Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.136673858_136673873dup | CA2692653759 | AGPAT2 | c.718_733dup (p.Val245GlyfsTer?) c.622_637dup (p.Val213GlyfsTer?) n.646_661dup | gnomAD v4 |
9 | g.136673857_136673874dup | CA591367750 | AGPAT2 | c.716_733dup (p.Leu244_Val245insAlaAspValProAlaLeu) c.620_637dup (p.Leu212_Val213insAlaAspValProAlaLeu) n.644_661dup | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136673858_136673876dup | CA2692653760 | AGPAT2 | c.715_733dup (p.Val245GlyfsTer?) c.619_637dup (p.Val213GlyfsTer?) n.643_661dup | gnomAD v4 |
9 | g.136673875_136673876insTCACTGGACGTCCGCC | CA2692653764 | AGPAT2 | c.724_725insAGTGAGGCGGACGTCC (p.Pro242GlnfsTer2) c.628_629insAGTGAGGCGGACGTCC (p.Pro210GlnfsTer2) n.652_653insAGTGAGGCGGACGTCC | gnomAD v4 |
9 | g.136673867_136673873dup | CA2692653765 | AGPAT2 | c.717_723dup (p.Pro242GlyfsTer?) c.621_627dup (p.Pro210GlyfsTer?) n.645_651dup | gnomAD v4 |
9 | g.136673869_136673874dup | CA2692653766 | AGPAT2 | c.716_721dup (p.Asp240_Val241insAlaAsp) c.620_625dup (p.Asp208_Val209insAlaAsp) n.644_649dup | gnomAD v4 |
9 | g.136673870_136673887dup | CA2692653767 | AGPAT2 | c.704_721dup (p.Asp240_Val241insGlyLeuThrAlaAlaAsp) c.608_625dup (p.Asp208_Val209insGlyLeuThrAlaAlaAsp) n.632_649dup | gnomAD v4 |
9 | g.136673871C>A | CA375577472 | AGPAT2 | c.718G>T (p.Asp240Tyr) c.622G>T (p.Asp208Tyr) n.646G>T | gnomAD v4 |
9 | g.136673871C>G | CA375577476 | AGPAT2 | c.718G>C (p.Asp240His) c.622G>C (p.Asp208His) n.646G>C | |
9 | g.136673871C>T | CA375577475 | AGPAT2 | c.718G>A (p.Asp240Asn) c.622G>A (p.Asp208Asn) n.646G>A | |
9 | g.136673872_136673875dup | CA591367757 | AGPAT2 | c.715_718dup (p.Asp240GlyfsTer?) c.619_622dup (p.Asp208GlyfsTer?) n.643_646dup | dbSNP gnomAD v2 gnomAD v4 |
9 | g.136673875_136673888del | CA1130033196 | AGPAT2 | c.705_718del (p.Leu236ArgfsTer?) c.609_622del (p.Leu204ArgfsTer?) n.633_646del | gnomAD v3 gnomAD v4 |
9 | g.136673872C>A | CA467737091 | AGPAT2 | c.717G>T (p.Ala239=) c.621G>T (p.Ala207=) n.645G>T | gnomAD v4 |
9 | g.136673872C>G | CA467737095 | AGPAT2 | c.717G>C (p.Ala239=) c.621G>C (p.Ala207=) n.645G>C | |
9 | g.136673872C>T | CA5342844 | AGPAT2 | c.717G>A (p.Ala239=) c.621G>A (p.Ala207=) n.645G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136673873G>A | CA5342845 | AGPAT2 | c.716C>T (p.Ala239Val) c.620C>T (p.Ala207Val) n.644C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136673873G>C | CA375577479 | AGPAT2 | c.716C>G (p.Ala239Gly) c.620C>G (p.Ala207Gly) n.644C>G | dbSNP gnomAD v2 gnomAD v4 |
9 | g.136673873G>T | CA375577480 | AGPAT2 | c.716C>A (p.Ala239Glu) c.620C>A (p.Ala207Glu) n.644C>A | gnomAD v4 |
9 | g.136673873dup | CA2579519884 | AGPAT2 | c.716dup (p.Asp240GlyfsTer?) c.620dup (p.Asp208GlyfsTer?) n.644dup | |
9 | g.136673874C>A | CA375577484 | AGPAT2 | c.715G>T (p.Ala239Ser) c.619G>T (p.Ala207Ser) n.643G>T | |
9 | g.136673874C>G | CA375577487 | AGPAT2 | c.715G>C (p.Ala239Pro) c.619G>C (p.Ala207Pro) n.643G>C | |
9 | g.136673874C>T | CA375577491 | AGPAT2 | c.715G>A (p.Ala239Thr) c.619G>A (p.Ala207Thr) n.643G>A | gnomAD v4 |
9 | g.136673875dup | CA591367763 | AGPAT2 | c.715dup (p.Ala239GlyfsTer?) c.619dup (p.Ala207GlyfsTer?) n.643dup | dbSNP gnomAD v2 gnomAD v4 |
9 | g.136673875C>A | CA467737117 | AGPAT2 | c.714G>T (p.Ala238=) c.618G>T (p.Ala206=) n.642G>T | gnomAD v4 |
9 | g.136673875C>G | CA467737119 | AGPAT2 | c.714G>C (p.Ala238=) c.618G>C (p.Ala206=) n.642G>C | dbSNP gnomAD v4 |
9 | g.136673875C>T | CA5342846 | AGPAT2 | c.714G>A (p.Ala238=) c.618G>A (p.Ala206=) n.642G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
9 | g.136673876G>A | CA5342847 | AGPAT2 | c.713C>T (p.Ala238Val) c.617C>T (p.Ala206Val) n.641C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
9 | g.136673876G>C | CA5342848 | AGPAT2 | c.713C>G (p.Ala238Gly) c.617C>G (p.Ala206Gly) n.641C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136673876G>T | CA375577502 | AGPAT2 | c.713C>A (p.Ala238Glu) c.617C>A (p.Ala206Glu) n.641C>A | gnomAD v4 |
9 | g.136673877_136673879del | CA591367767 | AGPAT2 | c.711_713del (p.Ala238del) c.615_617del (p.Ala206del) n.639_641del | dbSNP gnomAD v2 gnomAD v4 |
