Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
8 | g.143575411G>A | CA2688943804 | NAPRT | c.1291+12C>T (n.1291+12C>T) c.269+12C>T n.835+12C>T n.5C>T c.1210+12C>T (n.1210+12C>T) c.607+12C>T (n.607+12C>T) c.1510+12C>T (n.1510+12C>T) c.928+12C>T (n.928+12C>T) c.526+12C>T (n.526+12C>T) | gnomAD v4 |
8 | g.143575411G>C | CA2782557017 | NAPRT | c.1291+12C>G (n.1291+12C>G) c.269+12C>G n.835+12C>G n.5C>G c.1210+12C>G (n.1210+12C>G) c.607+12C>G (n.607+12C>G) c.1510+12C>G (n.1510+12C>G) c.928+12C>G (n.928+12C>G) c.526+12C>G (n.526+12C>G) | |
8 | g.143575412G>C | CA4912697 | NAPRT | c.1291+11C>G (n.1291+11C>G) c.269+11C>G n.835+11C>G n.4C>G c.1210+11C>G (n.1210+11C>G) c.607+11C>G (n.607+11C>G) c.1510+11C>G (n.1510+11C>G) c.928+11C>G (n.928+11C>G) c.526+11C>G (n.526+11C>G) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.143575412G= | CA1825861437 | NAPRT | c.1291+11C= (n.1291+11C=) c.269+11C= n.835+11C= n.4C= c.1210+11C= (n.1210+11C=) c.607+11C= (n.607+11C=) c.1510+11C= (n.1510+11C=) c.928+11C= (n.928+11C=) c.526+11C= (n.526+11C=) | |
8 | g.143575413A>G | CA2688943807 | NAPRT | c.1291+10T>C (n.1291+10T>C) c.269+10T>C n.835+10T>C n.3T>C c.1210+10T>C (n.1210+10T>C) c.607+10T>C (n.607+10T>C) c.1510+10T>C (n.1510+10T>C) c.928+10T>C (n.928+10T>C) c.526+10T>C (n.526+10T>C) | gnomAD v4 |
8 | g.143575414G>A | CA4912698 | NAPRT | c.1291+9C>T (n.1291+9C>T) c.269+9C>T n.835+9C>T n.2C>T c.1210+9C>T (n.1210+9C>T) c.607+9C>T (n.607+9C>T) c.1510+9C>T (n.1510+9C>T) c.928+9C>T (n.928+9C>T) c.526+9C>T (n.526+9C>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.143575414G>C | CA2688943809 | NAPRT | c.1291+9C>G (n.1291+9C>G) c.269+9C>G n.835+9C>G n.2C>G c.1210+9C>G (n.1210+9C>G) c.607+9C>G (n.607+9C>G) c.1510+9C>G (n.1510+9C>G) c.928+9C>G (n.928+9C>G) c.526+9C>G (n.526+9C>G) | gnomAD v4 |
8 | g.143575414G= | CA1825861438 | NAPRT | c.1291+9C= (n.1291+9C=) c.269+9C= n.835+9C= n.2C= c.1210+9C= (n.1210+9C=) c.607+9C= (n.607+9C=) c.1510+9C= (n.1510+9C=) c.928+9C= (n.928+9C=) c.526+9C= (n.526+9C=) | |
8 | g.143575415G>A | CA1825861440 | NAPRT | c.1291+8C>T (n.1291+8C>T) c.269+8C>T n.835+8C>T n.1C>T c.1210+8C>T (n.1210+8C>T) c.607+8C>T (n.607+8C>T) c.1510+8C>T (n.1510+8C>T) c.928+8C>T (n.928+8C>T) c.526+8C>T (n.526+8C>T) | dbSNP gnomAD v4 |
8 | g.143575415G= | CA1825861439 | NAPRT | c.1291+8C= (n.1291+8C=) c.269+8C= n.835+8C= n.1C= c.1210+8C= (n.1210+8C=) c.607+8C= (n.607+8C=) c.1510+8C= (n.1510+8C=) c.928+8C= (n.928+8C=) c.526+8C= (n.526+8C=) | |
8 | g.143575416G>A | CA2688943813 | NAPRT | c.1291+7C>T (n.1291+7C>T) c.269+7C>T n.835+7C>T c.1210+7C>T (n.1210+7C>T) c.607+7C>T (n.607+7C>T) c.1510+7C>T (n.1510+7C>T) c.928+7C>T (n.928+7C>T) c.526+7C>T (n.526+7C>T) | gnomAD v4 |
8 | g.143575416G>C | CA2688943814 | NAPRT | c.1291+7C>G (n.1291+7C>G) c.269+7C>G n.835+7C>G c.1210+7C>G (n.1210+7C>G) c.607+7C>G (n.607+7C>G) c.1510+7C>G (n.1510+7C>G) c.928+7C>G (n.928+7C>G) c.526+7C>G (n.526+7C>G) | gnomAD v4 |
8 | g.143575417C= | CA1825861441 | NAPRT | c.1291+6G= (n.1291+6G=) c.269+6G= n.835+6G= c.1210+6G= (n.1210+6G=) c.607+6G= (n.607+6G=) c.1510+6G= (n.1510+6G=) c.928+6G= (n.928+6G=) c.526+6G= (n.526+6G=) | |
8 | g.143575417C>T | CA4912699 | NAPRT | c.1291+6G>A (n.1291+6G>A) c.269+6G>A n.835+6G>A c.1210+6G>A (n.1210+6G>A) c.607+6G>A (n.607+6G>A) c.1510+6G>A (n.1510+6G>A) c.928+6G>A (n.928+6G>A) c.526+6G>A (n.526+6G>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.143575418C>A | CA2688943822 | NAPRT | c.1291+5G>T (n.1291+5G>T) c.269+5G>T n.835+5G>T c.1210+5G>T (n.1210+5G>T) c.607+5G>T (n.607+5G>T) c.1510+5G>T (n.1510+5G>T) c.928+5G>T (n.928+5G>T) c.526+5G>T (n.526+5G>T) | gnomAD v4 |
8 | g.143575418C= | CA1825861442 | NAPRT | c.1291+5G= (n.1291+5G=) c.269+5G= n.835+5G= c.1210+5G= (n.1210+5G=) c.607+5G= (n.607+5G=) c.1510+5G= (n.1510+5G=) c.928+5G= (n.928+5G=) c.526+5G= (n.526+5G=) | |
8 | g.143575418C>T | CA4912700 | NAPRT | c.1291+5G>A (n.1291+5G>A) c.269+5G>A n.835+5G>A c.1210+5G>A (n.1210+5G>A) c.607+5G>A (n.607+5G>A) c.1510+5G>A (n.1510+5G>A) c.928+5G>A (n.928+5G>A) c.526+5G>A (n.526+5G>A) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.143575419T>A | CA585728854 | NAPRT | c.1291+4A>T (n.1291+4A>T) c.269+4A>T n.835+4A>T c.1210+4A>T (n.1210+4A>T) c.607+4A>T (n.607+4A>T) c.1510+4A>T (n.1510+4A>T) c.928+4A>T (n.928+4A>T) c.526+4A>T (n.526+4A>T) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.143575419T>C | CA2688943825 | NAPRT | c.1291+4A>G (n.1291+4A>G) c.269+4A>G n.835+4A>G c.1210+4A>G (n.1210+4A>G) c.607+4A>G (n.607+4A>G) c.1510+4A>G (n.1510+4A>G) c.928+4A>G (n.928+4A>G) c.526+4A>G (n.526+4A>G) | gnomAD v4 |
8 | g.143575419T= | CA1825861443 | NAPRT | c.1291+4A= (n.1291+4A=) c.269+4A= n.835+4A= c.1210+4A= (n.1210+4A=) c.607+4A= (n.607+4A=) c.1510+4A= (n.1510+4A=) c.928+4A= (n.928+4A=) c.526+4A= (n.526+4A=) | |
8 | g.143575420C>T | CA2688943826 | NAPRT | c.1291+3G>A (n.1291+3G>A) c.269+3G>A n.835+3G>A c.1210+3G>A (n.1210+3G>A) c.607+3G>A (n.607+3G>A) c.1510+3G>A (n.1510+3G>A) c.928+3G>A (n.928+3G>A) c.526+3G>A (n.526+3G>A) | gnomAD v4 |
8 | g.143575421A= | CA1825861444 | NAPRT | c.1291+2T= (n.1291+2T=) c.269+2T= n.835+2T= c.1210+2T= (n.1210+2T=) c.607+2T= (n.607+2T=) c.1510+2T= (n.1510+2T=) c.928+2T= (n.928+2T=) c.526+2T= (n.526+2T=) | |
8 | g.143575421A>C | CA372450578 | NAPRT | c.1291+2T>G (n.1291+2T>G) c.269+2T>G n.835+2T>G c.1210+2T>G (n.1210+2T>G) c.607+2T>G (n.607+2T>G) c.1510+2T>G (n.1510+2T>G) c.928+2T>G (n.928+2T>G) c.526+2T>G (n.526+2T>G) | |
8 | g.143575421A>G | CA372450589 | NAPRT | c.1291+2T>C (n.1291+2T>C) c.269+2T>C n.835+2T>C c.1210+2T>C (n.1210+2T>C) c.607+2T>C (n.607+2T>C) c.1510+2T>C (n.1510+2T>C) c.928+2T>C (n.928+2T>C) c.526+2T>C (n.526+2T>C) | dbSNP |
8 | g.143575421A>T | CA372450598 | NAPRT | c.1291+2T>A (n.1291+2T>A) c.269+2T>A n.835+2T>A c.1210+2T>A (n.1210+2T>A) c.607+2T>A (n.607+2T>A) c.1510+2T>A (n.1510+2T>A) c.928+2T>A (n.928+2T>A) c.526+2T>A (n.526+2T>A) | |
8 | g.143575422C>A | CA4912701 | NAPRT | c.1291+1G>T (n.1291+1G>T) c.269+1G>T n.835+1G>T c.1210+1G>T (n.1210+1G>T) c.607+1G>T (n.607+1G>T) c.1510+1G>T (n.1510+1G>T) c.928+1G>T (n.928+1G>T) c.526+1G>T (n.526+1G>T) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.143575422C= | CA1825861445 | NAPRT | c.1291+1G= (n.1291+1G=) c.269+1G= n.835+1G= c.1210+1G= (n.1210+1G=) c.607+1G= (n.607+1G=) c.1510+1G= (n.1510+1G=) c.928+1G= (n.928+1G=) c.526+1G= (n.526+1G=) | |
8 | g.143575422C>G | CA372450628 | NAPRT | c.1291+1G>C (n.1291+1G>C) c.269+1G>C n.835+1G>C c.1210+1G>C (n.1210+1G>C) c.607+1G>C (n.607+1G>C) c.1510+1G>C (n.1510+1G>C) c.928+1G>C (n.928+1G>C) c.526+1G>C (n.526+1G>C) | |
8 | g.143575422C>T | CA187547731 | NAPRT | c.1291+1G>A (n.1291+1G>A) c.269+1G>A n.835+1G>A c.1210+1G>A (n.1210+1G>A) c.607+1G>A (n.607+1G>A) c.1510+1G>A (n.1510+1G>A) c.928+1G>A (n.928+1G>A) c.526+1G>A (n.526+1G>A) | dbSNP gnomAD v4 |
8 | g.143575423C>A | CA372450642 | NAPRT | c.1291G>T (p.Gly431Trp) c.269G>T n.835G>T c.1291G>T (p.Gly431Cys) c.1210G>T (p.Gly404Trp) c.607G>T (p.Gly203Trp) c.1510G>T (p.Gly504Trp) c.1510G>T (p.Gly504Cys) c.928G>T (p.Gly310Cys) c.526G>T (p.Gly176Trp) | |
8 | g.143575423C= | CA1825861446 | NAPRT | c.1291G= (p.Gly431=) c.269G= n.835G= c.1210G= (p.Gly404=) c.607G= (p.Gly203=) c.1510G= (p.Gly504=) c.928G= (p.Gly310=) c.526G= (p.Gly176=) | |
8 | g.143575423C>G | CA372450647 | NAPRT | c.1291G>C (p.Gly431Arg) c.269G>C n.835G>C c.1210G>C (p.Gly404Arg) c.607G>C (p.Gly203Arg) c.1510G>C (p.Gly504Arg) c.928G>C (p.Gly310Arg) c.526G>C (p.Gly176Arg) | |
8 | g.143575423C>T | CA4912702 | NAPRT | c.1291G>A (p.Gly431Arg) c.269G>A n.835G>A c.1291G>A (p.Gly431Ser) c.1210G>A (p.Gly404Arg) c.607G>A (p.Gly203Arg) c.1510G>A (p.Gly504Arg) c.1510G>A (p.Gly504Ser) c.928G>A (p.Gly310Ser) c.526G>A (p.Gly176Arg) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.143575424G>A | CA4912703 | NAPRT | c.1290C>T (p.Asp430=) c.268C>T n.834C>T c.1209C>T (p.Asp403=) c.606C>T (p.Asp202=) c.1509C>T (p.Asp503=) c.927C>T (p.Asp309=) c.525C>T (p.Asp175=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
8 | g.143575424G>C | CA372450656 | NAPRT | c.1290C>G (p.Asp430Glu) c.268C>G n.834C>G c.1209C>G (p.Asp403Glu) c.606C>G (p.Asp202Glu) c.1509C>G (p.Asp503Glu) c.927C>G (p.Asp309Glu) c.525C>G (p.Asp175Glu) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.143575424G= | CA1825861447 | NAPRT | c.1290C= (p.Asp430=) c.268C= n.834C= c.1209C= (p.Asp403=) c.606C= (p.Asp202=) c.1509C= (p.Asp503=) c.927C= (p.Asp309=) c.525C= (p.Asp175=) | |
8 | g.143575424G>T | CA372450652 | NAPRT | c.1290C>A (p.Asp430Glu) c.268C>A n.834C>A c.1209C>A (p.Asp403Glu) c.606C>A (p.Asp202Glu) c.1509C>A (p.Asp503Glu) c.927C>A (p.Asp309Glu) c.525C>A (p.Asp175Glu) | |
8 | g.143575425T>A | CA372450657 | NAPRT | c.1289A>T (p.Asp430Val) c.267A>T n.833A>T c.1208A>T (p.Asp403Val) c.605A>T (p.Asp202Val) c.1508A>T (p.Asp503Val) c.926A>T (p.Asp309Val) c.524A>T (p.Asp175Val) | |
8 | g.143575425T>C | CA372450658 | NAPRT | c.1289A>G (p.Asp430Gly) c.267A>G n.833A>G c.1208A>G (p.Asp403Gly) c.605A>G (p.Asp202Gly) c.1508A>G (p.Asp503Gly) c.926A>G (p.Asp309Gly) c.524A>G (p.Asp175Gly) | |
8 | g.143575425T>G | CA372450660 | NAPRT | c.1289A>C (p.Asp430Ala) c.267A>C n.833A>C c.1208A>C (p.Asp403Ala) c.605A>C (p.Asp202Ala) c.1508A>C (p.Asp503Ala) c.926A>C (p.Asp309Ala) c.524A>C (p.Asp175Ala) | |
8 | g.143575426C>A | CA372450665 | NAPRT | c.1288G>T (p.Asp430Tyr) c.266G>T n.832G>T c.1207G>T (p.Asp403Tyr) c.604G>T (p.Asp202Tyr) c.1507G>T (p.Asp503Tyr) c.925G>T (p.Asp309Tyr) c.523G>T (p.Asp175Tyr) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.143575426C= | CA1825861449 | NAPRT | c.1288G= (p.Asp430=) c.266G= n.832G= c.1207G= (p.Asp403=) c.604G= (p.Asp202=) c.1507G= (p.Asp503=) c.925G= (p.Asp309=) c.523G= (p.Asp175=) | |
