Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
9 | g.136674644_136674718dup | CA1130033669 | AGPAT2 | c.661+24_661+98dup (n.661+24_661+98dup) c.565+24_565+98dup (n.565+24_565+98dup) n.589+24_589+98dup | gnomAD v3 gnomAD v4 |
9 | g.136674703_136674714del | CA1130033698 | AGPAT2 | c.661+23_661+34del (n.661+23_661+34del) c.565+23_565+34del (n.565+23_565+34del) n.589+23_589+34del | gnomAD v3 gnomAD v4 |
9 | g.136674705_136674710del | CA2579519916 | AGPAT2 | c.661+27_661+32del (n.661+27_661+32del) c.565+27_565+32del (n.565+27_565+32del) n.589+27_589+32del | |
9 | g.136674705_136674711del | CA2692654178 | AGPAT2 | c.661+26_661+32del (n.661+26_661+32del) c.565+26_565+32del (n.565+26_565+32del) n.589+26_589+32del | gnomAD v4 |
9 | g.136674705_136674712del | CA2692654180 | AGPAT2 | c.661+25_661+32del (n.661+25_661+32del) c.565+25_565+32del (n.565+25_565+32del) n.589+25_589+32del | gnomAD v4 |
9 | g.136674705_136674709del | CA2692654182 | AGPAT2 | c.661+27_661+31del (n.661+27_661+31del) c.565+27_565+31del (n.565+27_565+31del) n.589+27_589+31del | gnomAD v4 |
9 | g.136674708A>G | CA5342876 | AGPAT2 | c.661+27T>C (n.661+27T>C) c.565+27T>C (n.565+27T>C) n.589+27T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674709C>A | CA2692654191 | AGPAT2 | c.661+26G>T (n.661+26G>T) c.565+26G>T (n.565+26G>T) n.589+26G>T | gnomAD v4 |
9 | g.136674709C>T | CA591183713 | AGPAT2 | c.661+26G>A (n.661+26G>A) c.565+26G>A (n.565+26G>A) n.589+26G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674711_136674712dup | CA2692654189 | AGPAT2 | c.661+25_661+26dup (n.661+25_661+26dup) c.565+25_565+26dup (n.565+25_565+26dup) n.589+25_589+26dup | gnomAD v4 |
9 | g.136674712del | CA2692654190 | AGPAT2 | c.661+26del (n.661+26del) c.565+26del (n.565+26del) n.589+26del | gnomAD v4 |
9 | g.136674710C>A | CA5342877 | AGPAT2 | c.661+25G>T (n.661+25G>T) c.565+25G>T (n.565+25G>T) n.589+25G>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674710C>G | CA2692654192 | AGPAT2 | c.661+25G>C (n.661+25G>C) c.565+25G>C (n.565+25G>C) n.589+25G>C | gnomAD v4 |
9 | g.136674710C>T | CA5342878 | AGPAT2 | c.661+25G>A (n.661+25G>A) c.565+25G>A (n.565+25G>A) n.589+25G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.136674711C>A | CA2692654193 | AGPAT2 | c.661+24G>T (n.661+24G>T) c.565+24G>T (n.565+24G>T) n.589+24G>T | gnomAD v4 |
9 | g.136674711C>T | CA2510724759 | AGPAT2 | c.661+24G>A (n.661+24G>A) c.565+24G>A (n.565+24G>A) n.589+24G>A | gnomAD v4 |
9 | g.136674712C>A | CA2692654194 | AGPAT2 | c.661+23G>T (n.661+23G>T) c.565+23G>T (n.565+23G>T) n.589+23G>T | gnomAD v4 |
9 | g.136674712C>G | CA2579519917 | AGPAT2 | c.661+23G>C (n.661+23G>C) c.565+23G>C (n.565+23G>C) n.589+23G>C | dbSNP gnomAD v4 |
9 | g.136674712C>T | CA5342879 | AGPAT2 | c.661+23G>A (n.661+23G>A) c.565+23G>A (n.565+23G>A) n.589+23G>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674713G>A | CA5342880 | AGPAT2 | c.661+22C>T (n.661+22C>T) c.565+22C>T (n.565+22C>T) n.589+22C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674713G>C | CA2720761020 | AGPAT2 | c.661+22C>G (n.661+22C>G) c.565+22C>G (n.565+22C>G) n.589+22C>G | dbSNP |
9 | g.136674713G>T | CA2692654195 | AGPAT2 | c.661+22C>A (n.661+22C>A) c.565+22C>A (n.565+22C>A) n.589+22C>A | gnomAD v4 |
9 | g.136674714G>A | CA591183723 | AGPAT2 | c.661+21C>T (n.661+21C>T) c.565+21C>T (n.565+21C>T) n.589+21C>T | dbSNP gnomAD v2 gnomAD v4 |
9 | g.136674714G>C | CA5342881 | AGPAT2 | c.661+21C>G (n.661+21C>G) c.565+21C>G (n.565+21C>G) n.589+21C>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674714G>T | CA591183725 | AGPAT2 | c.661+21C>A (n.661+21C>A) c.565+21C>A (n.565+21C>A) n.589+21C>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674715G>A | CA2692654197 | AGPAT2 | c.661+20C>T (n.661+20C>T) c.565+20C>T (n.565+20C>T) n.589+20C>T | gnomAD v4 |
9 | g.136674715G>C | CA2692654198 | AGPAT2 | c.661+20C>G (n.661+20C>G) c.565+20C>G (n.565+20C>G) n.589+20C>G | gnomAD v4 |
9 | g.136674715G>T | CA2692654196 | AGPAT2 | c.661+20C>A (n.661+20C>A) c.565+20C>A (n.565+20C>A) n.589+20C>A | gnomAD v4 |
9 | g.136674716T>C | CA1130033712 | AGPAT2 | c.661+19A>G (n.661+19A>G) c.565+19A>G (n.565+19A>G) n.589+19A>G | dbSNP gnomAD v3 gnomAD v4 |
9 | g.136674718_136674725del | CA5342882 | AGPAT2 | c.661+12_661+19del (n.661+12_661+19del) c.565+12_565+19del (n.565+12_565+19del) n.589+12_589+19del | dbSNP ExAC gnomAD v3 gnomAD v4 |
9 | g.136674717G>A | CA2692654199 | AGPAT2 | c.661+18C>T (n.661+18C>T) c.565+18C>T (n.565+18C>T) n.589+18C>T | gnomAD v4 |
9 | g.136674717G>T | CA5342883 | AGPAT2 | c.661+18C>A (n.661+18C>A) c.565+18C>A (n.565+18C>A) n.589+18C>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.136674718C>A | CA2692654200 | AGPAT2 | c.661+17G>T (n.661+17G>T) c.565+17G>T (n.565+17G>T) n.589+17G>T | gnomAD v4 |