9 | g.136673877_136673881del | CA1130033214 | AGPAT2 | c.709_713del (p.Thr237GlyfsTer?) c.613_617del (p.Thr205GlyfsTer?) n.637_641del | gnomAD v3 gnomAD v4 |
9 | g.136673877C>A | CA375577512 | AGPAT2 | c.712G>T (p.Ala238Ser) c.616G>T (p.Ala206Ser) n.640G>T | |
9 | g.136673877C>G | CA375577509 | AGPAT2 | c.712G>C (p.Ala238Pro) c.616G>C (p.Ala206Pro) n.640G>C | |
9 | g.136673877C>T | CA375577507 | AGPAT2 | c.712G>A (p.Ala238Thr) c.616G>A (p.Ala206Thr) n.640G>A | gnomAD v4 COSMIC |
9 | g.136673878_136673886del | CA2579519885 | AGPAT2 | c.704_712del (p.Gly235_Thr237del) c.608_616del (p.Gly203_Thr205del) n.632_640del | |
9 | g.136673878A>C | CA467737132 | AGPAT2 | c.711T>G (p.Thr237=) c.615T>G (p.Thr205=) n.639T>G | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136673878A>G | CA5342849 | AGPAT2 | c.711T>C (p.Thr237=) c.615T>C (p.Thr205=) n.639T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136673878A>T | CA467737135 | AGPAT2 | c.711T>A (p.Thr237=) c.615T>A (p.Thr205=) n.639T>A | gnomAD v4 |
9 | g.136673879del | CA861080724 | AGPAT2 | c.710del (p.Thr237MetfsTer16) c.614del (p.Thr205MetfsTer16) n.638del | dbSNP gnomAD v4 |
9 | g.136673879G>A | CA375577516 | AGPAT2 | c.710C>T (p.Thr237Ile) c.614C>T (p.Thr205Ile) n.638C>T | gnomAD v4 |
9 | g.136673879G>C | CA375577518 | AGPAT2 | c.710C>G (p.Thr237Ser) c.614C>G (p.Thr205Ser) n.638C>G | |
9 | g.136673879G>T | CA375577520 | AGPAT2 | c.710C>A (p.Thr237Asn) c.614C>A (p.Thr205Asn) n.638C>A | |
9 | g.136673880T>A | CA375577525 | AGPAT2 | c.709A>T (p.Thr237Ser) c.613A>T (p.Thr205Ser) n.637A>T | |
9 | g.136673880T>C | CA375577528 | AGPAT2 | c.709A>G (p.Thr237Ala) c.613A>G (p.Thr205Ala) n.637A>G | |
9 | g.136673880T>G | CA375577531 | AGPAT2 | c.709A>C (p.Thr237Pro) c.613A>C (p.Thr205Pro) n.637A>C | |
9 | g.136673881G>A | CA467737143 | AGPAT2 | c.708C>T (p.Leu236=) c.612C>T (p.Leu204=) n.636C>T | |
9 | g.136673881G>C | CA467737145 | AGPAT2 | c.708C>G (p.Leu236=) c.612C>G (p.Leu204=) n.636C>G | |
9 | g.136673881G>T | CA467737146 | AGPAT2 | c.708C>A (p.Leu236=) c.612C>A (p.Leu204=) n.636C>A | gnomAD v4 |
9 | g.136673882A>C | CA375577534 | AGPAT2 | c.707T>G (p.Leu236Arg) c.611T>G (p.Leu204Arg) n.635T>G | |
9 | g.136673882A>G | CA375577537 | AGPAT2 | c.707T>C (p.Leu236Pro) c.611T>C (p.Leu204Pro) n.635T>C | gnomAD v4 |
9 | g.136673882A>T | CA375577540 | AGPAT2 | c.707T>A (p.Leu236His) c.611T>A (p.Leu204His) n.635T>A | |
9 | g.136673883G>A | CA5342850 | AGPAT2 | c.706C>T (p.Leu236Phe) c.610C>T (p.Leu204Phe) n.634C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136673883G>C | CA375577545 | AGPAT2 | c.706C>G (p.Leu236Val) c.610C>G (p.Leu204Val) n.634C>G | gnomAD v4 |
9 | g.136673883G>T | CA375577548 | AGPAT2 | c.706C>A (p.Leu236Ile) c.610C>A (p.Leu204Ile) n.634C>A | gnomAD v4 |
9 | g.136673884G>A | CA467737152 | AGPAT2 | c.705C>T (p.Gly235=) c.609C>T (p.Gly203=) n.633C>T | dbSNP gnomAD v2 gnomAD v4 |
9 | g.136673884G>C | CA467737154 | AGPAT2 | c.705C>G (p.Gly235=) c.609C>G (p.Gly203=) n.633C>G | |
9 | g.136673884G>T | CA467737156 | AGPAT2 | c.705C>A (p.Gly235=) c.609C>A (p.Gly203=) n.633C>A | gnomAD v4 |
9 | g.136673884_136673885del | CA2692653768 | AGPAT2 | c.704_705del (p.Gly235AlafsTer?) c.608_609del (p.Gly203AlafsTer?) n.632_633del | gnomAD v4 |
9 | g.136673885C>A | CA375577556 | AGPAT2 | c.704G>T (p.Gly235Val) c.608G>T (p.Gly203Val) n.632G>T | gnomAD v4 |
9 | g.136673885C>G | CA375577552 | AGPAT2 | c.704G>C (p.Gly235Ala) c.608G>C (p.Gly203Ala) n.632G>C | gnomAD v4 |
9 | g.136673885C>T | CA375577555 | AGPAT2 | c.704G>A (p.Gly235Asp) c.608G>A (p.Gly203Asp) n.632G>A | gnomAD v4 |
9 | g.136673886dup | CA2692653769 | AGPAT2 | c.704dup (p.Leu236ProfsTer?) c.608dup (p.Leu204ProfsTer?) n.632dup | gnomAD v4 |
9 | g.136673886C>A | CA375577561 | AGPAT2 | c.703G>T (p.Gly235Cys) c.607G>T (p.Gly203Cys) n.631G>T | gnomAD v4 |
9 | g.136673886C>G | CA375577564 | AGPAT2 | c.703G>C (p.Gly235Arg) c.607G>C (p.Gly203Arg) n.631G>C | |