8 | g.143575426C>G | CA372450666 | NAPRT | c.1288G>C (p.Asp430His) c.266G>C n.832G>C c.1207G>C (p.Asp403His) c.604G>C (p.Asp202His) c.1507G>C (p.Asp503His) c.925G>C (p.Asp309His) c.523G>C (p.Asp175His) | |
8 | g.143575426C>T | CA372450668 | NAPRT | c.1288G>A (p.Asp430Asn) c.266G>A n.832G>A c.1207G>A (p.Asp403Asn) c.604G>A (p.Asp202Asn) c.1507G>A (p.Asp503Asn) c.925G>A (p.Asp309Asn) c.523G>A (p.Asp175Asn) | |
8 | g.143575426_143575427delinsCA | CA1825861448 | NAPRT | c.1287_1288delinsTG (p.Ser429=) c.265_266delinsTG n.831_832delinsTG c.1206_1207delinsTG (p.Ser402=) c.603_604delinsTG (p.Ser201=) c.1506_1507delinsTG (p.Ser502=) c.924_925delinsTG (p.Ser308=) c.522_523delinsTG (p.Ser174=) | |
8 | g.143575427del | CA4912704 | NAPRT | c.1287del (p.Asp430ThrfsTer11) c.265del n.831del c.1287del (p.Asp430ThrfsTer22) c.1206del (p.Asp403ThrfsTer11) c.603del (p.Asp202ThrfsTer11) c.1506del (p.Asp503ThrfsTer11) c.1506del (p.Asp503ThrfsTer22) c.924del (p.Asp309ThrfsTer22) c.522del (p.Asp175ThrfsTer11) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.143575427A>C | CA463512213 | NAPRT | c.1287T>G (p.Ser429=) c.265T>G n.831T>G c.1206T>G (p.Ser402=) c.603T>G (p.Ser201=) c.1506T>G (p.Ser502=) c.924T>G (p.Ser308=) c.522T>G (p.Ser174=) | |
8 | g.143575427A>G | CA463512216 | NAPRT | c.1287T>C (p.Ser429=) c.265T>C n.831T>C c.1206T>C (p.Ser402=) c.603T>C (p.Ser201=) c.1506T>C (p.Ser502=) c.924T>C (p.Ser308=) c.522T>C (p.Ser174=) | |
8 | g.143575427A>T | CA463512217 | NAPRT | c.1287T>A (p.Ser429=) c.265T>A n.831T>A c.1206T>A (p.Ser402=) c.603T>A (p.Ser201=) c.1506T>A (p.Ser502=) c.924T>A (p.Ser308=) c.522T>A (p.Ser174=) | |
8 | g.143575429_143575430del | CA2688943834 | NAPRT | c.1286_1287del (p.Ser429Ter) c.264_265del n.830_831del c.1205_1206del (p.Ser402Ter) c.602_603del (p.Ser201Ter) c.1505_1506del (p.Ser502Ter) c.923_924del (p.Ser308Ter) c.521_522del (p.Ser174Ter) | gnomAD v4 |
8 | g.143575428G>A | CA372450674 | NAPRT | c.1286C>T (p.Ser429Phe) c.264C>T n.830C>T c.1205C>T (p.Ser402Phe) c.602C>T (p.Ser201Phe) c.1505C>T (p.Ser502Phe) c.923C>T (p.Ser308Phe) c.521C>T (p.Ser174Phe) | |
8 | g.143575428G>C | CA372450683 | NAPRT | c.1286C>G (p.Ser429Cys) c.264C>G n.830C>G c.1205C>G (p.Ser402Cys) c.602C>G (p.Ser201Cys) c.1505C>G (p.Ser502Cys) c.923C>G (p.Ser308Cys) c.521C>G (p.Ser174Cys) | |
8 | g.143575428G>T | CA372450688 | NAPRT | c.1286C>A (p.Ser429Tyr) c.264C>A n.830C>A c.1205C>A (p.Ser402Tyr) c.602C>A (p.Ser201Tyr) c.1505C>A (p.Ser502Tyr) c.923C>A (p.Ser308Tyr) c.521C>A (p.Ser174Tyr) | |
8 | g.143575429A= | CA1825861450 | NAPRT | c.1285T= (p.Ser429=) c.263T= n.829T= c.1204T= (p.Ser402=) c.601T= (p.Ser201=) c.1504T= (p.Ser502=) c.922T= (p.Ser308=) c.520T= (p.Ser174=) | |
8 | g.143575429A>C | CA372450698 | NAPRT | c.1285T>G (p.Ser429Ala) c.263T>G n.829T>G c.1204T>G (p.Ser402Ala) c.601T>G (p.Ser201Ala) c.1504T>G (p.Ser502Ala) c.922T>G (p.Ser308Ala) c.520T>G (p.Ser174Ala) | |
8 | g.143575429A>G | CA4912705 | NAPRT | c.1285T>C (p.Ser429Pro) c.263T>C n.829T>C c.1204T>C (p.Ser402Pro) c.601T>C (p.Ser201Pro) c.1504T>C (p.Ser502Pro) c.922T>C (p.Ser308Pro) c.520T>C (p.Ser174Pro) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.143575429A>T | CA372450708 | NAPRT | c.1285T>A (p.Ser429Thr) c.263T>A n.829T>A c.1204T>A (p.Ser402Thr) c.601T>A (p.Ser201Thr) c.1504T>A (p.Ser502Thr) c.922T>A (p.Ser308Thr) c.520T>A (p.Ser174Thr) | |
8 | g.143575430G>A | CA4912706 | NAPRT | c.1284C>T (p.Gly428=) c.262C>T n.828C>T c.1203C>T (p.Gly401=) c.600C>T (p.Gly200=) c.1503C>T (p.Gly501=) c.921C>T (p.Gly307=) c.519C>T (p.Gly173=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.143575430G>C | CA463512231 | NAPRT | c.1284C>G (p.Gly428=) c.262C>G n.828C>G c.1203C>G (p.Gly401=) c.600C>G (p.Gly200=) c.1503C>G (p.Gly501=) c.921C>G (p.Gly307=) c.519C>G (p.Gly173=) | |
8 | g.143575430G= | CA1825861451 | NAPRT | c.1284C= (p.Gly428=) c.262C= n.828C= c.1203C= (p.Gly401=) c.600C= (p.Gly200=) c.1503C= (p.Gly501=) c.921C= (p.Gly307=) c.519C= (p.Gly173=) | |
8 | g.143575430G>T | CA463512229 | NAPRT | c.1284C>A (p.Gly428=) c.262C>A n.828C>A c.1203C>A (p.Gly401=) c.600C>A (p.Gly200=) c.1503C>A (p.Gly501=) c.921C>A (p.Gly307=) c.519C>A (p.Gly173=) | |
8 | g.143575431C>A | CA372450716 | NAPRT | c.1283G>T (p.Gly428Val) c.261G>T n.827G>T c.1202G>T (p.Gly401Val) c.599G>T (p.Gly200Val) c.1502G>T (p.Gly501Val) c.920G>T (p.Gly307Val) c.518G>T (p.Gly173Val) | |
8 | g.143575431C>G | CA372450720 | NAPRT | c.1283G>C (p.Gly428Ala) c.261G>C n.827G>C c.1202G>C (p.Gly401Ala) c.599G>C (p.Gly200Ala) c.1502G>C (p.Gly501Ala) c.920G>C (p.Gly307Ala) c.518G>C (p.Gly173Ala) | |
8 | g.143575431C>T | CA372450728 | NAPRT | c.1283G>A (p.Gly428Asp) c.261G>A n.827G>A c.1202G>A (p.Gly401Asp) c.599G>A (p.Gly200Asp) c.1502G>A (p.Gly501Asp) c.920G>A (p.Gly307Asp) c.518G>A (p.Gly173Asp) | |
8 | g.143575432C>A | CA372450729 | NAPRT | c.1282G>T (p.Gly428Cys) c.260G>T n.826G>T c.1066G>T c.1201G>T (p.Gly401Cys) c.598G>T (p.Gly200Cys) c.1501G>T (p.Gly501Cys) c.919G>T (p.Gly307Cys) c.517G>T (p.Gly173Cys) | gnomAD v4 |
8 | g.143575432C= | CA1825861452 | NAPRT | c.1282G= (p.Gly428=) c.260G= n.826G= c.1066G= c.1201G= (p.Gly401=) c.598G= (p.Gly200=) c.1501G= (p.Gly501=) c.919G= (p.Gly307=) c.517G= (p.Gly173=) | |
8 | g.143575432C>G | CA372450730 | NAPRT | c.1282G>C (p.Gly428Arg) c.260G>C n.826G>C c.1066G>C c.1201G>C (p.Gly401Arg) c.598G>C (p.Gly200Arg) c.1501G>C (p.Gly501Arg) c.919G>C (p.Gly307Arg) c.517G>C (p.Gly173Arg) | |
8 | g.143575432C>T | CA372450731 | NAPRT | c.1282G>A (p.Gly428Ser) c.260G>A n.826G>A c.1066G>A c.1201G>A (p.Gly401Ser) c.598G>A (p.Gly200Ser) c.1501G>A (p.Gly501Ser) c.919G>A (p.Gly307Ser) c.517G>A (p.Gly173Ser) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.143575433C>A | CA463512238 | NAPRT | c.1281G>T (p.Leu427=) c.259G>T n.825G>T c.1065G>T c.1200G>T (p.Leu400=) c.597G>T (p.Leu199=) c.1500G>T (p.Leu500=) c.918G>T (p.Leu306=) c.516G>T (p.Leu172=) | |
8 | g.143575433C>G | CA463512254 | NAPRT | c.1281G>C (p.Leu427=) c.259G>C n.825G>C c.1065G>C c.1200G>C (p.Leu400=) c.597G>C (p.Leu199=) c.1500G>C (p.Leu500=) c.918G>C (p.Leu306=) c.516G>C (p.Leu172=) | |
8 | g.143575433C>T | CA463512255 | NAPRT | c.1281G>A (p.Leu427=) c.259G>A n.825G>A c.1065G>A c.1200G>A (p.Leu400=) c.597G>A (p.Leu199=) c.1500G>A (p.Leu500=) c.918G>A (p.Leu306=) c.516G>A (p.Leu172=) | gnomAD v4 |
8 | g.143575434A= | CA1825861453 | NAPRT | c.1280T= (p.Leu427=) c.258T= n.824T= c.1064T= c.1199T= (p.Leu400=) c.596T= (p.Leu199=) c.1499T= (p.Leu500=) c.917T= (p.Leu306=) c.515T= (p.Leu172=) | |
8 | g.143575434A>C | CA372450735 | NAPRT | c.1280T>G (p.Leu427Arg) c.258T>G n.824T>G c.1064T>G c.1199T>G (p.Leu400Arg) c.596T>G (p.Leu199Arg) c.1499T>G (p.Leu500Arg) c.917T>G (p.Leu306Arg) c.515T>G (p.Leu172Arg) | |
8 | g.143575434A>G | CA4912707 | NAPRT | c.1280T>C (p.Leu427Pro) c.258T>C n.824T>C c.1064T>C c.1199T>C (p.Leu400Pro) c.596T>C (p.Leu199Pro) c.1499T>C (p.Leu500Pro) c.917T>C (p.Leu306Pro) c.515T>C (p.Leu172Pro) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.143575434A>T | CA372450742 | NAPRT | c.1280T>A (p.Leu427Gln) c.258T>A n.824T>A c.1064T>A c.1199T>A (p.Leu400Gln) c.596T>A (p.Leu199Gln) c.1499T>A (p.Leu500Gln) c.917T>A (p.Leu306Gln) c.515T>A (p.Leu172Gln) | |
8 | g.143575435G>A | CA463512256 | NAPRT | c.1279C>T (p.Leu427=) c.257C>T n.823C>T c.1063C>T c.1198C>T (p.Leu400=) c.595C>T (p.Leu199=) c.1498C>T (p.Leu500=) c.916C>T (p.Leu306=) c.514C>T (p.Leu172=) | gnomAD v4 |
8 | g.143575435G>C | CA372450753 | NAPRT | c.1279C>G (p.Leu427Val) c.257C>G n.823C>G c.1063C>G c.1198C>G (p.Leu400Val) c.595C>G (p.Leu199Val) c.1498C>G (p.Leu500Val) c.916C>G (p.Leu306Val) c.514C>G (p.Leu172Val) | |
8 | g.143575435G>T | CA372450768 | NAPRT | c.1279C>A (p.Leu427Met) c.257C>A n.823C>A c.1063C>A c.1198C>A (p.Leu400Met) c.595C>A (p.Leu199Met) c.1498C>A (p.Leu500Met) c.916C>A (p.Leu306Met) c.514C>A (p.Leu172Met) | gnomAD v4 |
8 | g.143575436del | CA2688943846 | NAPRT | c.1279del (p.Leu427TrpfsTer14) c.257del n.823del c.1063del c.1279del (p.Leu427TrpfsTer25) c.1198del (p.Leu400TrpfsTer14) c.595del (p.Leu199TrpfsTer14) c.1498del (p.Leu500TrpfsTer14) c.1498del (p.Leu500TrpfsTer25) c.916del (p.Leu306TrpfsTer25) c.514del (p.Leu172TrpfsTer14) | gnomAD v4 |
8 | g.143575436G>A | CA187547773 | NAPRT | c.1278C>T (p.Leu426=) c.256C>T n.822C>T c.1062C>T c.1197C>T (p.Leu399=) c.594C>T (p.Leu198=) c.1497C>T (p.Leu499=) c.915C>T (p.Leu305=) c.513C>T (p.Leu171=) | dbSNP |
8 | g.143575436G>C | CA463512257 | NAPRT | c.1278C>G (p.Leu426=) c.256C>G n.822C>G c.1062C>G c.1197C>G (p.Leu399=) c.594C>G (p.Leu198=) c.1497C>G (p.Leu499=) c.915C>G (p.Leu305=) c.513C>G (p.Leu171=) | |
8 | g.143575436G= | CA1825861454 | NAPRT | c.1278C= (p.Leu426=) c.256C= n.822C= c.1062C= c.1197C= (p.Leu399=) c.594C= (p.Leu198=) c.1497C= (p.Leu499=) c.915C= (p.Leu305=) c.513C= (p.Leu171=) | |
8 | g.143575436G>T | CA463512258 | NAPRT | c.1278C>A (p.Leu426=) c.256C>A n.822C>A c.1062C>A c.1197C>A (p.Leu399=) c.594C>A (p.Leu198=) c.1497C>A (p.Leu499=) c.915C>A (p.Leu305=) c.513C>A (p.Leu171=) | |
8 | g.143575437A>C | CA372450774 | NAPRT | c.1277T>G (p.Leu426Arg) c.255T>G n.821T>G c.1061T>G c.1196T>G (p.Leu399Arg) c.593T>G (p.Leu198Arg) c.1496T>G (p.Leu499Arg) c.914T>G (p.Leu305Arg) c.512T>G (p.Leu171Arg) | |
8 | g.143575437A>G | CA372450773 | NAPRT | c.1277T>C (p.Leu426Pro) c.255T>C n.821T>C c.1061T>C c.1196T>C (p.Leu399Pro) c.593T>C (p.Leu198Pro) c.1496T>C (p.Leu499Pro) c.914T>C (p.Leu305Pro) c.512T>C (p.Leu171Pro) | |
8 | g.143575437A>T | CA372450772 | NAPRT | c.1277T>A (p.Leu426His) c.255T>A n.821T>A c.1061T>A c.1196T>A (p.Leu399His) c.593T>A (p.Leu198His) c.1496T>A (p.Leu499His) c.914T>A (p.Leu305His) c.512T>A (p.Leu171His) | |