9 | g.136674718C>G | CA2692654201 | AGPAT2 | c.661+17G>C (n.661+17G>C) c.565+17G>C (n.565+17G>C) n.589+17G>C | gnomAD v4 |
9 | g.136674718C>T | CA2692654202 | AGPAT2 | c.661+17G>A (n.661+17G>A) c.565+17G>A (n.565+17G>A) n.589+17G>A | gnomAD v4 |
9 | g.136674719A>G | CA2692654203 | AGPAT2 | c.661+16T>C (n.661+16T>C) c.565+16T>C (n.565+16T>C) n.589+16T>C | gnomAD v4 |
9 | g.136674720C>A | CA2692654204 | AGPAT2 | c.661+15G>T (n.661+15G>T) c.565+15G>T (n.565+15G>T) n.589+15G>T | gnomAD v4 |
9 | g.136674720C>G | CA2692654205 | AGPAT2 | c.661+15G>C (n.661+15G>C) c.565+15G>C (n.565+15G>C) n.589+15G>C | gnomAD v4 |
9 | g.136674720C>T | CA591183726 | AGPAT2 | c.661+15G>A (n.661+15G>A) c.565+15G>A (n.565+15G>A) n.589+15G>A | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674721A>C | CA1130033715 | AGPAT2 | c.661+14T>G (n.661+14T>G) c.565+14T>G (n.565+14T>G) n.589+14T>G | dbSNP gnomAD v3 gnomAD v4 |
9 | g.136674721A>G | CA2692654206 | AGPAT2 | c.661+14T>C (n.661+14T>C) c.565+14T>C (n.565+14T>C) n.589+14T>C | gnomAD v4 |
9 | g.136674722C>A | CA2692654208 | AGPAT2 | c.661+13G>T (n.661+13G>T) c.565+13G>T (n.565+13G>T) n.589+13G>T | gnomAD v4 |
9 | g.136674722C>T | CA2692654207 | AGPAT2 | c.661+13G>A (n.661+13G>A) c.565+13G>A (n.565+13G>A) n.589+13G>A | gnomAD v4 |
9 | g.136674723A>G | CA5342885 | AGPAT2 | c.661+12T>C (n.661+12T>C) c.565+12T>C (n.565+12T>C) n.589+12T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674723A>T | CA2692654209 | AGPAT2 | c.661+12T>A (n.661+12T>A) c.565+12T>A (n.565+12T>A) n.589+12T>A | gnomAD v4 |
9 | g.136674723_136674724del | CA5342884 | AGPAT2 | c.661+11_661+12del (n.661+11_661+12del) c.565+11_565+12del (n.565+11_565+12del) n.589+11_589+12del | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674724T>C | CA2692654210 | AGPAT2 | c.661+11A>G (n.661+11A>G) c.565+11A>G (n.565+11A>G) n.589+11A>G | gnomAD v4 |
9 | g.136674725G>A | CA2692654211 | AGPAT2 | c.661+10C>T (n.661+10C>T) c.565+10C>T (n.565+10C>T) n.589+10C>T | gnomAD v4 |
9 | g.136674725G>T | CA5342887 | AGPAT2 | c.661+10C>A (n.661+10C>A) c.565+10C>A (n.565+10C>A) n.589+10C>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.136674726_136674728del | CA861081204 | AGPAT2 | c.661+8_661+10del (n.661+8_661+10del) c.565+8_565+10del (n.565+8_565+10del) n.589+8_589+10del | dbSNP gnomAD v4 |
9 | g.136674727_136674732dup | CA5342886 | AGPAT2 | c.661+5_661+10dup (n.661+5_661+10dup) c.565+5_565+10dup (n.565+5_565+10dup) n.589+5_589+10dup | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674726del | CA2497275517 | AGPAT2 | c.661+9del (n.661+9del) c.565+9del (n.565+9del) n.589+9del | dbSNP |
9 | g.136674726T>C | CA2692654212 | AGPAT2 | c.661+9A>G (n.661+9A>G) c.565+9A>G (n.565+9A>G) n.589+9A>G | gnomAD v4 |
9 | g.136674726T>G | CA2720854864 | AGPAT2 | c.661+9A>C (n.661+9A>C) c.565+9A>C (n.565+9A>C) n.589+9A>C | dbSNP |
9 | g.136674727G>A | CA5342889 | AGPAT2 | c.661+8C>T (n.661+8C>T) c.565+8C>T (n.565+8C>T) n.589+8C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674727G>C | CA5342888 | AGPAT2 | c.661+8C>G (n.661+8C>G) c.565+8C>G (n.565+8C>G) n.589+8C>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.136674727G>T | CA591183728 | AGPAT2 | c.661+8C>A (n.661+8C>A) c.565+8C>A (n.565+8C>A) n.589+8C>A | dbSNP gnomAD v2 gnomAD v4 |
9 | g.136674731dup | CA2692654213 | AGPAT2 | c.661+8dup (n.661+8dup) c.565+8dup (n.565+8dup) n.589+8dup | gnomAD v4 |
9 | g.136674731del | CA2579519918 | AGPAT2 | c.661+8del (n.661+8del) c.565+8del (n.565+8del) n.589+8del | gnomAD v4 |
9 | g.136674728G>A | CA861081213 | AGPAT2 | c.661+7C>T (n.661+7C>T) c.565+7C>T (n.565+7C>T) n.589+7C>T | dbSNP gnomAD v3 gnomAD v4 |
9 | g.136674728G>T | CA2692654214 | AGPAT2 | c.661+7C>A (n.661+7C>A) c.565+7C>A (n.565+7C>A) n.589+7C>A | gnomAD v4 |
9 | g.136674729G>A | CA2692654215 | AGPAT2 | c.661+6C>T (n.661+6C>T) c.565+6C>T (n.565+6C>T) n.589+6C>T | gnomAD v4 |
9 | g.136674729G>T | CA2692654216 | AGPAT2 | c.661+6C>A (n.661+6C>A) c.565+6C>A (n.565+6C>A) n.589+6C>A | gnomAD v4 |
9 | g.136674730G>A | CA5342890 | AGPAT2 | c.661+5C>T (n.661+5C>T) c.565+5C>T (n.565+5C>T) n.589+5C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674730G>T | CA2692654217 | AGPAT2 | c.661+5C>A (n.661+5C>A) c.565+5C>A (n.565+5C>A) n.589+5C>A | gnomAD v4 |
9 | g.136674731G>A | CA2579519919 | AGPAT2 | c.661+4C>T (n.661+4C>T) c.565+4C>T (n.565+4C>T) n.589+4C>T | gnomAD v4 |
9 | g.136674731G>C | CA591183729 | AGPAT2 | c.661+4C>G (n.661+4C>G) c.565+4C>G (n.565+4C>G) n.589+4C>G | dbSNP gnomAD v2 |
9 | g.136674731G>T | CA201627602 | AGPAT2 | c.661+4C>A (n.661+4C>A) c.565+4C>A (n.565+4C>A) n.589+4C>A | dbSNP gnomAD v4 |
9 | g.136674732T>C | CA2692654218 | AGPAT2 | c.661+3A>G (n.661+3A>G) c.565+3A>G (n.565+3A>G) n.589+3A>G | gnomAD v4 |
