Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.44352112T>A | CA399768727 | GRN | c.1277T>A (p.Leu426Gln) c.1136+360T>A (n.1136+360T>A) c.718T>A c.806T>A (p.Leu269Gln) | |
17 | g.44352112T>C | CA399768724 | GRN | c.1277T>C (p.Leu426Pro) c.1136+360T>C (n.1136+360T>C) c.718T>C c.806T>C (p.Leu269Pro) | dbSNP |
17 | g.44352112T>G | CA399768721 | GRN | c.1277T>G (p.Leu426Arg) c.1136+360T>G (n.1136+360T>G) c.718T>G c.806T>G (p.Leu269Arg) | |
17 | g.44352112T= | CA2261354505 | GRN | c.1277T= (p.Leu426=) c.1136+360T= (n.1136+360T=) c.718T= c.806T= (p.Leu269=) | |
17 | g.44352113G>A | CA290926716 | GRN | c.1278G>A (p.Leu426=) c.1136+361G>A (n.1136+361G>A) c.719G>A c.807G>A (p.Leu269=) | dbSNP gnomAD v4 |
17 | g.44352113G>C | CA500622225 | GRN | c.1278G>C (p.Leu426=) c.1136+361G>C (n.1136+361G>C) c.719G>C c.807G>C (p.Leu269=) | |
17 | g.44352113G= | CA2261354506 | GRN | c.1278G= (p.Leu426=) c.1136+361G= (n.1136+361G=) c.719G= c.807G= (p.Leu269=) | |
17 | g.44352113G>T | CA500622226 | GRN | c.1278G>T (p.Leu426=) c.1136+361G>T (n.1136+361G>T) c.719G>T c.807G>T (p.Leu269=) | |
17 | g.44352114_44352116del | CA2837994618 | GRN | c.1279_1281del (p.Glu427del) c.1136+362_1136+364del (n.1136+362_1136+364del) c.720_722del c.808_810del (p.Glu270del) | |
17 | g.44352114G>A | CA399768728 | GRN | c.1279G>A (p.Glu427Lys) c.1136+362G>A (n.1136+362G>A) c.720G>A c.808G>A (p.Glu270Lys) | |
17 | g.44352114G>C | CA399768730 | GRN | c.1279G>C (p.Glu427Gln) c.1136+362G>C (n.1136+362G>C) c.720G>C c.808G>C (p.Glu270Gln) | |
17 | g.44352114G>T | CA399768732 | GRN | c.1279G>T (p.Glu427Ter) c.1136+362G>T (n.1136+362G>T) c.720G>T c.808G>T (p.Glu270Ter) | |
17 | g.44352115A= | CA2261354507 | GRN | c.1280A= (p.Glu427=) c.1136+363A= (n.1136+363A=) c.721A= c.809A= (p.Glu270=) | |
17 | g.44352115A>C | CA399768734 | GRN | c.1280A>C (p.Glu427Ala) c.1136+363A>C (n.1136+363A>C) c.721A>C c.809A>C (p.Glu270Ala) | |
17 | g.44352115A>G | CA399768736 | GRN | c.1280A>G (p.Glu427Gly) c.1136+363A>G (n.1136+363A>G) c.721A>G c.809A>G (p.Glu270Gly) | dbSNP |
17 | g.44352115A>T | CA399768738 | GRN | c.1280A>T (p.Glu427Val) c.1136+363A>T (n.1136+363A>T) c.721A>T c.809A>T (p.Glu270Val) | |
17 | g.44352116G>A | CA8602162 | GRN | c.1281G>A (p.Glu427=) c.1136+364G>A (n.1136+364G>A) c.722G>A c.810G>A (p.Glu270=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.44352116G>C | CA399768741 | GRN | c.1281G>C (p.Glu427Asp) c.1136+364G>C (n.1136+364G>C) c.722G>C c.810G>C (p.Glu270Asp) | |
17 | g.44352116G= | CA2261354508 | GRN | c.1281G= (p.Glu427=) c.1136+364G= (n.1136+364G=) c.722G= c.810G= (p.Glu270=) | |
17 | g.44352116G>T | CA399768743 | GRN | c.1281G>T (p.Glu427Asp) c.1136+364G>T (n.1136+364G>T) c.722G>T c.810G>T (p.Glu270Asp) | |
17 | g.44352117A>C | CA399768745 | GRN | c.1282A>C (p.Lys428Gln) c.1136+365A>C (n.1136+365A>C) c.723A>C c.811A>C (p.Lys271Gln) | |
17 | g.44352117A>G | CA399768746 | GRN | c.1282A>G (p.Lys428Glu) c.1136+365A>G (n.1136+365A>G) c.723A>G c.811A>G (p.Lys271Glu) | |
17 | g.44352117A>T | CA399768747 | GRN | c.1282A>T (p.Lys428Ter) c.1136+365A>T (n.1136+365A>T) c.723A>T c.811A>T (p.Lys271Ter) | |
17 | g.44352118A>C | CA399768751 | GRN | c.1283A>C (p.Lys428Thr) c.1136+366A>C (n.1136+366A>C) c.724A>C c.812A>C (p.Lys271Thr) | |
17 | g.44352118A>G | CA399768753 | GRN | c.1283A>G (p.Lys428Arg) c.1136+366A>G (n.1136+366A>G) c.724A>G c.812A>G (p.Lys271Arg) | |
17 | g.44352118A>T | CA399768750 | GRN | c.1283A>T (p.Lys428Met) c.1136+366A>T (n.1136+366A>T) c.724A>T c.812A>T (p.Lys271Met) | |
17 | g.44352119G>A | CA500622233 | GRN | c.1284G>A (p.Lys428=) c.1136+367G>A (n.1136+367G>A) c.725G>A c.813G>A (p.Lys271=) | |
17 | g.44352119G>C | CA399768755 | GRN | c.1284G>C (p.Lys428Asn) c.1136+367G>C (n.1136+367G>C) c.725G>C c.813G>C (p.Lys271Asn) | |
17 | g.44352119G>T | CA399768756 | GRN | c.1284G>T (p.Lys428Asn) c.1136+367G>T (n.1136+367G>T) c.725G>T c.813G>T (p.Lys271Asn) | |
17 | g.44352120A>C | CA399768758 | GRN | c.1285A>C (p.Met429Leu) c.1136+368A>C (n.1136+368A>C) c.726A>C c.814A>C (p.Met272Leu) | |
17 | g.44352120A>G | CA399768759 | GRN | c.1285A>G (p.Met429Val) c.1136+368A>G (n.1136+368A>G) c.726A>G c.814A>G (p.Met272Val) | |
17 | g.44352120A>T | CA399768760 | GRN | c.1285A>T (p.Met429Leu) c.1136+368A>T (n.1136+368A>T) c.726A>T c.814A>T (p.Met272Leu) | |
17 | g.44352121T>A | CA399768764 | GRN | c.1286T>A (p.Met429Lys) c.1136+369T>A (n.1136+369T>A) c.727T>A c.815T>A (p.Met272Lys) | |
17 | g.44352121T>C | CA399768761 | GRN | c.1286T>C (p.Met429Thr) c.1136+369T>C (n.1136+369T>C) c.727T>C c.815T>C (p.Met272Thr) | gnomAD v4 |
17 | g.44352121T>G | CA399768762 | GRN | c.1286T>G (p.Met429Arg) c.1136+369T>G (n.1136+369T>G) c.727T>G c.815T>G (p.Met272Arg) | |
17 | g.44352122G>A | CA290926717 | GRN | c.1287G>A (p.Met429Ile) c.1136+370G>A (n.1136+370G>A) c.728G>A c.816G>A (p.Met272Ile) | dbSNP gnomAD v3 gnomAD v4 |
17 | g.44352122G>C | CA399768765 | GRN | c.1287G>C (p.Met429Ile) c.1136+370G>C (n.1136+370G>C) c.728G>C c.816G>C (p.Met272Ile) | |
17 | g.44352122G= | CA2261354509 | GRN | c.1287G= (p.Met429=) c.1136+370G= (n.1136+370G=) c.728G= c.816G= (p.Met272=) | |
17 | g.44352122G>T | CA399768767 | GRN | c.1287G>T (p.Met429Ile) c.1136+370G>T (n.1136+370G>T) c.728G>T c.816G>T (p.Met272Ile) | COSMIC |
17 | g.44352123C>A | CA399768769 | GRN | c.1288C>A (p.Pro430Thr) c.1136+371C>A (n.1136+371C>A) c.729C>A c.817C>A (p.Pro273Thr) | gnomAD v4 |
17 | g.44352123C= | CA2261354510 | GRN | c.1288C= (p.Pro430=) c.1136+371C= (n.1136+371C=) c.729C= c.817C= (p.Pro273=) | |
17 | g.44352123C>G | CA8602163 | GRN | c.1288C>G (p.Pro430Ala) c.1136+371C>G (n.1136+371C>G) c.729C>G c.817C>G (p.Pro273Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44352123C>T | CA399768771 | GRN | c.1288C>T (p.Pro430Ser) c.1136+371C>T (n.1136+371C>T) c.729C>T c.817C>T (p.Pro273Ser) | |
17 | g.44352124C>A | CA399768773 | GRN | c.1289C>A (p.Pro430His) c.1136+372C>A (n.1136+372C>A) c.730C>A c.818C>A (p.Pro273His) | |
17 | g.44352124C>G | CA399768774 | GRN | c.1289C>G (p.Pro430Arg) c.1136+372C>G (n.1136+372C>G) c.730C>G c.818C>G (p.Pro273Arg) | |
17 | g.44352124C>T | CA399768772 | GRN | c.1289C>T (p.Pro430Leu) c.1136+372C>T (n.1136+372C>T) c.730C>T c.818C>T (p.Pro273Leu) | gnomAD v4 |
17 | g.44352125T>A | CA500622239 | GRN | c.1290T>A (p.Pro430=) c.1136+373T>A (n.1136+373T>A) c.731T>A c.819T>A (p.Pro273=) | |