8 | g.143575438G>A | CA372450777 | NAPRT | c.1276C>T (p.Leu426Phe) c.254C>T n.820C>T c.1060C>T c.1195C>T (p.Leu399Phe) c.592C>T (p.Leu198Phe) c.1495C>T (p.Leu499Phe) c.913C>T (p.Leu305Phe) c.511C>T (p.Leu171Phe) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.143575438G>C | CA372450783 | NAPRT | c.1276C>G (p.Leu426Val) c.254C>G n.820C>G c.1060C>G c.1195C>G (p.Leu399Val) c.592C>G (p.Leu198Val) c.1495C>G (p.Leu499Val) c.913C>G (p.Leu305Val) c.511C>G (p.Leu171Val) | gnomAD v4 |
8 | g.143575438G= | CA1825861455 | NAPRT | c.1276C= (p.Leu426=) c.254C= n.820C= c.1060C= c.1195C= (p.Leu399=) c.592C= (p.Leu198=) c.1495C= (p.Leu499=) c.913C= (p.Leu305=) c.511C= (p.Leu171=) | |
8 | g.143575438G>T | CA372450789 | NAPRT | c.1276C>A (p.Leu426Ile) c.254C>A n.820C>A c.1060C>A c.1195C>A (p.Leu399Ile) c.592C>A (p.Leu198Ile) c.1495C>A (p.Leu499Ile) c.913C>A (p.Leu305Ile) c.511C>A (p.Leu171Ile) | |
8 | g.143575439C>A | CA463512259 | NAPRT | c.1275G>T (p.Arg425=) c.253G>T n.819G>T c.1059G>T c.1194G>T (p.Arg398=) c.591G>T (p.Arg197=) c.1494G>T (p.Arg498=) c.912G>T (p.Arg304=) c.510G>T (p.Arg170=) | |
8 | g.143575439C>G | CA463512260 | NAPRT | c.1275G>C (p.Arg425=) c.253G>C n.819G>C c.1059G>C c.1194G>C (p.Arg398=) c.591G>C (p.Arg197=) c.1494G>C (p.Arg498=) c.912G>C (p.Arg304=) c.510G>C (p.Arg170=) | gnomAD v4 |
8 | g.143575439C>T | CA463512261 | NAPRT | c.1275G>A (p.Arg425=) c.253G>A n.819G>A c.1059G>A c.1194G>A (p.Arg398=) c.591G>A (p.Arg197=) c.1494G>A (p.Arg498=) c.912G>A (p.Arg304=) c.510G>A (p.Arg170=) | |
8 | g.143575440C>A | CA372450793 | NAPRT | c.1274G>T (p.Arg425Leu) c.252G>T n.818G>T c.1058G>T c.1193G>T (p.Arg398Leu) c.590G>T (p.Arg197Leu) c.1493G>T (p.Arg498Leu) c.911G>T (p.Arg304Leu) c.509G>T (p.Arg170Leu) | |
8 | g.143575440C= | CA1825861456 | NAPRT | c.1274G= (p.Arg425=) c.252G= n.818G= c.1058G= c.1193G= (p.Arg398=) c.590G= (p.Arg197=) c.1493G= (p.Arg498=) c.911G= (p.Arg304=) c.509G= (p.Arg170=) | |
8 | g.143575440C>G | CA4912709 | NAPRT | c.1274G>C (p.Arg425Pro) c.252G>C n.818G>C c.1058G>C c.1193G>C (p.Arg398Pro) c.590G>C (p.Arg197Pro) c.1493G>C (p.Arg498Pro) c.911G>C (p.Arg304Pro) c.509G>C (p.Arg170Pro) | dbSNP ExAC gnomAD v3 gnomAD v4 |
8 | g.143575440C>T | CA4912708 | NAPRT | c.1274G>A (p.Arg425Gln) c.252G>A n.818G>A c.1058G>A c.1193G>A (p.Arg398Gln) c.590G>A (p.Arg197Gln) c.1493G>A (p.Arg498Gln) c.911G>A (p.Arg304Gln) c.509G>A (p.Arg170Gln) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.143575441G>A | CA4912710 | NAPRT | c.1273C>T (p.Arg425Trp) c.251C>T n.817C>T c.1057C>T c.1192C>T (p.Arg398Trp) c.589C>T (p.Arg197Trp) c.1492C>T (p.Arg498Trp) c.910C>T (p.Arg304Trp) c.508C>T (p.Arg170Trp) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.143575441G>C | CA372450805 | NAPRT | c.1273C>G (p.Arg425Gly) c.251C>G n.817C>G c.1057C>G c.1192C>G (p.Arg398Gly) c.589C>G (p.Arg197Gly) c.1492C>G (p.Arg498Gly) c.910C>G (p.Arg304Gly) c.508C>G (p.Arg170Gly) | |
8 | g.143575441G= | CA1825861457 | NAPRT | c.1273C= (p.Arg425=) c.251C= n.817C= c.1057C= c.1192C= (p.Arg398=) c.589C= (p.Arg197=) c.1492C= (p.Arg498=) c.910C= (p.Arg304=) c.508C= (p.Arg170=) | |
8 | g.143575441G>T | CA463512262 | NAPRT | c.1273C>A (p.Arg425=) c.251C>A n.817C>A c.1057C>A c.1192C>A (p.Arg398=) c.589C>A (p.Arg197=) c.1492C>A (p.Arg498=) c.910C>A (p.Arg304=) c.508C>A (p.Arg170=) | gnomAD v4 |
8 | g.143575442G>A | CA463512263 | NAPRT | c.1272C>T (p.Phe424=) c.250C>T n.816C>T c.1056C>T c.1191C>T (p.Phe397=) c.588C>T (p.Phe196=) c.1491C>T (p.Phe497=) c.909C>T (p.Phe303=) c.507C>T (p.Phe169=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.143575442G>C | CA372450810 | NAPRT | c.1272C>G (p.Phe424Leu) c.250C>G n.816C>G c.1056C>G c.1191C>G (p.Phe397Leu) c.588C>G (p.Phe196Leu) c.1491C>G (p.Phe497Leu) c.909C>G (p.Phe303Leu) c.507C>G (p.Phe169Leu) | |
8 | g.143575442G= | CA1825861458 | NAPRT | c.1272C= (p.Phe424=) c.250C= n.816C= c.1056C= c.1191C= (p.Phe397=) c.588C= (p.Phe196=) c.1491C= (p.Phe497=) c.909C= (p.Phe303=) c.507C= (p.Phe169=) | |
8 | g.143575442G>T | CA372450812 | NAPRT | c.1272C>A (p.Phe424Leu) c.250C>A n.816C>A c.1056C>A c.1191C>A (p.Phe397Leu) c.588C>A (p.Phe196Leu) c.1491C>A (p.Phe497Leu) c.909C>A (p.Phe303Leu) c.507C>A (p.Phe169Leu) | |
8 | g.143575443A>C | CA372450819 | NAPRT | c.1271T>G (p.Phe424Cys) c.249T>G n.815T>G c.1055T>G c.1190T>G (p.Phe397Cys) c.587T>G (p.Phe196Cys) c.1490T>G (p.Phe497Cys) c.908T>G (p.Phe303Cys) c.506T>G (p.Phe169Cys) | |
8 | g.143575443A>G | CA372450822 | NAPRT | c.1271T>C (p.Phe424Ser) c.249T>C n.815T>C c.1055T>C c.1190T>C (p.Phe397Ser) c.587T>C (p.Phe196Ser) c.1490T>C (p.Phe497Ser) c.908T>C (p.Phe303Ser) c.506T>C (p.Phe169Ser) | |
8 | g.143575443A>T | CA372450826 | NAPRT | c.1271T>A (p.Phe424Tyr) c.249T>A n.815T>A c.1055T>A c.1190T>A (p.Phe397Tyr) c.587T>A (p.Phe196Tyr) c.1490T>A (p.Phe497Tyr) c.908T>A (p.Phe303Tyr) c.506T>A (p.Phe169Tyr) | |
8 | g.143575444A= | CA1825861459 | NAPRT | c.1270T= (p.Phe424=) c.248T= n.814T= c.1054T= c.1189T= (p.Phe397=) c.586T= (p.Phe196=) c.1489T= (p.Phe497=) c.907T= (p.Phe303=) c.505T= (p.Phe169=) | |
8 | g.143575444A>C | CA372450839 | NAPRT | c.1270T>G (p.Phe424Val) c.248T>G n.814T>G c.1054T>G c.1189T>G (p.Phe397Val) c.586T>G (p.Phe196Val) c.1489T>G (p.Phe497Val) c.907T>G (p.Phe303Val) c.505T>G (p.Phe169Val) | |
8 | g.143575444A>G | CA4912711 | NAPRT | c.1270T>C (p.Phe424Leu) c.248T>C n.814T>C c.1054T>C c.1189T>C (p.Phe397Leu) c.586T>C (p.Phe196Leu) c.1489T>C (p.Phe497Leu) c.907T>C (p.Phe303Leu) c.505T>C (p.Phe169Leu) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.143575444A>T | CA372450829 | NAPRT | c.1270T>A (p.Phe424Ile) c.248T>A n.814T>A c.1054T>A c.1189T>A (p.Phe397Ile) c.586T>A (p.Phe196Ile) c.1489T>A (p.Phe497Ile) c.907T>A (p.Phe303Ile) c.505T>A (p.Phe169Ile) | |
8 | g.143575445A= | CA1825861460 | NAPRT | c.1269T= (p.Ala423=) c.247T= n.813T= c.1053T= c.1188T= (p.Ala396=) c.585T= (p.Ala195=) c.1488T= (p.Ala496=) c.906T= (p.Ala302=) c.504T= (p.Ala168=) | |
8 | g.143575445A>C | CA463512265 | NAPRT | c.1269T>G (p.Ala423=) c.247T>G n.813T>G c.1053T>G c.1188T>G (p.Ala396=) c.585T>G (p.Ala195=) c.1488T>G (p.Ala496=) c.906T>G (p.Ala302=) c.504T>G (p.Ala168=) | |
8 | g.143575445A>G | CA463512266 | NAPRT | c.1269T>C (p.Ala423=) c.247T>C n.813T>C c.1053T>C c.1188T>C (p.Ala396=) c.585T>C (p.Ala195=) c.1488T>C (p.Ala496=) c.906T>C (p.Ala302=) c.504T>C (p.Ala168=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.143575445A>T | CA463512268 | NAPRT | c.1269T>A (p.Ala423=) c.247T>A n.813T>A c.1053T>A c.1188T>A (p.Ala396=) c.585T>A (p.Ala195=) c.1488T>A (p.Ala496=) c.906T>A (p.Ala302=) c.504T>A (p.Ala168=) | |
8 | g.143575446G>A | CA4912713 | NAPRT | c.1268C>T (p.Ala423Val) c.246C>T n.812C>T c.1052C>T c.1187C>T (p.Ala396Val) c.584C>T (p.Ala195Val) c.1487C>T (p.Ala496Val) c.905C>T (p.Ala302Val) c.503C>T (p.Ala168Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.143575446G>C | CA4912712 | NAPRT | c.1268C>G (p.Ala423Gly) c.246C>G n.812C>G c.1052C>G c.1187C>G (p.Ala396Gly) c.584C>G (p.Ala195Gly) c.1487C>G (p.Ala496Gly) c.905C>G (p.Ala302Gly) c.503C>G (p.Ala168Gly) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.143575446G= | CA1825861461 | NAPRT | c.1268C= (p.Ala423=) c.246C= n.812C= c.1052C= c.1187C= (p.Ala396=) c.584C= (p.Ala195=) c.1487C= (p.Ala496=) c.905C= (p.Ala302=) c.503C= (p.Ala168=) | |
8 | g.143575446G>T | CA372450851 | NAPRT | c.1268C>A (p.Ala423Asp) c.246C>A n.812C>A c.1052C>A c.1187C>A (p.Ala396Asp) c.584C>A (p.Ala195Asp) c.1487C>A (p.Ala496Asp) c.905C>A (p.Ala302Asp) c.503C>A (p.Ala168Asp) | |
8 | g.143575447C>A | CA372450852 | NAPRT | c.1267G>T (p.Ala423Ser) c.245G>T n.811G>T c.1051G>T c.1186G>T (p.Ala396Ser) c.583G>T (p.Ala195Ser) c.1486G>T (p.Ala496Ser) c.904G>T (p.Ala302Ser) c.502G>T (p.Ala168Ser) | |
8 | g.143575447C>G | CA372450856 | NAPRT | c.1267G>C (p.Ala423Pro) c.245G>C n.811G>C c.1051G>C c.1186G>C (p.Ala396Pro) c.583G>C (p.Ala195Pro) c.1486G>C (p.Ala496Pro) c.904G>C (p.Ala302Pro) c.502G>C (p.Ala168Pro) | |
8 | g.143575447C>T | CA372450859 | NAPRT | c.1267G>A (p.Ala423Thr) c.245G>A n.811G>A c.1051G>A c.1186G>A (p.Ala396Thr) c.583G>A (p.Ala195Thr) c.1486G>A (p.Ala496Thr) c.904G>A (p.Ala302Thr) c.502G>A (p.Ala168Thr) | gnomAD v4 |
8 | g.143575448A= | CA1825861462 | NAPRT | c.1266T= (p.Ala422=) c.244T= n.810T= c.1050T= c.1185T= (p.Ala395=) c.582T= (p.Ala194=) c.1485T= (p.Ala495=) c.903T= (p.Ala301=) c.501T= (p.Ala167=) | |
8 | g.143575448A>C | CA463512275 | NAPRT | c.1266T>G (p.Ala422=) c.244T>G n.810T>G c.1050T>G c.1185T>G (p.Ala395=) c.582T>G (p.Ala194=) c.1485T>G (p.Ala495=) c.903T>G (p.Ala301=) c.501T>G (p.Ala167=) | gnomAD v4 |
8 | g.143575448A>G | CA463512277 | NAPRT | c.1266T>C (p.Ala422=) c.244T>C n.810T>C c.1050T>C c.1185T>C (p.Ala395=) c.582T>C (p.Ala194=) c.1485T>C (p.Ala495=) c.903T>C (p.Ala301=) c.501T>C (p.Ala167=) | dbSNP |
8 | g.143575448A>T | CA463512279 | NAPRT | c.1266T>A (p.Ala422=) c.244T>A n.810T>A c.1050T>A c.1185T>A (p.Ala395=) c.582T>A (p.Ala194=) c.1485T>A (p.Ala495=) c.903T>A (p.Ala301=) c.501T>A (p.Ala167=) | |
8 | g.143575449G>A | CA372450863 | NAPRT | c.1265C>T (p.Ala422Val) c.243C>T n.809C>T c.1049C>T c.1184C>T (p.Ala395Val) c.581C>T (p.Ala194Val) c.1484C>T (p.Ala495Val) c.902C>T (p.Ala301Val) c.500C>T (p.Ala167Val) | |
8 | g.143575449G>C | CA372450869 | NAPRT | c.1265C>G (p.Ala422Gly) c.243C>G n.809C>G c.1049C>G c.1184C>G (p.Ala395Gly) c.581C>G (p.Ala194Gly) c.1484C>G (p.Ala495Gly) c.902C>G (p.Ala301Gly) c.500C>G (p.Ala167Gly) | |
8 | g.143575449G>T | CA372450875 | NAPRT | c.1265C>A (p.Ala422Asp) c.243C>A n.809C>A c.1049C>A c.1184C>A (p.Ala395Asp) c.581C>A (p.Ala194Asp) c.1484C>A (p.Ala495Asp) c.902C>A (p.Ala301Asp) c.500C>A (p.Ala167Asp) | |