9 | g.136674733A>C | CA16042194 | AGPAT2 | c.661+2T>G (n.661+2T>G) c.565+2T>G (n.565+2T>G) n.589+2T>G | ClinVar dbSNP |
9 | g.136674733A>G | CA375578107 | AGPAT2 | c.661+2T>C (n.661+2T>C) c.565+2T>C (n.565+2T>C) n.589+2T>C | gnomAD v4 |
9 | g.136674733A>T | CA375578110 | AGPAT2 | c.661+2T>A (n.661+2T>A) c.565+2T>A (n.565+2T>A) n.589+2T>A | |
9 | g.136674733dup | CA2720874574 | AGPAT2 | c.661+2dup (n.661+2dup) c.565+2dup (n.565+2dup) n.589+2dup | dbSNP |
9 | g.136674734C>A | CA375578113 | AGPAT2 | c.661+1G>T (n.661+1G>T) c.565+1G>T (n.565+1G>T) n.589+1G>T | gnomAD v4 |
9 | g.136674734C>G | CA375578117 | AGPAT2 | c.661+1G>C (n.661+1G>C) c.565+1G>C (n.565+1G>C) n.589+1G>C | |
9 | g.136674734C>T | CA375578119 | AGPAT2 | c.661+1G>A (n.661+1G>A) c.565+1G>A (n.565+1G>A) n.589+1G>A | gnomAD v4 |
9 | g.136674735C>A | CA375578123 | AGPAT2 | c.661G>T (p.Gly221Ter) c.565G>T (p.Gly189Ter) n.589G>T | gnomAD v4 |
9 | g.136674735C>G | CA375578127 | AGPAT2 | c.661G>C (p.Gly221Arg) c.565G>C (p.Gly189Arg) n.589G>C | |
9 | g.136674735C>T | CA375578128 | AGPAT2 | c.661G>A (p.Gly221Arg) c.565G>A (p.Gly189Arg) n.589G>A | |
9 | g.136674736T>A | CA467737893 | AGPAT2 | c.660A>T (p.Ser220=) c.564A>T (p.Ser188=) n.588A>T | gnomAD v4 |
9 | g.136674736T>C | CA5342891 | AGPAT2 | c.660A>G (p.Ser220=) c.564A>G (p.Ser188=) n.588A>G | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674736T>G | CA467737898 | AGPAT2 | c.660A>C (p.Ser220=) c.564A>C (p.Ser188=) n.588A>C | gnomAD v4 |
9 | g.136674741_136674745del | CA861081233 | AGPAT2 | c.656_660del (p.Thr219ArgfsTer?) c.560_564del (p.Thr187ArgfsTer?) n.584_588del | ClinVar dbSNP gnomAD v3 gnomAD v4 |
9 | g.136674737del | CA2692654219 | AGPAT2 | c.659del (p.Ser220Ter) c.563del (p.Ser188Ter) n.587del | gnomAD v4 |
9 | g.136674737G>A | CA375578130 | AGPAT2 | c.659C>T (p.Ser220Leu) c.563C>T (p.Ser188Leu) n.587C>T | gnomAD v4 |
9 | g.136674737G>C | CA375578134 | AGPAT2 | c.659C>G (p.Ser220Ter) c.563C>G (p.Ser188Ter) n.587C>G | gnomAD v4 |
9 | g.136674737G>T | CA375578131 | AGPAT2 | c.659C>A (p.Ser220Ter) c.563C>A (p.Ser188Ter) n.587C>A | |
9 | g.136674738A>C | CA375578139 | AGPAT2 | c.658T>G (p.Ser220Ala) c.562T>G (p.Ser188Ala) n.586T>G | |
9 | g.136674738A>G | CA375578140 | AGPAT2 | c.658T>C (p.Ser220Pro) c.562T>C (p.Ser188Pro) n.586T>C | gnomAD v4 |
9 | g.136674738A>T | CA375578144 | AGPAT2 | c.658T>A (p.Ser220Thr) c.562T>A (p.Ser188Thr) n.586T>A | gnomAD v4 |
9 | g.136674739A>C | CA467737921 | AGPAT2 | c.657T>G (p.Thr219=) c.561T>G (p.Thr187=) n.585T>G | |
9 | g.136674739A>G | CA467737922 | AGPAT2 | c.657T>C (p.Thr219=) c.561T>C (p.Thr187=) n.585T>C | gnomAD v4 |
9 | g.136674739A>T | CA467737924 | AGPAT2 | c.657T>A (p.Thr219=) c.561T>A (p.Thr187=) n.585T>A | |
9 | g.136674740G>A | CA375578150 | AGPAT2 | c.656C>T (p.Thr219Ile) c.560C>T (p.Thr187Ile) n.584C>T | dbSNP gnomAD v2 gnomAD v4 |
9 | g.136674740G>C | CA375578155 | AGPAT2 | c.656C>G (p.Thr219Ser) c.560C>G (p.Thr187Ser) n.584C>G | |
9 | g.136674740G>T | CA375578159 | AGPAT2 | c.656C>A (p.Thr219Asn) c.560C>A (p.Thr187Asn) n.584C>A | |
9 | g.136674741T>A | CA375578163 | AGPAT2 | c.655A>T (p.Thr219Ser) c.559A>T (p.Thr187Ser) n.583A>T | |
9 | g.136674741T>C | CA375578166 | AGPAT2 | c.655A>G (p.Thr219Ala) c.559A>G (p.Thr187Ala) n.583A>G | dbSNP gnomAD v3 gnomAD v4 |
9 | g.136674741T>G | CA375578177 | AGPAT2 | c.655A>C (p.Thr219Pro) c.559A>C (p.Thr187Pro) n.583A>C | gnomAD v4 |
9 | g.136674742G>A | CA467737941 | AGPAT2 | c.654C>T (p.Phe218=) c.558C>T (p.Phe186=) n.582C>T | gnomAD v4 |
9 | g.136674742G>C | CA375578180 | AGPAT2 | c.654C>G (p.Phe218Leu) c.558C>G (p.Phe186Leu) n.582C>G | gnomAD v4 |
9 | g.136674742G>T | CA375578184 | AGPAT2 | c.654C>A (p.Phe218Leu) c.558C>A (p.Phe186Leu) n.582C>A | |
9 | g.136674745_136674747del | CA2579519920 | AGPAT2 | c.652_654del (p.Phe218del) c.556_558del (p.Phe186del) n.580_582del | gnomAD v4 |
9 | g.136674743A>C | CA375578192 | AGPAT2 | c.653T>G (p.Phe218Cys) c.557T>G (p.Phe186Cys) n.581T>G | |
9 | g.136674743A>G | CA375578196 | AGPAT2 | c.653T>C (p.Phe218Ser) c.557T>C (p.Phe186Ser) n.581T>C | gnomAD v4 |
9 | g.136674743A>T | CA375578191 | AGPAT2 | c.653T>A (p.Phe218Tyr) c.557T>A (p.Phe186Tyr) n.581T>A | gnomAD v4 |
9 | g.136674744del | CA2692654220 | AGPAT2 | c.653del (p.Phe218SerfsTer?) c.557del (p.Phe186SerfsTer?) n.581del | gnomAD v4 |
9 | g.136674744A>C | CA375578219 | AGPAT2 | c.652T>G (p.Phe218Val) c.556T>G (p.Phe186Val) n.580T>G | |
9 | g.136674744A>G | CA375578201 | AGPAT2 | c.652T>C (p.Phe218Leu) c.556T>C (p.Phe186Leu) n.580T>C | gnomAD v4 |
9 | g.136674744A>T | CA375578214 | AGPAT2 | c.652T>A (p.Phe218Ile) c.556T>A (p.Phe186Ile) n.580T>A | gnomAD v4 |
9 | g.136674745G>A | CA467737957 | AGPAT2 | c.651C>T (p.Phe217=) c.555C>T (p.Phe185=) n.579C>T | dbSNP gnomAD v2 gnomAD v4 |
