Chr Mutation (hg38) CAid Gene Transcript Linkouts
3g.169763862_169764683delinsATCCTAAGGAATTGAAGGTATGGATTTGGGACGGAATTACCTTGTCGTGATAAGTGGGCAGAATGGCCTGTTTGTTTCTTTCAACCTAGTGGGCCATTAGCTTATTTTCTTAAAGGAAATCAGAGCCAATTCTTGTGGGAGACTGCCGGCTGGGAGGGTTGGGGGTGGGGGGTGTGGAATAAATTTCTTTTCCGTCTTTCATTATGCCTAGTGTTCCGTTATTGGAACGCTAAGCTTGTGGGGGTTATATCCTACTGCTCAAGGTCATCGCCAAGGTCTAATTTTTCAAAAAAGAAACTTCTAACCTCTGGCATAAACCGATGACCATTAAAGGAACACAATTTCCAATGTTCATTTAGATCTTCTAATTAAATATTCATTAAATGTTAAATGATCTCTCAAAAAAAAATGACTGTTCTCCCACACCCCGTTGAGGGGACTGGTCGAGATCTACCTTGGGAGAAGCAAAAACCTCAACAAAATCTGCAGAGCAGGAACTAAGTTGTAATACAACCATAAAAGGCAACAAAAAGCGGAAGACGGGAGAACCCACGCAGGAACGGCTCCAGGCAACCCCGGCTCACTGCCCATTCATTTTGGCCGACTTTGGAGGTGCCTTCACGTCTCCTGCCAATTTGCAGCACACTGGCCCAGTCAGTCAGGTTTGGGGGTTCACAAGCCCCCATTGCCGGCGAGGGGTGACGGATGCGCACGATCGGCGTTCCCCCCACCAACAGGAAAGCGAACTGCATGTGTGAGCCGAGTCCTGGGTGCACGTCCCACAGCTCAGGGAATCGCGCCGCGCGCGGGGACTCGCTCCGTCA1419635826
3g.169763867_169764687delCA340670 ClinVar dbSNP
3g.169764645_169764683delinsAGCTCAGGGAATCGCGCCGCGCGCGGGGACTCGCTCCGTCA1419636256TERCn.378_416delinsACGGAGCGAGTCCCCGCGCGCGGCGCGATTCCCTGAGCT
3g.169764646G>ACA2696785TERCn.415C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.169764646G>CCA436714795TERCn.415C>G
dbSNP
3g.169764646G=CA1419636258TERCn.415C=
3g.169764646G>TCA436714796TERCn.415C>A
3g.169764646_169764683delCA87623658TERCn.378_415del
dbSNP
3g.169764647C>ACA436714797TERCn.414G>T
dbSNP gnomAD v4
3g.169764647C>GCA436714798TERCn.414G>C
3g.169764647C>TCA436714799TERCn.414G>A
gnomAD v4
3g.169764648T>ACA436714800TERCn.413A>T
dbSNP
3g.169764648T>CCA436714801TERCn.413A>G
3g.169764648T>GCA436714802TERCn.413A>C
3g.169764649C>ACA436714803TERCn.412G>T
gnomAD v4
3g.169764649C>GCA436714805TERCn.412G>C
3g.169764649C>TCA436714804TERCn.412G>A
dbSNP COSMIC
3g.169764650A=CA1419636259TERCn.411T=
3g.169764650A>CCA436714806TERCn.411T>G
3g.169764650A>GCA436714807TERCn.411T>C
3g.169764650A>TCA436714808TERCn.411T>A
dbSNP
3g.169764651G>ACA436714809TERCn.410C>T
dbSNP gnomAD v2
3g.169764651G>CCA343767TERCn.410C>G
ClinVar dbSNP
3g.169764651G=CA1419636260TERCn.410C=
3g.169764651G>TCA436714810TERCn.410C>A
dbSNP gnomAD v4
3g.169764652G>ACA2696786TERCn.409C>T
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
3g.169764652G>CCA436714811TERCn.409C>G
3g.169764652G=CA1419636261TERCn.409C=
3g.169764652G>TCA436714812TERCn.409C>A
3g.169764653G>ACA436714813TERCn.408C>T
ClinVar dbSNP gnomAD v4 COSMIC
3g.169764653G>CCA340671TERCn.408C>G
ClinVar dbSNP
3g.169764653G=CA1419636262TERCn.408C=
3g.169764653G>TCA87623705TERCn.408C>A
dbSNP
3g.169764653_169764654delinsGACA1419636263TERCn.407_408delinsTC
3g.169764653_169764654delinsTTCA658822145TERCn.407_408delinsAA
ClinVar dbSNP
3g.169764654A>CCA436714816TERCn.407T>G
3g.169764654A>GCA436714815TERCn.407T>C
dbSNP
3g.169764654A>TCA436714814TERCn.407T>A
3g.169764655A>CCA436714817TERCn.406T>G
3g.169764655A>GCA436714818TERCn.406T>C
3g.169764655A>TCA436714819TERCn.406T>A
3g.169764656T>ACA436714820TERCn.405A>T
3g.169764656T>CCA87623713TERCn.405A>G
ClinVar dbSNP gnomAD v3 gnomAD v4
3g.169764656T>GCA436714821TERCn.405A>C
3g.169764656T=CA1419636264TERCn.405A=
3g.169764657C>ACA436714822TERCn.404G>T
ClinVar dbSNP gnomAD v4
3g.169764657C>GCA436714823TERCn.404G>C
3g.169764657C>TCA436714824TERCn.404G>A
gnomAD v4
3g.169764658G>ACA2696787TERCn.403C>T
dbSNP ExAC gnomAD v2 gnomAD v4
3g.169764658G>CCA436714825TERCn.403C>G

Number of alleles fetched