8 | g.143575450C>A | CA187547807 | NAPRT | c.1264G>T (p.Ala422Ser) c.242G>T n.808G>T c.1048G>T c.1183G>T (p.Ala395Ser) c.580G>T (p.Ala194Ser) c.1483G>T (p.Ala495Ser) c.901G>T (p.Ala301Ser) c.499G>T (p.Ala167Ser) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.143575450C= | CA1825861463 | NAPRT | c.1264G= (p.Ala422=) c.242G= n.808G= c.1048G= c.1183G= (p.Ala395=) c.580G= (p.Ala194=) c.1483G= (p.Ala495=) c.901G= (p.Ala301=) c.499G= (p.Ala167=) | |
8 | g.143575450C>G | CA372450882 | NAPRT | c.1264G>C (p.Ala422Pro) c.242G>C n.808G>C c.1048G>C c.1183G>C (p.Ala395Pro) c.580G>C (p.Ala194Pro) c.1483G>C (p.Ala495Pro) c.901G>C (p.Ala301Pro) c.499G>C (p.Ala167Pro) | |
8 | g.143575450C>T | CA4912714 | NAPRT | c.1264G>A (p.Ala422Thr) c.242G>A n.808G>A c.1048G>A c.1183G>A (p.Ala395Thr) c.580G>A (p.Ala194Thr) c.1483G>A (p.Ala495Thr) c.901G>A (p.Ala301Thr) c.499G>A (p.Ala167Thr) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.143575451C>A | CA372450890 | NAPRT | c.1263G>T (p.Lys421Asn) c.241G>T n.807G>T c.1047G>T c.1182G>T (p.Lys394Asn) c.579G>T (p.Lys193Asn) c.1482G>T (p.Lys494Asn) c.900G>T (p.Lys300Asn) c.498G>T (p.Lys166Asn) | |
8 | g.143575451C>G | CA372450893 | NAPRT | c.1263G>C (p.Lys421Asn) c.241G>C n.807G>C c.1047G>C c.1182G>C (p.Lys394Asn) c.579G>C (p.Lys193Asn) c.1482G>C (p.Lys494Asn) c.900G>C (p.Lys300Asn) c.498G>C (p.Lys166Asn) | |
8 | g.143575451C>T | CA463512281 | NAPRT | c.1263G>A (p.Lys421=) c.241G>A n.807G>A c.1047G>A c.1182G>A (p.Lys394=) c.579G>A (p.Lys193=) c.1482G>A (p.Lys494=) c.900G>A (p.Lys300=) c.498G>A (p.Lys166=) | gnomAD v4 |
8 | g.143575452T>A | CA372450894 | NAPRT | c.1262A>T (p.Lys421Met) c.240A>T n.806A>T c.1046A>T c.1181A>T (p.Lys394Met) c.578A>T (p.Lys193Met) c.1481A>T (p.Lys494Met) c.899A>T (p.Lys300Met) c.497A>T (p.Lys166Met) | |
8 | g.143575452T>C | CA372450896 | NAPRT | c.1262A>G (p.Lys421Arg) c.240A>G n.806A>G c.1046A>G c.1181A>G (p.Lys394Arg) c.578A>G (p.Lys193Arg) c.1481A>G (p.Lys494Arg) c.899A>G (p.Lys300Arg) c.497A>G (p.Lys166Arg) | COSMIC COSMIC COSMIC |
8 | g.143575452T>G | CA372450895 | NAPRT | c.1262A>C (p.Lys421Thr) c.240A>C n.806A>C c.1046A>C c.1181A>C (p.Lys394Thr) c.578A>C (p.Lys193Thr) c.1481A>C (p.Lys494Thr) c.899A>C (p.Lys300Thr) c.497A>C (p.Lys166Thr) | |
8 | g.143575453T>A | CA372450901 | NAPRT | c.1261A>T (p.Lys421Ter) c.239A>T n.805A>T c.1045A>T c.1180A>T (p.Lys394Ter) c.577A>T (p.Lys193Ter) c.1480A>T (p.Lys494Ter) c.898A>T (p.Lys300Ter) c.496A>T (p.Lys166Ter) | |
8 | g.143575453T>C | CA372450906 | NAPRT | c.1261A>G (p.Lys421Glu) c.239A>G n.805A>G c.1045A>G c.1180A>G (p.Lys394Glu) c.577A>G (p.Lys193Glu) c.1480A>G (p.Lys494Glu) c.898A>G (p.Lys300Glu) c.496A>G (p.Lys166Glu) | dbSNP gnomAD v4 |
8 | g.143575453T>G | CA372450902 | NAPRT | c.1261A>C (p.Lys421Gln) c.239A>C n.805A>C c.1045A>C c.1180A>C (p.Lys394Gln) c.577A>C (p.Lys193Gln) c.1480A>C (p.Lys494Gln) c.898A>C (p.Lys300Gln) c.496A>C (p.Lys166Gln) | |
8 | g.143575454G>A | CA463512292 | NAPRT | c.1260C>T (p.Ser420=) c.238C>T n.804C>T c.1044C>T c.1179C>T (p.Ser393=) c.576C>T (p.Ser192=) c.1479C>T (p.Ser493=) c.897C>T (p.Ser299=) c.495C>T (p.Ser165=) | |
8 | g.143575454G>C | CA372450907 | NAPRT | c.1260C>G (p.Ser420Arg) c.238C>G n.804C>G c.1044C>G c.1179C>G (p.Ser393Arg) c.576C>G (p.Ser192Arg) c.1479C>G (p.Ser493Arg) c.897C>G (p.Ser299Arg) c.495C>G (p.Ser165Arg) | |
8 | g.143575454G>T | CA372450910 | NAPRT | c.1260C>A (p.Ser420Arg) c.238C>A n.804C>A c.1044C>A c.1179C>A (p.Ser393Arg) c.576C>A (p.Ser192Arg) c.1479C>A (p.Ser493Arg) c.897C>A (p.Ser299Arg) c.495C>A (p.Ser165Arg) | |
8 | g.143575455C>A | CA372450915 | NAPRT | c.1259G>T (p.Ser420Ile) c.237G>T n.803G>T c.1043G>T c.1178G>T (p.Ser393Ile) c.575G>T (p.Ser192Ile) c.1478G>T (p.Ser493Ile) c.896G>T (p.Ser299Ile) c.494G>T (p.Ser165Ile) | |
8 | g.143575455C= | CA1825861464 | NAPRT | c.1259G= (p.Ser420=) c.237G= n.803G= c.1043G= c.1178G= (p.Ser393=) c.575G= (p.Ser192=) c.1478G= (p.Ser493=) c.896G= (p.Ser299=) c.494G= (p.Ser165=) | |
8 | g.143575455C>G | CA372450923 | NAPRT | c.1259G>C (p.Ser420Thr) c.237G>C n.803G>C c.1043G>C c.1178G>C (p.Ser393Thr) c.575G>C (p.Ser192Thr) c.1478G>C (p.Ser493Thr) c.896G>C (p.Ser299Thr) c.494G>C (p.Ser165Thr) | |
8 | g.143575455C>T | CA372450928 | NAPRT | c.1259G>A (p.Ser420Asn) c.237G>A n.803G>A c.1043G>A c.1178G>A (p.Ser393Asn) c.575G>A (p.Ser192Asn) c.1478G>A (p.Ser493Asn) c.896G>A (p.Ser299Asn) c.494G>A (p.Ser165Asn) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.143575456T>A | CA372450931 | NAPRT | c.1258A>T (p.Ser420Cys) c.236A>T n.802A>T c.1042A>T c.1177A>T (p.Ser393Cys) c.574A>T (p.Ser192Cys) c.1477A>T (p.Ser493Cys) c.895A>T (p.Ser299Cys) c.493A>T (p.Ser165Cys) | |
8 | g.143575456T>C | CA372450933 | NAPRT | c.1258A>G (p.Ser420Gly) c.236A>G n.802A>G c.1042A>G c.1177A>G (p.Ser393Gly) c.574A>G (p.Ser192Gly) c.1477A>G (p.Ser493Gly) c.895A>G (p.Ser299Gly) c.493A>G (p.Ser165Gly) | gnomAD v4 |
8 | g.143575456T>G | CA372450935 | NAPRT | c.1258A>C (p.Ser420Arg) c.236A>C n.802A>C c.1042A>C c.1177A>C (p.Ser393Arg) c.574A>C (p.Ser192Arg) c.1477A>C (p.Ser493Arg) c.895A>C (p.Ser299Arg) c.493A>C (p.Ser165Arg) | |
8 | g.143575457C>A | CA463512307 | NAPRT | c.1257G>T (p.Gly419=) c.235G>T n.801G>T c.1041G>T c.1176G>T (p.Gly392=) c.573G>T (p.Gly191=) c.1476G>T (p.Gly492=) c.894G>T (p.Gly298=) c.492G>T (p.Gly164=) | gnomAD v4 |
8 | g.143575457C>G | CA463512304 | NAPRT | c.1257G>C (p.Gly419=) c.235G>C n.801G>C c.1041G>C c.1176G>C (p.Gly392=) c.573G>C (p.Gly191=) c.1476G>C (p.Gly492=) c.894G>C (p.Gly298=) c.492G>C (p.Gly164=) | |
8 | g.143575457C>T | CA463512306 | NAPRT | c.1257G>A (p.Gly419=) c.235G>A n.801G>A c.1041G>A c.1176G>A (p.Gly392=) c.573G>A (p.Gly191=) c.1476G>A (p.Gly492=) c.894G>A (p.Gly298=) c.492G>A (p.Gly164=) | |
8 | g.143575459dup | CA2688943881 | NAPRT | c.1257dup (p.Ser420GlufsTer11) c.235dup n.801dup c.1041dup c.1176dup (p.Ser393GlufsTer11) c.573dup (p.Ser192GlufsTer11) c.1476dup (p.Ser493GlufsTer11) c.894dup (p.Ser299GlufsTer11) c.492dup (p.Ser165GlufsTer11) | gnomAD v4 |
8 | g.143575457_143575465delinsCCCAGGCAA | CA1825861465 | NAPRT | c.1249_1257delinsTTGCCTGGG (p.Leu417=) c.227_235delinsTTGCCTGGG n.793_801delinsTTGCCTGGG c.1033_1041delinsTTGCCTGGG c.1168_1176delinsTTGCCTGGG (p.Leu390=) c.565_573delinsTTGCCTGGG (p.Leu189=) c.1468_1476delinsTTGCCTGGG (p.Leu490=) c.886_894delinsTTGCCTGGG (p.Leu296=) c.484_492delinsTTGCCTGGG (p.Leu162=) | |
8 | g.143575458C>A | CA372450945 | NAPRT | c.1256G>T (p.Gly419Val) c.234G>T n.800G>T c.1040G>T c.1175G>T (p.Gly392Val) c.572G>T (p.Gly191Val) c.1475G>T (p.Gly492Val) c.893G>T (p.Gly298Val) c.491G>T (p.Gly164Val) | |
8 | g.143575458C>G | CA372450952 | NAPRT | c.1256G>C (p.Gly419Ala) c.234G>C n.800G>C c.1040G>C c.1175G>C (p.Gly392Ala) c.572G>C (p.Gly191Ala) c.1475G>C (p.Gly492Ala) c.893G>C (p.Gly298Ala) c.491G>C (p.Gly164Ala) | |
8 | g.143575458C>T | CA372450957 | NAPRT | c.1256G>A (p.Gly419Glu) c.234G>A n.800G>A c.1040G>A c.1175G>A (p.Gly392Glu) c.572G>A (p.Gly191Glu) c.1475G>A (p.Gly492Glu) c.893G>A (p.Gly298Glu) c.491G>A (p.Gly164Glu) | |
8 | g.143575459_143575466del | CA4912715 | NAPRT | c.1249_1256del (p.Leu417GlufsTer11) c.227_234del n.793_800del c.1033_1040del c.1168_1175del (p.Leu390GlufsTer11) c.565_572del (p.Leu189GlufsTer11) c.1468_1475del (p.Leu490GlufsTer11) c.886_893del (p.Leu296GlufsTer11) c.484_491del (p.Leu162GlufsTer11) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.143575459C>A | CA372450976 | NAPRT | c.1255G>T (p.Gly419Trp) c.233G>T n.799G>T c.1039G>T c.1174G>T (p.Gly392Trp) c.571G>T (p.Gly191Trp) c.1474G>T (p.Gly492Trp) c.892G>T (p.Gly298Trp) c.490G>T (p.Gly164Trp) | |
8 | g.143575459C>G | CA372450967 | NAPRT | c.1255G>C (p.Gly419Arg) c.233G>C n.799G>C c.1039G>C c.1174G>C (p.Gly392Arg) c.571G>C (p.Gly191Arg) c.1474G>C (p.Gly492Arg) c.892G>C (p.Gly298Arg) c.490G>C (p.Gly164Arg) | |
8 | g.143575459C>T | CA372450972 | NAPRT | c.1255G>A (p.Gly419Arg) c.233G>A n.799G>A c.1039G>A c.1174G>A (p.Gly392Arg) c.571G>A (p.Gly191Arg) c.1474G>A (p.Gly492Arg) c.892G>A (p.Gly298Arg) c.490G>A (p.Gly164Arg) | |
8 | g.143575460A>C | CA463512312 | NAPRT | c.1254T>G (p.Pro418=) c.232T>G n.798T>G c.1038T>G c.1173T>G (p.Pro391=) c.570T>G (p.Pro190=) c.1473T>G (p.Pro491=) c.891T>G (p.Pro297=) c.489T>G (p.Pro163=) | |
8 | g.143575460A>G | CA463512313 | NAPRT | c.1254T>C (p.Pro418=) c.232T>C n.798T>C c.1038T>C c.1173T>C (p.Pro391=) c.570T>C (p.Pro190=) c.1473T>C (p.Pro491=) c.891T>C (p.Pro297=) c.489T>C (p.Pro163=) | gnomAD v4 |
8 | g.143575460A>T | CA463512316 | NAPRT | c.1254T>A (p.Pro418=) c.232T>A n.798T>A c.1038T>A c.1173T>A (p.Pro391=) c.570T>A (p.Pro190=) c.1473T>A (p.Pro491=) c.891T>A (p.Pro297=) c.489T>A (p.Pro163=) | |
8 | g.143575461G>A | CA372450984 | NAPRT | c.1253C>T (p.Pro418Leu) c.231C>T n.797C>T c.1037C>T c.1172C>T (p.Pro391Leu) c.569C>T (p.Pro190Leu) c.1472C>T (p.Pro491Leu) c.890C>T (p.Pro297Leu) c.488C>T (p.Pro163Leu) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.143575461G>C | CA372450988 | NAPRT | c.1253C>G (p.Pro418Arg) c.231C>G n.797C>G c.1037C>G c.1172C>G (p.Pro391Arg) c.569C>G (p.Pro190Arg) c.1472C>G (p.Pro491Arg) c.890C>G (p.Pro297Arg) c.488C>G (p.Pro163Arg) | |
8 | g.143575461G= | CA1825861466 | NAPRT | c.1253C= (p.Pro418=) c.231C= n.797C= c.1037C= c.1172C= (p.Pro391=) c.569C= (p.Pro190=) c.1472C= (p.Pro491=) c.890C= (p.Pro297=) c.488C= (p.Pro163=) | |
8 | g.143575461G>T | CA372450991 | NAPRT | c.1253C>A (p.Pro418His) c.231C>A n.797C>A c.1037C>A c.1172C>A (p.Pro391His) c.569C>A (p.Pro190His) c.1472C>A (p.Pro491His) c.890C>A (p.Pro297His) c.488C>A (p.Pro163His) | gnomAD v4 |