9 | g.136674745G>C | CA375578223 | AGPAT2 | c.651C>G (p.Phe217Leu) c.555C>G (p.Phe185Leu) n.579C>G | |
9 | g.136674745G>T | CA375578227 | AGPAT2 | c.651C>A (p.Phe217Leu) c.555C>A (p.Phe185Leu) n.579C>A | |
9 | g.136674746A>C | CA375578232 | AGPAT2 | c.650T>G (p.Phe217Cys) c.554T>G (p.Phe185Cys) n.578T>G | |
9 | g.136674746A>G | CA375578238 | AGPAT2 | c.650T>C (p.Phe217Ser) c.554T>C (p.Phe185Ser) n.578T>C | gnomAD v4 |
9 | g.136674746A>T | CA375578242 | AGPAT2 | c.650T>A (p.Phe217Tyr) c.554T>A (p.Phe185Tyr) n.578T>A | |
9 | g.136674746_136674748del | CA591183730 | AGPAT2 | c.648_650del (p.Lys216_Phe217delinsAsn) c.552_554del (p.Lys184_Phe185delinsAsn) n.576_578del | gnomAD v2 |
9 | g.136674747A>C | CA375578246 | AGPAT2 | c.649T>G (p.Phe217Val) c.553T>G (p.Phe185Val) n.577T>G | |
9 | g.136674747A>G | CA375578249 | AGPAT2 | c.649T>C (p.Phe217Leu) c.553T>C (p.Phe185Leu) n.577T>C | gnomAD v4 |
9 | g.136674747A>T | CA375578253 | AGPAT2 | c.649T>A (p.Phe217Ile) c.553T>A (p.Phe185Ile) n.577T>A | |
9 | g.136674748C>A | CA375578261 | AGPAT2 | c.648G>T (p.Lys216Asn) c.552G>T (p.Lys184Asn) n.576G>T | gnomAD v4 |
9 | g.136674748C>G | CA375578264 | AGPAT2 | c.648G>C (p.Lys216Asn) c.552G>C (p.Lys184Asn) n.576G>C | gnomAD v4 |
9 | g.136674748C>T | CA467737982 | AGPAT2 | c.648G>A (p.Lys216=) c.552G>A (p.Lys184=) n.576G>A | dbSNP gnomAD v4 |
9 | g.136674754_136674756del | CA5342892 | AGPAT2 | c.646_648del (p.Lys216del) c.550_552del (p.Lys184del) n.574_576del | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674749T>A | CA5342893 | AGPAT2 | c.647A>T (p.Lys216Met) c.551A>T (p.Lys184Met) n.575A>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674749T>C | CA375578268 | AGPAT2 | c.647A>G (p.Lys216Arg) c.551A>G (p.Lys184Arg) n.575A>G | gnomAD v4 |
9 | g.136674749T>G | CA375578271 | AGPAT2 | c.647A>C (p.Lys216Thr) c.551A>C (p.Lys184Thr) n.575A>C | |
9 | g.136674749T= | CA2580617654 | AGPAT2 | c.647A= (p.Lys216=) c.551A= (p.Lys184=) n.575A= | |
9 | g.136674749_136674750delinsAA | CA2580080924 | AGPAT2 | c.646_647delinsTT (p.Lys216Leu) c.550_551delinsTT (p.Lys184Leu) n.574_575delinsTT | ClinVar |
9 | g.136674749_136674750delinsTT | CA2580615409 | AGPAT2 | c.646_647delinsAA (p.Lys216=) c.550_551delinsAA (p.Lys184=) n.574_575delinsAA | |
9 | g.136674750T>A | CA5342894 | AGPAT2 | c.646A>T (p.Lys216Ter) c.550A>T (p.Lys184Ter) n.574A>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674750T>C | CA375578278 | AGPAT2 | c.646A>G (p.Lys216Glu) c.550A>G (p.Lys184Glu) n.574A>G | gnomAD v4 |
9 | g.136674750T>G | CA375578281 | AGPAT2 | c.646A>C (p.Lys216Gln) c.550A>C (p.Lys184Gln) n.574A>C | |
9 | g.136674751C>A | CA5342895 | AGPAT2 | c.645G>T (p.Lys215Asn) c.549G>T (p.Lys183Asn) n.573G>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.136674751C>G | CA375578290 | AGPAT2 | c.645G>C (p.Lys215Asn) c.549G>C (p.Lys183Asn) n.573G>C | |
9 | g.136674751C>T | CA5342896 | AGPAT2 | c.645G>A (p.Lys215=) c.549G>A (p.Lys183=) n.573G>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.136674752T>A | CA375578296 | AGPAT2 | c.644A>T (p.Lys215Met) c.548A>T (p.Lys183Met) n.572A>T | |
9 | g.136674752T>C | CA375578314 | AGPAT2 | c.644A>G (p.Lys215Arg) c.548A>G (p.Lys183Arg) n.572A>G | gnomAD v4 |
9 | g.136674752T>G | CA375578320 | AGPAT2 | c.644A>C (p.Lys215Thr) c.548A>C (p.Lys183Thr) n.572A>C | |
9 | g.136674753T>A | CA277949 | AGPAT2 | c.643A>T (p.Lys215Ter) c.547A>T (p.Lys183Ter) n.571A>T | ClinVar dbSNP |
9 | g.136674753T>C | CA375578333 | AGPAT2 | c.643A>G (p.Lys215Glu) c.547A>G (p.Lys183Glu) n.571A>G | gnomAD v4 |
9 | g.136674753T>G | CA375578339 | AGPAT2 | c.643A>C (p.Lys215Gln) c.547A>C (p.Lys183Gln) n.571A>C | |
9 | g.136674754C>A | CA375578340 | AGPAT2 | c.642G>T (p.Lys214Asn) c.546G>T (p.Lys182Asn) n.570G>T | gnomAD v4 |
9 | g.136674754C>G | CA375578341 | AGPAT2 | c.642G>C (p.Lys214Asn) c.546G>C (p.Lys182Asn) n.570G>C | |
9 | g.136674754C>T | CA201627646 | AGPAT2 | c.642G>A (p.Lys214=) c.546G>A (p.Lys182=) n.570G>A | dbSNP gnomAD v3 gnomAD v4 |
9 | g.136674755T>A | CA375578347 | AGPAT2 | c.641A>T (p.Lys214Met) c.545A>T (p.Lys182Met) n.569A>T | COSMIC |
9 | g.136674755T>C | CA375578359 | AGPAT2 | c.641A>G (p.Lys214Arg) c.545A>G (p.Lys182Arg) n.569A>G | gnomAD v4 |
9 | g.136674755T>G | CA375578372 | AGPAT2 | c.641A>C (p.Lys214Thr) c.545A>C (p.Lys182Thr) n.569A>C | |
9 | g.136674756T>A | CA375578373 | AGPAT2 | c.640A>T (p.Lys214Ter) c.544A>T (p.Lys182Ter) n.568A>T | |
9 | g.136674756T>C | CA5342897 | AGPAT2 | c.640A>G (p.Lys214Glu) c.544A>G (p.Lys182Glu) n.568A>G | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674756T>G | CA375578377 | AGPAT2 | c.640A>C (p.Lys214Gln) c.544A>C (p.Lys182Gln) n.568A>C | |
9 | g.136674757G>A | CA467738055 | AGPAT2 | c.639C>T (p.Thr213=) c.543C>T (p.Thr181=) n.567C>T | gnomAD v4 |