9 | g.136673886C>T | CA5342851 | AGPAT2 | c.703G>A (p.Gly235Ser) c.607G>A (p.Gly203Ser) n.631G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136673887G>A | CA151608 | AGPAT2 | c.702C>T (p.Ser234=) c.606C>T (p.Ser202=) n.630C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136673887G>C | CA375577571 | AGPAT2 | c.702C>G (p.Ser234Arg) c.606C>G (p.Ser202Arg) n.630C>G | |
9 | g.136673887G>T | CA375577575 | AGPAT2 | c.702C>A (p.Ser234Arg) c.606C>A (p.Ser202Arg) n.630C>A | gnomAD v4 |
9 | g.136673888C>A | CA375577578 | AGPAT2 | c.701G>T (p.Ser234Ile) c.605G>T (p.Ser202Ile) n.629G>T | |
9 | g.136673888C>G | CA375577581 | AGPAT2 | c.701G>C (p.Ser234Thr) c.605G>C (p.Ser202Thr) n.629G>C | |
9 | g.136673888C>T | CA375577584 | AGPAT2 | c.701G>A (p.Ser234Asn) c.605G>A (p.Ser202Asn) n.629G>A | |
9 | g.136673889_136673905del | CA2692653770 | AGPAT2 | c.685_701del (p.Glu229ArgfsTer?) c.589_605del (p.Glu197ArgfsTer?) n.613_629del | gnomAD v4 |
9 | g.136673889T>A | CA375577588 | AGPAT2 | c.700A>T (p.Ser234Cys) c.604A>T (p.Ser202Cys) n.628A>T | |
9 | g.136673889T>C | CA375577590 | AGPAT2 | c.700A>G (p.Ser234Gly) c.604A>G (p.Ser202Gly) n.628A>G | gnomAD v4 |
9 | g.136673889T>G | CA375577594 | AGPAT2 | c.700A>C (p.Ser234Arg) c.604A>C (p.Ser202Arg) n.628A>C | |
9 | g.136673890G>A | CA467737165 | AGPAT2 | c.699C>T (p.Thr233=) c.603C>T (p.Thr201=) n.627C>T | gnomAD v4 |
9 | g.136673890G>C | CA467737166 | AGPAT2 | c.699C>G (p.Thr233=) c.603C>G (p.Thr201=) n.627C>G | |
9 | g.136673890G>T | CA467737167 | AGPAT2 | c.699C>A (p.Thr233=) c.603C>A (p.Thr201=) n.627C>A | gnomAD v4 |
9 | g.136673891G>A | CA5342852 | AGPAT2 | c.698C>T (p.Thr233Ile) c.602C>T (p.Thr201Ile) n.626C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136673891G>C | CA375577600 | AGPAT2 | c.698C>G (p.Thr233Ser) c.602C>G (p.Thr201Ser) n.626C>G | |
9 | g.136673891G>T | CA375577599 | AGPAT2 | c.698C>A (p.Thr233Asn) c.602C>A (p.Thr201Asn) n.626C>A | ClinVar dbSNP gnomAD v4 |
9 | g.136673892T>A | CA375577605 | AGPAT2 | c.697A>T (p.Thr233Ser) c.601A>T (p.Thr201Ser) n.625A>T | |
9 | g.136673892T>C | CA375577610 | AGPAT2 | c.697A>G (p.Thr233Ala) c.601A>G (p.Thr201Ala) n.625A>G | |
9 | g.136673892T>G | CA375577607 | AGPAT2 | c.697A>C (p.Thr233Pro) c.601A>C (p.Thr201Pro) n.625A>C | |
9 | g.136673893G>A | CA467737170 | AGPAT2 | c.696C>T (p.Pro232=) c.600C>T (p.Pro200=) n.624C>T | gnomAD v4 |
9 | g.136673893G>C | CA467737174 | AGPAT2 | c.696C>G (p.Pro232=) c.600C>G (p.Pro200=) n.624C>G | |
9 | g.136673893G>T | CA467737172 | AGPAT2 | c.696C>A (p.Pro232=) c.600C>A (p.Pro200=) n.624C>A | |
9 | g.136673894G>A | CA375577613 | AGPAT2 | c.695C>T (p.Pro232Leu) c.599C>T (p.Pro200Leu) n.623C>T | gnomAD v4 |
9 | g.136673894G>C | CA375577617 | AGPAT2 | c.695C>G (p.Pro232Arg) c.599C>G (p.Pro200Arg) n.623C>G | |
9 | g.136673894G>T | CA375577615 | AGPAT2 | c.695C>A (p.Pro232His) c.599C>A (p.Pro200His) n.623C>A | gnomAD v4 |
9 | g.136673895G>A | CA375577620 | AGPAT2 | c.694C>T (p.Pro232Ser) c.598C>T (p.Pro200Ser) n.622C>T | gnomAD v4 |
9 | g.136673895G>C | CA375577622 | AGPAT2 | c.694C>G (p.Pro232Ala) c.598C>G (p.Pro200Ala) n.622C>G | |
9 | g.136673895G>T | CA375577625 | AGPAT2 | c.694C>A (p.Pro232Thr) c.598C>A (p.Pro200Thr) n.622C>A | |
9 | g.136673896G>A | CA467737175 | AGPAT2 | c.693C>T (p.Ile231=) c.597C>T (p.Ile199=) n.621C>T | gnomAD v4 |
9 | g.136673896G>C | CA375577632 | AGPAT2 | c.693C>G (p.Ile231Met) c.597C>G (p.Ile199Met) n.621C>G | |
9 | g.136673896G>T | CA467737176 | AGPAT2 | c.693C>A (p.Ile231=) c.597C>A (p.Ile199=) n.621C>A | |
9 | g.136673897A>C | CA375577635 | AGPAT2 | c.692T>G (p.Ile231Ser) c.596T>G (p.Ile199Ser) n.620T>G | |
9 | g.136673897A>G | CA5342853 | AGPAT2 | c.692T>C (p.Ile231Thr) c.596T>C (p.Ile199Thr) n.620T>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.136673897A>T | CA375577636 | AGPAT2 | c.692T>A (p.Ile231Asn) c.596T>A (p.Ile199Asn) n.620T>A | dbSNP gnomAD v4 |
9 | g.136673898T>A | CA375577640 | AGPAT2 | c.691A>T (p.Ile231Phe) c.595A>T (p.Ile199Phe) n.619A>T | gnomAD v4 |
9 | g.136673898T>C | CA375577643 | AGPAT2 | c.691A>G (p.Ile231Val) c.595A>G (p.Ile199Val) n.619A>G | |
9 | g.136673898T>G | CA375577646 | AGPAT2 | c.691A>C (p.Ile231Leu) c.595A>C (p.Ile199Leu) n.619A>C | |
9 | g.136673899G>A | CA467737179 | AGPAT2 | c.690C>T (p.Ala230=) c.594C>T (p.Ala198=) n.618C>T | gnomAD v4 |