17 | g.44352125T>C | CA500622240 | GRN | c.1290T>C (p.Pro430=) c.1136+373T>C (n.1136+373T>C) c.731T>C c.819T>C (p.Pro273=) | gnomAD v4 |
17 | g.44352125T>G | CA500622241 | GRN | c.1290T>G (p.Pro430=) c.1136+373T>G (n.1136+373T>G) c.731T>G c.819T>G (p.Pro273=) | |
17 | g.44352126G>A | CA399768775 | GRN | c.1291G>A (p.Ala431Thr) c.1136+374G>A (n.1136+374G>A) c.732G>A c.820G>A (p.Ala274Thr) | |
17 | g.44352126G>C | CA399768777 | GRN | c.1291G>C (p.Ala431Pro) c.1136+374G>C (n.1136+374G>C) c.732G>C c.820G>C (p.Ala274Pro) | |
17 | g.44352126G>T | CA399768776 | GRN | c.1291G>T (p.Ala431Ser) c.1136+374G>T (n.1136+374G>T) c.732G>T c.820G>T (p.Ala274Ser) | |
17 | g.44352127C>A | CA399768778 | GRN | c.1292C>A (p.Ala431Asp) c.1136+375C>A (n.1136+375C>A) c.733C>A c.821C>A (p.Ala274Asp) | |
17 | g.44352127C>G | CA399768779 | GRN | c.1292C>G (p.Ala431Gly) c.1136+375C>G (n.1136+375C>G) c.733C>G c.821C>G (p.Ala274Gly) | |
17 | g.44352127C>T | CA399768780 | GRN | c.1292C>T (p.Ala431Val) c.1136+375C>T (n.1136+375C>T) c.733C>T c.821C>T (p.Ala274Val) | COSMIC |
17 | g.44352128C>A | CA500622244 | GRN | c.1293C>A (p.Ala431=) c.1136+376C>A (n.1136+376C>A) c.734C>A c.822C>A (p.Ala274=) | |
17 | g.44352128C= | CA2261354511 | GRN | c.1293C= (p.Ala431=) c.1136+376C= (n.1136+376C=) c.734C= c.822C= (p.Ala274=) | |
17 | g.44352128C>G | CA500622245 | GRN | c.1293C>G (p.Ala431=) c.1136+376C>G (n.1136+376C>G) c.734C>G c.822C>G (p.Ala274=) | |
17 | g.44352128C>T | CA8602164 | GRN | c.1293C>T (p.Ala431=) c.1136+376C>T (n.1136+376C>T) c.734C>T c.822C>T (p.Ala274=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44352129C>A | CA399768781 | GRN | c.1294C>A (p.Arg432Ser) c.1136+377C>A (n.1136+377C>A) c.735C>A c.823C>A (p.Arg275Ser) | |
17 | g.44352129C= | CA2261354512 | GRN | c.1294C= (p.Arg432=) c.1136+377C= (n.1136+377C=) c.735C= c.823C= (p.Arg275=) | |
17 | g.44352129C>G | CA8602165 | GRN | c.1294C>G (p.Arg432Gly) c.1136+377C>G (n.1136+377C>G) c.735C>G c.823C>G (p.Arg275Gly) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.44352129C>T | CA225333 | GRN | c.1294C>T (p.Arg432Cys) c.1136+377C>T (n.1136+377C>T) c.735C>T c.823C>T (p.Arg275Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44352130G>A | CA290926750 | GRN | c.1295G>A (p.Arg432His) c.1136+378G>A (n.1136+378G>A) c.736G>A c.824G>A (p.Arg275His) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44352130G>C | CA399768782 | GRN | c.1295G>C (p.Arg432Pro) c.1136+378G>C (n.1136+378G>C) c.736G>C c.824G>C (p.Arg275Pro) | |
17 | g.44352130G= | CA2261354513 | GRN | c.1295G= (p.Arg432=) c.1136+378G= (n.1136+378G=) c.736G= c.824G= (p.Arg275=) | |
17 | g.44352130G>T | CA399768785 | GRN | c.1295G>T (p.Arg432Leu) c.1136+378G>T (n.1136+378G>T) c.736G>T c.824G>T (p.Arg275Leu) | gnomAD v4 |
17 | g.44352131C>A | CA500622249 | GRN | c.1296C>A (p.Arg432=) c.1136+379C>A (n.1136+379C>A) c.737C>A c.825C>A (p.Arg275=) | gnomAD v4 |
17 | g.44352131C>G | CA500622252 | GRN | c.1296C>G (p.Arg432=) c.1136+379C>G (n.1136+379C>G) c.737C>G c.825C>G (p.Arg275=) | |
17 | g.44352131C>T | CA500622250 | GRN | c.1296C>T (p.Arg432=) c.1136+379C>T (n.1136+379C>T) c.737C>T c.825C>T (p.Arg275=) | |
17 | g.44352132C>A | CA500622254 | GRN | c.1297C>A (p.Arg433=) c.1136+380C>A (n.1136+380C>A) c.738C>A c.826C>A (p.Arg276=) | gnomAD v4 |
17 | g.44352132C= | CA2261354514 | GRN | c.1297C= (p.Arg433=) c.1136+380C= (n.1136+380C=) c.738C= c.826C= (p.Arg276=) | |
17 | g.44352132C>G | CA399768787 | GRN | c.1297C>G (p.Arg433Gly) c.1136+380C>G (n.1136+380C>G) c.738C>G c.826C>G (p.Arg276Gly) | |
17 | g.44352132C>T | CA225336 | GRN | c.1297C>T (p.Arg433Trp) c.1136+380C>T (n.1136+380C>T) c.738C>T c.826C>T (p.Arg276Trp) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44352132_44352133delinsCG | CA2261354515 | GRN | c.1297_1298delinsCG (p.Arg433=) c.1136+380_1136+381delinsCG (n.1136+380_1136+381delinsCG) c.738_739delinsCG c.826_827delinsCG (p.Arg276=) | |
17 | g.44352133G>A | CA200816 | GRN | c.1298G>A (p.Arg433Gln) c.1136+381G>A (n.1136+381G>A) c.739G>A c.827G>A (p.Arg276Gln) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44352133G>C | CA399768792 | GRN | c.1298G>C (p.Arg433Pro) c.1136+381G>C (n.1136+381G>C) c.739G>C c.827G>C (p.Arg276Pro) | |
17 | g.44352133G= | CA2261354516 | GRN | c.1298G= (p.Arg433=) c.1136+381G= (n.1136+381G=) c.739G= c.827G= (p.Arg276=) | |
17 | g.44352133G>T | CA399768794 | GRN | c.1298G>T (p.Arg433Leu) c.1136+381G>T (n.1136+381G>T) c.739G>T c.827G>T (p.Arg276Leu) | |
17 | g.44352135del | CA626224248 | GRN | c.1300del (p.Ala434LeufsTer?) c.1136+383del (n.1136+383del) c.741del c.829del (p.Ala277LeufsTer?) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.44352134G>A | CA500622257 | GRN | c.1299G>A (p.Arg433=) c.1136+382G>A (n.1136+382G>A) c.740G>A c.828G>A (p.Arg276=) | |
17 | g.44352134G>C | CA500622258 | GRN | c.1299G>C (p.Arg433=) c.1136+382G>C (n.1136+382G>C) c.740G>C c.828G>C (p.Arg276=) | dbSNP gnomAD v4 |
17 | g.44352134G= | CA2261354517 | GRN | c.1299G= (p.Arg433=) c.1136+382G= (n.1136+382G=) c.740G= c.828G= (p.Arg276=) | |
17 | g.44352134G>T | CA500622259 | GRN | c.1299G>T (p.Arg433=) c.1136+382G>T (n.1136+382G>T) c.740G>T c.828G>T (p.Arg276=) | |
17 | g.44352135G>A | CA399768796 | GRN | c.1300G>A (p.Ala434Thr) c.1136+383G>A (n.1136+383G>A) c.741G>A c.829G>A (p.Ala277Thr) | gnomAD v4 |
17 | g.44352135G>C | CA399768800 | GRN | c.1300G>C (p.Ala434Pro) c.1136+383G>C (n.1136+383G>C) c.741G>C c.829G>C (p.Ala277Pro) | |
17 | g.44352135G>T | CA399768798 | GRN | c.1300G>T (p.Ala434Ser) c.1136+383G>T (n.1136+383G>T) c.741G>T c.829G>T (p.Ala277Ser) | |
17 | g.44352136C>A | CA399768802 | GRN | c.1301C>A (p.Ala434Asp) c.1136+384C>A (n.1136+384C>A) c.742C>A c.830C>A (p.Ala277Asp) | |
17 | g.44352136C= | CA2261354518 | GRN | c.1301C= (p.Ala434=) c.1136+384C= (n.1136+384C=) c.742C= c.830C= (p.Ala277=) | |
17 | g.44352136C>G | CA399768804 | GRN | c.1301C>G (p.Ala434Gly) c.1136+384C>G (n.1136+384C>G) c.742C>G c.830C>G (p.Ala277Gly) | |
17 | g.44352136C>T | CA8602166 | GRN | c.1301C>T (p.Ala434Val) c.1136+384C>T (n.1136+384C>T) c.742C>T c.830C>T (p.Ala277Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.44352137T>A | CA500622262 | GRN | c.1302T>A (p.Ala434=) c.1136+385T>A (n.1136+385T>A) c.743T>A c.831T>A (p.Ala277=) | |
