Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.143575407dupCA1825861431NAPRTc.1291+21dup (n.1291+21dup)
c.269+21dup
n.835+21dup
n.14dup
c.1210+21dup (n.1210+21dup)
c.607+21dup (n.607+21dup)
c.1510+21dup (n.1510+21dup)
c.928+21dup (n.928+21dup)
c.526+21dup (n.526+21dup)
dbSNP gnomAD v4
8g.143575407delCA585728849NAPRTc.1291+21del (n.1291+21del)
c.269+21del
n.835+21del
n.14del
c.1210+21del (n.1210+21del)
c.607+21del (n.607+21del)
c.1510+21del (n.1510+21del)
c.928+21del (n.928+21del)
c.526+21del (n.526+21del)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.143575407G>ACA585728853NAPRTc.1291+16C>T (n.1291+16C>T)
c.269+16C>T
n.835+16C>T
n.9C>T
c.1210+16C>T (n.1210+16C>T)
c.607+16C>T (n.607+16C>T)
c.1510+16C>T (n.1510+16C>T)
c.928+16C>T (n.928+16C>T)
c.526+16C>T (n.526+16C>T)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
8g.143575407G=CA1825861436NAPRTc.1291+16C= (n.1291+16C=)
c.269+16C=
n.835+16C=
n.9C=
c.1210+16C= (n.1210+16C=)
c.607+16C= (n.607+16C=)
c.1510+16C= (n.1510+16C=)
c.928+16C= (n.928+16C=)
c.526+16C= (n.526+16C=)
8g.143575407G>TCA848763504NAPRTc.1291+16C>A (n.1291+16C>A)
c.269+16C>A
n.835+16C>A
n.9C>A
c.1210+16C>A (n.1210+16C>A)
c.607+16C>A (n.607+16C>A)
c.1510+16C>A (n.1510+16C>A)
c.928+16C>A (n.928+16C>A)
c.526+16C>A (n.526+16C>A)
dbSNP gnomAD v3 gnomAD v4
8g.143575410G>TCA2688943802NAPRTc.1291+13C>A (n.1291+13C>A)
c.269+13C>A
n.835+13C>A
n.6C>A
c.1210+13C>A (n.1210+13C>A)
c.607+13C>A (n.607+13C>A)
c.1510+13C>A (n.1510+13C>A)
c.928+13C>A (n.928+13C>A)
c.526+13C>A (n.526+13C>A)
gnomAD v4
8g.143575411G>ACA2688943804NAPRTc.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
8g.143575411G>CCA2782557017NAPRTc.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)
8g.143575412G>CCA4912697NAPRTc.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
8g.143575412G=CA1825861437NAPRTc.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=)
8g.143575413A>GCA2688943807NAPRTc.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
8g.143575414G>ACA4912698NAPRTc.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
8g.143575414G>CCA2688943809NAPRTc.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
8g.143575414G=CA1825861438NAPRTc.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=)
8g.143575415G>ACA1825861440NAPRTc.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
8g.143575415G=CA1825861439NAPRTc.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=)
8g.143575416G>ACA2688943813NAPRTc.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
8g.143575416G>CCA2688943814NAPRTc.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
8g.143575417C=CA1825861441NAPRTc.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=)
8g.143575417C>TCA4912699NAPRTc.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
8g.143575418C>ACA2688943822NAPRTc.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
8g.143575418C=CA1825861442NAPRTc.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=)
8g.143575418C>TCA4912700NAPRTc.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
8g.143575419T>ACA585728854NAPRTc.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
8g.143575419T>CCA2688943825NAPRTc.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
8g.143575419T=CA1825861443NAPRTc.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=)
8g.143575420C>TCA2688943826NAPRTc.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
8g.143575421A=CA1825861444NAPRTc.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=)
8g.143575421A>CCA372450578NAPRTc.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)
8g.143575421A>GCA372450589NAPRTc.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
8g.143575421A>TCA372450598NAPRTc.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)
8g.143575422C>ACA4912701NAPRTc.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
8g.143575422C=CA1825861445NAPRTc.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=)
8g.143575422C>GCA372450628NAPRTc.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)
8g.143575422C>TCA187547731NAPRTc.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
8g.143575423C>ACA372450642NAPRTc.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)
8g.143575423C=CA1825861446NAPRTc.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=)
8g.143575423C>GCA372450647NAPRTc.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)
8g.143575423C>TCA4912702NAPRTc.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
8g.143575424G>ACA4912703NAPRTc.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
8g.143575424G>CCA372450656NAPRTc.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
8g.143575424G=CA1825861447NAPRTc.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=)
8g.143575424G>TCA372450652NAPRTc.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)
8g.143575425T>ACA372450657NAPRTc.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)
8g.143575425T>CCA372450658NAPRTc.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)
8g.143575425T>GCA372450660NAPRTc.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)
8g.143575426C>ACA372450665NAPRTc.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
8g.143575426C=CA1825861449NAPRTc.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=)
8g.143575426C>GCA372450666NAPRTc.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)
8g.143575426C>TCA372450668NAPRTc.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)
8g.143575426_143575427delinsCACA1825861448NAPRTc.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=)
8g.143575427delCA4912704NAPRTc.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
8g.143575427A>CCA463512213NAPRTc.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=)
8g.143575427A>GCA463512216NAPRTc.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=)
8g.143575427A>TCA463512217NAPRTc.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=)
8g.143575429_143575430delCA2688943834NAPRTc.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
8g.143575428G>ACA372450674NAPRTc.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)
8g.143575428G>CCA372450683NAPRTc.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)