9 | g.136673899G>C | CA467737177 | AGPAT2 | c.690C>G (p.Ala230=) c.594C>G (p.Ala198=) n.618C>G | |
9 | g.136673899G>T | CA467737178 | AGPAT2 | c.690C>A (p.Ala230=) c.594C>A (p.Ala198=) n.618C>A | |
9 | g.136673900G>A | CA375577651 | AGPAT2 | c.689C>T (p.Ala230Val) c.593C>T (p.Ala198Val) n.617C>T | gnomAD v4 |
9 | g.136673900G>C | CA375577653 | AGPAT2 | c.689C>G (p.Ala230Gly) c.593C>G (p.Ala198Gly) n.617C>G | |
9 | g.136673900G>T | CA375577654 | AGPAT2 | c.689C>A (p.Ala230Asp) c.593C>A (p.Ala198Asp) n.617C>A | gnomAD v4 |
9 | g.136673901C>A | CA375577662 | AGPAT2 | c.688G>T (p.Ala230Ser) c.592G>T (p.Ala198Ser) n.616G>T | gnomAD v4 |
9 | g.136673901C>G | CA375577658 | AGPAT2 | c.688G>C (p.Ala230Pro) c.592G>C (p.Ala198Pro) n.616G>C | |
9 | g.136673901C>T | CA375577656 | AGPAT2 | c.688G>A (p.Ala230Thr) c.592G>A (p.Ala198Thr) n.616G>A | gnomAD v4 |
9 | g.136673902T>A | CA375577665 | AGPAT2 | c.687A>T (p.Glu229Asp) c.591A>T (p.Glu197Asp) n.615A>T | |
9 | g.136673902T>C | CA467737180 | AGPAT2 | c.687A>G (p.Glu229=) c.591A>G (p.Glu197=) n.615A>G | gnomAD v4 |
9 | g.136673902T>G | CA375577667 | AGPAT2 | c.687A>C (p.Glu229Asp) c.591A>C (p.Glu197Asp) n.615A>C | |
9 | g.136673903del | CA2692653771 | AGPAT2 | c.687del (p.Ala230ProfsTer23) c.591del (p.Ala198ProfsTer23) n.615del | gnomAD v4 |
9 | g.136673903T>A | CA375577671 | AGPAT2 | c.686A>T (p.Glu229Val) c.590A>T (p.Glu197Val) n.614A>T | |
9 | g.136673903T>C | CA375577673 | AGPAT2 | c.686A>G (p.Glu229Gly) c.590A>G (p.Glu197Gly) n.614A>G | |
9 | g.136673903T>G | CA375577676 | AGPAT2 | c.686A>C (p.Glu229Ala) c.590A>C (p.Glu197Ala) n.614A>C | |
9 | g.136673904C>A | CA375577678 | AGPAT2 | c.685G>T (p.Glu229Ter) c.589G>T (p.Glu197Ter) n.613G>T | ClinVar dbSNP gnomAD v4 |
9 | g.136673904C>G | CA375577679 | AGPAT2 | c.685G>C (p.Glu229Gln) c.589G>C (p.Glu197Gln) n.613G>C | |
9 | g.136673904C>T | CA375577680 | AGPAT2 | c.685G>A (p.Glu229Lys) c.589G>A (p.Glu197Lys) n.613G>A | dbSNP gnomAD v2 |
9 | g.136673905C>A | CA467737181 | AGPAT2 | c.684G>T (p.Leu228=) c.588G>T (p.Leu196=) n.612G>T | gnomAD v4 |
9 | g.136673905C>G | CA467737182 | AGPAT2 | c.684G>C (p.Leu228=) c.588G>C (p.Leu196=) n.612G>C | |
9 | g.136673905C>T | CA467737183 | AGPAT2 | c.684G>A (p.Leu228=) c.588G>A (p.Leu196=) n.612G>A | gnomAD v4 |
9 | g.136673906A>C | CA375577681 | AGPAT2 | c.683T>G (p.Leu228Arg) c.587T>G (p.Leu196Arg) n.611T>G | |
9 | g.136673906A>G | CA277946 | AGPAT2 | c.683T>C (p.Leu228Pro) c.587T>C (p.Leu196Pro) n.611T>C | ClinVar dbSNP gnomAD v4 |
9 | g.136673906A>T | CA375577682 | AGPAT2 | c.683T>A (p.Leu228Gln) c.587T>A (p.Leu196Gln) n.611T>A | |
9 | g.136673907G>A | CA467737186 | AGPAT2 | c.682C>T (p.Leu228=) c.586C>T (p.Leu196=) n.610C>T | gnomAD v4 |
9 | g.136673907G>C | CA375577687 | AGPAT2 | c.682C>G (p.Leu228Val) c.586C>G (p.Leu196Val) n.610C>G | gnomAD v4 |
9 | g.136673907G>T | CA375577690 | AGPAT2 | c.682C>A (p.Leu228Met) c.586C>A (p.Leu196Met) n.610C>A | |
9 | g.136673908C>A | CA467737190 | AGPAT2 | c.681G>T (p.Val227=) c.585G>T (p.Val195=) n.609G>T | gnomAD v4 |
9 | g.136673908C>G | CA467737192 | AGPAT2 | c.681G>C (p.Val227=) c.585G>C (p.Val195=) n.609G>C | |
9 | g.136673908C>T | CA467737194 | AGPAT2 | c.681G>A (p.Val227=) c.585G>A (p.Val195=) n.609G>A | dbSNP gnomAD v2 gnomAD v4 |
9 | g.136673908_136673922del | CA2692653772 | AGPAT2 | c.667_681del (p.Val223_Val227del) c.571_585del (p.Val191_Val195del) n.595_609del | gnomAD v4 |
9 | g.136673909A>C | CA375577703 | AGPAT2 | c.680T>G (p.Val227Gly) c.584T>G (p.Val195Gly) n.608T>G | |
9 | g.136673909A>G | CA375577709 | AGPAT2 | c.680T>C (p.Val227Ala) c.584T>C (p.Val195Ala) n.608T>C | gnomAD v4 |
9 | g.136673909A>T | CA375577694 | AGPAT2 | c.680T>A (p.Val227Glu) c.584T>A (p.Val195Glu) n.608T>A | |
9 | g.136673910C>A | CA375577715 | AGPAT2 | c.679G>T (p.Val227Leu) c.583G>T (p.Val195Leu) n.607G>T | |
9 | g.136673910C>G | CA375577717 | AGPAT2 | c.679G>C (p.Val227Leu) c.583G>C (p.Val195Leu) n.607G>C | |
9 | g.136673910C>T | CA5342854 | AGPAT2 | c.679G>A (p.Val227Met) c.583G>A (p.Val195Met) n.607G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.136673911C>A | CA375577721 | AGPAT2 | c.678G>T (p.Gln226His) c.582G>T (p.Gln194His) n.606G>T | gnomAD v4 |