8 | g.143575462G>A | CA372451003 | NAPRT | c.1252C>T (p.Pro418Ser) c.230C>T n.796C>T c.1036C>T c.1171C>T (p.Pro391Ser) c.568C>T (p.Pro190Ser) c.1471C>T (p.Pro491Ser) c.889C>T (p.Pro297Ser) c.487C>T (p.Pro163Ser) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.143575462G>C | CA372451010 | NAPRT | c.1252C>G (p.Pro418Ala) c.230C>G n.796C>G c.1036C>G c.1171C>G (p.Pro391Ala) c.568C>G (p.Pro190Ala) c.1471C>G (p.Pro491Ala) c.889C>G (p.Pro297Ala) c.487C>G (p.Pro163Ala) | |
8 | g.143575462G= | CA1825861467 | NAPRT | c.1252C= (p.Pro418=) c.230C= n.796C= c.1036C= c.1171C= (p.Pro391=) c.568C= (p.Pro190=) c.1471C= (p.Pro491=) c.889C= (p.Pro297=) c.487C= (p.Pro163=) | |
8 | g.143575462G>T | CA372451013 | NAPRT | c.1252C>A (p.Pro418Thr) c.230C>A n.796C>A c.1036C>A c.1171C>A (p.Pro391Thr) c.568C>A (p.Pro190Thr) c.1471C>A (p.Pro491Thr) c.889C>A (p.Pro297Thr) c.487C>A (p.Pro163Thr) | |
8 | g.143575463C>A | CA372451022 | NAPRT | c.1251G>T (p.Leu417Phe) c.229G>T n.795G>T c.1035G>T c.1170G>T (p.Leu390Phe) c.567G>T (p.Leu189Phe) c.1470G>T (p.Leu490Phe) c.888G>T (p.Leu296Phe) c.486G>T (p.Leu162Phe) | |
8 | g.143575463C= | CA1825861468 | NAPRT | c.1251G= (p.Leu417=) c.229G= n.795G= c.1035G= c.1170G= (p.Leu390=) c.567G= (p.Leu189=) c.1470G= (p.Leu490=) c.888G= (p.Leu296=) c.486G= (p.Leu162=) | |
8 | g.143575463C>G | CA372451037 | NAPRT | c.1251G>C (p.Leu417Phe) c.229G>C n.795G>C c.1035G>C c.1170G>C (p.Leu390Phe) c.567G>C (p.Leu189Phe) c.1470G>C (p.Leu490Phe) c.888G>C (p.Leu296Phe) c.486G>C (p.Leu162Phe) | |
8 | g.143575463C>T | CA4912716 | NAPRT | c.1251G>A (p.Leu417=) c.229G>A n.795G>A c.1035G>A c.1170G>A (p.Leu390=) c.567G>A (p.Leu189=) c.1470G>A (p.Leu490=) c.888G>A (p.Leu296=) c.486G>A (p.Leu162=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.143575464A>C | CA372451051 | NAPRT | c.1250T>G (p.Leu417Trp) c.228T>G n.794T>G c.1034T>G c.1169T>G (p.Leu390Trp) c.566T>G (p.Leu189Trp) c.1469T>G (p.Leu490Trp) c.887T>G (p.Leu296Trp) c.485T>G (p.Leu162Trp) | |
8 | g.143575464A>G | CA372451054 | NAPRT | c.1250T>C (p.Leu417Ser) c.228T>C n.794T>C c.1034T>C c.1169T>C (p.Leu390Ser) c.566T>C (p.Leu189Ser) c.1469T>C (p.Leu490Ser) c.887T>C (p.Leu296Ser) c.485T>C (p.Leu162Ser) | |
8 | g.143575464A>T | CA372451059 | NAPRT | c.1250T>A (p.Leu417Ter) c.228T>A n.794T>A c.1034T>A c.1169T>A (p.Leu390Ter) c.566T>A (p.Leu189Ter) c.1469T>A (p.Leu490Ter) c.887T>A (p.Leu296Ter) c.485T>A (p.Leu162Ter) | |
8 | g.143575465A>C | CA372451066 | NAPRT | c.1249T>G (p.Leu417Val) c.227T>G n.793T>G c.1033T>G c.1168T>G (p.Leu390Val) c.565T>G (p.Leu189Val) c.1468T>G (p.Leu490Val) c.886T>G (p.Leu296Val) c.484T>G (p.Leu162Val) | |
8 | g.143575465A>G | CA463512331 | NAPRT | c.1249T>C (p.Leu417=) c.227T>C n.793T>C c.1033T>C c.1168T>C (p.Leu390=) c.565T>C (p.Leu189=) c.1468T>C (p.Leu490=) c.886T>C (p.Leu296=) c.484T>C (p.Leu162=) | |
8 | g.143575465A>T | CA372451063 | NAPRT | c.1249T>A (p.Leu417Met) c.227T>A n.793T>A c.1033T>A c.1168T>A (p.Leu390Met) c.565T>A (p.Leu189Met) c.1468T>A (p.Leu490Met) c.886T>A (p.Leu296Met) c.484T>A (p.Leu162Met) | gnomAD v4 |
8 | g.143575466C>A | CA4912718 | NAPRT | c.1248G>T (p.Thr416=) c.226G>T n.792G>T c.1032G>T c.1167G>T (p.Thr389=) c.564G>T (p.Thr188=) c.1467G>T (p.Thr489=) c.885G>T (p.Thr295=) c.483G>T (p.Thr161=) | dbSNP ExAC gnomAD v2 |
8 | g.143575466C= | CA1825861469 | NAPRT | c.1248G= (p.Thr416=) c.226G= n.792G= c.1032G= c.1167G= (p.Thr389=) c.564G= (p.Thr188=) c.1467G= (p.Thr489=) c.885G= (p.Thr295=) c.483G= (p.Thr161=) | |
8 | g.143575466C>G | CA463512337 | NAPRT | c.1248G>C (p.Thr416=) c.226G>C n.792G>C c.1032G>C c.1167G>C (p.Thr389=) c.564G>C (p.Thr188=) c.1467G>C (p.Thr489=) c.885G>C (p.Thr295=) c.483G>C (p.Thr161=) | |
8 | g.143575466C>T | CA4912717 | NAPRT | c.1248G>A (p.Thr416=) c.226G>A n.792G>A c.1032G>A c.1167G>A (p.Thr389=) c.564G>A (p.Thr188=) c.1467G>A (p.Thr489=) c.885G>A (p.Thr295=) c.483G>A (p.Thr161=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.143575467G>A | CA4912720 | NAPRT | c.1247C>T (p.Thr416Met) c.225C>T n.791C>T c.1031C>T c.1166C>T (p.Thr389Met) c.563C>T (p.Thr188Met) c.1466C>T (p.Thr489Met) c.884C>T (p.Thr295Met) c.482C>T (p.Thr161Met) | dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC |
8 | g.143575467G>C | CA372451082 | NAPRT | c.1247C>G (p.Thr416Arg) c.225C>G n.791C>G c.1031C>G c.1166C>G (p.Thr389Arg) c.563C>G (p.Thr188Arg) c.1466C>G (p.Thr489Arg) c.884C>G (p.Thr295Arg) c.482C>G (p.Thr161Arg) | gnomAD v4 |
8 | g.143575467G= | CA1825861470 | NAPRT | c.1247C= (p.Thr416=) c.225C= n.791C= c.1031C= c.1166C= (p.Thr389=) c.563C= (p.Thr188=) c.1466C= (p.Thr489=) c.884C= (p.Thr295=) c.482C= (p.Thr161=) | |
8 | g.143575467G>T | CA4912719 | NAPRT | c.1247C>A (p.Thr416Lys) c.225C>A n.791C>A c.1031C>A c.1166C>A (p.Thr389Lys) c.563C>A (p.Thr188Lys) c.1466C>A (p.Thr489Lys) c.884C>A (p.Thr295Lys) c.482C>A (p.Thr161Lys) | dbSNP ExAC gnomAD v2 |
8 | g.143575468T>A | CA372451085 | NAPRT | c.1246A>T (p.Thr416Ser) c.224A>T n.790A>T c.1030A>T c.1165A>T (p.Thr389Ser) c.562A>T (p.Thr188Ser) c.1465A>T (p.Thr489Ser) c.883A>T (p.Thr295Ser) c.481A>T (p.Thr161Ser) | |
8 | g.143575468T>C | CA372451087 | NAPRT | c.1246A>G (p.Thr416Ala) c.224A>G n.790A>G c.1030A>G c.1165A>G (p.Thr389Ala) c.562A>G (p.Thr188Ala) c.1465A>G (p.Thr489Ala) c.883A>G (p.Thr295Ala) c.481A>G (p.Thr161Ala) | |
8 | g.143575468T>G | CA372451091 | NAPRT | c.1246A>C (p.Thr416Pro) c.224A>C n.790A>C c.1030A>C c.1165A>C (p.Thr389Pro) c.562A>C (p.Thr188Pro) c.1465A>C (p.Thr489Pro) c.883A>C (p.Thr295Pro) c.481A>C (p.Thr161Pro) | |
8 | g.143575469C>A | CA372451097 | NAPRT | c.1245G>T (p.Gln415His) c.223G>T n.789G>T c.1029G>T c.1164G>T (p.Gln388His) c.561G>T (p.Gln187His) c.1464G>T (p.Gln488His) c.882G>T (p.Gln294His) c.480G>T (p.Gln160His) | |
8 | g.143575469C>G | CA372451101 | NAPRT | c.1245G>C (p.Gln415His) c.223G>C n.789G>C c.1029G>C c.1164G>C (p.Gln388His) c.561G>C (p.Gln187His) c.1464G>C (p.Gln488His) c.882G>C (p.Gln294His) c.480G>C (p.Gln160His) | |
8 | g.143575469C>T | CA463512345 | NAPRT | c.1245G>A (p.Gln415=) c.223G>A n.789G>A c.1029G>A c.1164G>A (p.Gln388=) c.561G>A (p.Gln187=) c.1464G>A (p.Gln488=) c.882G>A (p.Gln294=) c.480G>A (p.Gln160=) | |
8 | g.143575470T>A | CA372451106 | NAPRT | c.1244A>T (p.Gln415Leu) c.222A>T n.788A>T c.1028A>T c.1163A>T (p.Gln388Leu) c.560A>T (p.Gln187Leu) c.1463A>T (p.Gln488Leu) c.881A>T (p.Gln294Leu) c.479A>T (p.Gln160Leu) | |
8 | g.143575470T>C | CA372451108 | NAPRT | c.1244A>G (p.Gln415Arg) c.222A>G n.788A>G c.1028A>G c.1163A>G (p.Gln388Arg) c.560A>G (p.Gln187Arg) c.1463A>G (p.Gln488Arg) c.881A>G (p.Gln294Arg) c.479A>G (p.Gln160Arg) | |
8 | g.143575470T>G | CA372451109 | NAPRT | c.1244A>C (p.Gln415Pro) c.222A>C n.788A>C c.1028A>C c.1163A>C (p.Gln388Pro) c.560A>C (p.Gln187Pro) c.1463A>C (p.Gln488Pro) c.881A>C (p.Gln294Pro) c.479A>C (p.Gln160Pro) | |
8 | g.143575471G>A | CA372451122 | NAPRT | c.1243C>T (p.Gln415Ter) c.221C>T n.787C>T c.1027C>T c.1162C>T (p.Gln388Ter) c.559C>T (p.Gln187Ter) c.1462C>T (p.Gln488Ter) c.880C>T (p.Gln294Ter) c.478C>T (p.Gln160Ter) | |
8 | g.143575471G>C | CA372451117 | NAPRT | c.1243C>G (p.Gln415Glu) c.221C>G n.787C>G c.1027C>G c.1162C>G (p.Gln388Glu) c.559C>G (p.Gln187Glu) c.1462C>G (p.Gln488Glu) c.880C>G (p.Gln294Glu) c.478C>G (p.Gln160Glu) | |
8 | g.143575471G>T | CA372451113 | NAPRT | c.1243C>A (p.Gln415Lys) c.221C>A n.787C>A c.1027C>A c.1162C>A (p.Gln388Lys) c.559C>A (p.Gln187Lys) c.1462C>A (p.Gln488Lys) c.880C>A (p.Gln294Lys) c.478C>A (p.Gln160Lys) | |
8 | g.143575472C>A | CA372451126 | NAPRT | c.1242G>T (p.Lys414Asn) c.220G>T n.786G>T c.1026G>T c.1161G>T (p.Lys387Asn) c.558G>T (p.Lys186Asn) c.1461G>T (p.Lys487Asn) c.879G>T (p.Lys293Asn) c.477G>T (p.Lys159Asn) | |
8 | g.143575472C>G | CA372451128 | NAPRT | c.1242G>C (p.Lys414Asn) c.220G>C n.786G>C c.1026G>C c.1161G>C (p.Lys387Asn) c.558G>C (p.Lys186Asn) c.1461G>C (p.Lys487Asn) c.879G>C (p.Lys293Asn) c.477G>C (p.Lys159Asn) | |
8 | g.143575472C>T | CA463512361 | NAPRT | c.1242G>A (p.Lys414=) c.220G>A n.786G>A c.1026G>A c.1161G>A (p.Lys387=) c.558G>A (p.Lys186=) c.1461G>A (p.Lys487=) c.879G>A (p.Lys293=) c.477G>A (p.Lys159=) | gnomAD v4 |
8 | g.143575473T>A | CA372451137 | NAPRT | c.1241A>T (p.Lys414Met) c.219A>T n.785A>T c.1025A>T c.1160A>T (p.Lys387Met) c.557A>T (p.Lys186Met) c.1460A>T (p.Lys487Met) c.878A>T (p.Lys293Met) c.476A>T (p.Lys159Met) | |
8 | g.143575473T>C | CA372451140 | NAPRT | c.1241A>G (p.Lys414Arg) c.219A>G n.785A>G c.1025A>G c.1160A>G (p.Lys387Arg) c.557A>G (p.Lys186Arg) c.1460A>G (p.Lys487Arg) c.878A>G (p.Lys293Arg) c.476A>G (p.Lys159Arg) | gnomAD v4 |
8 | g.143575473T>G | CA372451142 | NAPRT | c.1241A>C (p.Lys414Thr) c.219A>C n.785A>C c.1025A>C c.1160A>C (p.Lys387Thr) c.557A>C (p.Lys186Thr) c.1460A>C (p.Lys487Thr) c.878A>C (p.Lys293Thr) c.476A>C (p.Lys159Thr) | |
8 | g.143575474T>A | CA372451145 | NAPRT | c.1240A>T (p.Lys414Ter) c.218A>T n.784A>T c.1024A>T c.1159A>T (p.Lys387Ter) c.556A>T (p.Lys186Ter) c.1459A>T (p.Lys487Ter) c.877A>T (p.Lys293Ter) c.475A>T (p.Lys159Ter) | |
8 | g.143575474T>C | CA372451147 | NAPRT | c.1240A>G (p.Lys414Glu) c.218A>G n.784A>G c.1024A>G c.1159A>G (p.Lys387Glu) c.556A>G (p.Lys186Glu) c.1459A>G (p.Lys487Glu) c.877A>G (p.Lys293Glu) c.475A>G (p.Lys159Glu) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.143575474T>G | CA372451149 | NAPRT | c.1240A>C (p.Lys414Gln) c.218A>C n.784A>C c.1024A>C c.1159A>C (p.Lys387Gln) c.556A>C (p.Lys186Gln) c.1459A>C (p.Lys487Gln) c.877A>C (p.Lys293Gln) c.475A>C (p.Lys159Gln) | |
8 | g.143575474T= | CA1825861471 | NAPRT | c.1240A= (p.Lys414=) c.218A= n.784A= c.1024A= c.1159A= (p.Lys387=) c.556A= (p.Lys186=) c.1459A= (p.Lys487=) c.877A= (p.Lys293=) c.475A= (p.Lys159=) | |