9 | g.136674757G>C | CA467738056 | AGPAT2 | c.639C>G (p.Thr213=) c.543C>G (p.Thr181=) n.567C>G | |
9 | g.136674757G>T | CA467738058 | AGPAT2 | c.639C>A (p.Thr213=) c.543C>A (p.Thr181=) n.567C>A | gnomAD v4 |
9 | g.136674758del | CA2692654221 | AGPAT2 | c.639del (p.Lys214ArgfsTer?) c.543del (p.Lys182ArgfsTer?) n.567del | gnomAD v4 |
9 | g.136674758G>A | CA5342898 | AGPAT2 | c.638C>T (p.Thr213Ile) c.542C>T (p.Thr181Ile) n.566C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.136674758G>C | CA375578386 | AGPAT2 | c.638C>G (p.Thr213Ser) c.542C>G (p.Thr181Ser) n.566C>G | dbSNP gnomAD v4 |
9 | g.136674758G>T | CA375578392 | AGPAT2 | c.638C>A (p.Thr213Asn) c.542C>A (p.Thr181Asn) n.566C>A | gnomAD v4 |
9 | g.136674759T>A | CA375578404 | AGPAT2 | c.637A>T (p.Thr213Ser) c.541A>T (p.Thr181Ser) n.565A>T | |
9 | g.136674759T>C | CA375578407 | AGPAT2 | c.637A>G (p.Thr213Ala) c.541A>G (p.Thr181Ala) n.565A>G | gnomAD v4 |
9 | g.136674759T>G | CA375578421 | AGPAT2 | c.637A>C (p.Thr213Pro) c.541A>C (p.Thr181Pro) n.565A>C | |
9 | g.136674760G>A | CA467738083 | AGPAT2 | c.636C>T (p.Asn212=) c.540C>T (p.Asn180=) n.564C>T | gnomAD v4 |
9 | g.136674760G>C | CA375578426 | AGPAT2 | c.636C>G (p.Asn212Lys) c.540C>G (p.Asn180Lys) n.564C>G | |
9 | g.136674760G>T | CA375578444 | AGPAT2 | c.636C>A (p.Asn212Lys) c.540C>A (p.Asn180Lys) n.564C>A | |
9 | g.136674761T>A | CA375578457 | AGPAT2 | c.635A>T (p.Asn212Ile) c.539A>T (p.Asn180Ile) n.563A>T | gnomAD v4 |
9 | g.136674761T>C | CA375578460 | AGPAT2 | c.635A>G (p.Asn212Ser) c.539A>G (p.Asn180Ser) n.563A>G | gnomAD v4 |
9 | g.136674761T>G | CA5342899 | AGPAT2 | c.635A>C (p.Asn212Thr) c.539A>C (p.Asn180Thr) n.563A>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674762T>A | CA375578467 | AGPAT2 | c.634A>T (p.Asn212Tyr) c.538A>T (p.Asn180Tyr) n.562A>T | |
9 | g.136674762T>C | CA375578480 | AGPAT2 | c.634A>G (p.Asn212Asp) c.538A>G (p.Asn180Asp) n.562A>G | gnomAD v4 |
9 | g.136674762T>G | CA375578482 | AGPAT2 | c.634A>C (p.Asn212His) c.538A>C (p.Asn180His) n.562A>C | |
9 | g.136674763G>A | CA5342900 | AGPAT2 | c.633C>T (p.Tyr211=) c.537C>T (p.Tyr179=) n.561C>T | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.136674763G>C | CA375578488 | AGPAT2 | c.633C>G (p.Tyr211Ter) c.537C>G (p.Tyr179Ter) n.561C>G | |
9 | g.136674763G>T | CA375578501 | AGPAT2 | c.633C>A (p.Tyr211Ter) c.537C>A (p.Tyr179Ter) n.561C>A | |
9 | g.136674764T>A | CA375578503 | AGPAT2 | c.632A>T (p.Tyr211Phe) c.536A>T (p.Tyr179Phe) n.560A>T | |
9 | g.136674764T>C | CA375578504 | AGPAT2 | c.632A>G (p.Tyr211Cys) c.536A>G (p.Tyr179Cys) n.560A>G | gnomAD v4 |
9 | g.136674764T>G | CA375578506 | AGPAT2 | c.632A>C (p.Tyr211Ser) c.536A>C (p.Tyr179Ser) n.560A>C | |
9 | g.136674765A>C | CA375578511 | AGPAT2 | c.631T>G (p.Tyr211Asp) c.535T>G (p.Tyr179Asp) n.559T>G | |
9 | g.136674765A>G | CA375578517 | AGPAT2 | c.631T>C (p.Tyr211His) c.535T>C (p.Tyr179His) n.559T>C | gnomAD v4 |
9 | g.136674765A>T | CA375578533 | AGPAT2 | c.631T>A (p.Tyr211Asn) c.535T>A (p.Tyr179Asn) n.559T>A | gnomAD v4 |
9 | g.136674767_136674769del | CA2692654222 | AGPAT2 | c.629_631del (p.Phe210del) c.533_535del (p.Phe178del) n.557_559del | gnomAD v4 |
9 | g.136674766G>A | CA467738142 | AGPAT2 | c.630C>T (p.Phe210=) c.534C>T (p.Phe178=) n.558C>T | gnomAD v4 |
9 | g.136674766G>C | CA375578544 | AGPAT2 | c.630C>G (p.Phe210Leu) c.534C>G (p.Phe178Leu) n.558C>G | |
9 | g.136674766G>T | CA375578539 | AGPAT2 | c.630C>A (p.Phe210Leu) c.534C>A (p.Phe178Leu) n.558C>A | |
9 | g.136674767A>C | CA375578553 | AGPAT2 | c.629T>G (p.Phe210Cys) c.533T>G (p.Phe178Cys) n.557T>G | |
9 | g.136674767A>G | CA5342902 | AGPAT2 | c.629T>C (p.Phe210Ser) c.533T>C (p.Phe178Ser) n.557T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674767A>T | CA375578557 | AGPAT2 | c.629T>A (p.Phe210Tyr) c.533T>A (p.Phe178Tyr) n.557T>A | |
9 | g.136674768dup | CA1130033743 | AGPAT2 | c.629dup (p.Tyr211LeufsTer?) c.533dup (p.Tyr179LeufsTer?) n.557dup | dbSNP gnomAD v3 gnomAD v4 |
9 | g.136674768del | CA2692654223 | AGPAT2 | c.629del (p.Phe210SerfsTer?) c.533del (p.Phe178SerfsTer?) n.557del | gnomAD v4 |
9 | g.136674768A>C | CA375578558 | AGPAT2 | c.628T>G (p.Phe210Val) c.532T>G (p.Phe178Val) n.556T>G | |
9 | g.136674768A>G | CA375578562 | AGPAT2 | c.628T>C (p.Phe210Leu) c.532T>C (p.Phe178Leu) n.556T>C | gnomAD v4 |
9 | g.136674768A>T | CA375578563 | AGPAT2 | c.628T>A (p.Phe210Ile) c.532T>A (p.Phe178Ile) n.556T>A | gnomAD v4 |
9 | g.136674773_136674775del | CA5342901 | AGPAT2 | c.626_628del (p.Ser209del) c.530_532del (p.Ser177del) n.554_556del | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674769G>A | CA467738176 | AGPAT2 | c.627C>T (p.Ser209=) c.531C>T (p.Ser177=) n.555C>T | gnomAD v4 |
9 | g.136674769G>C | CA467738171 | AGPAT2 | c.627C>G (p.Ser209=) c.531C>G (p.Ser177=) n.555C>G | gnomAD v4 |