9 | g.136673911C>G | CA375577722 | AGPAT2 | c.678G>C (p.Gln226His) c.582G>C (p.Gln194His) n.606G>C | |
9 | g.136673911C>T | CA467737204 | AGPAT2 | c.678G>A (p.Gln226=) c.582G>A (p.Gln194=) n.606G>A | ClinVar dbSNP gnomAD v2 gnomAD v4 |
9 | g.136673912T>A | CA375577726 | AGPAT2 | c.677A>T (p.Gln226Leu) c.581A>T (p.Gln194Leu) n.605A>T | gnomAD v4 |
9 | g.136673912T>C | CA375577730 | AGPAT2 | c.677A>G (p.Gln226Arg) c.581A>G (p.Gln194Arg) n.605A>G | dbSNP gnomAD v4 |
9 | g.136673912T>G | CA375577734 | AGPAT2 | c.677A>C (p.Gln226Pro) c.581A>C (p.Gln194Pro) n.605A>C | |
9 | g.136673913G>A | CA16042193 | AGPAT2 | c.676C>T (p.Gln226Ter) c.580C>T (p.Gln194Ter) n.604C>T | ClinVar dbSNP gnomAD v4 |
9 | g.136673913G>C | CA375577739 | AGPAT2 | c.676C>G (p.Gln226Glu) c.580C>G (p.Gln194Glu) n.604C>G | |
9 | g.136673913G>T | CA375577742 | AGPAT2 | c.676C>A (p.Gln226Lys) c.580C>A (p.Gln194Lys) n.604C>A | gnomAD v4 |
9 | g.136673914C>A | CA467737213 | AGPAT2 | c.675G>T (p.Val225=) c.579G>T (p.Val193=) n.603G>T | gnomAD v4 |
9 | g.136673914C>G | CA5342855 | AGPAT2 | c.675G>C (p.Val225=) c.579G>C (p.Val193=) n.603G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.136673914C>T | CA5342856 | AGPAT2 | c.675G>A (p.Val225=) c.579G>A (p.Val193=) n.603G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.136673915A>C | CA375577747 | AGPAT2 | c.674T>G (p.Val225Gly) c.578T>G (p.Val193Gly) n.602T>G | |
9 | g.136673915A>G | CA5342857 | AGPAT2 | c.674T>C (p.Val225Ala) c.578T>C (p.Val193Ala) n.602T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136673915A>T | CA375577750 | AGPAT2 | c.674T>A (p.Val225Glu) c.578T>A (p.Val193Glu) n.602T>A | |
9 | g.136673916C>A | CA375577751 | AGPAT2 | c.673G>T (p.Val225Leu) c.577G>T (p.Val193Leu) n.601G>T | gnomAD v4 |
9 | g.136673916C>G | CA375577753 | AGPAT2 | c.673G>C (p.Val225Leu) c.577G>C (p.Val193Leu) n.601G>C | gnomAD v4 |
9 | g.136673916C>T | CA375577759 | AGPAT2 | c.673G>A (p.Val225Met) c.577G>A (p.Val193Met) n.601G>A | gnomAD v4 |
9 | g.136673917T>A | CA467737228 | AGPAT2 | c.672A>T (p.Thr224=) c.576A>T (p.Thr192=) n.600A>T | |
9 | g.136673917T>C | CA467737235 | AGPAT2 | c.672A>G (p.Thr224=) c.576A>G (p.Thr192=) n.600A>G | |
9 | g.136673917T>G | CA467737231 | AGPAT2 | c.672A>C (p.Thr224=) c.576A>C (p.Thr192=) n.600A>C | |
9 | g.136673918G>A | CA375577763 | AGPAT2 | c.671C>T (p.Thr224Ile) c.575C>T (p.Thr192Ile) n.599C>T | gnomAD v4 |
9 | g.136673918G>C | CA201626932 | AGPAT2 | c.671C>G (p.Thr224Arg) c.575C>G (p.Thr192Arg) n.599C>G | dbSNP |
9 | g.136673918G>T | CA375577767 | AGPAT2 | c.671C>A (p.Thr224Lys) c.575C>A (p.Thr192Lys) n.599C>A | gnomAD v4 |
9 | g.136673919T>A | CA375577768 | AGPAT2 | c.670A>T (p.Thr224Ser) c.574A>T (p.Thr192Ser) n.598A>T | |
9 | g.136673919T>C | CA375577769 | AGPAT2 | c.670A>G (p.Thr224Ala) c.574A>G (p.Thr192Ala) n.598A>G | gnomAD v4 |
9 | g.136673919T>G | CA375577770 | AGPAT2 | c.670A>C (p.Thr224Pro) c.574A>C (p.Thr192Pro) n.598A>C | |
9 | g.136673920G>A | CA201626936 | AGPAT2 | c.669C>T (p.Val223=) c.573C>T (p.Val191=) n.597C>T | dbSNP gnomAD v2 gnomAD v4 |
9 | g.136673920G>C | CA467737257 | AGPAT2 | c.669C>G (p.Val223=) c.573C>G (p.Val191=) n.597C>G | |
9 | g.136673920G>T | CA467737260 | AGPAT2 | c.669C>A (p.Val223=) c.573C>A (p.Val191=) n.597C>A | gnomAD v4 |
9 | g.136673921A>C | CA375577778 | AGPAT2 | c.668T>G (p.Val223Gly) c.572T>G (p.Val191Gly) n.596T>G | |
9 | g.136673921A>G | CA375577775 | AGPAT2 | c.668T>C (p.Val223Ala) c.572T>C (p.Val191Ala) n.596T>C | dbSNP gnomAD v4 |
9 | g.136673921A>T | CA375577773 | AGPAT2 | c.668T>A (p.Val223Asp) c.572T>A (p.Val191Asp) n.596T>A | gnomAD v4 |
9 | g.136673922C>A | CA375577781 | AGPAT2 | c.667G>T (p.Val223Phe) c.571G>T (p.Val191Phe) n.595G>T | gnomAD v4 |
9 | g.136673922C>G | CA201626941 | AGPAT2 | c.667G>C (p.Val223Leu) c.571G>C (p.Val191Leu) n.595G>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136673922C>T | CA375577791 | AGPAT2 | c.667G>A (p.Val223Ile) c.571G>A (p.Val191Ile) n.595G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136673923T>A | CA467737289 | AGPAT2 | c.666A>T (p.Thr222=) c.570A>T (p.Thr190=) n.594A>T | gnomAD v4 |