8 | g.143575475C>A | CA372451153 | NAPRT | c.1239G>T (p.Glu413Asp) c.217G>T n.783G>T c.1023G>T c.1158G>T (p.Glu386Asp) c.555G>T (p.Glu185Asp) c.1458G>T (p.Glu486Asp) c.876G>T (p.Glu292Asp) c.474G>T (p.Glu158Asp) | |
8 | g.143575475C>G | CA372451156 | NAPRT | c.1239G>C (p.Glu413Asp) c.217G>C n.783G>C c.1023G>C c.1158G>C (p.Glu386Asp) c.555G>C (p.Glu185Asp) c.1458G>C (p.Glu486Asp) c.876G>C (p.Glu292Asp) c.474G>C (p.Glu158Asp) | |
8 | g.143575475C>T | CA463512376 | NAPRT | c.1239G>A (p.Glu413=) c.217G>A n.783G>A c.1023G>A c.1158G>A (p.Glu386=) c.555G>A (p.Glu185=) c.1458G>A (p.Glu486=) c.876G>A (p.Glu292=) c.474G>A (p.Glu158=) | gnomAD v4 |
8 | g.143575476T>A | CA372451157 | NAPRT | c.1238A>T (p.Glu413Val) c.216A>T n.782A>T c.1022A>T c.1157A>T (p.Glu386Val) c.554A>T (p.Glu185Val) c.1457A>T (p.Glu486Val) c.875A>T (p.Glu292Val) c.473A>T (p.Glu158Val) | |
8 | g.143575476T>C | CA372451158 | NAPRT | c.1238A>G (p.Glu413Gly) c.216A>G n.782A>G c.1022A>G c.1157A>G (p.Glu386Gly) c.554A>G (p.Glu185Gly) c.1457A>G (p.Glu486Gly) c.875A>G (p.Glu292Gly) c.473A>G (p.Glu158Gly) | gnomAD v4 |
8 | g.143575476T>G | CA372451159 | NAPRT | c.1238A>C (p.Glu413Ala) c.216A>C n.782A>C c.1022A>C c.1157A>C (p.Glu386Ala) c.554A>C (p.Glu185Ala) c.1457A>C (p.Glu486Ala) c.875A>C (p.Glu292Ala) c.473A>C (p.Glu158Ala) | |
8 | g.143575477C>A | CA372451163 | NAPRT | c.1237G>T (p.Glu413Ter) c.215G>T n.781G>T c.1021G>T c.1156G>T (p.Glu386Ter) c.553G>T (p.Glu185Ter) c.1456G>T (p.Glu486Ter) c.874G>T (p.Glu292Ter) c.472G>T (p.Glu158Ter) | gnomAD v4 COSMIC COSMIC COSMIC |
8 | g.143575477C= | CA1825861472 | NAPRT | c.1237G= (p.Glu413=) c.215G= n.781G= c.1021G= c.1156G= (p.Glu386=) c.553G= (p.Glu185=) c.1456G= (p.Glu486=) c.874G= (p.Glu292=) c.472G= (p.Glu158=) | |
8 | g.143575477C>G | CA372451167 | NAPRT | c.1237G>C (p.Glu413Gln) c.215G>C n.781G>C c.1021G>C c.1156G>C (p.Glu386Gln) c.553G>C (p.Glu185Gln) c.1456G>C (p.Glu486Gln) c.874G>C (p.Glu292Gln) c.472G>C (p.Glu158Gln) | |
8 | g.143575477C>T | CA187547822 | NAPRT | c.1237G>A (p.Glu413Lys) c.215G>A n.781G>A c.1021G>A c.1156G>A (p.Glu386Lys) c.553G>A (p.Glu185Lys) c.1456G>A (p.Glu486Lys) c.874G>A (p.Glu292Lys) c.472G>A (p.Glu158Lys) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC COSMIC |
8 | g.143575478G>A | CA187547830 | NAPRT | c.1236C>T (p.Pro412=) c.214C>T n.780C>T c.1020C>T c.1155C>T (p.Pro385=) c.552C>T (p.Pro184=) c.1455C>T (p.Pro485=) c.873C>T (p.Pro291=) c.471C>T (p.Pro157=) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.143575478G>C | CA4912721 | NAPRT | c.1236C>G (p.Pro412=) c.214C>G n.780C>G c.1020C>G c.1155C>G (p.Pro385=) c.552C>G (p.Pro184=) c.1455C>G (p.Pro485=) c.873C>G (p.Pro291=) c.471C>G (p.Pro157=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.143575478G= | CA1825861473 | NAPRT | c.1236C= (p.Pro412=) c.214C= n.780C= c.1020C= c.1155C= (p.Pro385=) c.552C= (p.Pro184=) c.1455C= (p.Pro485=) c.873C= (p.Pro291=) c.471C= (p.Pro157=) | |
8 | g.143575478G>T | CA463512393 | NAPRT | c.1236C>A (p.Pro412=) c.214C>A n.780C>A c.1020C>A c.1155C>A (p.Pro385=) c.552C>A (p.Pro184=) c.1455C>A (p.Pro485=) c.873C>A (p.Pro291=) c.471C>A (p.Pro157=) | |
8 | g.143575479G>A | CA372451170 | NAPRT | c.1235C>T (p.Pro412Leu) c.213C>T n.779C>T c.1019C>T c.1154C>T (p.Pro385Leu) c.551C>T (p.Pro184Leu) c.1454C>T (p.Pro485Leu) c.872C>T (p.Pro291Leu) c.470C>T (p.Pro157Leu) | gnomAD v4 |
8 | g.143575479G>C | CA372451173 | NAPRT | c.1235C>G (p.Pro412Arg) c.213C>G n.779C>G c.1019C>G c.1154C>G (p.Pro385Arg) c.551C>G (p.Pro184Arg) c.1454C>G (p.Pro485Arg) c.872C>G (p.Pro291Arg) c.470C>G (p.Pro157Arg) | |
8 | g.143575479G>T | CA372451175 | NAPRT | c.1235C>A (p.Pro412His) c.213C>A n.779C>A c.1019C>A c.1154C>A (p.Pro385His) c.551C>A (p.Pro184His) c.1454C>A (p.Pro485His) c.872C>A (p.Pro291His) c.470C>A (p.Pro157His) | |
8 | g.143575480G>A | CA372451189 | NAPRT | c.1234C>T (p.Pro412Ser) c.212C>T n.778C>T c.1018C>T c.1153C>T (p.Pro385Ser) c.550C>T (p.Pro184Ser) c.1453C>T (p.Pro485Ser) c.871C>T (p.Pro291Ser) c.469C>T (p.Pro157Ser) | gnomAD v4 |
8 | g.143575480G>C | CA372451186 | NAPRT | c.1234C>G (p.Pro412Ala) c.212C>G n.778C>G c.1018C>G c.1153C>G (p.Pro385Ala) c.550C>G (p.Pro184Ala) c.1453C>G (p.Pro485Ala) c.871C>G (p.Pro291Ala) c.469C>G (p.Pro157Ala) | |
8 | g.143575480G>T | CA372451183 | NAPRT | c.1234C>A (p.Pro412Thr) c.212C>A n.778C>A c.1018C>A c.1153C>A (p.Pro385Thr) c.550C>A (p.Pro184Thr) c.1453C>A (p.Pro485Thr) c.871C>A (p.Pro291Thr) c.469C>A (p.Pro157Thr) | |
8 | g.143575481G>A | CA4912722 | NAPRT | c.1233C>T (p.Asp411=) c.211C>T n.777C>T c.1017C>T c.1152C>T (p.Asp384=) c.549C>T (p.Asp183=) c.1452C>T (p.Asp484=) c.870C>T (p.Asp290=) c.468C>T (p.Asp156=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.143575481G>C | CA372451195 | NAPRT | c.1233C>G (p.Asp411Glu) c.211C>G n.777C>G c.1017C>G c.1152C>G (p.Asp384Glu) c.549C>G (p.Asp183Glu) c.1452C>G (p.Asp484Glu) c.870C>G (p.Asp290Glu) c.468C>G (p.Asp156Glu) | |
8 | g.143575481G= | CA1825861474 | NAPRT | c.1233C= (p.Asp411=) c.211C= n.777C= c.1017C= c.1152C= (p.Asp384=) c.549C= (p.Asp183=) c.1452C= (p.Asp484=) c.870C= (p.Asp290=) c.468C= (p.Asp156=) | |
8 | g.143575481G>T | CA372451196 | NAPRT | c.1233C>A (p.Asp411Glu) c.211C>A n.777C>A c.1017C>A c.1152C>A (p.Asp384Glu) c.549C>A (p.Asp183Glu) c.1452C>A (p.Asp484Glu) c.870C>A (p.Asp290Glu) c.468C>A (p.Asp156Glu) | |
8 | g.143575482T>A | CA372451200 | NAPRT | c.1232A>T (p.Asp411Val) c.210A>T n.776A>T c.1016A>T c.1151A>T (p.Asp384Val) c.548A>T (p.Asp183Val) c.1451A>T (p.Asp484Val) c.869A>T (p.Asp290Val) c.467A>T (p.Asp156Val) | |
8 | g.143575482T>C | CA372451202 | NAPRT | c.1232A>G (p.Asp411Gly) c.210A>G n.776A>G c.1016A>G c.1151A>G (p.Asp384Gly) c.548A>G (p.Asp183Gly) c.1451A>G (p.Asp484Gly) c.869A>G (p.Asp290Gly) c.467A>G (p.Asp156Gly) | |
8 | g.143575482T>G | CA372451204 | NAPRT | c.1232A>C (p.Asp411Ala) c.210A>C n.776A>C c.1016A>C c.1151A>C (p.Asp384Ala) c.548A>C (p.Asp183Ala) c.1451A>C (p.Asp484Ala) c.869A>C (p.Asp290Ala) c.467A>C (p.Asp156Ala) | |
8 | g.143575483C>A | CA372451216 | NAPRT | c.1231G>T (p.Asp411Tyr) c.209G>T n.775G>T c.1015G>T c.1150G>T (p.Asp384Tyr) c.547G>T (p.Asp183Tyr) c.1450G>T (p.Asp484Tyr) c.868G>T (p.Asp290Tyr) c.466G>T (p.Asp156Tyr) | |
8 | g.143575483C= | CA1825861475 | NAPRT | c.1231G= (p.Asp411=) c.209G= n.775G= c.1015G= c.1150G= (p.Asp384=) c.547G= (p.Asp183=) c.1450G= (p.Asp484=) c.868G= (p.Asp290=) c.466G= (p.Asp156=) | |
8 | g.143575483C>G | CA372451208 | NAPRT | c.1231G>C (p.Asp411His) c.209G>C n.775G>C c.1015G>C c.1150G>C (p.Asp384His) c.547G>C (p.Asp183His) c.1450G>C (p.Asp484His) c.868G>C (p.Asp290His) c.466G>C (p.Asp156His) | |
8 | g.143575483C>T | CA4912723 | NAPRT | c.1231G>A (p.Asp411Asn) c.209G>A n.775G>A c.1015G>A c.1150G>A (p.Asp384Asn) c.547G>A (p.Asp183Asn) c.1450G>A (p.Asp484Asn) c.868G>A (p.Asp290Asn) c.466G>A (p.Asp156Asn) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.143575484C>A | CA372451218 | NAPRT | c.1230G>T (p.Glu410Asp) c.208G>T n.774G>T c.1014G>T c.1149G>T (p.Glu383Asp) c.546G>T (p.Glu182Asp) c.1449G>T (p.Glu483Asp) c.867G>T (p.Glu289Asp) c.465G>T (p.Glu155Asp) | gnomAD v4 |
8 | g.143575484C>G | CA372451221 | NAPRT | c.1230G>C (p.Glu410Asp) c.208G>C n.774G>C c.1014G>C c.1149G>C (p.Glu383Asp) c.546G>C (p.Glu182Asp) c.1449G>C (p.Glu483Asp) c.867G>C (p.Glu289Asp) c.465G>C (p.Glu155Asp) | |
8 | g.143575484C>T | CA463375938 | NAPRT | c.1230G>A (p.Glu410=) c.208G>A n.774G>A c.1014G>A c.1149G>A (p.Glu383=) c.546G>A (p.Glu182=) c.1449G>A (p.Glu483=) c.867G>A (p.Glu289=) c.465G>A (p.Glu155=) | |
8 | g.143575485T>A | CA372451225 | NAPRT | c.1229A>T (p.Glu410Val) c.207A>T n.773A>T c.1013A>T c.1148A>T (p.Glu383Val) c.545A>T (p.Glu182Val) c.1448A>T (p.Glu483Val) c.866A>T (p.Glu289Val) c.464A>T (p.Glu155Val) | |
8 | g.143575485T>C | CA372451229 | NAPRT | c.1229A>G (p.Glu410Gly) c.207A>G n.773A>G c.1013A>G c.1148A>G (p.Glu383Gly) c.545A>G (p.Glu182Gly) c.1448A>G (p.Glu483Gly) c.866A>G (p.Glu289Gly) c.464A>G (p.Glu155Gly) | gnomAD v4 |
8 | g.143575485T>G | CA372451230 | NAPRT | c.1229A>C (p.Glu410Ala) c.207A>C n.773A>C c.1013A>C c.1148A>C (p.Glu383Ala) c.545A>C (p.Glu182Ala) c.1448A>C (p.Glu483Ala) c.866A>C (p.Glu289Ala) c.464A>C (p.Glu155Ala) | |
8 | g.143575486C>A | CA372451234 | NAPRT | c.1228G>T (p.Glu410Ter) c.206G>T n.772G>T c.1012G>T c.1147G>T (p.Glu383Ter) c.544G>T (p.Glu182Ter) c.1447G>T (p.Glu483Ter) c.865G>T (p.Glu289Ter) c.463G>T (p.Glu155Ter) | gnomAD v4 |
8 | g.143575486C= | CA1825861476 | NAPRT | c.1228G= (p.Glu410=) c.206G= n.772G= c.1012G= c.1147G= (p.Glu383=) c.544G= (p.Glu182=) c.1447G= (p.Glu483=) c.865G= (p.Glu289=) c.463G= (p.Glu155=) | |
8 | g.143575486C>G | CA372451236 | NAPRT | c.1228G>C (p.Glu410Gln) c.206G>C n.772G>C c.1012G>C c.1147G>C (p.Glu383Gln) c.544G>C (p.Glu182Gln) c.1447G>C (p.Glu483Gln) c.865G>C (p.Glu289Gln) c.463G>C (p.Glu155Gln) | |
8 | g.143575486C>T | CA4912724 | NAPRT | c.1228G>A (p.Glu410Lys) c.206G>A n.772G>A c.1012G>A c.1147G>A (p.Glu383Lys) c.544G>A (p.Glu182Lys) c.1447G>A (p.Glu483Lys) c.865G>A (p.Glu289Lys) c.463G>A (p.Glu155Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.143575487G>A | CA4912725 | NAPRT | c.1227C>T (p.Thr409=) c.205C>T n.771C>T c.1011C>T c.1146C>T (p.Thr382=) c.543C>T (p.Thr181=) c.1446C>T (p.Thr482=) c.864C>T (p.Thr288=) c.462C>T (p.Thr154=) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.143575487G>C | CA463375939 | NAPRT | c.1227C>G (p.Thr409=) c.205C>G n.771C>G c.1011C>G c.1146C>G (p.Thr382=) c.543C>G (p.Thr181=) c.1446C>G (p.Thr482=) c.864C>G (p.Thr288=) c.462C>G (p.Thr154=) | COSMIC COSMIC COSMIC |
8 | g.143575487G= | CA1825861477 | NAPRT | c.1227C= (p.Thr409=) c.205C= n.771C= c.1011C= c.1146C= (p.Thr382=) c.543C= (p.Thr181=) c.1446C= (p.Thr482=) c.864C= (p.Thr288=) c.462C= (p.Thr154=) | |