17 | g.44352137T>C | CA500622263 | GRN | c.1302T>C (p.Ala434=) c.1136+385T>C (n.1136+385T>C) c.743T>C c.831T>C (p.Ala277=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44352137T>G | CA500622264 | GRN | c.1302T>G (p.Ala434=) c.1136+385T>G (n.1136+385T>G) c.743T>G c.831T>G (p.Ala277=) | |
17 | g.44352137T= | CA2261354519 | GRN | c.1302T= (p.Ala434=) c.1136+385T= (n.1136+385T=) c.743T= c.831T= (p.Ala277=) | |
17 | g.44352138T>A | CA399768805 | GRN | c.1303T>A (p.Ser435Thr) c.1136+386T>A (n.1136+386T>A) c.744T>A c.832T>A (p.Ser278Thr) | |
17 | g.44352138T>C | CA399768806 | GRN | c.1303T>C (p.Ser435Pro) c.1136+386T>C (n.1136+386T>C) c.744T>C c.832T>C (p.Ser278Pro) | |
17 | g.44352138T>G | CA399768808 | GRN | c.1303T>G (p.Ser435Ala) c.1136+386T>G (n.1136+386T>G) c.744T>G c.832T>G (p.Ser278Ala) | |
17 | g.44352139C>A | CA399768810 | GRN | c.1304C>A (p.Ser435Tyr) c.1136+387C>A (n.1136+387C>A) c.745C>A c.833C>A (p.Ser278Tyr) | |
17 | g.44352139C>G | CA399768812 | GRN | c.1304C>G (p.Ser435Cys) c.1136+387C>G (n.1136+387C>G) c.745C>G c.833C>G (p.Ser278Cys) | |
17 | g.44352139C>T | CA399768814 | GRN | c.1304C>T (p.Ser435Phe) c.1136+387C>T (n.1136+387C>T) c.745C>T c.833C>T (p.Ser278Phe) | COSMIC |
17 | g.44352140C>A | CA500622269 | GRN | c.1305C>A (p.Ser435=) c.1137-389C>A (n.1137-389C>A) c.746C>A c.834C>A (p.Ser278=) | |
17 | g.44352140C>G | CA500622270 | GRN | c.1305C>G (p.Ser435=) c.1137-389C>G (n.1137-389C>G) c.746C>G c.834C>G (p.Ser278=) | |
17 | g.44352140C>T | CA500622271 | GRN | c.1305C>T (p.Ser435=) c.1137-389C>T (n.1137-389C>T) c.746C>T c.834C>T (p.Ser278=) | |
17 | g.44352140_44352141del | CA2809588881 | GRN | c.1305_1306del (p.Leu436IlefsTer9) c.1137-389_1137-388del (n.1137-389_1137-388del) c.746_747del c.834_835del (p.Leu279IlefsTer9) | |
17 | g.44352141T>A | CA399768818 | GRN | c.1306T>A (p.Leu436Ile) c.1137-388T>A (n.1137-388T>A) c.747T>A c.835T>A (p.Leu279Ile) | |
17 | g.44352141T>C | CA500622275 | GRN | c.1306T>C (p.Leu436=) c.1137-388T>C (n.1137-388T>C) c.747T>C c.835T>C (p.Leu279=) | dbSNP |
17 | g.44352141T>G | CA399768821 | GRN | c.1306T>G (p.Leu436Val) c.1137-388T>G (n.1137-388T>G) c.747T>G c.835T>G (p.Leu279Val) | |
17 | g.44352142T>A | CA399768826 | GRN | c.1307T>A (p.Leu436Ter) c.1137-387T>A (n.1137-387T>A) c.748T>A c.836T>A (p.Leu279Ter) | |
17 | g.44352142T>C | CA399768829 | GRN | c.1307T>C (p.Leu436Ser) c.1137-387T>C (n.1137-387T>C) c.748T>C c.836T>C (p.Leu279Ser) | dbSNP gnomAD v3 gnomAD v4 |
17 | g.44352142T>G | CA399768828 | GRN | c.1307T>G (p.Leu436Ter) c.1137-387T>G (n.1137-387T>G) c.748T>G c.836T>G (p.Leu279Ter) | |
17 | g.44352142T= | CA2261354520 | GRN | c.1307T= (p.Leu436=) c.1137-387T= (n.1137-387T=) c.748T= c.836T= (p.Leu279=) | |
17 | g.44352143A>C | CA399768833 | GRN | c.1308A>C (p.Leu436Phe) c.1137-386A>C (n.1137-386A>C) c.749A>C c.837A>C (p.Leu279Phe) | |
17 | g.44352143A>G | CA500622276 | GRN | c.1308A>G (p.Leu436=) c.1137-386A>G (n.1137-386A>G) c.749A>G c.837A>G (p.Leu279=) | |
17 | g.44352143A>T | CA399768836 | GRN | c.1308A>T (p.Leu436Phe) c.1137-386A>T (n.1137-386A>T) c.749A>T c.837A>T (p.Leu279Phe) | |
17 | g.44352144T>A | CA399768840 | GRN | c.1309T>A (p.Ser437Thr) c.1137-385T>A (n.1137-385T>A) c.750T>A c.838T>A (p.Ser280Thr) | |
17 | g.44352144T>C | CA399768843 | GRN | c.1309T>C (p.Ser437Pro) c.1137-385T>C (n.1137-385T>C) c.750T>C c.838T>C (p.Ser280Pro) | |
17 | g.44352144T>G | CA399768845 | GRN | c.1309T>G (p.Ser437Ala) c.1137-385T>G (n.1137-385T>G) c.750T>G c.838T>G (p.Ser280Ala) | |
17 | g.44352145C>A | CA399768849 | GRN | c.1310C>A (p.Ser437Tyr) c.1137-384C>A (n.1137-384C>A) c.751C>A c.839C>A (p.Ser280Tyr) | |
17 | g.44352145C>G | CA399768851 | GRN | c.1310C>G (p.Ser437Cys) c.1137-384C>G (n.1137-384C>G) c.751C>G c.839C>G (p.Ser280Cys) | |
17 | g.44352145C>T | CA399768853 | GRN | c.1310C>T (p.Ser437Phe) c.1137-384C>T (n.1137-384C>T) c.751C>T c.839C>T (p.Ser280Phe) | |
17 | g.44352146C>A | CA500622280 | GRN | c.1311C>A (p.Ser437=) c.1137-383C>A (n.1137-383C>A) c.752C>A c.840C>A (p.Ser280=) | |
17 | g.44352146C= | CA2261354521 | GRN | c.1311C= (p.Ser437=) c.1137-383C= (n.1137-383C=) c.752C= c.840C= (p.Ser280=) | |
17 | g.44352146C>G | CA8602167 | GRN | c.1311C>G (p.Ser437=) c.1137-383C>G (n.1137-383C>G) c.752C>G c.840C>G (p.Ser280=) | dbSNP ExAC gnomAD v2 |
17 | g.44352146C>T | CA290926758 | GRN | c.1311C>T (p.Ser437=) c.1137-383C>T (n.1137-383C>T) c.752C>T c.840C>T (p.Ser280=) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.44352147C>A | CA399768862 | GRN | c.1312C>A (p.His438Asn) c.1137-382C>A (n.1137-382C>A) c.753C>A c.841C>A (p.His281Asn) | |
17 | g.44352147C>G | CA399768866 | GRN | c.1312C>G (p.His438Asp) c.1137-382C>G (n.1137-382C>G) c.753C>G c.841C>G (p.His281Asp) | |
17 | g.44352147C>T | CA399768868 | GRN | c.1312C>T (p.His438Tyr) c.1137-382C>T (n.1137-382C>T) c.753C>T c.841C>T (p.His281Tyr) | |
17 | g.44352148A>C | CA399768872 | GRN | c.1313A>C (p.His438Pro) c.1137-381A>C (n.1137-381A>C) c.754A>C c.842A>C (p.His281Pro) | |
17 | g.44352148A>G | CA399768877 | GRN | c.1313A>G (p.His438Arg) c.1137-381A>G (n.1137-381A>G) c.754A>G c.842A>G (p.His281Arg) | |
17 | g.44352148A>T | CA399768875 | GRN | c.1313A>T (p.His438Leu) c.1137-381A>T (n.1137-381A>T) c.754A>T c.842A>T (p.His281Leu) | |
17 | g.44352149C>A | CA399768880 | GRN | c.1314C>A (p.His438Gln) c.1137-380C>A (n.1137-380C>A) c.755C>A c.843C>A (p.His281Gln) | |
17 | g.44352149C= | CA2261354522 | GRN | c.1314C= (p.His438=) c.1137-380C= (n.1137-380C=) c.755C= c.843C= (p.His281=) | |
17 | g.44352149C>G | CA399768883 | GRN | c.1314C>G (p.His438Gln) c.1137-380C>G (n.1137-380C>G) c.755C>G c.843C>G (p.His281Gln) | |
17 | g.44352149C>T | CA500622284 | GRN | c.1314C>T (p.His438=) c.1137-380C>T (n.1137-380C>T) c.755C>T c.843C>T (p.His281=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44352152del | CA2579758278 | GRN | c.1317del (p.Arg440GlufsTer?) c.1137-377del (n.1137-377del) c.758del c.846del (p.Arg283GlufsTer?) | |
17 | g.44352150C>A | CA399768886 | GRN | c.1315C>A (p.Pro439Thr) c.1137-379C>A (n.1137-379C>A) c.756C>A c.844C>A (p.Pro282Thr) | |
17 | g.44352150C>G | CA399768889 | GRN | c.1315C>G (p.Pro439Ala) c.1137-379C>G (n.1137-379C>G) c.756C>G c.844C>G (p.Pro282Ala) | |
17 | g.44352150C>T | CA399768891 | GRN | c.1315C>T (p.Pro439Ser) c.1137-379C>T (n.1137-379C>T) c.756C>T c.844C>T (p.Pro282Ser) | |
17 | g.44352151C>A | CA399768895 | GRN | c.1316C>A (p.Pro439His) c.1137-378C>A (n.1137-378C>A) c.757C>A c.845C>A (p.Pro282His) | |