9 | g.136673923T>C | CA467737292 | AGPAT2 | c.666A>G (p.Thr222=) c.570A>G (p.Thr190=) n.594A>G | gnomAD v4 |
9 | g.136673923T>G | CA467737294 | AGPAT2 | c.666A>C (p.Thr222=) c.570A>C (p.Thr190=) n.594A>C | |
9 | g.136673924_136673925del | CA2692653773 | AGPAT2 | c.665_666del (p.Thr222SerfsTer?) c.569_570del (p.Thr190SerfsTer?) n.593_594del | gnomAD v4 |
9 | g.136673924G>A | CA375577795 | AGPAT2 | c.665C>T (p.Thr222Ile) c.569C>T (p.Thr190Ile) n.593C>T | dbSNP gnomAD v4 |
9 | g.136673924G>C | CA375577796 | AGPAT2 | c.665C>G (p.Thr222Arg) c.569C>G (p.Thr190Arg) n.593C>G | gnomAD v4 |
9 | g.136673924G>T | CA375577797 | AGPAT2 | c.665C>A (p.Thr222Lys) c.569C>A (p.Thr190Lys) n.593C>A | gnomAD v4 |
9 | g.136673925T>A | CA375577802 | AGPAT2 | c.664A>T (p.Thr222Ser) c.568A>T (p.Thr190Ser) n.592A>T | gnomAD v4 |
9 | g.136673925T>C | CA375577809 | AGPAT2 | c.664A>G (p.Thr222Ala) c.568A>G (p.Thr190Ala) n.592A>G | |
9 | g.136673925T>G | CA375577811 | AGPAT2 | c.664A>C (p.Thr222Pro) c.568A>C (p.Thr190Pro) n.592A>C | |
9 | g.136673926T>A | CA467737313 | AGPAT2 | c.663A>T (p.Gly221=) c.567A>T (p.Gly189=) n.591A>T | |
9 | g.136673926T>C | CA467737314 | AGPAT2 | c.663A>G (p.Gly221=) c.567A>G (p.Gly189=) n.591A>G | |
9 | g.136673926T>G | CA467737317 | AGPAT2 | c.663A>C (p.Gly221=) c.567A>C (p.Gly189=) n.591A>C | |
9 | g.136673927C>A | CA375577813 | AGPAT2 | c.662G>T (p.Gly221Val) c.566G>T (p.Gly189Val) n.590G>T | gnomAD v4 |
9 | g.136673927C>G | CA375577816 | AGPAT2 | c.662G>C (p.Gly221Ala) c.566G>C (p.Gly189Ala) n.590G>C | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136673927C>T | CA375577822 | AGPAT2 | c.662G>A (p.Gly221Glu) c.566G>A (p.Gly189Glu) n.590G>A | gnomAD v4 |
9 | g.136673928del | CA5342858 | AGPAT2 | c.662del c.566del n.590del | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136673928C>A | CA375577829 | AGPAT2 | c.662-1G>T (n.662-1G>T) c.566-1G>T (n.566-1G>T) n.590-1G>T | gnomAD v4 |
9 | g.136673928C>G | CA375577832 | AGPAT2 | c.662-1G>C (n.662-1G>C) c.566-1G>C (n.566-1G>C) n.590-1G>C | |
9 | g.136673928C>T | CA375577839 | AGPAT2 | c.662-1G>A (n.662-1G>A) c.566-1G>A (n.566-1G>A) n.590-1G>A | gnomAD v4 |
9 | g.136673929T>A | CA375577842 | AGPAT2 | c.662-2A>T (n.662-2A>T) c.566-2A>T (n.566-2A>T) n.590-2A>T | |
9 | g.136673929T>C | CA375577855 | AGPAT2 | c.662-2A>G (n.662-2A>G) c.566-2A>G (n.566-2A>G) n.590-2A>G | gnomAD v4 |
9 | g.136673929T>G | CA375577854 | AGPAT2 | c.662-2A>C (n.662-2A>C) c.566-2A>C (n.566-2A>C) n.590-2A>C | ClinVar dbSNP gnomAD v4 |
9 | g.136673930G>A | CA861080825 | AGPAT2 | c.662-3C>T (n.662-3C>T) c.566-3C>T (n.566-3C>T) n.590-3C>T | dbSNP gnomAD v4 |
9 | g.136673930G>T | CA2692653774 | AGPAT2 | c.662-3C>A (n.662-3C>A) c.566-3C>A (n.566-3C>A) n.590-3C>A | gnomAD v4 |
9 | g.136673931T>A | CA2692653775 | AGPAT2 | c.662-4A>T (n.662-4A>T) c.566-4A>T (n.566-4A>T) n.590-4A>T | gnomAD v4 |
9 | g.136673931T>C | CA2692653776 | AGPAT2 | c.662-4A>G (n.662-4A>G) c.566-4A>G (n.566-4A>G) n.590-4A>G | gnomAD v4 |
9 | g.136673932G>A | CA5342861 | AGPAT2 | c.662-5C>T (n.662-5C>T) c.566-5C>T (n.566-5C>T) n.590-5C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136673932G>C | CA5342859 | AGPAT2 | c.662-5C>G (n.662-5C>G) c.566-5C>G (n.566-5C>G) n.590-5C>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136673932G>T | CA5342860 | AGPAT2 | c.662-5C>A (n.662-5C>A) c.566-5C>A (n.566-5C>A) n.590-5C>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136673936dup | CA591367772 | AGPAT2 | c.662-5dup (n.662-5dup) c.566-5dup (n.566-5dup) n.590-5dup | dbSNP gnomAD v2 gnomAD v4 |
9 | g.136673936del | CA2692653777 | AGPAT2 | c.662-5del (n.662-5del) c.566-5del (n.566-5del) n.590-5del | gnomAD v4 |
9 | g.136673933G>A | CA591367773 | AGPAT2 | c.662-6C>T (n.662-6C>T) c.566-6C>T (n.566-6C>T) n.590-6C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136673933G>T | CA2692653778 | AGPAT2 | c.662-6C>A (n.662-6C>A) c.566-6C>A (n.566-6C>A) n.590-6C>A | gnomAD v4 |
9 | g.136673934G>A | CA591367774 | AGPAT2 | c.662-7C>T (n.662-7C>T) c.566-7C>T (n.566-7C>T) n.590-7C>T | dbSNP gnomAD v2 gnomAD v4 |
