A | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.136673784T>A | CA375577079 | AGPAT2 | c.805A>T (p.Thr269Ser) c.709A>T (p.Thr237Ser) n.733A>T | |
| 9 | g.136673784T>C | CA375577081 | AGPAT2 | c.805A>G (p.Thr269Ala) c.709A>G (p.Thr237Ala) n.733A>G | |
| 9 | g.136673784T>G | CA375577083 | AGPAT2 | c.805A>C (p.Thr269Pro) c.709A>C (p.Thr237Pro) n.733A>C | |
| 9 | g.136673787_136673800del | CA2692653749 | AGPAT2 | c.792_805del (p.Gln264HisfsTer?) c.696_709del (p.Gln232HisfsTer?) n.720_733del | gnomAD v4 |
| 9 | g.136673785G>A | CA467736958 | AGPAT2 | c.804C>T (p.Ala268=) c.708C>T (p.Ala236=) n.732C>T | |
| 9 | g.136673785G>C | CA467736959 | AGPAT2 | c.804C>G (p.Ala268=) c.708C>G (p.Ala236=) n.732C>G | |
| 9 | g.136673785G>T | CA467736960 | AGPAT2 | c.804C>A (p.Ala268=) c.708C>A (p.Ala236=) n.732C>A | |
| 9 | g.136673786G>A | CA5342809 | AGPAT2 | c.803C>T (p.Ala268Val) c.707C>T (p.Ala236Val) n.731C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136673786G>C | CA375577087 | AGPAT2 | c.803C>G (p.Ala268Gly) c.707C>G (p.Ala236Gly) n.731C>G | |
| 9 | g.136673786G>T | CA375577085 | AGPAT2 | c.803C>A (p.Ala268Asp) c.707C>A (p.Ala236Asp) n.731C>A | gnomAD v4 |
| 9 | g.136673787C>A | CA375577090 | AGPAT2 | c.802G>T (p.Ala268Ser) c.706G>T (p.Ala236Ser) n.730G>T | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.136673787C>G | CA375577093 | AGPAT2 | c.802G>C (p.Ala268Pro) c.706G>C (p.Ala236Pro) n.730G>C | dbSNP gnomAD v3 gnomAD v4 |
| 9 | g.136673787C>T | CA375577092 | AGPAT2 | c.802G>A (p.Ala268Thr) c.706G>A (p.Ala236Thr) n.730G>A | gnomAD v4 COSMIC |
| 9 | g.136673790del | CA2692653750 | AGPAT2 | c.802del (p.Ala268ProfsTer19) c.706del (p.Ala236ProfsTer19) n.730del | gnomAD v4 |
| 9 | g.136673788C>A | CA467736962 | AGPAT2 | c.801G>T (p.Gly267=) c.705G>T (p.Gly235=) n.729G>T | gnomAD v4 |
| 9 | g.136673788C>G | CA467736963 | AGPAT2 | c.801G>C (p.Gly267=) c.705G>C (p.Gly235=) n.729G>C | |
| 9 | g.136673788C>T | CA5342810 | AGPAT2 | c.801G>A (p.Gly267=) c.705G>A (p.Gly235=) n.729G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136673789C>A | CA375577098 | AGPAT2 | c.800G>T (p.Gly267Val) c.704G>T (p.Gly235Val) n.728G>T | |
| 9 | g.136673789C>G | CA375577096 | AGPAT2 | c.800G>C (p.Gly267Ala) c.704G>C (p.Gly235Ala) n.728G>C | |
| 9 | g.136673789C>T | CA375577100 | AGPAT2 | c.800G>A (p.Gly267Glu) c.704G>A (p.Gly235Glu) n.728G>A | gnomAD v4 |
| 9 | g.136673789_136673792del | CA591367746 | AGPAT2 | c.797_800del (p.Asn266ArgfsTer20) c.701_704del (p.Asn234ArgfsTer20) n.725_728del | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.136673790C>A | CA375577103 | AGPAT2 | c.799G>T (p.Gly267Trp) c.703G>T (p.Gly235Trp) n.727G>T | gnomAD v4 |
| 9 | g.136673790C>G | CA375577104 | AGPAT2 | c.799G>C (p.Gly267Arg) c.703G>C (p.Gly235Arg) n.727G>C | dbSNP |
| 9 | g.136673790C>T | CA5342811 | AGPAT2 | c.799G>A (p.Gly267Arg) c.703G>A (p.Gly235Arg) n.727G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136673791G>A | CA5342812 | AGPAT2 | c.798C>T (p.Asn266=) c.702C>T (p.Asn234=) n.726C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136673791G>C | CA375577108 | AGPAT2 | c.798C>G (p.Asn266Lys) c.702C>G (p.Asn234Lys) n.726C>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136673791G>T | CA375577111 | AGPAT2 | c.798C>A (p.Asn266Lys) c.702C>A (p.Asn234Lys) n.726C>A | |