17 | g.44352151C= | CA2261354523 | GRN | c.1316C= (p.Pro439=) c.1137-378C= (n.1137-378C=) c.757C= c.845C= (p.Pro282=) | |
17 | g.44352151C>G | CA8602168 | GRN | c.1316C>G (p.Pro439Arg) c.1137-378C>G (n.1137-378C>G) c.757C>G c.845C>G (p.Pro282Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44352151C>T | CA399768897 | GRN | c.1316C>T (p.Pro439Leu) c.1137-378C>T (n.1137-378C>T) c.757C>T c.845C>T (p.Pro282Leu) | dbSNP gnomAD v3 gnomAD v4 |
17 | g.44352152C>A | CA500622286 | GRN | c.1317C>A (p.Pro439=) c.1137-377C>A (n.1137-377C>A) c.758C>A c.846C>A (p.Pro282=) | |
17 | g.44352152C>G | CA500622289 | GRN | c.1317C>G (p.Pro439=) c.1137-377C>G (n.1137-377C>G) c.758C>G c.846C>G (p.Pro282=) | |
17 | g.44352152C>T | CA500622288 | GRN | c.1317C>T (p.Pro439=) c.1137-377C>T (n.1137-377C>T) c.758C>T c.846C>T (p.Pro282=) | |
17 | g.44352152_44352153del | CA2576290563 | GRN | c.1317_1318del (p.Asp441HisfsTer4) c.1137-377_1137-376del (n.1137-377_1137-376del) c.758_759del c.846_847del (p.Asp284HisfsTer4) | ClinVar |
17 | g.44352153A>C | CA500622291 | GRN | c.1318A>C (p.Arg440=) c.1137-376A>C (n.1137-376A>C) c.759A>C c.847A>C (p.Arg283=) | |
17 | g.44352153A>G | CA399768901 | GRN | c.1318A>G (p.Arg440Gly) c.1137-376A>G (n.1137-376A>G) c.759A>G c.847A>G (p.Arg283Gly) | gnomAD v4 |
17 | g.44352153A>T | CA399768903 | GRN | c.1318A>T (p.Arg440Ter) c.1137-376A>T (n.1137-376A>T) c.759A>T c.847A>T (p.Arg283Ter) | |
17 | g.44352154G>A | CA399768913 | GRN | c.1319G>A (p.Arg440Lys) c.1137-375G>A (n.1137-375G>A) c.760G>A c.848G>A (p.Arg283Lys) | |
17 | g.44352154G>C | CA399768911 | GRN | c.1319G>C (p.Arg440Thr) c.1137-375G>C (n.1137-375G>C) c.760G>C c.848G>C (p.Arg283Thr) | |
17 | g.44352154G>T | CA399768907 | GRN | c.1319G>T (p.Arg440Ile) c.1137-375G>T (n.1137-375G>T) c.760G>T c.848G>T (p.Arg283Ile) | |
17 | g.44352155A>C | CA399768917 | GRN | c.1320A>C (p.Arg440Ser) c.1137-374A>C (n.1137-374A>C) c.761A>C c.849A>C (p.Arg283Ser) | |
17 | g.44352155A>G | CA500622296 | GRN | c.1320A>G (p.Arg440=) c.1137-374A>G (n.1137-374A>G) c.761A>G c.849A>G (p.Arg283=) | |
17 | g.44352155A>T | CA399768919 | GRN | c.1320A>T (p.Arg440Ser) c.1137-374A>T (n.1137-374A>T) c.761A>T c.849A>T (p.Arg283Ser) | |
17 | g.44352156G>A | CA399768922 | GRN | c.1321G>A (p.Asp441Asn) c.1137-373G>A (n.1137-373G>A) c.762G>A c.850G>A (p.Asp284Asn) | |
17 | g.44352156G>C | CA399768925 | GRN | c.1321G>C (p.Asp441His) c.1137-373G>C (n.1137-373G>C) c.762G>C c.850G>C (p.Asp284His) | |
17 | g.44352156G>T | CA399768928 | GRN | c.1321G>T (p.Asp441Tyr) c.1137-373G>T (n.1137-373G>T) c.762G>T c.850G>T (p.Asp284Tyr) | |
17 | g.44352157A>C | CA399768930 | GRN | c.1322A>C (p.Asp441Ala) c.1137-372A>C (n.1137-372A>C) c.763A>C c.851A>C (p.Asp284Ala) | |
17 | g.44352157A>G | CA399768937 | GRN | c.1322A>G (p.Asp441Gly) c.1137-372A>G (n.1137-372A>G) c.763A>G c.851A>G (p.Asp284Gly) | |
17 | g.44352157A>T | CA399768940 | GRN | c.1322A>T (p.Asp441Val) c.1137-372A>T (n.1137-372A>T) c.763A>T c.851A>T (p.Asp284Val) | |
17 | g.44352158C>A | CA399768944 | GRN | c.1323C>A (p.Asp441Glu) c.1137-371C>A (n.1137-371C>A) c.764C>A c.852C>A (p.Asp284Glu) | |
17 | g.44352158C>G | CA399768947 | GRN | c.1323C>G (p.Asp441Glu) c.1137-371C>G (n.1137-371C>G) c.764C>G c.852C>G (p.Asp284Glu) | |
17 | g.44352158C>T | CA500622303 | GRN | c.1323C>T (p.Asp441=) c.1137-371C>T (n.1137-371C>T) c.764C>T c.852C>T (p.Asp284=) | |
17 | g.44352159A= | CA2261354524 | GRN | c.1324A= (p.Ile442=) c.1137-370A= (n.1137-370A=) c.765A= c.853A= (p.Ile285=) | |
17 | g.44352159A>C | CA399768950 | GRN | c.1324A>C (p.Ile442Leu) c.1137-370A>C (n.1137-370A>C) c.765A>C c.853A>C (p.Ile285Leu) | dbSNP gnomAD v3 gnomAD v4 |
17 | g.44352159A>G | CA290926765 | GRN | c.1324A>G (p.Ile442Val) c.1137-370A>G (n.1137-370A>G) c.765A>G c.853A>G (p.Ile285Val) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.44352159A>T | CA399768955 | GRN | c.1324A>T (p.Ile442Phe) c.1137-370A>T (n.1137-370A>T) c.765A>T c.853A>T (p.Ile285Phe) | |
17 | g.44352160T>A | CA399768960 | GRN | c.1325T>A (p.Ile442Asn) c.1137-369T>A (n.1137-369T>A) c.766T>A c.854T>A (p.Ile285Asn) | |
17 | g.44352160T>C | CA399768963 | GRN | c.1325T>C (p.Ile442Thr) c.1137-369T>C (n.1137-369T>C) c.766T>C c.854T>C (p.Ile285Thr) | |
17 | g.44352160T>G | CA399768965 | GRN | c.1325T>G (p.Ile442Ser) c.1137-369T>G (n.1137-369T>G) c.766T>G c.854T>G (p.Ile285Ser) | |
17 | g.44352161C>A | CA500622305 | GRN | c.1326C>A (p.Ile442=) c.1137-368C>A (n.1137-368C>A) c.767C>A c.855C>A (p.Ile285=) | |
17 | g.44352161C= | CA2261354525 | GRN | c.1326C= (p.Ile442=) c.1137-368C= (n.1137-368C=) c.767C= c.855C= (p.Ile285=) | |
17 | g.44352161C>G | CA8602170 | GRN | c.1326C>G (p.Ile442Met) c.1137-368C>G (n.1137-368C>G) c.767C>G c.855C>G (p.Ile285Met) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44352161C>T | CA8602169 | GRN | c.1326C>T (p.Ile442=) c.1137-368C>T (n.1137-368C>T) c.767C>T c.855C>T (p.Ile285=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44352162G>A | CA8602171 | GRN | c.1327G>A (p.Gly443Ser) c.1137-367G>A (n.1137-367G>A) c.768G>A c.856G>A (p.Gly286Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44352162G>C | CA399768975 | GRN | c.1327G>C (p.Gly443Arg) c.1137-367G>C (n.1137-367G>C) c.768G>C c.856G>C (p.Gly286Arg) | ClinVar gnomAD v4 |
17 | g.44352162G= | CA2261354526 | GRN | c.1327G= (p.Gly443=) c.1137-367G= (n.1137-367G=) c.768G= c.856G= (p.Gly286=) | |
17 | g.44352162G>T | CA399768978 | GRN | c.1327G>T (p.Gly443Cys) c.1137-367G>T (n.1137-367G>T) c.768G>T c.856G>T (p.Gly286Cys) | |
17 | g.44352163G>A | CA399768981 | GRN | c.1328G>A (p.Gly443Asp) c.1137-366G>A (n.1137-366G>A) c.769G>A c.857G>A (p.Gly286Asp) | gnomAD v4 |
17 | g.44352163G>C | CA399768984 | GRN | c.1328G>C (p.Gly443Ala) c.1137-366G>C (n.1137-366G>C) c.769G>C c.857G>C (p.Gly286Ala) | |
17 | g.44352163G>T | CA399768986 | GRN | c.1328G>T (p.Gly443Val) c.1137-366G>T (n.1137-366G>T) c.769G>T c.857G>T (p.Gly286Val) | |
17 | g.44352164C>A | CA500622308 | GRN | c.1329C>A (p.Gly443=) c.1137-365C>A (n.1137-365C>A) c.770C>A c.858C>A (p.Gly286=) | |
17 | g.44352164C= | CA2261354527 | GRN | c.1329C= (p.Gly443=) c.1137-365C= (n.1137-365C=) c.770C= c.858C= (p.Gly286=) | |
17 | g.44352164C>G | CA500622309 | GRN | c.1329C>G (p.Gly443=) c.1137-365C>G (n.1137-365C>G) c.770C>G c.858C>G (p.Gly286=) | |