9 | g.136673934G>T | CA2692653779 | AGPAT2 | c.662-7C>A (n.662-7C>A) c.566-7C>A (n.566-7C>A) n.590-7C>A | gnomAD v4 |
9 | g.136673935G>A | CA5342862 | AGPAT2 | c.662-8C>T (n.662-8C>T) c.566-8C>T (n.566-8C>T) n.590-8C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.136673935G>T | CA2692653780 | AGPAT2 | c.662-8C>A (n.662-8C>A) c.566-8C>A (n.566-8C>A) n.590-8C>A | gnomAD v4 |
9 | g.136673936G>A | CA5342863 | AGPAT2 | c.662-9C>T (n.662-9C>T) c.566-9C>T (n.566-9C>T) n.590-9C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136673936G>C | CA2692653781 | AGPAT2 | c.662-9C>G (n.662-9C>G) c.566-9C>G (n.566-9C>G) n.590-9C>G | gnomAD v4 |
9 | g.136673937A>G | CA2692653782 | AGPAT2 | c.662-10T>C (n.662-10T>C) c.566-10T>C (n.566-10T>C) n.590-10T>C | gnomAD v4 |
9 | g.136673938A>G | CA2692653783 | AGPAT2 | c.662-11T>C (n.662-11T>C) c.566-11T>C (n.566-11T>C) n.590-11T>C | dbSNP gnomAD v4 |
9 | g.136673938A>T | CA5342864 | AGPAT2 | c.662-11T>A (n.662-11T>A) c.566-11T>A (n.566-11T>A) n.590-11T>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136673939G>A | CA2692653784 | AGPAT2 | c.662-12C>T (n.662-12C>T) c.566-12C>T (n.566-12C>T) n.590-12C>T | gnomAD v4 |
9 | g.136673939G>T | CA2692653785 | AGPAT2 | c.662-12C>A (n.662-12C>A) c.566-12C>A (n.566-12C>A) n.590-12C>A | gnomAD v4 |
9 | g.136673940C>A | CA2692653786 | AGPAT2 | c.662-13G>T (n.662-13G>T) c.566-13G>T (n.566-13G>T) n.590-13G>T | gnomAD v4 |
9 | g.136673940C>G | CA2579519886 | AGPAT2 | c.662-13G>C (n.662-13G>C) c.566-13G>C (n.566-13G>C) n.590-13G>C | |
9 | g.136673941A>G | CA2692653787 | AGPAT2 | c.662-14T>C (n.662-14T>C) c.566-14T>C (n.566-14T>C) n.590-14T>C | gnomAD v4 |
9 | g.136673943C>A | CA2692653789 | AGPAT2 | c.662-16G>T (n.662-16G>T) c.566-16G>T (n.566-16G>T) n.590-16G>T | gnomAD v4 |
9 | g.136673943C>T | CA2692653788 | AGPAT2 | c.662-16G>A (n.662-16G>A) c.566-16G>A (n.566-16G>A) n.590-16G>A | gnomAD v4 |
9 | g.136673945G>A | CA861080839 | AGPAT2 | c.662-18C>T (n.662-18C>T) c.566-18C>T (n.566-18C>T) n.590-18C>T | dbSNP |
9 | g.136673945G>T | CA2692653790 | AGPAT2 | c.662-18C>A (n.662-18C>A) c.566-18C>A (n.566-18C>A) n.590-18C>A | gnomAD v4 |
9 | g.136673947C>A | CA2692653791 | AGPAT2 | c.662-20G>T (n.662-20G>T) c.566-20G>T (n.566-20G>T) n.590-20G>T | gnomAD v4 |
9 | g.136673947C>T | CA201626971 | AGPAT2 | c.662-20G>A (n.662-20G>A) c.566-20G>A (n.566-20G>A) n.590-20G>A | dbSNP gnomAD v4 |
9 | g.136673949_136673974dup | CA5342865 | AGPAT2 | c.662-45_662-20dup (n.662-45_662-20dup) c.566-45_566-20dup (n.566-45_566-20dup) n.590-45_590-20dup | dbSNP ExAC gnomAD v2 |
9 | g.136673948C>A | CA2692653792 | AGPAT2 | c.662-21G>T (n.662-21G>T) c.566-21G>T (n.566-21G>T) n.590-21G>T | gnomAD v4 |
9 | g.136673948C>G | CA2692653793 | AGPAT2 | c.662-21G>C (n.662-21G>C) c.566-21G>C (n.566-21G>C) n.590-21G>C | gnomAD v4 |
9 | g.136673948C>T | CA2579519887 | AGPAT2 | c.662-21G>A (n.662-21G>A) c.566-21G>A (n.566-21G>A) n.590-21G>A | |
9 | g.136673949T>C | CA2692653794 | AGPAT2 | c.662-22A>G (n.662-22A>G) c.566-22A>G (n.566-22A>G) n.590-22A>G | gnomAD v4 |
9 | g.136673950C>A | CA2692653795 | AGPAT2 | c.662-23G>T (n.662-23G>T) c.566-23G>T (n.566-23G>T) n.590-23G>T | gnomAD v4 |
9 | g.136673950C>T | CA2692653796 | AGPAT2 | c.662-23G>A (n.662-23G>A) c.566-23G>A (n.566-23G>A) n.590-23G>A | gnomAD v4 |
9 | g.136673951del | CA2692653797 | AGPAT2 | c.662-24del (n.662-24del) c.566-24del (n.566-24del) n.590-24del | gnomAD v4 |
9 | g.136673951A>C | CA2720854572 | AGPAT2 | c.662-24T>G (n.662-24T>G) c.566-24T>G (n.566-24T>G) n.590-24T>G | dbSNP |
9 | g.136673951A>G | CA2692653798 | AGPAT2 | c.662-24T>C (n.662-24T>C) c.566-24T>C (n.566-24T>C) n.590-24T>C | gnomAD v4 |
9 | g.136673952G>A | CA201626974 | AGPAT2 | c.662-25C>T (n.662-25C>T) c.566-25C>T (n.566-25C>T) n.590-25C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136673952G>C | CA201626977 | AGPAT2 | c.662-25C>G (n.662-25C>G) c.566-25C>G (n.566-25C>G) n.590-25C>G | dbSNP |
9 | g.136673952G>T | CA2692653799 | AGPAT2 | c.662-25C>A (n.662-25C>A) c.566-25C>A (n.566-25C>A) n.590-25C>A | gnomAD v4 |