9 | g.136674769G>T | CA467738173 | AGPAT2 | c.627C>A (p.Ser209=) c.531C>A (p.Ser177=) n.555C>A | gnomAD v4 |
9 | g.136674770G>A | CA375578575 | AGPAT2 | c.626C>T (p.Ser209Phe) c.530C>T (p.Ser177Phe) n.554C>T | gnomAD v4 |
9 | g.136674770G>C | CA375578565 | AGPAT2 | c.626C>G (p.Ser209Cys) c.530C>G (p.Ser177Cys) n.554C>G | |
9 | g.136674770G>T | CA5342903 | AGPAT2 | c.626C>A (p.Ser209Tyr) c.530C>A (p.Ser177Tyr) n.554C>A | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.136674772_136674776del | CA913189691 | AGPAT2 | c.622_626del (p.Ser208LeufsTer?) c.526_530del (p.Ser176LeufsTer?) n.550_554del | ClinVar dbSNP |
9 | g.136674771A>C | CA375578591 | AGPAT2 | c.625T>G (p.Ser209Ala) c.529T>G (p.Ser177Ala) n.553T>G | |
9 | g.136674771A>G | CA375578593 | AGPAT2 | c.625T>C (p.Ser209Pro) c.529T>C (p.Ser177Pro) n.553T>C | gnomAD v4 |
9 | g.136674771A>T | CA375578596 | AGPAT2 | c.625T>A (p.Ser209Thr) c.529T>A (p.Ser177Thr) n.553T>A | |
9 | g.136674772G>A | CA467738195 | AGPAT2 | c.624C>T (p.Ser208=) c.528C>T (p.Ser176=) n.552C>T | dbSNP gnomAD v2 gnomAD v4 |
9 | g.136674772G>C | CA467738199 | AGPAT2 | c.624C>G (p.Ser208=) c.528C>G (p.Ser176=) n.552C>G | gnomAD v4 |
9 | g.136674772G>T | CA467738197 | AGPAT2 | c.624C>A (p.Ser208=) c.528C>A (p.Ser176=) n.552C>A | gnomAD v4 |
9 | g.136674773G>A | CA201627675 | AGPAT2 | c.623C>T (p.Ser208Phe) c.527C>T (p.Ser176Phe) n.551C>T | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
9 | g.136674773G>C | CA375578605 | AGPAT2 | c.623C>G (p.Ser208Cys) c.527C>G (p.Ser176Cys) n.551C>G | |
9 | g.136674773G>T | CA375578606 | AGPAT2 | c.623C>A (p.Ser208Tyr) c.527C>A (p.Ser176Tyr) n.551C>A | |
9 | g.136674774A>C | CA375578610 | AGPAT2 | c.622T>G (p.Ser208Ala) c.526T>G (p.Ser176Ala) n.550T>G | |
9 | g.136674774A>G | CA5342904 | AGPAT2 | c.622T>C (p.Ser208Pro) c.526T>C (p.Ser176Pro) n.550T>C | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674774A>T | CA375578608 | AGPAT2 | c.622T>A (p.Ser208Thr) c.526T>A (p.Ser176Thr) n.550T>A | gnomAD v4 |
9 | g.136674775G>A | CA467738219 | AGPAT2 | c.621C>T (p.Phe207=) c.525C>T (p.Phe175=) n.549C>T | ClinVar gnomAD v4 |
9 | g.136674775G>C | CA375578613 | AGPAT2 | c.621C>G (p.Phe207Leu) c.525C>G (p.Phe175Leu) n.549C>G | gnomAD v4 |
9 | g.136674775G>T | CA375578614 | AGPAT2 | c.621C>A (p.Phe207Leu) c.525C>A (p.Phe175Leu) n.549C>A | |
9 | g.136674779_136674782del | CA591183731 | AGPAT2 | c.618_621del (p.Phe207ProfsTer?) c.522_525del (p.Phe175ProfsTer?) n.546_549del | gnomAD v2 gnomAD v4 |
9 | g.136674776A>C | CA375578617 | AGPAT2 | c.620T>G (p.Phe207Cys) c.524T>G (p.Phe175Cys) n.548T>G | |
9 | g.136674776A>G | CA375578618 | AGPAT2 | c.620T>C (p.Phe207Ser) c.524T>C (p.Phe175Ser) n.548T>C | gnomAD v4 |
9 | g.136674776A>T | CA375578622 | AGPAT2 | c.620T>A (p.Phe207Tyr) c.524T>A (p.Phe175Tyr) n.548T>A | |
9 | g.136674777del | CA2692654224 | AGPAT2 | c.620del (p.Phe207SerfsTer?) c.524del (p.Phe175SerfsTer?) n.548del | gnomAD v4 |
9 | g.136674777A>C | CA375578630 | AGPAT2 | c.619T>G (p.Phe207Val) c.523T>G (p.Phe175Val) n.547T>G | |
9 | g.136674777A>G | CA375578628 | AGPAT2 | c.619T>C (p.Phe207Leu) c.523T>C (p.Phe175Leu) n.547T>C | gnomAD v4 |
9 | g.136674777A>T | CA375578629 | AGPAT2 | c.619T>A (p.Phe207Ile) c.523T>A (p.Phe175Ile) n.547T>A | gnomAD v4 |
9 | g.136674778G>A | CA5342905 | AGPAT2 | c.618C>T (p.Ser206=) c.522C>T (p.Ser174=) n.546C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674778G>C | CA467738236 | AGPAT2 | c.618C>G (p.Ser206=) c.522C>G (p.Ser174=) n.546C>G | |
9 | g.136674778G>T | CA467738238 | AGPAT2 | c.618C>A (p.Ser206=) c.522C>A (p.Ser174=) n.546C>A | |
9 | g.136674779G>A | CA5342906 | AGPAT2 | c.617C>T (p.Ser206Phe) c.521C>T (p.Ser174Phe) n.545C>T | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.136674779G>C | CA375578635 | AGPAT2 | c.617C>G (p.Ser206Cys) c.521C>G (p.Ser174Cys) n.545C>G | |
9 | g.136674779G>T | CA375578636 | AGPAT2 | c.617C>A (p.Ser206Tyr) c.521C>A (p.Ser174Tyr) n.545C>A | |
9 | g.136674780A>C | CA375578637 | AGPAT2 | c.616T>G (p.Ser206Ala) c.520T>G (p.Ser174Ala) n.544T>G | |
9 | g.136674780A>G | CA375578646 | AGPAT2 | c.616T>C (p.Ser206Pro) c.520T>C (p.Ser174Pro) n.544T>C | gnomAD v4 |
9 | g.136674780A>T | CA375578650 | AGPAT2 | c.616T>A (p.Ser206Thr) c.520T>A (p.Ser174Thr) n.544T>A | |
9 | g.136674781A>C | CA467738254 | AGPAT2 | c.615T>G (p.Ser205=) c.519T>G (p.Ser173=) n.543T>G | |
9 | g.136674781A>G | CA467738256 | AGPAT2 | c.615T>C (p.Ser205=) c.519T>C (p.Ser173=) n.543T>C | gnomAD v4 |
9 | g.136674781A>T | CA467738259 | AGPAT2 | c.615T>A (p.Ser205=) c.519T>A (p.Ser173=) n.543T>A | gnomAD v4 |
9 | g.136674782G>A | CA375578653 | AGPAT2 | c.614C>T (p.Ser205Phe) c.518C>T (p.Ser173Phe) n.542C>T | gnomAD v4 |
9 | g.136674782G>C | CA375578654 | AGPAT2 | c.614C>G (p.Ser205Cys) c.518C>G (p.Ser173Cys) n.542C>G | |