8g.143575428G>TCA372450688NAPRTc.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)
8g.143575429A=CA1825861450NAPRTc.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=)
8g.143575429A>CCA372450698NAPRTc.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)
8g.143575429A>GCA4912705NAPRTc.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
8g.143575429A>TCA372450708NAPRTc.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)
8g.143575430G>ACA4912706NAPRTc.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
8g.143575430G>CCA463512231NAPRTc.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=)
8g.143575430G=CA1825861451NAPRTc.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=)
8g.143575430G>TCA463512229NAPRTc.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=)
8g.143575431C>ACA372450716NAPRTc.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)
8g.143575431C>GCA372450720NAPRTc.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)
8g.143575431C>TCA372450728NAPRTc.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)
8g.143575432C>ACA372450729NAPRTc.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
8g.143575432C=CA1825861452NAPRTc.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=)
8g.143575432C>GCA372450730NAPRTc.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)
8g.143575432C>TCA372450731NAPRTc.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
8g.143575433C>ACA463512238NAPRTc.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=)
8g.143575433C>GCA463512254NAPRTc.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=)
8g.143575433C>TCA463512255NAPRTc.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
8g.143575434A=CA1825861453NAPRTc.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=)
8g.143575434A>CCA372450735NAPRTc.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)
8g.143575434A>GCA4912707NAPRTc.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
8g.143575434A>TCA372450742NAPRTc.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)
8g.143575435G>ACA463512256NAPRTc.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
8g.143575435G>CCA372450753NAPRTc.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)
8g.143575435G>TCA372450768NAPRTc.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
8g.143575436delCA2688943846NAPRTc.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
8g.143575436G>ACA187547773NAPRTc.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
8g.143575436G>CCA463512257NAPRTc.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=)
8g.143575436G=CA1825861454NAPRTc.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=)
8g.143575436G>TCA463512258NAPRTc.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=)
8g.143575437A>CCA372450774NAPRTc.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)
8g.143575437A>GCA372450773NAPRTc.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)
8g.143575437A>TCA372450772NAPRTc.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)
8g.143575438G>ACA372450777NAPRTc.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
8g.143575438G>CCA372450783NAPRTc.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
8g.143575438G=CA1825861455NAPRTc.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=)
8g.143575438G>TCA372450789NAPRTc.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)
8g.143575439C>ACA463512259NAPRTc.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=)
8g.143575439C>GCA463512260NAPRTc.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
8g.143575439C>TCA463512261NAPRTc.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=)
8g.143575440C>ACA372450793NAPRTc.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)
8g.143575440C=CA1825861456NAPRTc.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=)
8g.143575440C>GCA4912709NAPRTc.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
8g.143575440C>TCA4912708NAPRTc.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
8g.143575441G>ACA4912710NAPRTc.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
8g.143575441G>CCA372450805NAPRTc.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)
8g.143575441G=CA1825861457NAPRTc.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=)
8g.143575441G>TCA463512262NAPRTc.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
8g.143575442G>ACA463512263NAPRTc.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
8g.143575442G>CCA372450810NAPRTc.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)
8g.143575442G=CA1825861458NAPRTc.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=)
8g.143575442G>TCA372450812NAPRTc.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)
8g.143575443A>CCA372450819NAPRTc.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)
8g.143575443A>GCA372450822NAPRTc.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)
8g.143575443A>TCA372450826NAPRTc.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)
8g.143575444A=CA1825861459NAPRTc.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=)
8g.143575444A>CCA372450839NAPRTc.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)
8g.143575444A>GCA4912711NAPRTc.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
8g.143575444A>TCA372450829NAPRTc.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)
8g.143575445A=CA1825861460NAPRTc.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=)
8g.143575445A>CCA463512265NAPRTc.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=)
8g.143575445A>GCA463512266NAPRTc.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
8g.143575445A>TCA463512268NAPRTc.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=)
8g.143575446G>ACA4912713NAPRTc.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
8g.143575446G>CCA4912712NAPRTc.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
8g.143575446G=CA1825861461NAPRTc.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=)
8g.143575446G>TCA372450851NAPRTc.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)
8g.143575447C>ACA372450852NAPRTc.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)