| 9 | g.136673792T>A | CA375577113 | AGPAT2 | c.797A>T (p.Asn266Ile) c.701A>T (p.Asn234Ile) n.725A>T | |
| 9 | g.136673792T>C | CA375577114 | AGPAT2 | c.797A>G (p.Asn266Ser) c.701A>G (p.Asn234Ser) n.725A>G | |
| 9 | g.136673792T>G | CA375577115 | AGPAT2 | c.797A>C (p.Asn266Thr) c.701A>C (p.Asn234Thr) n.725A>C | dbSNP gnomAD v4 |
| 9 | g.136673793T>A | CA375577118 | AGPAT2 | c.796A>T (p.Asn266Tyr) c.700A>T (p.Asn234Tyr) n.724A>T | |
| 9 | g.136673793T>C | CA375577119 | AGPAT2 | c.796A>G (p.Asn266Asp) c.700A>G (p.Asn234Asp) n.724A>G | |
| 9 | g.136673793T>G | CA375577121 | AGPAT2 | c.796A>C (p.Asn266His) c.700A>C (p.Asn234His) n.724A>C | |
| 9 | g.136673794C>A | CA375577125 | AGPAT2 | c.795G>T (p.Glu265Asp) c.699G>T (p.Glu233Asp) n.723G>T | gnomAD v4 |
| 9 | g.136673794C>G | CA375577122 | AGPAT2 | c.795G>C (p.Glu265Asp) c.699G>C (p.Glu233Asp) n.723G>C | |
| 9 | g.136673794C>T | CA5342813 | AGPAT2 | c.795G>A (p.Glu265=) c.699G>A (p.Glu233=) n.723G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.136673795T>A | CA375577127 | AGPAT2 | c.794A>T (p.Glu265Val) c.698A>T (p.Glu233Val) n.722A>T | |
| 9 | g.136673795T>C | CA375577128 | AGPAT2 | c.794A>G (p.Glu265Gly) c.698A>G (p.Glu233Gly) n.722A>G | |
| 9 | g.136673795T>G | CA375577130 | AGPAT2 | c.794A>C (p.Glu265Ala) c.698A>C (p.Glu233Ala) n.722A>C | |
| 9 | g.136673795_136673855del | CA2692653751 | AGPAT2 | c.734_794del (p.Val245GlyfsTer22) c.638_698del (p.Val213GlyfsTer22) n.662_722del | gnomAD v4 |
| 9 | g.136673796C>A | CA375577133 | AGPAT2 | c.793G>T (p.Glu265Ter) c.697G>T (p.Glu233Ter) n.721G>T | |
| 9 | g.136673796C>G | CA375577134 | AGPAT2 | c.793G>C (p.Glu265Gln) c.697G>C (p.Glu233Gln) n.721G>C | |
| 9 | g.136673796C>T | CA375577135 | AGPAT2 | c.793G>A (p.Glu265Lys) c.697G>A (p.Glu233Lys) n.721G>A | |
| 9 | g.136673797C>A | CA375577138 | AGPAT2 | c.792G>T (p.Gln264His) c.696G>T (p.Gln232His) n.720G>T | gnomAD v4 |
| 9 | g.136673797C>G | CA375577140 | AGPAT2 | c.792G>C (p.Gln264His) c.696G>C (p.Gln232His) n.720G>C | |
| 9 | g.136673797C>T | CA467736971 | AGPAT2 | c.792G>A (p.Gln264=) c.696G>A (p.Gln232=) n.720G>A | gnomAD v4 |
| 9 | g.136673798T>A | CA375577142 | AGPAT2 | c.791A>T (p.Gln264Leu) c.695A>T (p.Gln232Leu) n.719A>T | |
| 9 | g.136673798T>C | CA375577144 | AGPAT2 | c.791A>G (p.Gln264Arg) c.695A>G (p.Gln232Arg) n.719A>G | |
| 9 | g.136673798T>G | CA375577146 | AGPAT2 | c.791A>C (p.Gln264Pro) c.695A>C (p.Gln232Pro) n.719A>C | |
| 9 | g.136673799G>A | CA5342814 | AGPAT2 | c.790C>T (p.Gln264Ter) c.694C>T (p.Gln232Ter) n.718C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136673799G>C | CA375577148 | AGPAT2 | c.790C>G (p.Gln264Glu) c.694C>G (p.Gln232Glu) n.718C>G | |
| 9 | g.136673799G>T | CA375577147 | AGPAT2 | c.790C>A (p.Gln264Lys) c.694C>A (p.Gln232Lys) n.718C>A | |
| 9 | g.136673804dup | CA2692653752 | AGPAT2 | c.790dup (p.Gln264ProfsTer?) c.694dup (p.Gln232ProfsTer?) n.718dup | gnomAD v4 |
| 9 | g.136673804del | CA2692653753 | AGPAT2 | c.790del (p.Gln264ArgfsTer23) c.694del (p.Gln232ArgfsTer23) n.718del | gnomAD v4 |
| 9 | g.136673800G>A | CA201626782 | AGPAT2 | c.789C>T (p.Pro263=) c.693C>T (p.Pro231=) n.717C>T | dbSNP |
| 9 | g.136673800G>C | CA467736976 | AGPAT2 | c.789C>G (p.Pro263=) c.693C>G (p.Pro231=) n.717C>G | |