9 | g.136674782G>T | CA375578655 | AGPAT2 | c.614C>A (p.Ser205Tyr) c.518C>A (p.Ser173Tyr) n.542C>A | |
9 | g.136674783A>C | CA375578656 | AGPAT2 | c.613T>G (p.Ser205Ala) c.517T>G (p.Ser173Ala) n.541T>G | |
9 | g.136674783A>G | CA375578657 | AGPAT2 | c.613T>C (p.Ser205Pro) c.517T>C (p.Ser173Pro) n.541T>C | gnomAD v4 |
9 | g.136674783A>T | CA375578658 | AGPAT2 | c.613T>A (p.Ser205Thr) c.517T>A (p.Ser173Thr) n.541T>A | |
9 | g.136674784G>A | CA5342907 | AGPAT2 | c.612C>T (p.Tyr204=) c.516C>T (p.Tyr172=) n.540C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674784G>C | CA375578668 | AGPAT2 | c.612C>G (p.Tyr204Ter) c.516C>G (p.Tyr172Ter) n.540C>G | |
9 | g.136674784G>T | CA375578667 | AGPAT2 | c.612C>A (p.Tyr204Ter) c.516C>A (p.Tyr172Ter) n.540C>A | gnomAD v4 |
9 | g.136674785T>A | CA375578669 | AGPAT2 | c.611A>T (p.Tyr204Phe) c.515A>T (p.Tyr172Phe) n.539A>T | |
9 | g.136674785T>C | CA5342908 | AGPAT2 | c.611A>G (p.Tyr204Cys) c.515A>G (p.Tyr172Cys) n.539A>G | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.136674785T>G | CA375578678 | AGPAT2 | c.611A>C (p.Tyr204Ser) c.515A>C (p.Tyr172Ser) n.539A>C | |
9 | g.136674786A>C | CA375578679 | AGPAT2 | c.610T>G (p.Tyr204Asp) c.514T>G (p.Tyr172Asp) n.538T>G | |
9 | g.136674786A>G | CA375578680 | AGPAT2 | c.610T>C (p.Tyr204His) c.514T>C (p.Tyr172His) n.538T>C | gnomAD v4 |
9 | g.136674786A>T | CA375578684 | AGPAT2 | c.610T>A (p.Tyr204Asn) c.514T>A (p.Tyr172Asn) n.538T>A | |
9 | g.136674787C>A | CA467738276 | AGPAT2 | c.609G>T (p.Val203=) c.513G>T (p.Val171=) n.537G>T | gnomAD v4 |
9 | g.136674787C>G | CA467738277 | AGPAT2 | c.609G>C (p.Val203=) c.513G>C (p.Val171=) n.537G>C | |
9 | g.136674787C>T | CA467738279 | AGPAT2 | c.609G>A (p.Val203=) c.513G>A (p.Val171=) n.537G>A | gnomAD v4 |
9 | g.136674788A>C | CA375578688 | AGPAT2 | c.608T>G (p.Val203Gly) c.512T>G (p.Val171Gly) n.536T>G | |
9 | g.136674788A>G | CA375578689 | AGPAT2 | c.608T>C (p.Val203Ala) c.512T>C (p.Val171Ala) n.536T>C | dbSNP gnomAD v4 |
9 | g.136674788A>T | CA375578690 | AGPAT2 | c.608T>A (p.Val203Glu) c.512T>A (p.Val171Glu) n.536T>A | |
9 | g.136674789C>A | CA375578697 | AGPAT2 | c.607G>T (p.Val203Leu) c.511G>T (p.Val171Leu) n.535G>T | gnomAD v4 |
9 | g.136674789C>G | CA375578701 | AGPAT2 | c.607G>C (p.Val203Leu) c.511G>C (p.Val171Leu) n.535G>C | |
9 | g.136674789C>T | CA375578711 | AGPAT2 | c.607G>A (p.Val203Met) c.511G>A (p.Val171Met) n.535G>A | gnomAD v4 |
9 | g.136674790del | CA645547675 | AGPAT2 | c.607del (p.Val203CysfsTer?) c.511del (p.Val171CysfsTer?) n.535del | COSMIC |
9 | g.136674790C>A | CA467738295 | AGPAT2 | c.606G>T (p.Val202=) c.510G>T (p.Val170=) n.534G>T | gnomAD v4 |
9 | g.136674790C>G | CA467738296 | AGPAT2 | c.606G>C (p.Val202=) c.510G>C (p.Val170=) n.534G>C | |
9 | g.136674790C>T | CA467738306 | AGPAT2 | c.606G>A (p.Val202=) c.510G>A (p.Val170=) n.534G>A | gnomAD v4 |
9 | g.136674791A>C | CA375578751 | AGPAT2 | c.605T>G (p.Val202Gly) c.509T>G (p.Val170Gly) n.533T>G | |
9 | g.136674791A>G | CA375578740 | AGPAT2 | c.605T>C (p.Val202Ala) c.509T>C (p.Val170Ala) n.533T>C | |
9 | g.136674791A>T | CA375578748 | AGPAT2 | c.605T>A (p.Val202Glu) c.509T>A (p.Val170Glu) n.533T>A | |
9 | g.136674792del | CA2692654225 | AGPAT2 | c.604del (p.Val202TrpfsTer?) c.508del (p.Val170TrpfsTer?) n.532del | gnomAD v4 |
9 | g.136674792C>A | CA375578753 | AGPAT2 | c.604G>T (p.Val202Leu) c.508G>T (p.Val170Leu) n.532G>T | dbSNP gnomAD v4 |
9 | g.136674792C>G | CA375578757 | AGPAT2 | c.604G>C (p.Val202Leu) c.508G>C (p.Val170Leu) n.532G>C | gnomAD v4 |
9 | g.136674792C>T | CA5342909 | AGPAT2 | c.604G>A (p.Val202Met) c.508G>A (p.Val170Met) n.532G>A | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674793G>A | CA467738315 | AGPAT2 | c.603C>T (p.Pro201=) c.507C>T (p.Pro169=) n.531C>T | dbSNP gnomAD v2 gnomAD v4 |
9 | g.136674793G>C | CA467738317 | AGPAT2 | c.603C>G (p.Pro201=) c.507C>G (p.Pro169=) n.531C>G | dbSNP gnomAD v4 |
9 | g.136674793G>T | CA5342910 | AGPAT2 | c.603C>A (p.Pro201=) c.507C>A (p.Pro169=) n.531C>A | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674796del | CA2497275518 | AGPAT2 | c.603del (p.Val202TrpfsTer?) c.507del (p.Val170TrpfsTer?) n.531del | dbSNP gnomAD v4 |
9 | g.136674794G>A | CA375578792 | AGPAT2 | c.602C>T (p.Pro201Leu) c.506C>T (p.Pro169Leu) n.530C>T | gnomAD v4 |
9 | g.136674794G>C | CA375578795 | AGPAT2 | c.602C>G (p.Pro201Arg) c.506C>G (p.Pro169Arg) n.530C>G | |
9 | g.136674794G>T | CA375578799 | AGPAT2 | c.602C>A (p.Pro201His) c.506C>A (p.Pro169His) n.530C>A | gnomAD v4 |
9 | g.136674795G>A | CA375578810 | AGPAT2 | c.601C>T (p.Pro201Ser) c.505C>T (p.Pro169Ser) n.529C>T | dbSNP gnomAD v4 |
9 | g.136674795G>C | CA375578832 | AGPAT2 | c.601C>G (p.Pro201Ala) c.505C>G (p.Pro169Ala) n.529C>G | |