9 | g.136673953T>C | CA861080843 | AGPAT2 | c.662-26A>G (n.662-26A>G) c.566-26A>G (n.566-26A>G) n.590-26A>G | dbSNP gnomAD v3 gnomAD v4 |
9 | g.136673954G>A | CA2692653800 | AGPAT2 | c.662-27C>T (n.662-27C>T) c.566-27C>T (n.566-27C>T) n.590-27C>T | gnomAD v4 |
9 | g.136673954G>T | CA2692653801 | AGPAT2 | c.662-27C>A (n.662-27C>A) c.566-27C>A (n.566-27C>A) n.590-27C>A | gnomAD v4 |
9 | g.136673955G>A | CA2579519888 | AGPAT2 | c.662-28C>T (n.662-28C>T) c.566-28C>T (n.566-28C>T) n.590-28C>T | |
9 | g.136673955G>C | CA2692653802 | AGPAT2 | c.662-28C>G (n.662-28C>G) c.566-28C>G (n.566-28C>G) n.590-28C>G | gnomAD v4 |
9 | g.136673955G>T | CA2692653803 | AGPAT2 | c.662-28C>A (n.662-28C>A) c.566-28C>A (n.566-28C>A) n.590-28C>A | gnomAD v4 |
9 | g.136673956C>A | CA2692653804 | AGPAT2 | c.662-29G>T (n.662-29G>T) c.566-29G>T (n.566-29G>T) n.590-29G>T | gnomAD v4 |
9 | g.136673956C>T | CA591367775 | AGPAT2 | c.662-29G>A (n.662-29G>A) c.566-29G>A (n.566-29G>A) n.590-29G>A | dbSNP gnomAD v2 gnomAD v4 |
9 | g.136673957C>T | CA861080846 | AGPAT2 | c.662-30G>A (n.662-30G>A) c.566-30G>A (n.566-30G>A) n.590-30G>A | dbSNP gnomAD v3 gnomAD v4 |
9 | g.136673958T>C | CA2692653805 | AGPAT2 | c.662-31A>G (n.662-31A>G) c.566-31A>G (n.566-31A>G) n.590-31A>G | gnomAD v4 |
9 | g.136673959del | CA2497275508 | AGPAT2 | c.662-32del (n.662-32del) c.566-32del (n.566-32del) n.590-32del | dbSNP |
9 | g.136673959G>A | CA2692653806 | AGPAT2 | c.662-32C>T (n.662-32C>T) c.566-32C>T (n.566-32C>T) n.590-32C>T | dbSNP gnomAD v4 |
9 | g.136673959G>T | CA2692653807 | AGPAT2 | c.662-32C>A (n.662-32C>A) c.566-32C>A (n.566-32C>A) n.590-32C>A | gnomAD v4 |
9 | g.136673960T>A | CA2692653808 | AGPAT2 | c.662-33A>T (n.662-33A>T) c.566-33A>T (n.566-33A>T) n.590-33A>T | gnomAD v4 |
9 | g.136673960T>C | CA2692653809 | AGPAT2 | c.662-33A>G (n.662-33A>G) c.566-33A>G (n.566-33A>G) n.590-33A>G | gnomAD v4 |
9 | g.136673961G>A | CA2692653810 | AGPAT2 | c.662-34C>T (n.662-34C>T) c.566-34C>T (n.566-34C>T) n.590-34C>T | gnomAD v4 |
9 | g.136673961G>T | CA2692653811 | AGPAT2 | c.662-34C>A (n.662-34C>A) c.566-34C>A (n.566-34C>A) n.590-34C>A | gnomAD v4 |
9 | g.136673962G>A | CA591367776 | AGPAT2 | c.662-35C>T (n.662-35C>T) c.566-35C>T (n.566-35C>T) n.590-35C>T | dbSNP gnomAD v2 gnomAD v4 |
9 | g.136673962G>T | CA2692653812 | AGPAT2 | c.662-35C>A (n.662-35C>A) c.566-35C>A (n.566-35C>A) n.590-35C>A | gnomAD v4 |
9 | g.136673963G>A | CA2692653813 | AGPAT2 | c.662-36C>T (n.662-36C>T) c.566-36C>T (n.566-36C>T) n.590-36C>T | gnomAD v4 |
9 | g.136673963G>T | CA2692653814 | AGPAT2 | c.662-36C>A (n.662-36C>A) c.566-36C>A (n.566-36C>A) n.590-36C>A | gnomAD v4 |
9 | g.136673964G>C | CA2692653815 | AGPAT2 | c.662-37C>G (n.662-37C>G) c.566-37C>G (n.566-37C>G) n.590-37C>G | gnomAD v4 |
9 | g.136673964G>T | CA2550120002 | AGPAT2 | c.662-37C>A (n.662-37C>A) c.566-37C>A (n.566-37C>A) n.590-37C>A | gnomAD v4 |
9 | g.136673965A>G | CA2579519889 | AGPAT2 | c.662-38T>C (n.662-38T>C) c.566-38T>C (n.566-38T>C) n.590-38T>C | dbSNP |
9 | g.136673966G>A | CA2692653816 | AGPAT2 | c.662-39C>T (n.662-39C>T) c.566-39C>T (n.566-39C>T) n.590-39C>T | gnomAD v4 |
9 | g.136673966G>T | CA2692653817 | AGPAT2 | c.662-39C>A (n.662-39C>A) c.566-39C>A (n.566-39C>A) n.590-39C>A | gnomAD v4 |
9 | g.136673967C>A | CA2692653818 | AGPAT2 | c.662-40G>T (n.662-40G>T) c.566-40G>T (n.566-40G>T) n.590-40G>T | gnomAD v4 |
9 | g.136673967C>T | CA2692653819 | AGPAT2 | c.662-40G>A (n.662-40G>A) c.566-40G>A (n.566-40G>A) n.590-40G>A | gnomAD v4 |
9 | g.136673968T>C | CA591367777 | AGPAT2 | c.662-41A>G (n.662-41A>G) c.566-41A>G (n.566-41A>G) n.590-41A>G | dbSNP gnomAD v2 gnomAD v4 |
9 | g.136673969G>T | CA2786279726 | AGPAT2 | c.662-42C>A (n.662-42C>A) c.566-42C>A (n.566-42C>A) n.590-42C>A | |
9 | g.136673972del | CA591367778 | AGPAT2 | c.662-42del (n.662-42del) c.566-42del (n.566-42del) n.590-42del | gnomAD v2 gnomAD v4 |
9 | g.136673970G>A | CA5342866 | AGPAT2 | c.662-43C>T (n.662-43C>T) c.566-43C>T (n.566-43C>T) n.590-43C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.136673971G>T | CA5342867 | AGPAT2 | c.662-44C>A (n.662-44C>A) c.566-44C>A (n.566-44C>A) n.590-44C>A | dbSNP ExAC gnomAD v2 gnomAD v4 |