| 9 | g.136673800G>T | CA5342815 | AGPAT2 | c.789C>A (p.Pro263=) c.693C>A (p.Pro231=) n.717C>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136673801G>A | CA5342816 | AGPAT2 | c.788C>T (p.Pro263Leu) c.692C>T (p.Pro231Leu) n.716C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136673801G>C | CA375577152 | AGPAT2 | c.788C>G (p.Pro263Arg) c.692C>G (p.Pro231Arg) n.716C>G | ClinVar |
| 9 | g.136673801G= | CA2580903229 | AGPAT2 | c.788C= (p.Pro263=) c.692C= (p.Pro231=) n.716C= | |
| 9 | g.136673801G>T | CA375577153 | AGPAT2 | c.788C>A (p.Pro263His) c.692C>A (p.Pro231His) n.716C>A | |
| 9 | g.136673802G>A | CA375577155 | AGPAT2 | c.787C>T (p.Pro263Ser) c.691C>T (p.Pro231Ser) n.715C>T | |
| 9 | g.136673802G>C | CA375577157 | AGPAT2 | c.787C>G (p.Pro263Ala) c.691C>G (p.Pro231Ala) n.715C>G | gnomAD v4 |
| 9 | g.136673802G>T | CA375577159 | AGPAT2 | c.787C>A (p.Pro263Thr) c.691C>A (p.Pro231Thr) n.715C>A | |
| 9 | g.136673803G>A | CA5342817 | AGPAT2 | c.786C>T (p.Thr262=) c.690C>T (p.Thr230=) n.714C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136673803G>C | CA467736979 | AGPAT2 | c.786C>G (p.Thr262=) c.690C>G (p.Thr230=) n.714C>G | |
| 9 | g.136673803G>T | CA5342818 | AGPAT2 | c.786C>A (p.Thr262=) c.690C>A (p.Thr230=) n.714C>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136673804G>A | CA5342819 | AGPAT2 | c.785C>T (p.Thr262Ile) c.689C>T (p.Thr230Ile) n.713C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136673804G>C | CA375577164 | AGPAT2 | c.785C>G (p.Thr262Ser) c.689C>G (p.Thr230Ser) n.713C>G | |
| 9 | g.136673804G>T | CA375577166 | AGPAT2 | c.785C>A (p.Thr262Asn) c.689C>A (p.Thr230Asn) n.713C>A | gnomAD v4 |
| 9 | g.136673805T>A | CA375577170 | AGPAT2 | c.784A>T (p.Thr262Ser) c.688A>T (p.Thr230Ser) n.712A>T | |
| 9 | g.136673805T>C | CA375577172 | AGPAT2 | c.784A>G (p.Thr262Ala) c.688A>G (p.Thr230Ala) n.712A>G | |
| 9 | g.136673805T>G | CA375577168 | AGPAT2 | c.784A>C (p.Thr262Pro) c.688A>C (p.Thr230Pro) n.712A>C | |
| 9 | g.136673806C>A | CA375577174 | AGPAT2 | c.783G>T (p.Lys261Asn) c.687G>T (p.Lys229Asn) n.711G>T | gnomAD v4 |
| 9 | g.136673806C>G | CA375577176 | AGPAT2 | c.783G>C (p.Lys261Asn) c.687G>C (p.Lys229Asn) n.711G>C | |
| 9 | g.136673806C>T | CA5342820 | AGPAT2 | c.783G>A (p.Lys261=) c.687G>A (p.Lys229=) n.711G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136673807T>A | CA375577179 | AGPAT2 | c.782A>T (p.Lys261Met) c.686A>T (p.Lys229Met) n.710A>T | |
| 9 | g.136673807T>C | CA5342821 | AGPAT2 | c.782A>G (p.Lys261Arg) c.686A>G (p.Lys229Arg) n.710A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 9 | g.136673807T>G | CA375577182 | AGPAT2 | c.782A>C (p.Lys261Thr) c.686A>C (p.Lys229Thr) n.710A>C | |
| 9 | g.136673808T>A | CA375577187 | AGPAT2 | c.781A>T (p.Lys261Ter) c.685A>T (p.Lys229Ter) n.709A>T | |
| 9 | g.136673808T>C | CA5342822 | AGPAT2 | c.781A>G (p.Lys261Glu) c.685A>G (p.Lys229Glu) n.709A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
| 9 | g.136673808T>G | CA375577185 | AGPAT2 | c.781A>C (p.Lys261Gln) c.685A>C (p.Lys229Gln) n.709A>C | |
| 9 | g.136673809G>A | CA201626808 | AGPAT2 | c.780C>T (p.Ser260=) c.684C>T (p.Ser228=) n.708C>T | dbSNP gnomAD v4 |
| 9 | g.136673809G>C | CA467736986 | AGPAT2 | c.780C>G (p.Ser260=) c.684C>G (p.Ser228=) n.708C>G | dbSNP gnomAD v2 gnomAD v4 |
| 9 | g.136673809G>T | CA467736985 | AGPAT2 | c.780C>A (p.Ser260=) c.684C>A (p.Ser228=) n.708C>A |