8 | g.143575487G>T | CA463375940 | NAPRT | c.1227C>A (p.Thr409=) c.205C>A n.771C>A c.1011C>A c.1146C>A (p.Thr382=) c.543C>A (p.Thr181=) c.1446C>A (p.Thr482=) c.864C>A (p.Thr288=) c.462C>A (p.Thr154=) | |
8 | g.143575488G>A | CA4912726 | NAPRT | c.1226C>T (p.Thr409Ile) c.204C>T n.770C>T c.1010C>T c.1145C>T (p.Thr382Ile) c.542C>T (p.Thr181Ile) c.1445C>T (p.Thr482Ile) c.863C>T (p.Thr288Ile) c.461C>T (p.Thr154Ile) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.143575488G>C | CA372451249 | NAPRT | c.1226C>G (p.Thr409Ser) c.204C>G n.770C>G c.1010C>G c.1145C>G (p.Thr382Ser) c.542C>G (p.Thr181Ser) c.1445C>G (p.Thr482Ser) c.863C>G (p.Thr288Ser) c.461C>G (p.Thr154Ser) | |
8 | g.143575488G= | CA1825861478 | NAPRT | c.1226C= (p.Thr409=) c.204C= n.770C= c.1010C= c.1145C= (p.Thr382=) c.542C= (p.Thr181=) c.1445C= (p.Thr482=) c.863C= (p.Thr288=) c.461C= (p.Thr154=) | |
8 | g.143575488G>T | CA372451250 | NAPRT | c.1226C>A (p.Thr409Asn) c.204C>A n.770C>A c.1010C>A c.1145C>A (p.Thr382Asn) c.542C>A (p.Thr181Asn) c.1445C>A (p.Thr482Asn) c.863C>A (p.Thr288Asn) c.461C>A (p.Thr154Asn) | |
8 | g.143575489T>A | CA372451254 | NAPRT | c.1225A>T (p.Thr409Ser) c.203A>T n.769A>T c.1009A>T c.1144A>T (p.Thr382Ser) c.541A>T (p.Thr181Ser) c.1444A>T (p.Thr482Ser) c.862A>T (p.Thr288Ser) c.460A>T (p.Thr154Ser) | gnomAD v4 |
8 | g.143575489T>C | CA372451261 | NAPRT | c.1225A>G (p.Thr409Ala) c.203A>G n.769A>G c.1009A>G c.1144A>G (p.Thr382Ala) c.541A>G (p.Thr181Ala) c.1444A>G (p.Thr482Ala) c.862A>G (p.Thr288Ala) c.460A>G (p.Thr154Ala) | |
8 | g.143575489T>G | CA372451258 | NAPRT | c.1225A>C (p.Thr409Pro) c.203A>C n.769A>C c.1009A>C c.1144A>C (p.Thr382Pro) c.541A>C (p.Thr181Pro) c.1444A>C (p.Thr482Pro) c.862A>C (p.Thr288Pro) c.460A>C (p.Thr154Pro) | |
8 | g.143575490C>A | CA463375941 | NAPRT | c.1224G>T (p.Leu408=) c.202G>T n.768G>T c.1008G>T c.1143G>T (p.Leu381=) c.540G>T (p.Leu180=) c.1443G>T (p.Leu481=) c.861G>T (p.Leu287=) c.459G>T (p.Leu153=) | gnomAD v4 |
8 | g.143575490C>G | CA463375942 | NAPRT | c.1224G>C (p.Leu408=) c.202G>C n.768G>C c.1008G>C c.1143G>C (p.Leu381=) c.540G>C (p.Leu180=) c.1443G>C (p.Leu481=) c.861G>C (p.Leu287=) c.459G>C (p.Leu153=) | |
8 | g.143575490C>T | CA463375943 | NAPRT | c.1224G>A (p.Leu408=) c.202G>A n.768G>A c.1008G>A c.1143G>A (p.Leu381=) c.540G>A (p.Leu180=) c.1443G>A (p.Leu481=) c.861G>A (p.Leu287=) c.459G>A (p.Leu153=) | |
8 | g.143575491A>C | CA372451262 | NAPRT | c.1223T>G (p.Leu408Arg) c.201T>G n.767T>G c.1007T>G c.1142T>G (p.Leu381Arg) c.539T>G (p.Leu180Arg) c.1442T>G (p.Leu481Arg) c.860T>G (p.Leu287Arg) c.458T>G (p.Leu153Arg) | |
8 | g.143575491A>G | CA372451263 | NAPRT | c.1223T>C (p.Leu408Pro) c.201T>C n.767T>C c.1007T>C c.1142T>C (p.Leu381Pro) c.539T>C (p.Leu180Pro) c.1442T>C (p.Leu481Pro) c.860T>C (p.Leu287Pro) c.458T>C (p.Leu153Pro) | |
8 | g.143575491A>T | CA372451264 | NAPRT | c.1223T>A (p.Leu408Gln) c.201T>A n.767T>A c.1007T>A c.1142T>A (p.Leu381Gln) c.539T>A (p.Leu180Gln) c.1442T>A (p.Leu481Gln) c.860T>A (p.Leu287Gln) c.458T>A (p.Leu153Gln) | |
8 | g.143575492G>A | CA463375944 | NAPRT | c.1222C>T (p.Leu408=) c.200C>T n.766C>T c.1006C>T c.1141C>T (p.Leu381=) c.538C>T (p.Leu180=) c.1441C>T (p.Leu481=) c.859C>T (p.Leu287=) c.457C>T (p.Leu153=) | |
8 | g.143575492G>C | CA372451265 | NAPRT | c.1222C>G (p.Leu408Val) c.200C>G n.766C>G c.1006C>G c.1141C>G (p.Leu381Val) c.538C>G (p.Leu180Val) c.1441C>G (p.Leu481Val) c.859C>G (p.Leu287Val) c.457C>G (p.Leu153Val) | |
8 | g.143575492G>T | CA372451267 | NAPRT | c.1222C>A (p.Leu408Met) c.200C>A n.766C>A c.1006C>A c.1141C>A (p.Leu381Met) c.538C>A (p.Leu180Met) c.1441C>A (p.Leu481Met) c.859C>A (p.Leu287Met) c.457C>A (p.Leu153Met) | |
8 | g.143575493C>A | CA372451270 | NAPRT | c.1221G>T (p.Lys407Asn) c.199G>T n.765G>T c.1005G>T c.1140G>T (p.Lys380Asn) c.537G>T (p.Lys179Asn) c.1440G>T (p.Lys480Asn) c.858G>T (p.Lys286Asn) c.456G>T (p.Lys152Asn) | |
8 | g.143575493C>G | CA372451273 | NAPRT | c.1221G>C (p.Lys407Asn) c.199G>C n.765G>C c.1005G>C c.1140G>C (p.Lys380Asn) c.537G>C (p.Lys179Asn) c.1440G>C (p.Lys480Asn) c.858G>C (p.Lys286Asn) c.456G>C (p.Lys152Asn) | |
8 | g.143575493C>T | CA463375945 | NAPRT | c.1221G>A (p.Lys407=) c.199G>A n.765G>A c.1005G>A c.1140G>A (p.Lys380=) c.537G>A (p.Lys179=) c.1440G>A (p.Lys480=) c.858G>A (p.Lys286=) c.456G>A (p.Lys152=) | |
8 | g.143575494T>A | CA372451278 | NAPRT | c.1220A>T (p.Lys407Met) c.198A>T n.764A>T c.1004A>T c.1139A>T (p.Lys380Met) c.536A>T (p.Lys179Met) c.1439A>T (p.Lys480Met) c.857A>T (p.Lys286Met) c.455A>T (p.Lys152Met) | |
8 | g.143575494T>C | CA372451291 | NAPRT | c.1220A>G (p.Lys407Arg) c.198A>G n.764A>G c.1004A>G c.1139A>G (p.Lys380Arg) c.536A>G (p.Lys179Arg) c.1439A>G (p.Lys480Arg) c.857A>G (p.Lys286Arg) c.455A>G (p.Lys152Arg) | |
8 | g.143575494T>G | CA372451294 | NAPRT | c.1220A>C (p.Lys407Thr) c.198A>C n.764A>C c.1004A>C c.1139A>C (p.Lys380Thr) c.536A>C (p.Lys179Thr) c.1439A>C (p.Lys480Thr) c.857A>C (p.Lys286Thr) c.455A>C (p.Lys152Thr) | |
8 | g.143575495T>A | CA372451299 | NAPRT | c.1219A>T (p.Lys407Ter) c.197A>T n.763A>T c.1003A>T c.1138A>T (p.Lys380Ter) c.535A>T (p.Lys179Ter) c.1438A>T (p.Lys480Ter) c.856A>T (p.Lys286Ter) c.454A>T (p.Lys152Ter) | |
8 | g.143575495T>C | CA372451302 | NAPRT | c.1219A>G (p.Lys407Glu) c.197A>G n.763A>G c.1003A>G c.1138A>G (p.Lys380Glu) c.535A>G (p.Lys179Glu) c.1438A>G (p.Lys480Glu) c.856A>G (p.Lys286Glu) c.454A>G (p.Lys152Glu) | gnomAD v4 |
8 | g.143575495T>G | CA372451305 | NAPRT | c.1219A>C (p.Lys407Gln) c.197A>C n.763A>C c.1003A>C c.1138A>C (p.Lys380Gln) c.535A>C (p.Lys179Gln) c.1438A>C (p.Lys480Gln) c.856A>C (p.Lys286Gln) c.454A>C (p.Lys152Gln) | |
8 | g.143575496C>A | CA372451309 | NAPRT | c.1218G>T (p.Met406Ile) c.196G>T n.762G>T c.1002G>T c.1137G>T (p.Met379Ile) c.534G>T (p.Met178Ile) c.1437G>T (p.Met479Ile) c.855G>T (p.Met285Ile) c.453G>T (p.Met151Ile) | |
8 | g.143575496C= | CA1825861479 | NAPRT | c.1218G= (p.Met406=) c.196G= n.762G= c.1002G= c.1137G= (p.Met379=) c.534G= (p.Met178=) c.1437G= (p.Met479=) c.855G= (p.Met285=) c.453G= (p.Met151=) | |
8 | g.143575496C>G | CA372451315 | NAPRT | c.1218G>C (p.Met406Ile) c.196G>C n.762G>C c.1002G>C c.1137G>C (p.Met379Ile) c.534G>C (p.Met178Ile) c.1437G>C (p.Met479Ile) c.855G>C (p.Met285Ile) c.453G>C (p.Met151Ile) | |
8 | g.143575496C>T | CA372451312 | NAPRT | c.1218G>A (p.Met406Ile) c.196G>A n.762G>A c.1002G>A c.1137G>A (p.Met379Ile) c.534G>A (p.Met178Ile) c.1437G>A (p.Met479Ile) c.855G>A (p.Met285Ile) c.453G>A (p.Met151Ile) | dbSNP gnomAD v3 gnomAD v4 |
8 | g.143575497A>C | CA372451320 | NAPRT | c.1217T>G (p.Met406Arg) c.195T>G n.761T>G c.1001T>G c.1136T>G (p.Met379Arg) c.533T>G (p.Met178Arg) c.1436T>G (p.Met479Arg) c.854T>G (p.Met285Arg) c.452T>G (p.Met151Arg) | |
8 | g.143575497A>G | CA372451323 | NAPRT | c.1217T>C (p.Met406Thr) c.195T>C n.761T>C c.1001T>C c.1136T>C (p.Met379Thr) c.533T>C (p.Met178Thr) c.1436T>C (p.Met479Thr) c.854T>C (p.Met285Thr) c.452T>C (p.Met151Thr) | |
8 | g.143575497A>T | CA372451329 | NAPRT | c.1217T>A (p.Met406Lys) c.195T>A n.761T>A c.1001T>A c.1136T>A (p.Met379Lys) c.533T>A (p.Met178Lys) c.1436T>A (p.Met479Lys) c.854T>A (p.Met285Lys) c.452T>A (p.Met151Lys) | |
8 | g.143575498T>A | CA372451332 | NAPRT | c.1216A>T (p.Met406Leu) c.194A>T n.760A>T c.1000A>T c.1135A>T (p.Met379Leu) c.532A>T (p.Met178Leu) c.1435A>T (p.Met479Leu) c.853A>T (p.Met285Leu) c.451A>T (p.Met151Leu) | |
8 | g.143575498T>C | CA372451335 | NAPRT | c.1216A>G (p.Met406Val) c.194A>G n.760A>G c.1000A>G c.1135A>G (p.Met379Val) c.532A>G (p.Met178Val) c.1435A>G (p.Met479Val) c.853A>G (p.Met285Val) c.451A>G (p.Met151Val) | |
8 | g.143575498T>G | CA372451337 | NAPRT | c.1216A>C (p.Met406Leu) c.194A>C n.760A>C c.1000A>C c.1135A>C (p.Met379Leu) c.532A>C (p.Met178Leu) c.1435A>C (p.Met479Leu) c.853A>C (p.Met285Leu) c.451A>C (p.Met151Leu) | |
8 | g.143575499T>A | CA463375946 | NAPRT | c.1215A>T (p.Arg405=) c.193A>T n.759A>T c.999A>T c.1134A>T (p.Arg378=) c.531A>T (p.Arg177=) c.1434A>T (p.Arg478=) c.852A>T (p.Arg284=) c.450A>T (p.Arg150=) | |
8 | g.143575499T>C | CA463375947 | NAPRT | c.1215A>G (p.Arg405=) c.193A>G n.759A>G c.999A>G c.1134A>G (p.Arg378=) c.531A>G (p.Arg177=) c.1434A>G (p.Arg478=) c.852A>G (p.Arg284=) c.450A>G (p.Arg150=) | |
8 | g.143575499T>G | CA463375948 | NAPRT | c.1215A>C (p.Arg405=) c.193A>C n.759A>C c.999A>C c.1134A>C (p.Arg378=) c.531A>C (p.Arg177=) c.1434A>C (p.Arg478=) c.852A>C (p.Arg284=) c.450A>C (p.Arg150=) | |
8 | g.143575500C>A | CA372451341 | NAPRT | c.1214G>T (p.Arg405Leu) c.192G>T n.758G>T c.998G>T c.1133G>T (p.Arg378Leu) c.530G>T (p.Arg177Leu) c.1433G>T (p.Arg478Leu) c.851G>T (p.Arg284Leu) c.449G>T (p.Arg150Leu) | dbSNP |
8 | g.143575500C= | CA1825861480 | NAPRT | c.1214G= (p.Arg405=) c.192G= n.758G= c.998G= c.1133G= (p.Arg378=) c.530G= (p.Arg177=) c.1433G= (p.Arg478=) c.851G= (p.Arg284=) c.449G= (p.Arg150=) | |
8 | g.143575500C>G | CA372451347 | NAPRT | c.1214G>C (p.Arg405Pro) c.192G>C n.758G>C c.998G>C c.1133G>C (p.Arg378Pro) c.530G>C (p.Arg177Pro) c.1433G>C (p.Arg478Pro) c.851G>C (p.Arg284Pro) c.449G>C (p.Arg150Pro) | gnomAD v4 |
8 | g.143575500C>T | CA4912727 | NAPRT | c.1214G>A (p.Arg405Gln) c.192G>A n.758G>A c.998G>A c.1133G>A (p.Arg378Gln) c.530G>A (p.Arg177Gln) c.1433G>A (p.Arg478Gln) c.851G>A (p.Arg284Gln) c.449G>A (p.Arg150Gln) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.143575501G>A | CA4912728 | NAPRT | c.1213C>T (p.Arg405Ter) c.191C>T n.757C>T c.997C>T c.1132C>T (p.Arg378Ter) c.529C>T (p.Arg177Ter) c.1432C>T (p.Arg478Ter) c.850C>T (p.Arg284Ter) c.448C>T (p.Arg150Ter) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC COSMIC |