17 | g.44352164C>T | CA500622310 | GRN | c.1329C>T (p.Gly443=) c.1137-365C>T (n.1137-365C>T) c.770C>T c.858C>T (p.Gly286=) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.44352165T>A | CA399768989 | GRN | c.1330T>A (p.Cys444Ser) c.1137-364T>A (n.1137-364T>A) c.771T>A c.859T>A (p.Cys287Ser) | |
17 | g.44352165T>C | CA399768992 | GRN | c.1330T>C (p.Cys444Arg) c.1137-364T>C (n.1137-364T>C) c.771T>C c.859T>C (p.Cys287Arg) | ClinVar |
17 | g.44352165T>G | CA399768995 | GRN | c.1330T>G (p.Cys444Gly) c.1137-364T>G (n.1137-364T>G) c.771T>G c.859T>G (p.Cys287Gly) | |
17 | g.44352166G>A | CA8602172 | GRN | c.1331G>A (p.Cys444Tyr) c.1137-363G>A (n.1137-363G>A) c.772G>A c.860G>A (p.Cys287Tyr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.44352166G>C | CA399769000 | GRN | c.1331G>C (p.Cys444Ser) c.1137-363G>C (n.1137-363G>C) c.772G>C c.860G>C (p.Cys287Ser) | |
17 | g.44352166G= | CA2261354528 | GRN | c.1331G= (p.Cys444=) c.1137-363G= (n.1137-363G=) c.772G= c.860G= (p.Cys287=) | |
17 | g.44352166G>T | CA399769003 | GRN | c.1331G>T (p.Cys444Phe) c.1137-363G>T (n.1137-363G>T) c.772G>T c.860G>T (p.Cys287Phe) | |
17 | g.44352167T>A | CA399769006 | GRN | c.1332T>A (p.Cys444Ter) c.1137-362T>A (n.1137-362T>A) c.773T>A c.861T>A (p.Cys287Ter) | |
17 | g.44352167T>C | CA500622314 | GRN | c.1332T>C (p.Cys444=) c.1137-362T>C (n.1137-362T>C) c.773T>C c.861T>C (p.Cys287=) | |
17 | g.44352167T>G | CA399769009 | GRN | c.1332T>G (p.Cys444Trp) c.1137-362T>G (n.1137-362T>G) c.773T>G c.861T>G (p.Cys287Trp) | |
17 | g.44352168G>A | CA8602173 | GRN | c.1333G>A (p.Asp445Asn) c.1137-361G>A (n.1137-361G>A) c.774G>A c.862G>A (p.Asp288Asn) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.44352168G>C | CA399769013 | GRN | c.1333G>C (p.Asp445His) c.1137-361G>C (n.1137-361G>C) c.774G>C c.862G>C (p.Asp288His) | |
17 | g.44352168G= | CA2261354529 | GRN | c.1333G= (p.Asp445=) c.1137-361G= (n.1137-361G=) c.774G= c.862G= (p.Asp288=) | |
17 | g.44352168G>T | CA399769015 | GRN | c.1333G>T (p.Asp445Tyr) c.1137-361G>T (n.1137-361G>T) c.774G>T c.862G>T (p.Asp288Tyr) | |
17 | g.44352169A>C | CA399769019 | GRN | c.1334A>C (p.Asp445Ala) c.1137-360A>C (n.1137-360A>C) c.775A>C c.863A>C (p.Asp288Ala) | |
17 | g.44352169A>G | CA399769021 | GRN | c.1334A>G (p.Asp445Gly) c.1137-360A>G (n.1137-360A>G) c.775A>G c.863A>G (p.Asp288Gly) | |
17 | g.44352169A>T | CA399769024 | GRN | c.1334A>T (p.Asp445Val) c.1137-360A>T (n.1137-360A>T) c.775A>T c.863A>T (p.Asp288Val) | |
17 | g.44352170C>A | CA399769029 | GRN | c.1335C>A (p.Asp445Glu) c.1137-359C>A (n.1137-359C>A) c.776C>A c.864C>A (p.Asp288Glu) | gnomAD v4 |
17 | g.44352170C>G | CA399769030 | GRN | c.1335C>G (p.Asp445Glu) c.1137-359C>G (n.1137-359C>G) c.776C>G c.864C>G (p.Asp288Glu) | |
17 | g.44352170C>T | CA500622317 | GRN | c.1335C>T (p.Asp445=) c.1137-359C>T (n.1137-359C>T) c.776C>T c.864C>T (p.Asp288=) | COSMIC |
17 | g.44352171C>A | CA399769032 | GRN | c.1336C>A (p.Gln446Lys) c.1137-358C>A (n.1137-358C>A) c.777C>A c.865C>A (p.Gln289Lys) | |
17 | g.44352171C>G | CA399769036 | GRN | c.1336C>G (p.Gln446Glu) c.1137-358C>G (n.1137-358C>G) c.777C>G c.865C>G (p.Gln289Glu) | |
17 | g.44352171C>T | CA399769038 | GRN | c.1336C>T (p.Gln446Ter) c.1137-358C>T (n.1137-358C>T) c.777C>T c.865C>T (p.Gln289Ter) | gnomAD v4 |
17 | g.44352172A= | CA2261354530 | GRN | c.1337A= (p.Gln446=) c.1137-357A= (n.1137-357A=) c.778A= c.866A= (p.Gln289=) | |
17 | g.44352172A>C | CA399769041 | GRN | c.1337A>C (p.Gln446Pro) c.1137-357A>C (n.1137-357A>C) c.778A>C c.866A>C (p.Gln289Pro) | |
17 | g.44352172A>G | CA399769044 | GRN | c.1337A>G (p.Gln446Arg) c.1137-357A>G (n.1137-357A>G) c.778A>G c.866A>G (p.Gln289Arg) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44352172A>T | CA8602174 | GRN | c.1337A>T (p.Gln446Leu) c.1137-357A>T (n.1137-357A>T) c.778A>T c.866A>T (p.Gln289Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.44352173G>A | CA500622321 | GRN | c.1338G>A (p.Gln446=) c.1137-356G>A (n.1137-356G>A) c.779G>A c.867G>A (p.Gln289=) | |
17 | g.44352173G>C | CA399769049 | GRN | c.1338G>C (p.Gln446His) c.1137-356G>C (n.1137-356G>C) c.779G>C c.867G>C (p.Gln289His) | |
17 | g.44352173G>T | CA399769052 | GRN | c.1338G>T (p.Gln446His) c.1137-356G>T (n.1137-356G>T) c.779G>T c.867G>T (p.Gln289His) | |
17 | g.44352174C>A | CA399769055 | GRN | c.1339C>A (p.His447Asn) c.1137-355C>A (n.1137-355C>A) c.780C>A c.868C>A (p.His290Asn) | |
17 | g.44352174C= | CA2261354531 | GRN | c.1339C= (p.His447=) c.1137-355C= (n.1137-355C=) c.780C= c.868C= (p.His290=) | |
17 | g.44352174C>G | CA399769058 | GRN | c.1339C>G (p.His447Asp) c.1137-355C>G (n.1137-355C>G) c.780C>G c.868C>G (p.His290Asp) | |
17 | g.44352174C>T | CA399769061 | GRN | c.1339C>T (p.His447Tyr) c.1137-355C>T (n.1137-355C>T) c.780C>T c.868C>T (p.His290Tyr) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.44352175A>C | CA399769064 | GRN | c.1340A>C (p.His447Pro) c.1137-354A>C (n.1137-354A>C) c.781A>C c.869A>C (p.His290Pro) | COSMIC |
17 | g.44352175A>G | CA399769067 | GRN | c.1340A>G (p.His447Arg) c.1137-354A>G (n.1137-354A>G) c.781A>G c.869A>G (p.His290Arg) | |
17 | g.44352175A>T | CA399769069 | GRN | c.1340A>T (p.His447Leu) c.1137-354A>T (n.1137-354A>T) c.781A>T c.869A>T (p.His290Leu) | |
17 | g.44352176C>A | CA399769073 | GRN | c.1341C>A (p.His447Gln) c.1137-353C>A (n.1137-353C>A) c.782C>A c.870C>A (p.His290Gln) | |
17 | g.44352176C= | CA2261354532 | GRN | c.1341C= (p.His447=) c.1137-353C= (n.1137-353C=) c.782C= c.870C= (p.His290=) | |
17 | g.44352176C>G | CA399769075 | GRN | c.1341C>G (p.His447Gln) c.1137-353C>G (n.1137-353C>G) c.782C>G c.870C>G (p.His290Gln) | |
17 | g.44352176C>T | CA225339 | GRN | c.1341C>T (p.His447=) c.1137-353C>T (n.1137-353C>T) c.782C>T c.870C>T (p.His290=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44352177A>C | CA399769080 | GRN | c.1342A>C (p.Thr448Pro) c.1137-352A>C (n.1137-352A>C) c.783A>C c.871A>C (p.Thr291Pro) | |
17 | g.44352177A>G | CA399769082 | GRN | c.1342A>G (p.Thr448Ala) c.1137-352A>G (n.1137-352A>G) c.783A>G c.871A>G (p.Thr291Ala) | gnomAD v4 COSMIC |
17 | g.44352177A>T | CA399769085 | GRN | c.1342A>T (p.Thr448Ser) c.1137-352A>T (n.1137-352A>T) c.783A>T c.871A>T (p.Thr291Ser) | |
17 | g.44352180_44352200del | CA2576290564 | GRN | c.1345_1365del (p.Ser449_Thr455del) c.1137-349_1137-329del (n.1137-349_1137-329del) c.786_806del c.874_894del (p.Ser292_Thr298del) | gnomAD v4 |