9 | g.136674795G>T | CA375578841 | AGPAT2 | c.601C>A (p.Pro201Thr) c.505C>A (p.Pro169Thr) n.529C>A | gnomAD v4 COSMIC |
9 | g.136674796G>A | CA5342911 | AGPAT2 | c.600C>T (p.Val200=) c.504C>T (p.Val168=) n.528C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674796G>C | CA467738332 | AGPAT2 | c.600C>G (p.Val200=) c.504C>G (p.Val168=) n.528C>G | |
9 | g.136674796G>T | CA467738328 | AGPAT2 | c.600C>A (p.Val200=) c.504C>A (p.Val168=) n.528C>A | gnomAD v4 |
9 | g.136674797A>C | CA375578882 | AGPAT2 | c.599T>G (p.Val200Gly) c.503T>G (p.Val168Gly) n.527T>G | |
9 | g.136674797A>G | CA375578857 | AGPAT2 | c.599T>C (p.Val200Ala) c.503T>C (p.Val168Ala) n.527T>C | gnomAD v4 |
9 | g.136674797A>T | CA375578856 | AGPAT2 | c.599T>A (p.Val200Asp) c.503T>A (p.Val168Asp) n.527T>A | |
9 | g.136674798C>A | CA201627695 | AGPAT2 | c.598G>T (p.Val200Phe) c.502G>T (p.Val168Phe) n.526G>T | dbSNP gnomAD v4 |
9 | g.136674798C>G | CA5342912 | AGPAT2 | c.598G>C (p.Val200Leu) c.502G>C (p.Val168Leu) n.526G>C | dbSNP ExAC gnomAD v2 gnomAD v4 |
9 | g.136674798C>T | CA375578889 | AGPAT2 | c.598G>A (p.Val200Ile) c.502G>A (p.Val168Ile) n.526G>A | dbSNP gnomAD v2 gnomAD v4 |
9 | g.136674799del | CA2692654226 | AGPAT2 | c.597del (p.Ile199MetfsTer?) c.501del (p.Ile167MetfsTer?) n.525del | gnomAD v4 |
9 | g.136674799G>A | CA5342913 | AGPAT2 | c.597C>T (p.Ile199=) c.501C>T (p.Ile167=) n.525C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674799G>C | CA375578891 | AGPAT2 | c.597C>G (p.Ile199Met) c.501C>G (p.Ile167Met) n.525C>G | |
9 | g.136674799G>T | CA467738339 | AGPAT2 | c.597C>A (p.Ile199=) c.501C>A (p.Ile167=) n.525C>A | gnomAD v4 |
9 | g.136674800A>C | CA375578900 | AGPAT2 | c.596T>G (p.Ile199Ser) c.500T>G (p.Ile167Ser) n.524T>G | |
9 | g.136674800A>G | CA375578906 | AGPAT2 | c.596T>C (p.Ile199Thr) c.500T>C (p.Ile167Thr) n.524T>C | dbSNP gnomAD v4 |
9 | g.136674800A>T | CA375578921 | AGPAT2 | c.596T>A (p.Ile199Asn) c.500T>A (p.Ile167Asn) n.524T>A | |
9 | g.136674801T>A | CA375578928 | AGPAT2 | c.595A>T (p.Ile199Phe) c.499A>T (p.Ile167Phe) n.523A>T | |
9 | g.136674801T>C | CA375578934 | AGPAT2 | c.595A>G (p.Ile199Val) c.499A>G (p.Ile167Val) n.523A>G | gnomAD v4 |
9 | g.136674801T>G | CA375578937 | AGPAT2 | c.595A>C (p.Ile199Leu) c.499A>C (p.Ile167Leu) n.523A>C | |
9 | g.136674802G>A | CA5342914 | AGPAT2 | c.594C>T (p.Pro198=) c.498C>T (p.Pro166=) n.522C>T | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
9 | g.136674802G>C | CA467738543 | AGPAT2 | c.594C>G (p.Pro198=) c.498C>G (p.Pro166=) n.522C>G | |
9 | g.136674802G>T | CA467738541 | AGPAT2 | c.594C>A (p.Pro198=) c.498C>A (p.Pro166=) n.522C>A | gnomAD v4 |
9 | g.136674804del | CA2692654227 | AGPAT2 | c.594del (p.Ile199SerfsTer?) c.498del (p.Ile167SerfsTer?) n.522del | gnomAD v4 |
9 | g.136674803G>A | CA375578965 | AGPAT2 | c.593C>T (p.Pro198Leu) c.497C>T (p.Pro166Leu) n.521C>T | gnomAD v4 |
9 | g.136674803G>C | CA375578968 | AGPAT2 | c.593C>G (p.Pro198Arg) c.497C>G (p.Pro166Arg) n.521C>G | |
9 | g.136674803G>T | CA375578970 | AGPAT2 | c.593C>A (p.Pro198His) c.497C>A (p.Pro166His) n.521C>A | gnomAD v4 |
9 | g.136674804G>A | CA375578979 | AGPAT2 | c.592C>T (p.Pro198Ser) c.496C>T (p.Pro166Ser) n.520C>T | dbSNP gnomAD v4 |
9 | g.136674804G>C | CA375578973 | AGPAT2 | c.592C>G (p.Pro198Ala) c.496C>G (p.Pro166Ala) n.520C>G | |
9 | g.136674804G>T | CA375578975 | AGPAT2 | c.592C>A (p.Pro198Thr) c.496C>A (p.Pro166Thr) n.520C>A | gnomAD v4 |
9 | g.136674805C>A | CA467738550 | AGPAT2 | c.591G>T (p.Val197=) c.495G>T (p.Val165=) n.519G>T | gnomAD v4 |
9 | g.136674805C>G | CA467738554 | AGPAT2 | c.591G>C (p.Val197=) c.495G>C (p.Val165=) n.519G>C | gnomAD v4 |
9 | g.136674805C>T | CA467738552 | AGPAT2 | c.591G>A (p.Val197=) c.495G>A (p.Val165=) n.519G>A | dbSNP gnomAD v4 |
9 | g.136674806A>C | CA375578980 | AGPAT2 | c.590T>G (p.Val197Gly) c.494T>G (p.Val165Gly) n.518T>G | |
9 | g.136674806A>G | CA375578983 | AGPAT2 | c.590T>C (p.Val197Ala) c.494T>C (p.Val165Ala) n.518T>C | gnomAD v4 |
9 | g.136674806A>T | CA375578986 | AGPAT2 | c.590T>A (p.Val197Glu) c.494T>A (p.Val165Glu) n.518T>A | |
9 | g.136674807C>A | CA375578988 | AGPAT2 | c.589G>T (p.Val197Leu) c.493G>T (p.Val165Leu) n.517G>T | gnomAD v4 |
9 | g.136674807C>G | CA375578989 | AGPAT2 | c.589G>C (p.Val197Leu) c.493G>C (p.Val165Leu) n.517G>C | gnomAD v4 |
9 | g.136674807C>T | CA375578990 | AGPAT2 | c.589G>A (p.Val197Met) c.493G>A (p.Val165Met) n.517G>A | gnomAD v4 |
9 | g.136674808C>A | CA375578992 | AGPAT2 | c.589-1G>T (n.589-1G>T) c.493-1G>T (n.493-1G>T) n.517-1G>T | gnomAD v4 |
9 | g.136674808C>G | CA375578994 | AGPAT2 | c.589-1G>C (n.589-1G>C) c.493-1G>C (n.493-1G>C) n.517-1G>C | |
9 | g.136674808C>T | CA375578997 | AGPAT2 | c.589-1G>A (n.589-1G>A) c.493-1G>A (n.493-1G>A) n.517-1G>A | dbSNP gnomAD v4 |