8 | g.143575501G>C | CA372451358 | NAPRT | c.1213C>G (p.Arg405Gly) c.191C>G n.757C>G c.997C>G c.1132C>G (p.Arg378Gly) c.529C>G (p.Arg177Gly) c.1432C>G (p.Arg478Gly) c.850C>G (p.Arg284Gly) c.448C>G (p.Arg150Gly) | |
8 | g.143575501G= | CA1825861481 | NAPRT | c.1213C= (p.Arg405=) c.191C= n.757C= c.997C= c.1132C= (p.Arg378=) c.529C= (p.Arg177=) c.1432C= (p.Arg478=) c.850C= (p.Arg284=) c.448C= (p.Arg150=) | |
8 | g.143575501G>T | CA463375949 | NAPRT | c.1213C>A (p.Arg405=) c.191C>A n.757C>A c.997C>A c.1132C>A (p.Arg378=) c.529C>A (p.Arg177=) c.1432C>A (p.Arg478=) c.850C>A (p.Arg284=) c.448C>A (p.Arg150=) | |
8 | g.143575502T>A | CA463375950 | NAPRT | c.1212A>T (p.Pro404=) c.190A>T n.756A>T c.996A>T c.1131A>T (p.Pro377=) c.528A>T (p.Pro176=) c.1431A>T (p.Pro477=) c.849A>T (p.Pro283=) c.447A>T (p.Pro149=) | |
8 | g.143575502T>C | CA4912729 | NAPRT | c.1212A>G (p.Pro404=) c.190A>G n.756A>G c.996A>G c.1131A>G (p.Pro377=) c.528A>G (p.Pro176=) c.1431A>G (p.Pro477=) c.849A>G (p.Pro283=) c.447A>G (p.Pro149=) | dbSNP ExAC gnomAD v3 gnomAD v4 |
8 | g.143575502T>G | CA463375951 | NAPRT | c.1212A>C (p.Pro404=) c.190A>C n.756A>C c.996A>C c.1131A>C (p.Pro377=) c.528A>C (p.Pro176=) c.1431A>C (p.Pro477=) c.849A>C (p.Pro283=) c.447A>C (p.Pro149=) | |
8 | g.143575502T= | CA1825861482 | NAPRT | c.1212A= (p.Pro404=) c.190A= n.756A= c.996A= c.1131A= (p.Pro377=) c.528A= (p.Pro176=) c.1431A= (p.Pro477=) c.849A= (p.Pro283=) c.447A= (p.Pro149=) | |
8 | g.143575503G>A | CA372451368 | NAPRT | c.1211C>T (p.Pro404Leu) c.189C>T n.755C>T c.995C>T c.1130C>T (p.Pro377Leu) c.527C>T (p.Pro176Leu) c.1430C>T (p.Pro477Leu) c.848C>T (p.Pro283Leu) c.446C>T (p.Pro149Leu) | gnomAD v4 COSMIC COSMIC COSMIC |
8 | g.143575503G>C | CA372451365 | NAPRT | c.1211C>G (p.Pro404Arg) c.189C>G n.755C>G c.995C>G c.1130C>G (p.Pro377Arg) c.527C>G (p.Pro176Arg) c.1430C>G (p.Pro477Arg) c.848C>G (p.Pro283Arg) c.446C>G (p.Pro149Arg) | |
8 | g.143575503G>T | CA372451371 | NAPRT | c.1211C>A (p.Pro404Gln) c.189C>A n.755C>A c.995C>A c.1130C>A (p.Pro377Gln) c.527C>A (p.Pro176Gln) c.1430C>A (p.Pro477Gln) c.848C>A (p.Pro283Gln) c.446C>A (p.Pro149Gln) | |
8 | g.143575504del | CA2688943991 | NAPRT | c.1211del (p.Pro404HisfsTer3) c.189del n.755del c.995del c.1130del (p.Pro377HisfsTer3) c.527del (p.Pro176HisfsTer3) c.1430del (p.Pro477HisfsTer3) c.848del (p.Pro283HisfsTer3) c.446del (p.Pro149HisfsTer3) | gnomAD v4 |
8 | g.143575504G>A | CA372451374 | NAPRT | c.1210C>T (p.Pro404Ser) c.188C>T n.754C>T c.994C>T c.1129C>T (p.Pro377Ser) c.526C>T (p.Pro176Ser) c.1429C>T (p.Pro477Ser) c.847C>T (p.Pro283Ser) c.445C>T (p.Pro149Ser) | gnomAD v4 |
8 | g.143575504G>C | CA372451380 | NAPRT | c.1210C>G (p.Pro404Ala) c.188C>G n.754C>G c.994C>G c.1129C>G (p.Pro377Ala) c.526C>G (p.Pro176Ala) c.1429C>G (p.Pro477Ala) c.847C>G (p.Pro283Ala) c.445C>G (p.Pro149Ala) | |
8 | g.143575504G>T | CA372451377 | NAPRT | c.1210C>A (p.Pro404Thr) c.188C>A n.754C>A c.994C>A c.1129C>A (p.Pro377Thr) c.526C>A (p.Pro176Thr) c.1429C>A (p.Pro477Thr) c.847C>A (p.Pro283Thr) c.445C>A (p.Pro149Thr) | |
8 | g.143575505C>A | CA372451382 | NAPRT | c.1209G>T (p.Gln403His) c.187G>T n.753G>T c.993G>T c.1128G>T (p.Gln376His) c.525G>T (p.Gln175His) c.1428G>T (p.Gln476His) c.846G>T (p.Gln282His) c.444G>T (p.Gln148His) | |
8 | g.143575505C>G | CA372451385 | NAPRT | c.1209G>C (p.Gln403His) c.187G>C n.753G>C c.993G>C c.1128G>C (p.Gln376His) c.525G>C (p.Gln175His) c.1428G>C (p.Gln476His) c.846G>C (p.Gln282His) c.444G>C (p.Gln148His) | |
8 | g.143575505C>T | CA463375952 | NAPRT | c.1209G>A (p.Gln403=) c.187G>A n.753G>A c.993G>A c.1128G>A (p.Gln376=) c.525G>A (p.Gln175=) c.1428G>A (p.Gln476=) c.846G>A (p.Gln282=) c.444G>A (p.Gln148=) | |
8 | g.143575509_143575601del | CA4912730 | NAPRT | c.1188+25_1209del c.166+25_187del n.732+25_753del c.972+25_993del c.1108-72_1128del c.504+25_525del c.1407+25_1428del c.826-72_846del c.424-72_444del | ExAC |
8 | g.143575506T>A | CA372451390 | NAPRT | c.1208A>T (p.Gln403Leu) c.186A>T n.752A>T c.992A>T c.1127A>T (p.Gln376Leu) c.524A>T (p.Gln175Leu) c.1427A>T (p.Gln476Leu) c.845A>T (p.Gln282Leu) c.443A>T (p.Gln148Leu) | |
8 | g.143575506T>C | CA372451392 | NAPRT | c.1208A>G (p.Gln403Arg) c.186A>G n.752A>G c.992A>G c.1127A>G (p.Gln376Arg) c.524A>G (p.Gln175Arg) c.1427A>G (p.Gln476Arg) c.845A>G (p.Gln282Arg) c.443A>G (p.Gln148Arg) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.143575506T>G | CA372451395 | NAPRT | c.1208A>C (p.Gln403Pro) c.186A>C n.752A>C c.992A>C c.1127A>C (p.Gln376Pro) c.524A>C (p.Gln175Pro) c.1427A>C (p.Gln476Pro) c.845A>C (p.Gln282Pro) c.443A>C (p.Gln148Pro) | |
8 | g.143575506T= | CA1825861483 | NAPRT | c.1208A= (p.Gln403=) c.186A= n.752A= c.992A= c.1127A= (p.Gln376=) c.524A= (p.Gln175=) c.1427A= (p.Gln476=) c.845A= (p.Gln282=) c.443A= (p.Gln148=) | |
8 | g.143575507G>A | CA372451399 | NAPRT | c.1207C>T (p.Gln403Ter) c.185C>T n.751C>T c.991C>T c.1126C>T (p.Gln376Ter) c.523C>T (p.Gln175Ter) c.1426C>T (p.Gln476Ter) c.844C>T (p.Gln282Ter) c.442C>T (p.Gln148Ter) | gnomAD v4 |
8 | g.143575507G>C | CA372451402 | NAPRT | c.1207C>G (p.Gln403Glu) c.185C>G n.751C>G c.991C>G c.1126C>G (p.Gln376Glu) c.523C>G (p.Gln175Glu) c.1426C>G (p.Gln476Glu) c.844C>G (p.Gln282Glu) c.442C>G (p.Gln148Glu) | |
8 | g.143575507G>T | CA372451406 | NAPRT | c.1207C>A (p.Gln403Lys) c.185C>A n.751C>A c.991C>A c.1126C>A (p.Gln376Lys) c.523C>A (p.Gln175Lys) c.1426C>A (p.Gln476Lys) c.844C>A (p.Gln282Lys) c.442C>A (p.Gln148Lys) | |
8 | g.143575508G>A | CA463375953 | NAPRT | c.1206C>T (p.Gly402=) c.184C>T n.750C>T c.990C>T c.1125C>T (p.Gly375=) c.522C>T (p.Gly174=) c.1425C>T (p.Gly475=) c.843C>T (p.Gly281=) c.441C>T (p.Gly147=) | gnomAD v4 |
8 | g.143575508G>C | CA463375954 | NAPRT | c.1206C>G (p.Gly402=) c.184C>G n.750C>G c.990C>G c.1125C>G (p.Gly375=) c.522C>G (p.Gly174=) c.1425C>G (p.Gly475=) c.843C>G (p.Gly281=) c.441C>G (p.Gly147=) | gnomAD v4 |
8 | g.143575508G= | CA1825861484 | NAPRT | c.1206C= (p.Gly402=) c.184C= n.750C= c.990C= c.1125C= (p.Gly375=) c.522C= (p.Gly174=) c.1425C= (p.Gly475=) c.843C= (p.Gly281=) c.441C= (p.Gly147=) | |
8 | g.143575508G>T | CA187547938 | NAPRT | c.1206C>A (p.Gly402=) c.184C>A n.750C>A c.990C>A c.1125C>A (p.Gly375=) c.522C>A (p.Gly174=) c.1425C>A (p.Gly475=) c.843C>A (p.Gly281=) c.441C>A (p.Gly147=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.143575508_143575509delinsGC | CA1825861485 | NAPRT | c.1205_1206delinsGC (p.Gly402=) c.183_184delinsGC n.749_750delinsGC c.989_990delinsGC c.1124_1125delinsGC (p.Gly375=) c.521_522delinsGC (p.Gly174=) c.1424_1425delinsGC (p.Gly475=) c.842_843delinsGC (p.Gly281=) c.440_441delinsGC (p.Gly147=) | |
8 | g.143575509C>A | CA4912733 | NAPRT | c.1205G>T (p.Gly402Val) c.183G>T n.749G>T c.989G>T c.1124G>T (p.Gly375Val) c.521G>T (p.Gly174Val) c.1424G>T (p.Gly475Val) c.842G>T (p.Gly281Val) c.440G>T (p.Gly147Val) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.143575509C= | CA1825861486 | NAPRT | c.1205G= (p.Gly402=) c.183G= n.749G= c.989G= c.1124G= (p.Gly375=) c.521G= (p.Gly174=) c.1424G= (p.Gly475=) c.842G= (p.Gly281=) c.440G= (p.Gly147=) | |
8 | g.143575509C>G | CA4912731 | NAPRT | c.1205G>C (p.Gly402Ala) c.183G>C n.749G>C c.989G>C c.1124G>C (p.Gly375Ala) c.521G>C (p.Gly174Ala) c.1424G>C (p.Gly475Ala) c.842G>C (p.Gly281Ala) c.440G>C (p.Gly147Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 |
8 | g.143575509C>T | CA4912732 | NAPRT | c.1205G>A (p.Gly402Asp) c.183G>A n.749G>A c.989G>A c.1124G>A (p.Gly375Asp) c.521G>A (p.Gly174Asp) c.1424G>A (p.Gly475Asp) c.842G>A (p.Gly281Asp) c.440G>A (p.Gly147Asp) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.143575514dup | CA585421614 | NAPRT | c.1205dup (p.Gln403ProfsTer28) c.183dup n.749dup c.989dup c.1124dup (p.Gln376ProfsTer28) c.521dup (p.Gln175ProfsTer28) c.1424dup (p.Gln476ProfsTer28) c.842dup (p.Gln282ProfsTer28) c.440dup (p.Gln148ProfsTer28) | dbSNP gnomAD v2 gnomAD v4 |
8 | g.143575514del | CA463375955 | NAPRT | c.1205del (p.Gly402AlafsTer5) c.183del n.749del c.989del c.1124del (p.Gly375AlafsTer5) c.521del (p.Gly174AlafsTer5) c.1424del (p.Gly475AlafsTer5) c.842del (p.Gly281AlafsTer5) c.440del (p.Gly147AlafsTer5) | dbSNP gnomAD v2 gnomAD v4 COSMIC COSMIC COSMIC |
8 | g.143575510C>A | CA4912734 | NAPRT | c.1204G>T (p.Gly402Cys) c.182G>T n.748G>T c.988G>T c.1123G>T (p.Gly375Cys) c.520G>T (p.Gly174Cys) c.1423G>T (p.Gly475Cys) c.841G>T (p.Gly281Cys) c.439G>T (p.Gly147Cys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
8 | g.143575510C= | CA1825861487 | NAPRT | c.1204G= (p.Gly402=) c.182G= n.748G= c.988G= c.1123G= (p.Gly375=) c.520G= (p.Gly174=) c.1423G= (p.Gly475=) c.841G= (p.Gly281=) c.439G= (p.Gly147=) | |
8 | g.143575510C>G | CA372451411 | NAPRT | c.1204G>C (p.Gly402Arg) c.182G>C n.748G>C c.988G>C c.1123G>C (p.Gly375Arg) c.520G>C (p.Gly174Arg) c.1423G>C (p.Gly475Arg) c.841G>C (p.Gly281Arg) c.439G>C (p.Gly147Arg) | |
8 | g.143575510C>T | CA372451412 | NAPRT | c.1204G>A (p.Gly402Ser) c.182G>A n.748G>A c.988G>A c.1123G>A (p.Gly375Ser) c.520G>A (p.Gly174Ser) c.1423G>A (p.Gly475Ser) c.841G>A (p.Gly281Ser) c.439G>A (p.Gly147Ser) | gnomAD v4 |
8 | g.143575511C>A | CA463375956 | NAPRT | c.1203G>T (p.Gly401=) c.181G>T n.747G>T c.987G>T c.1122G>T (p.Gly374=) c.519G>T (p.Gly173=) c.1422G>T (p.Gly474=) c.840G>T (p.Gly280=) c.438G>T (p.Gly146=) | |
8 | g.143575511C>G | CA463375957 | NAPRT | c.1203G>C (p.Gly401=) c.181G>C n.747G>C c.987G>C c.1122G>C (p.Gly374=) c.519G>C (p.Gly173=) c.1422G>C (p.Gly474=) c.840G>C (p.Gly280=) c.438G>C (p.Gly146=) | |
8 | g.143575511C>T | CA463375958 | NAPRT | c.1203G>A (p.Gly401=) c.181G>A n.747G>A c.987G>A c.1122G>A (p.Gly374=) c.519G>A (p.Gly173=) c.1422G>A (p.Gly474=) c.840G>A (p.Gly280=) c.438G>A (p.Gly146=) | gnomAD v4 |