17 | g.44352178C>A | CA399769088 | GRN | c.1343C>A (p.Thr448Asn) c.1137-351C>A (n.1137-351C>A) c.784C>A c.872C>A (p.Thr291Asn) | |
17 | g.44352178C= | CA2261354533 | GRN | c.1343C= (p.Thr448=) c.1137-351C= (n.1137-351C=) c.784C= c.872C= (p.Thr291=) | |
17 | g.44352178C>G | CA399769094 | GRN | c.1343C>G (p.Thr448Ser) c.1137-351C>G (n.1137-351C>G) c.784C>G c.872C>G (p.Thr291Ser) | |
17 | g.44352178C>T | CA399769091 | GRN | c.1343C>T (p.Thr448Ile) c.1137-351C>T (n.1137-351C>T) c.784C>T c.872C>T (p.Thr291Ile) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
17 | g.44352179C>A | CA500622331 | GRN | c.1344C>A (p.Thr448=) c.1137-350C>A (n.1137-350C>A) c.785C>A c.873C>A (p.Thr291=) | |
17 | g.44352179C= | CA2261354534 | GRN | c.1344C= (p.Thr448=) c.1137-350C= (n.1137-350C=) c.785C= c.873C= (p.Thr291=) | |
17 | g.44352179C>G | CA500622333 | GRN | c.1344C>G (p.Thr448=) c.1137-350C>G (n.1137-350C>G) c.785C>G c.873C>G (p.Thr291=) | ClinVar gnomAD v4 |
17 | g.44352179C>T | CA500622335 | GRN | c.1344C>T (p.Thr448=) c.1137-350C>T (n.1137-350C>T) c.785C>T c.873C>T (p.Thr291=) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
17 | g.44352180A>C | CA399769097 | GRN | c.1345A>C (p.Ser449Arg) c.1137-349A>C (n.1137-349A>C) c.786A>C c.874A>C (p.Ser292Arg) | |
17 | g.44352180A>G | CA399769107 | GRN | c.1345A>G (p.Ser449Gly) c.1137-349A>G (n.1137-349A>G) c.786A>G c.874A>G (p.Ser292Gly) | |
17 | g.44352180A>T | CA399769099 | GRN | c.1345A>T (p.Ser449Cys) c.1137-349A>T (n.1137-349A>T) c.786A>T c.874A>T (p.Ser292Cys) | |
17 | g.44352180_44352201delinsAGCTGCCCGGTGGGGCAGACCT | CA2261354535 | GRN | c.1345_1366delinsAGCTGCCCGGTGGGGCAGACCT (p.Ser449=) c.1137-349_1137-328delinsAGCTGCCCGGTGGGGCAGACCT (n.1137-349_1137-328delinsAGCTGCCCGGTGGGGCAGACCT) c.786_807delinsAGCTGCCCGGTGGGGCAGACCT c.874_895delinsAGCTGCCCGGTGGGGCAGACCT (p.Ser292=) | |
17 | g.44352181G>A | CA8602176 | GRN | c.1346G>A (p.Ser449Asn) c.1137-348G>A (n.1137-348G>A) c.787G>A c.875G>A (p.Ser292Asn) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.44352181G>C | CA399769113 | GRN | c.1346G>C (p.Ser449Thr) c.1137-348G>C (n.1137-348G>C) c.787G>C c.875G>C (p.Ser292Thr) | gnomAD v4 |
17 | g.44352181G= | CA2261354536 | GRN | c.1346G= (p.Ser449=) c.1137-348G= (n.1137-348G=) c.787G= c.875G= (p.Ser292=) | |
17 | g.44352181G>T | CA399769116 | GRN | c.1346G>T (p.Ser449Ile) c.1137-348G>T (n.1137-348G>T) c.787G>T c.875G>T (p.Ser292Ile) | |
17 | g.44352189_44352209del | CA8602175 | GRN | c.1354_1374del (p.Val452_Pro458del) c.1137-340_1137-320del (n.1137-340_1137-320del) c.795_815del c.883_903del (p.Val295_Pro301del) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44352182C>A | CA399769124 | GRN | c.1347C>A (p.Ser449Arg) c.1137-347C>A (n.1137-347C>A) c.788C>A c.876C>A (p.Ser292Arg) | gnomAD v4 |
17 | g.44352182C= | CA2261354537 | GRN | c.1347C= (p.Ser449=) c.1137-347C= (n.1137-347C=) c.788C= c.876C= (p.Ser292=) | |
17 | g.44352182C>G | CA399769119 | GRN | c.1347C>G (p.Ser449Arg) c.1137-347C>G (n.1137-347C>G) c.788C>G c.876C>G (p.Ser292Arg) | ClinVar dbSNP gnomAD v4 |
17 | g.44352182C>T | CA290926791 | GRN | c.1347C>T (p.Ser449=) c.1137-347C>T (n.1137-347C>T) c.788C>T c.876C>T (p.Ser292=) | dbSNP gnomAD v4 |
17 | g.44352183T>A | CA399769127 | GRN | c.1348T>A (p.Cys450Ser) c.1137-346T>A (n.1137-346T>A) c.789T>A c.877T>A (p.Cys293Ser) | |
17 | g.44352183T>C | CA399769130 | GRN | c.1348T>C (p.Cys450Arg) c.1137-346T>C (n.1137-346T>C) c.789T>C c.877T>C (p.Cys293Arg) | |
17 | g.44352183T>G | CA399769133 | GRN | c.1348T>G (p.Cys450Gly) c.1137-346T>G (n.1137-346T>G) c.789T>G c.877T>G (p.Cys293Gly) | |
17 | g.44352184G>A | CA399769135 | GRN | c.1349G>A (p.Cys450Tyr) c.1137-345G>A (n.1137-345G>A) c.790G>A c.878G>A (p.Cys293Tyr) | |
17 | g.44352184G>C | CA399769138 | GRN | c.1349G>C (p.Cys450Ser) c.1137-345G>C (n.1137-345G>C) c.790G>C c.878G>C (p.Cys293Ser) | |
17 | g.44352184G>T | CA399769141 | GRN | c.1349G>T (p.Cys450Phe) c.1137-345G>T (n.1137-345G>T) c.790G>T c.878G>T (p.Cys293Phe) | |
17 | g.44352185C>A | CA399769144 | GRN | c.1350C>A (p.Cys450Ter) c.1137-344C>A (n.1137-344C>A) c.791C>A c.879C>A (p.Cys293Ter) | |
17 | g.44352185C>G | CA399769147 | GRN | c.1350C>G (p.Cys450Trp) c.1137-344C>G (n.1137-344C>G) c.791C>G c.879C>G (p.Cys293Trp) | |
17 | g.44352185C>T | CA500622339 | GRN | c.1350C>T (p.Cys450=) c.1137-344C>T (n.1137-344C>T) c.791C>T c.879C>T (p.Cys293=) | |
17 | g.44352186C>A | CA399769150 | GRN | c.1351C>A (p.Pro451Thr) c.1137-343C>A (n.1137-343C>A) c.792C>A c.880C>A (p.Pro294Thr) | |
17 | g.44352186C>G | CA399769153 | GRN | c.1351C>G (p.Pro451Ala) c.1137-343C>G (n.1137-343C>G) c.792C>G c.880C>G (p.Pro294Ala) | gnomAD v4 |
17 | g.44352186C>T | CA399769154 | GRN | c.1351C>T (p.Pro451Ser) c.1137-343C>T (n.1137-343C>T) c.792C>T c.880C>T (p.Pro294Ser) | |
17 | g.44352187C>A | CA399769159 | GRN | c.1352C>A (p.Pro451Gln) c.1137-342C>A (n.1137-342C>A) c.793C>A c.881C>A (p.Pro294Gln) | |
17 | g.44352187C= | CA2261354538 | GRN | c.1352C= (p.Pro451=) c.1137-342C= (n.1137-342C=) c.793C= c.881C= (p.Pro294=) | |
17 | g.44352187C>G | CA399769162 | GRN | c.1352C>G (p.Pro451Arg) c.1137-342C>G (n.1137-342C>G) c.793C>G c.881C>G (p.Pro294Arg) | |
17 | g.44352187C>T | CA8602177 | GRN | c.1352C>T (p.Pro451Leu) c.1137-342C>T (n.1137-342C>T) c.793C>T c.881C>T (p.Pro294Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44352188G>A | CA500622342 | GRN | c.1353G>A (p.Pro451=) c.1137-341G>A (n.1137-341G>A) c.794G>A c.882G>A (p.Pro294=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44352188G>C | CA500622343 | GRN | c.1353G>C (p.Pro451=) c.1137-341G>C (n.1137-341G>C) c.794G>C c.882G>C (p.Pro294=) | |
17 | g.44352188G= | CA2261354539 | GRN | c.1353G= (p.Pro451=) c.1137-341G= (n.1137-341G=) c.794G= c.882G= (p.Pro294=) | |
17 | g.44352188G>T | CA500622344 | GRN | c.1353G>T (p.Pro451=) c.1137-341G>T (n.1137-341G>T) c.794G>T c.882G>T (p.Pro294=) | gnomAD v4 |
17 | g.44352189del | CA2638210586 | GRN | c.1354del (p.Val452TrpfsTer?) c.1137-340del (n.1137-340del) c.795del c.883del (p.Val295TrpfsTer?) | gnomAD v4 |
17 | g.44352189G>A | CA399769166 | GRN | c.1354G>A (p.Val452Met) c.1137-340G>A (n.1137-340G>A) c.795G>A c.883G>A (p.Val295Met) | |
17 | g.44352189G>C | CA399769167 | GRN | c.1354G>C (p.Val452Leu) c.1137-340G>C (n.1137-340G>C) c.795G>C c.883G>C (p.Val295Leu) | |
17 | g.44352189G>T | CA399769170 | GRN | c.1354G>T (p.Val452Leu) c.1137-340G>T (n.1137-340G>T) c.795G>T c.883G>T (p.Val295Leu) | gnomAD v4 |