8g.143575447C>GCA372450856NAPRTc.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)
8g.143575447C>TCA372450859NAPRTc.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
8g.143575448A=CA1825861462NAPRTc.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=)
8g.143575448A>CCA463512275NAPRTc.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
8g.143575448A>GCA463512277NAPRTc.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
8g.143575448A>TCA463512279NAPRTc.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=)
8g.143575449G>ACA372450863NAPRTc.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)
8g.143575449G>CCA372450869NAPRTc.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)
8g.143575449G>TCA372450875NAPRTc.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)
8g.143575450C>ACA187547807NAPRTc.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
8g.143575450C=CA1825861463NAPRTc.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=)
8g.143575450C>GCA372450882NAPRTc.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)
8g.143575450C>TCA4912714NAPRTc.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
8g.143575451C>ACA372450890NAPRTc.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)
8g.143575451C>GCA372450893NAPRTc.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)
8g.143575451C>TCA463512281NAPRTc.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
8g.143575452T>ACA372450894NAPRTc.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)
8g.143575452T>CCA372450896NAPRTc.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
8g.143575452T>GCA372450895NAPRTc.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)
8g.143575453T>ACA372450901NAPRTc.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)
8g.143575453T>CCA372450906NAPRTc.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
8g.143575453T>GCA372450902NAPRTc.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)
8g.143575454G>ACA463512292NAPRTc.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=)
8g.143575454G>CCA372450907NAPRTc.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)
8g.143575454G>TCA372450910NAPRTc.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)
8g.143575455C>ACA372450915NAPRTc.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)
8g.143575455C=CA1825861464NAPRTc.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=)
8g.143575455C>GCA372450923NAPRTc.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)
8g.143575455C>TCA372450928NAPRTc.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
8g.143575456T>ACA372450931NAPRTc.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)
8g.143575456T>CCA372450933NAPRTc.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
8g.143575456T>GCA372450935NAPRTc.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)
8g.143575457C>ACA463512307NAPRTc.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
8g.143575457C>GCA463512304NAPRTc.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=)
8g.143575457C>TCA463512306NAPRTc.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=)
8g.143575459dupCA2688943881NAPRTc.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
8g.143575457_143575465delinsCCCAGGCAACA1825861465NAPRTc.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=)
8g.143575458C>ACA372450945NAPRTc.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)
8g.143575458C>GCA372450952NAPRTc.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)
8g.143575458C>TCA372450957NAPRTc.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)
8g.143575459_143575466delCA4912715NAPRTc.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
8g.143575459C>ACA372450976NAPRTc.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)
8g.143575459C>GCA372450967NAPRTc.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)
8g.143575459C>TCA372450972NAPRTc.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)
8g.143575460A>CCA463512312NAPRTc.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=)
8g.143575460A>GCA463512313NAPRTc.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
8g.143575460A>TCA463512316NAPRTc.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=)
8g.143575461G>ACA372450984NAPRTc.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
8g.143575461G>CCA372450988NAPRTc.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)
8g.143575461G=CA1825861466NAPRTc.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=)
8g.143575461G>TCA372450991NAPRTc.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
8g.143575462G>ACA372451003NAPRTc.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
8g.143575462G>CCA372451010NAPRTc.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)
8g.143575462G=CA1825861467NAPRTc.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=)
8g.143575462G>TCA372451013NAPRTc.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)
8g.143575463C>ACA372451022NAPRTc.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)
8g.143575463C=CA1825861468NAPRTc.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=)
8g.143575463C>GCA372451037NAPRTc.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)
8g.143575463C>TCA4912716NAPRTc.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
8g.143575464A>CCA372451051NAPRTc.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)
8g.143575464A>GCA372451054NAPRTc.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)
8g.143575464A>TCA372451059NAPRTc.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)
8g.143575465A>CCA372451066NAPRTc.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)
8g.143575465A>GCA463512331NAPRTc.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=)
8g.143575465A>TCA372451063NAPRTc.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
8g.143575466C>ACA4912718NAPRTc.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
8g.143575466C=CA1825861469NAPRTc.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=)
8g.143575466C>GCA463512337NAPRTc.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=)
8g.143575466C>TCA4912717NAPRTc.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
