Chr Mutation (hg38) CAid Gene Transcript Linkouts
8g.18400285C>ACA370635549NAT2c.282C>A (p.Tyr94Ter)
c.-57-52C>A (p.=)
8g.18400285C>GCA370635550NAT2c.282C>G (p.Tyr94Ter)
c.-57-52C>G (p.=)
8g.18400285C>TCA4651588NAT2c.282C>T (p.Tyr94=)
c.-57-52C>T (p.=)
ClinVar dbSNP ExAC gnomAD
8g.18400286A>CCA370635551NAT2c.283A>C (p.Ile95Leu)
c.-57-51A>C (p.=)
8g.18400286A>GCA370635552NAT2c.283A>G (p.Ile95Val)
c.-57-51A>G (p.=)
8g.18400286A>TCA370635553NAT2c.283A>T (p.Ile95Phe)
c.-57-51A>T (p.=)
8g.18400287T>ACA370635554NAT2c.284T>A (p.Ile95Asn)
c.-57-50T>A (p.=)
8g.18400287T>CCA370635555NAT2c.284T>C (p.Ile95Thr)
c.-57-50T>C (p.=)
gnomAD
8g.18400287T>GCA370635556NAT2c.284T>G (p.Ile95Ser)
c.-57-50T>G (p.=)
8g.18400288C>ACA459881100NAT2c.285C>A (p.Ile95=)
c.-57-49C>A (p.=)
8g.18400288C>GCA173519910NAT2c.285C>G (p.Ile95Met)
c.-57-49C>G (p.=)
dbSNP gnomAD
8g.18400288C>TCA459881101NAT2c.285C>T (p.Ile95=)
c.-57-49C>T (p.=)
COSMIC
8g.18400288_18400289delinsTTCA645546244NAT2c.285_286delinsTT (p.Pro96Ser)
c.-57-49_-57-48delinsTT (p.=)
COSMIC
8g.18400289C>ACA370635559NAT2c.286C>A (p.Pro96Thr)
c.-57-48C>A (p.=)
8g.18400289C>GCA370635558NAT2c.286C>G (p.Pro96Ala)
c.-57-48C>G (p.=)
8g.18400289C>TCA370635557NAT2c.286C>T (p.Pro96Ser)
c.-57-48C>T (p.=)
8g.18400290C>ACA370635560NAT2c.287C>A (p.Pro96His)
c.-57-47C>A (p.=)
gnomAD
8g.18400290C>GCA370635561NAT2c.287C>G (p.Pro96Arg)
c.-57-47C>G (p.=)
8g.18400290C>TCA4651589NAT2c.287C>T (p.Pro96Leu)
c.-57-47C>T (p.=)
dbSNP ExAC gnomAD COSMIC
8g.18400291T>ACA459881102NAT2c.288T>A (p.Pro96=)
c.-57-46T>A (p.=)
8g.18400291T>CCA459881103NAT2c.288T>C (p.Pro96=)
c.-57-46T>C (p.=)
8g.18400291T>GCA459881104NAT2c.288T>G (p.Pro96=)
c.-57-46T>G (p.=)
8g.18400292C>ACA370635562NAT2c.289C>A (p.Pro97Thr)
c.-57-45C>A (p.=)
8g.18400292C>GCA370635563NAT2c.289C>G (p.Pro97Ala)
c.-57-45C>G (p.=)
gnomAD
8g.18400292C>TCA370635564NAT2c.289C>T (p.Pro97Ser)
c.-57-45C>T (p.=)
8g.18400293C>ACA370635565NAT2c.290C>A (p.Pro97Gln)
c.-57-44C>A (p.=)
8g.18400293C>GCA370635566NAT2c.290C>G (p.Pro97Arg)
c.-57-44C>G (p.=)
8g.18400293C>TCA370635567NAT2c.290C>T (p.Pro97Leu)
c.-57-44C>T (p.=)
8g.18400294A>CCA459881105NAT2c.291A>C (p.Pro97=)
c.-57-43A>C (p.=)
8g.18400294A>GCA173519911NAT2c.291A>G (p.Pro97=)
c.-57-43A>G (p.=)
dbSNP
8g.18400294A>TCA459881106NAT2c.291A>T (p.Pro97=)
c.-57-43A>T (p.=)
8g.18400295G>ACA173519912NAT2c.292G>A (p.Val98Ile)
c.-57-42G>A (p.=)
dbSNP gnomAD
8g.18400295G>CCA370635568NAT2c.292G>C (p.Val98Leu)
c.-57-42G>C (p.=)
8g.18400295G>TCA370635569NAT2c.292G>T (p.Val98Phe)
c.-57-42G>T (p.=)
8g.18400296T>ACA370635571NAT2c.293T>A (p.Val98Asp)
c.-57-41T>A (p.=)
8g.18400296T>CCA370635572NAT2c.293T>C (p.Val98Ala)
c.-57-41T>C (p.=)
8g.18400296T>GCA370635570NAT2c.293T>G (p.Val98Gly)
c.-57-41T>G (p.=)
8g.18400297T>ACA459881107NAT2c.294T>A (p.Val98=)
c.-57-40T>A (p.=)
8g.18400297T>CCA459881108NAT2c.294T>C (p.Val98=)
c.-57-40T>C (p.=)
8g.18400297T>GCA459881109NAT2c.294T>G (p.Val98=)
c.-57-40T>G (p.=)
8g.18400298A>CCA370635573NAT2c.295A>C (p.Asn99His)
c.-57-39A>C (p.=)
8g.18400298A>GCA4651590NAT2c.295A>G (p.Asn99Asp)
c.-57-39A>G (p.=)
dbSNP ExAC gnomAD
8g.18400298A>TCA370635574NAT2c.295A>T (p.Asn99Tyr)
c.-57-39A>T (p.=)
8g.18400299A>CCA370635575NAT2c.296A>C (p.Asn99Thr)
c.-57-38A>C (p.=)
8g.18400299A>GCA370635576NAT2c.296A>G (p.Asn99Ser)
c.-57-38A>G (p.=)
8g.18400299A>TCA370635577NAT2c.296A>T (p.Asn99Ile)
c.-57-38A>T (p.=)
COSMIC
8g.18400300C>ACA370635578NAT2c.297C>A (p.Asn99Lys)
c.-57-37C>A (p.=)
8g.18400300C>GCA370635579NAT2c.297C>G (p.Asn99Lys)
c.-57-37C>G (p.=)
8g.18400300C>TCA459881110NAT2c.297C>T (p.Asn99=)
c.-57-37C>T (p.=)
8g.18400301A>CCA370635580NAT2c.298A>C (p.Lys100Gln)
c.-57-36A>C (p.=)

Number of alleles fetched