17 | g.44352190T>A | CA8602179 | GRN | c.1355T>A (p.Val452Glu) c.1137-339T>A (n.1137-339T>A) c.796T>A c.884T>A (p.Val295Glu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44352190T>C | CA8602178 | GRN | c.1355T>C (p.Val452Ala) c.1137-339T>C (n.1137-339T>C) c.796T>C c.884T>C (p.Val295Ala) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44352190T>G | CA399769173 | GRN | c.1355T>G (p.Val452Gly) c.1137-339T>G (n.1137-339T>G) c.796T>G c.884T>G (p.Val295Gly) | dbSNP |
17 | g.44352190T= | CA2261354541 | GRN | c.1355T= (p.Val452=) c.1137-339T= (n.1137-339T=) c.796T= c.884T= (p.Val295=) | |
17 | g.44352190_44352191delinsTG | CA2261354540 | GRN | c.1355_1356delinsTG (p.Val452=) c.1137-339_1137-338delinsTG (n.1137-339_1137-338delinsTG) c.796_797delinsTG c.884_885delinsTG (p.Val295=) | |
17 | g.44352191G>A | CA500622346 | GRN | c.1356G>A (p.Val452=) c.1137-338G>A (n.1137-338G>A) c.797G>A c.885G>A (p.Val295=) | |
17 | g.44352191G>C | CA500622347 | GRN | c.1356G>C (p.Val452=) c.1137-338G>C (n.1137-338G>C) c.797G>C c.885G>C (p.Val295=) | |
17 | g.44352191G>T | CA500622348 | GRN | c.1356G>T (p.Val452=) c.1137-338G>T (n.1137-338G>T) c.797G>T c.885G>T (p.Val295=) | |
17 | g.44352194dup | CA2695226239 | GRN | c.1359dup (p.Gln454AlafsTer?) c.1137-335dup (n.1137-335dup) c.800dup c.888dup (p.Gln297AlafsTer?) | |
17 | g.44352194del | CA290926818 | GRN | c.1359del (p.Gln454ArgfsTer?) c.1137-335del (n.1137-335del) c.800del c.888del (p.Gln297ArgfsTer?) | dbSNP |
17 | g.44352192G>A | CA8602180 | GRN | c.1357G>A (p.Gly453Arg) c.1137-337G>A (n.1137-337G>A) c.798G>A c.886G>A (p.Gly296Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44352192G>C | CA399769176 | GRN | c.1357G>C (p.Gly453Arg) c.1137-337G>C (n.1137-337G>C) c.798G>C c.886G>C (p.Gly296Arg) | |
17 | g.44352192G= | CA2261354542 | GRN | c.1357G= (p.Gly453=) c.1137-337G= (n.1137-337G=) c.798G= c.886G= (p.Gly296=) | |
17 | g.44352192G>T | CA399769178 | GRN | c.1357G>T (p.Gly453Trp) c.1137-337G>T (n.1137-337G>T) c.798G>T c.886G>T (p.Gly296Trp) | |
17 | g.44352195_44352217del | CA2638210599 | GRN | c.1360_1382del (p.Gln454TrpfsTer?) c.1137-334_1137-312del (n.1137-334_1137-312del) c.801_823del c.889_911del (p.Gln297TrpfsTer?) | gnomAD v4 |
17 | g.44352193G>A | CA399769182 | GRN | c.1358G>A (p.Gly453Glu) c.1137-336G>A (n.1137-336G>A) c.799G>A c.887G>A (p.Gly296Glu) | |
17 | g.44352193G>C | CA399769184 | GRN | c.1358G>C (p.Gly453Ala) c.1137-336G>C (n.1137-336G>C) c.799G>C c.887G>C (p.Gly296Ala) | |
17 | g.44352193G= | CA2261354543 | GRN | c.1358G= (p.Gly453=) c.1137-336G= (n.1137-336G=) c.799G= c.887G= (p.Gly296=) | |
17 | g.44352193G>T | CA399769180 | GRN | c.1358G>T (p.Gly453Val) c.1137-336G>T (n.1137-336G>T) c.799G>T c.887G>T (p.Gly296Val) | dbSNP |
17 | g.44352194G>A | CA500622351 | GRN | c.1359G>A (p.Gly453=) c.1137-335G>A (n.1137-335G>A) c.800G>A c.888G>A (p.Gly296=) | |
17 | g.44352194G>C | CA500622352 | GRN | c.1359G>C (p.Gly453=) c.1137-335G>C (n.1137-335G>C) c.800G>C c.888G>C (p.Gly296=) | |
17 | g.44352194G>T | CA500622353 | GRN | c.1359G>T (p.Gly453=) c.1137-335G>T (n.1137-335G>T) c.800G>T c.888G>T (p.Gly296=) | |
17 | g.44352195C>A | CA399769187 | GRN | c.1360C>A (p.Gln454Lys) c.1137-334C>A (n.1137-334C>A) c.801C>A c.889C>A (p.Gln297Lys) | |
17 | g.44352195C>G | CA399769188 | GRN | c.1360C>G (p.Gln454Glu) c.1137-334C>G (n.1137-334C>G) c.801C>G c.889C>G (p.Gln297Glu) | |
17 | g.44352195C>T | CA399769190 | GRN | c.1360C>T (p.Gln454Ter) c.1137-334C>T (n.1137-334C>T) c.801C>T c.889C>T (p.Gln297Ter) | |
17 | g.44352196A>C | CA399769193 | GRN | c.1361A>C (p.Gln454Pro) c.1137-333A>C (n.1137-333A>C) c.802A>C c.890A>C (p.Gln297Pro) | |
17 | g.44352196A>G | CA399769194 | GRN | c.1361A>G (p.Gln454Arg) c.1137-333A>G (n.1137-333A>G) c.802A>G c.890A>G (p.Gln297Arg) | |
17 | g.44352196A>T | CA399769196 | GRN | c.1361A>T (p.Gln454Leu) c.1137-333A>T (n.1137-333A>T) c.802A>T c.890A>T (p.Gln297Leu) | |
17 | g.44352197G>A | CA500622354 | GRN | c.1362G>A (p.Gln454=) c.1137-332G>A (n.1137-332G>A) c.803G>A c.891G>A (p.Gln297=) | |
17 | g.44352197G>C | CA399769198 | GRN | c.1362G>C (p.Gln454His) c.1137-332G>C (n.1137-332G>C) c.803G>C c.891G>C (p.Gln297His) | |
17 | g.44352197G>T | CA399769200 | GRN | c.1362G>T (p.Gln454His) c.1137-332G>T (n.1137-332G>T) c.803G>T c.891G>T (p.Gln297His) | |
17 | g.44352198A= | CA2261354544 | GRN | c.1363A= (p.Thr455=) c.1137-331A= (n.1137-331A=) c.804A= c.892A= (p.Thr298=) | |
17 | g.44352198A>C | CA399769203 | GRN | c.1363A>C (p.Thr455Pro) c.1137-331A>C (n.1137-331A>C) c.804A>C c.892A>C (p.Thr298Pro) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.44352198A>G | CA399769205 | GRN | c.1363A>G (p.Thr455Ala) c.1137-331A>G (n.1137-331A>G) c.804A>G c.892A>G (p.Thr298Ala) | |
17 | g.44352198A>T | CA399769206 | GRN | c.1363A>T (p.Thr455Ser) c.1137-331A>T (n.1137-331A>T) c.804A>T c.892A>T (p.Thr298Ser) | |
17 | g.44352199C>A | CA399769210 | GRN | c.1364C>A (p.Thr455Asn) c.1137-330C>A (n.1137-330C>A) c.805C>A c.893C>A (p.Thr298Asn) | |
17 | g.44352199C= | CA2261354545 | GRN | c.1364C= (p.Thr455=) c.1137-330C= (n.1137-330C=) c.805C= c.893C= (p.Thr298=) | |
17 | g.44352199C>G | CA399769212 | GRN | c.1364C>G (p.Thr455Ser) c.1137-330C>G (n.1137-330C>G) c.805C>G c.893C>G (p.Thr298Ser) | |
17 | g.44352199C>T | CA399769209 | GRN | c.1364C>T (p.Thr455Ile) c.1137-330C>T (n.1137-330C>T) c.805C>T c.893C>T (p.Thr298Ile) | |
17 | g.44352200C>A | CA500622356 | GRN | c.1365C>A (p.Thr455=) c.1137-329C>A (n.1137-329C>A) c.806C>A c.894C>A (p.Thr298=) | |
17 | g.44352200C= | CA2261354546 | GRN | c.1365C= (p.Thr455=) c.1137-329C= (n.1137-329C=) c.806C= c.894C= (p.Thr298=) | |
17 | g.44352200C>G | CA500622357 | GRN | c.1365C>G (p.Thr455=) c.1137-329C>G (n.1137-329C>G) c.806C>G c.894C>G (p.Thr298=) | dbSNP |
17 | g.44352200C>T | CA500622358 | GRN | c.1365C>T (p.Thr455=) c.1137-329C>T (n.1137-329C>T) c.806C>T c.894C>T (p.Thr298=) | gnomAD v4 |
17 | g.44352204_44352206dup | CA2261354547 | GRN | c.1369_1371dup (p.Cys457_Pro458insCys) c.1137-325_1137-323dup (n.1137-325_1137-323dup) c.810_812dup c.898_900dup (p.Cys300_Pro301insCys) | dbSNP |
17 | g.44352201T>A | CA399769214 | GRN | c.1366T>A (p.Cys456Ser) c.1137-328T>A (n.1137-328T>A) c.807T>A c.895T>A (p.Cys299Ser) | |