8g.143575467G>ACA4912720NAPRTc.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
8g.143575467G>CCA372451082NAPRTc.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
8g.143575467G=CA1825861470NAPRTc.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=)
8g.143575467G>TCA4912719NAPRTc.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
8g.143575468T>ACA372451085NAPRTc.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)
8g.143575468T>CCA372451087NAPRTc.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)
8g.143575468T>GCA372451091NAPRTc.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)
8g.143575469C>ACA372451097NAPRTc.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)
8g.143575469C>GCA372451101NAPRTc.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)
8g.143575469C>TCA463512345NAPRTc.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=)
8g.143575470T>ACA372451106NAPRTc.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)
8g.143575470T>CCA372451108NAPRTc.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)
8g.143575470T>GCA372451109NAPRTc.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)
8g.143575471G>ACA372451122NAPRTc.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)
8g.143575471G>CCA372451117NAPRTc.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)
8g.143575471G>TCA372451113NAPRTc.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)
8g.143575472C>ACA372451126NAPRTc.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)
8g.143575472C>GCA372451128NAPRTc.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)
8g.143575472C>TCA463512361NAPRTc.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
8g.143575473T>ACA372451137NAPRTc.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)
8g.143575473T>CCA372451140NAPRTc.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
8g.143575473T>GCA372451142NAPRTc.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)
8g.143575474T>ACA372451145NAPRTc.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)
8g.143575474T>CCA372451147NAPRTc.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
8g.143575474T>GCA372451149NAPRTc.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)
8g.143575474T=CA1825861471NAPRTc.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=)
8g.143575475C>ACA372451153NAPRTc.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)
8g.143575475C>GCA372451156NAPRTc.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)
8g.143575475C>TCA463512376NAPRTc.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
8g.143575476T>ACA372451157NAPRTc.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)
8g.143575476T>CCA372451158NAPRTc.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
8g.143575476T>GCA372451159NAPRTc.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)
8g.143575477C>ACA372451163NAPRTc.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
8g.143575477C=CA1825861472NAPRTc.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=)
8g.143575477C>GCA372451167NAPRTc.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)
8g.143575477C>TCA187547822NAPRTc.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
8g.143575478G>ACA187547830NAPRTc.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
8g.143575478G>CCA4912721NAPRTc.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
8g.143575478G=CA1825861473NAPRTc.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=)
8g.143575478G>TCA463512393NAPRTc.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=)
8g.143575479G>ACA372451170NAPRTc.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
8g.143575479G>CCA372451173NAPRTc.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)
8g.143575479G>TCA372451175NAPRTc.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)
8g.143575480G>ACA372451189NAPRTc.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
8g.143575480G>CCA372451186NAPRTc.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)
8g.143575480G>TCA372451183NAPRTc.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)
8g.143575481G>ACA4912722NAPRTc.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
8g.143575481G>CCA372451195NAPRTc.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)
8g.143575481G=CA1825861474NAPRTc.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=)
8g.143575481G>TCA372451196NAPRTc.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)
8g.143575482T>ACA372451200NAPRTc.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)
8g.143575482T>CCA372451202NAPRTc.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)
8g.143575482T>GCA372451204NAPRTc.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)
8g.143575483C>ACA372451216NAPRTc.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)
8g.143575483C=CA1825861475NAPRTc.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=)
8g.143575483C>GCA372451208NAPRTc.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)
8g.143575483C>TCA4912723NAPRTc.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
8g.143575484C>ACA372451218NAPRTc.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
8g.143575484C>GCA372451221NAPRTc.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)
8g.143575484C>TCA463375938NAPRTc.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=)
8g.143575485T>ACA372451225NAPRTc.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)
8g.143575485T>CCA372451229NAPRTc.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
8g.143575485T>GCA372451230NAPRTc.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)
8g.143575486C>ACA372451234NAPRTc.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
8g.143575486C=CA1825861476NAPRTc.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=)
8g.143575486C>GCA372451236NAPRTc.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)
8g.143575486C>TCA4912724NAPRTc.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
8g.143575487G>ACA4912725NAPRTc.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
8g.143575487G>CCA463375939NAPRTc.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
8g.143575487G=CA1825861477NAPRTc.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=)