17 | g.44352201T>C | CA290926827 | GRN | c.1366T>C (p.Cys456Arg) c.1137-328T>C (n.1137-328T>C) c.807T>C c.895T>C (p.Cys299Arg) | dbSNP gnomAD v3 gnomAD v4 |
17 | g.44352201T>G | CA399769217 | GRN | c.1366T>G (p.Cys456Gly) c.1137-328T>G (n.1137-328T>G) c.807T>G c.895T>G (p.Cys299Gly) | |
17 | g.44352201T= | CA2261354548 | GRN | c.1366T= (p.Cys456=) c.1137-328T= (n.1137-328T=) c.807T= c.895T= (p.Cys299=) | |
17 | g.44352202G>A | CA399769221 | GRN | c.1367G>A (p.Cys456Tyr) c.1137-327G>A (n.1137-327G>A) c.1G>A c.808G>A c.896G>A (p.Cys299Tyr) | gnomAD v4 |
17 | g.44352202G>C | CA399769225 | GRN | c.1367G>C (p.Cys456Ser) c.1137-327G>C (n.1137-327G>C) c.1G>C c.808G>C c.896G>C (p.Cys299Ser) | dbSNP gnomAD v2 |
17 | g.44352202G= | CA2261354549 | GRN | c.1367G= (p.Cys456=) c.1137-327G= (n.1137-327G=) c.1G= c.808G= c.896G= (p.Cys299=) | |
17 | g.44352202G>T | CA399769227 | GRN | c.1367G>T (p.Cys456Phe) c.1137-327G>T (n.1137-327G>T) c.1G>T c.808G>T c.896G>T (p.Cys299Phe) | |
17 | g.44352203C>A | CA399769230 | GRN | c.1368C>A (p.Cys456Ter) c.1137-326C>A (n.1137-326C>A) c.2C>A c.809C>A c.897C>A (p.Cys299Ter) | |
17 | g.44352203C>G | CA399769233 | GRN | c.1368C>G (p.Cys456Trp) c.1137-326C>G (n.1137-326C>G) c.2C>G c.809C>G c.897C>G (p.Cys299Trp) | |
17 | g.44352203C>T | CA500622363 | GRN | c.1368C>T (p.Cys456=) c.1137-326C>T (n.1137-326C>T) c.2C>T c.809C>T c.897C>T (p.Cys299=) | gnomAD v4 |
17 | g.44352204T>A | CA399769236 | GRN | c.1369T>A (p.Cys457Ser) c.1137-325T>A (n.1137-325T>A) c.3T>A c.810T>A c.898T>A (p.Cys300Ser) | |
17 | g.44352204T>C | CA399769239 | GRN | c.1369T>C (p.Cys457Arg) c.1137-325T>C (n.1137-325T>C) c.3T>C c.810T>C c.898T>C (p.Cys300Arg) | |
17 | g.44352204T>G | CA399769242 | GRN | c.1369T>G (p.Cys457Gly) c.1137-325T>G (n.1137-325T>G) c.3T>G c.810T>G c.898T>G (p.Cys300Gly) | |
17 | g.44352205G>A | CA399769245 | GRN | c.1370G>A (p.Cys457Tyr) c.1137-324G>A (n.1137-324G>A) c.4G>A c.811G>A c.899G>A (p.Cys300Tyr) | dbSNP |
17 | g.44352205G>C | CA399769247 | GRN | c.1370G>C (p.Cys457Ser) c.1137-324G>C (n.1137-324G>C) c.4G>C c.811G>C c.899G>C (p.Cys300Ser) | |
17 | g.44352205G= | CA2261354551 | GRN | c.1370G= (p.Cys457=) c.1137-324G= (n.1137-324G=) c.4G= c.811G= c.899G= (p.Cys300=) | |
17 | g.44352205G>T | CA399769249 | GRN | c.1370G>T (p.Cys457Phe) c.1137-324G>T (n.1137-324G>T) c.4G>T c.811G>T c.899G>T (p.Cys300Phe) | |
17 | g.44352205_44352206delinsGC | CA2261354550 | GRN | c.1370_1371delinsGC (p.Cys457=) c.1137-324_1137-323delinsGC (n.1137-324_1137-323delinsGC) c.4_5delinsGC c.811_812delinsGC c.899_900delinsGC (p.Cys300=) | |
17 | g.44352206C>A | CA399769257 | GRN | c.1371C>A (p.Cys457Ter) c.1137-323C>A (n.1137-323C>A) c.5C>A c.812C>A c.900C>A (p.Cys300Ter) | |
17 | g.44352206C>G | CA399769254 | GRN | c.1371C>G (p.Cys457Trp) c.1137-323C>G (n.1137-323C>G) c.5C>G c.812C>G c.900C>G (p.Cys300Trp) | |
17 | g.44352206C>T | CA500622367 | GRN | c.1371C>T (p.Cys457=) c.1137-323C>T (n.1137-323C>T) c.5C>T c.812C>T c.900C>T (p.Cys300=) | |
17 | g.44352208del | CA626224249 | GRN | c.1373del (p.Pro458ArgfsTer?) c.1137-321del (n.1137-321del) c.7del c.814del c.902del (p.Pro301ArgfsTer?) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.44352207C>A | CA399769261 | GRN | c.1372C>A (p.Pro458Thr) c.1137-322C>A (n.1137-322C>A) c.6C>A c.813C>A c.901C>A (p.Pro301Thr) | |
17 | g.44352207C>G | CA399769266 | GRN | c.1372C>G (p.Pro458Ala) c.1137-322C>G (n.1137-322C>G) c.6C>G c.813C>G c.901C>G (p.Pro301Ala) | |
17 | g.44352207C>T | CA399769263 | GRN | c.1372C>T (p.Pro458Ser) c.1137-322C>T (n.1137-322C>T) c.6C>T c.813C>T c.901C>T (p.Pro301Ser) | |
17 | g.44352208C>A | CA399769270 | GRN | c.1373C>A (p.Pro458Gln) c.1137-321C>A (n.1137-321C>A) c.7C>A c.814C>A c.902C>A (p.Pro301Gln) | dbSNP gnomAD v2 |
17 | g.44352208C= | CA2261354552 | GRN | c.1373C= (p.Pro458=) c.1137-321C= (n.1137-321C=) c.7C= c.814C= c.902C= (p.Pro301=) | |
17 | g.44352208C>G | CA399769274 | GRN | c.1373C>G (p.Pro458Arg) c.1137-321C>G (n.1137-321C>G) c.7C>G c.814C>G c.902C>G (p.Pro301Arg) | ClinVar dbSNP |
17 | g.44352208C>T | CA225342 | GRN | c.1373C>T (p.Pro458Leu) c.1137-321C>T (n.1137-321C>T) c.7C>T c.814C>T c.902C>T (p.Pro301Leu) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44352208_44352209insAGG | CA2809588882 | GRN | c.1373_1374insAGG (p.Pro458_Ser459insGly) c.1137-321_1137-320insAGG (n.1137-321_1137-320insAGG) c.7_8insAGG c.814_815insAGG c.902_903insAGG (p.Pro301_Ser302insGly) | |
17 | g.44352209G>A | CA8602181 | GRN | c.1374G>A (p.Pro458=) c.1137-320G>A (n.1137-320G>A) c.8G>A c.815G>A c.903G>A (p.Pro301=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.44352209G>C | CA500622369 | GRN | c.1374G>C (p.Pro458=) c.1137-320G>C (n.1137-320G>C) c.8G>C c.815G>C c.903G>C (p.Pro301=) | ClinVar |
17 | g.44352209G= | CA2261354553 | GRN | c.1374G= (p.Pro458=) c.1137-320G= (n.1137-320G=) c.8G= c.815G= c.903G= (p.Pro301=) | |
17 | g.44352209G>T | CA500622371 | GRN | c.1374G>T (p.Pro458=) c.1137-320G>T (n.1137-320G>T) c.8G>T c.815G>T c.903G>T (p.Pro301=) | |
17 | g.44352210A>C | CA399769279 | GRN | c.1375A>C (p.Ser459Arg) c.1137-319A>C (n.1137-319A>C) c.9A>C c.816A>C c.904A>C (p.Ser302Arg) | |
17 | g.44352210A>G | CA399769282 | GRN | c.1375A>G (p.Ser459Gly) c.1137-319A>G (n.1137-319A>G) c.9A>G c.816A>G c.904A>G (p.Ser302Gly) | |
17 | g.44352210A>T | CA399769285 | GRN | c.1375A>T (p.Ser459Cys) c.1137-319A>T (n.1137-319A>T) c.9A>T c.816A>T c.904A>T (p.Ser302Cys) | |
17 | g.44352211G>A | CA399769288 | GRN | c.1376G>A (p.Ser459Asn) c.1137-318G>A (n.1137-318G>A) c.10G>A c.817G>A c.905G>A (p.Ser302Asn) | |
17 | g.44352211G>C | CA399769290 | GRN | c.1376G>C (p.Ser459Thr) c.1137-318G>C (n.1137-318G>C) c.10G>C c.817G>C c.905G>C (p.Ser302Thr) | |
17 | g.44352211G>T | CA399769293 | GRN | c.1376G>T (p.Ser459Ile) c.1137-318G>T (n.1137-318G>T) c.10G>T c.817G>T c.905G>T (p.Ser302Ile) | gnomAD v4 |
17 | g.44352212C>A | CA399769296 | GRN | c.1377C>A (p.Ser459Arg) c.1137-317C>A (n.1137-317C>A) c.11C>A c.818C>A c.906C>A (p.Ser302Arg) | |
17 | g.44352212C= | CA2261354554 | GRN | c.1377C= (p.Ser459=) c.1137-317C= (n.1137-317C=) c.11C= c.818C= c.906C= (p.Ser302=) | |
17 | g.44352212C>G | CA399769299 | GRN | c.1377C>G (p.Ser459Arg) c.1137-317C>G (n.1137-317C>G) c.11C>G c.818C>G c.906C>G (p.Ser302Arg) | dbSNP |
17 | g.44352212C>T | CA500622373 | GRN | c.1377C>T (p.Ser459=) c.1137-317C>T (n.1137-317C>T) c.11C>T c.818C>T c.906C>T (p.Ser302=) | dbSNP gnomAD v4 |