8g.143575487G>TCA463375940NAPRTc.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=)
8g.143575488G>ACA4912726NAPRTc.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
8g.143575488G>CCA372451249NAPRTc.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)
8g.143575488G=CA1825861478NAPRTc.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=)
8g.143575488G>TCA372451250NAPRTc.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)
8g.143575489T>ACA372451254NAPRTc.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
8g.143575489T>CCA372451261NAPRTc.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)
8g.143575489T>GCA372451258NAPRTc.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)
8g.143575490C>ACA463375941NAPRTc.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
8g.143575490C>GCA463375942NAPRTc.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=)
8g.143575490C>TCA463375943NAPRTc.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=)
8g.143575491A>CCA372451262NAPRTc.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)
8g.143575491A>GCA372451263NAPRTc.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)
8g.143575491A>TCA372451264NAPRTc.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)
8g.143575492G>ACA463375944NAPRTc.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=)
8g.143575492G>CCA372451265NAPRTc.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)
8g.143575492G>TCA372451267NAPRTc.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)
8g.143575493C>ACA372451270NAPRTc.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)
8g.143575493C>GCA372451273NAPRTc.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)
8g.143575493C>TCA463375945NAPRTc.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=)
8g.143575494T>ACA372451278NAPRTc.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)
8g.143575494T>CCA372451291NAPRTc.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)
8g.143575494T>GCA372451294NAPRTc.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)
8g.143575495T>ACA372451299NAPRTc.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)
8g.143575495T>CCA372451302NAPRTc.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
8g.143575495T>GCA372451305NAPRTc.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)
8g.143575496C>ACA372451309NAPRTc.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)
8g.143575496C=CA1825861479NAPRTc.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=)
8g.143575496C>GCA372451315NAPRTc.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)
8g.143575496C>TCA372451312NAPRTc.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
8g.143575497A>CCA372451320NAPRTc.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)
8g.143575497A>GCA372451323NAPRTc.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)
8g.143575497A>TCA372451329NAPRTc.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)
8g.143575498T>ACA372451332NAPRTc.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)
8g.143575498T>CCA372451335NAPRTc.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)
8g.143575498T>GCA372451337NAPRTc.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)
8g.143575499T>ACA463375946NAPRTc.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=)
8g.143575499T>CCA463375947NAPRTc.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=)
8g.143575499T>GCA463375948NAPRTc.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=)
8g.143575500C>ACA372451341NAPRTc.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
8g.143575500C=CA1825861480NAPRTc.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=)
8g.143575500C>GCA372451347NAPRTc.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
8g.143575500C>TCA4912727NAPRTc.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
8g.143575501G>ACA4912728NAPRTc.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
8g.143575501G>CCA372451358NAPRTc.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)
8g.143575501G=CA1825861481NAPRTc.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=)
8g.143575501G>TCA463375949NAPRTc.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=)
8g.143575502T>ACA463375950NAPRTc.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=)
8g.143575502T>CCA4912729NAPRTc.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
8g.143575502T>GCA463375951NAPRTc.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=)
8g.143575502T=CA1825861482NAPRTc.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=)
8g.143575503G>ACA372451368NAPRTc.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
8g.143575503G>CCA372451365NAPRTc.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)
8g.143575503G>TCA372451371NAPRTc.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)
8g.143575504delCA2688943991NAPRTc.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
8g.143575504G>ACA372451374NAPRTc.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
8g.143575504G>CCA372451380NAPRTc.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)
8g.143575504G>TCA372451377NAPRTc.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)
8g.143575505C>ACA372451382NAPRTc.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)
8g.143575505C>GCA372451385NAPRTc.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)
8g.143575505C>TCA463375952NAPRTc.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=)
8g.143575509_143575601delCA4912730NAPRTc.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
8g.143575506T>ACA372451390NAPRTc.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)
8g.143575506T>CCA372451392NAPRTc.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
8g.143575506T>GCA372451395NAPRTc.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)
8g.143575506T=CA1825861483NAPRTc.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=)
8g.143575507G>ACA372451399NAPRTc.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
8g.143575507G>CCA372451402NAPRTc.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)
8g.143575507G>TCA372451406NAPRTc.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)

Number of alleles fetched