Chr Mutation (hg38) CAid Gene Transcript Linkouts
18g.31524601_31524604delinsCTAACA2293857170DSG2n.659+16_659+19delinsCTAA
c.659+16_659+19delinsCTAA
c.828+16_828+19delinsCTAA (n.828+16_828+19delinsCTAA)
c.294+16_294+19delinsCTAA (n.294+16_294+19delinsCTAA)
18g.31524605_31524607delCA629148139DSG2n.659+20_659+22del
c.659+20_659+22del
c.828+20_828+22del (n.828+20_828+22del)
c.294+20_294+22del (n.294+20_294+22del)
 ClinVar dbSNP gnomAD v2 gnomAD v4
18g.31524603A>GCA2812000634DSG2n.659+18A>G
c.659+18A>G
c.828+18A>G (n.828+18A>G)
c.294+18A>G (n.294+18A>G)
18g.31524604A>CCA2641406215DSG2n.659+19A>C
c.659+19A>C
c.828+19A>C (n.828+19A>C)
c.294+19A>C (n.294+19A>C)
 gnomAD v4
18g.31524605_31524606delCA2641406214DSG2n.659+20_659+21del
c.659+20_659+21del
c.828+20_828+21del (n.828+20_828+21del)
c.294+20_294+21del (n.294+20_294+21del)
 ClinVar gnomAD v4
18g.31524607A>CCA2576480511DSG2n.659+22A>C
c.659+22A>C
c.828+22A>C (n.828+22A>C)
c.294+22A>C (n.294+22A>C)
18g.31524609T>CCA2293857174DSG2n.659+24T>C
c.659+24T>C
c.828+24T>C (n.828+24T>C)
c.294+24T>C (n.294+24T>C)
 dbSNP gnomAD v4
18g.31524609T=CA2293857175DSG2n.659+24T=
c.659+24T=
c.828+24T= (n.828+24T=)
c.294+24T= (n.294+24T=)
18g.31524610G>CCA2641406216DSG2n.659+25G>C
c.659+25G>C
c.828+25G>C (n.828+25G>C)
c.294+25G>C (n.294+25G>C)
 gnomAD v4
18g.31524610_31524614delinsGTACCCA2293857177DSG2n.659+25_659+29delinsGTACC
c.659+25_659+29delinsGTACC
c.828+25_828+29delinsGTACC (n.828+25_828+29delinsGTACC)
c.294+25_294+29delinsGTACC (n.294+25_294+29delinsGTACC)
18g.31524611T>GCA629148140DSG2n.659+26T>G
c.659+26T>G
c.828+26T>G (n.828+26T>G)
c.294+26T>G (n.294+26T>G)
 dbSNP gnomAD v2 gnomAD v4
18g.31524611T=CA2293857180DSG2n.659+26T=
c.659+26T=
c.828+26T= (n.828+26T=)
c.294+26T= (n.294+26T=)
18g.31524613_31524616delCA2293857181DSG2n.659+28_659+31del
c.659+28_659+31del
c.828+28_828+31del (n.828+28_828+31del)
c.294+28_294+31del (n.294+28_294+31del)
 dbSNP
18g.31524614C>TCA629148141DSG2n.659+29C>T
c.659+29C>T
c.828+29C>T (n.828+29C>T)
c.294+29C>T (n.294+29C>T)
 gnomAD v2
18g.31524614_31524618delinsCTATTCA2293857183DSG2n.659+29_659+33delinsCTATT
c.659+29_659+33delinsCTATT
c.828+29_828+33delinsCTATT (n.828+29_828+33delinsCTATT)
c.294+29_294+33delinsCTATT (n.294+29_294+33delinsCTATT)
18g.31524622_31524625delCA629148142DSG2n.659+37_659+40del
c.659+37_659+40del
c.828+37_828+40del (n.828+37_828+40del)
c.294+37_294+40del (n.294+37_294+40del)
 dbSNP gnomAD v2 gnomAD v4
18g.31524616A=CA2293857185DSG2n.659+31A=
c.659+31A=
c.828+31A= (n.828+31A=)
c.294+31A= (n.294+31A=)
18g.31524616A>GCA629148143DSG2n.659+31A>G
c.659+31A>G
c.828+31A>G (n.828+31A>G)
c.294+31A>G (n.294+31A>G)
 dbSNP gnomAD v2 gnomAD v4
18g.31524617T>CCA629148144DSG2n.659+32T>C
c.659+32T>C
c.828+32T>C (n.828+32T>C)
c.294+32T>C (n.294+32T>C)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
18g.31524617T=CA2293857187DSG2n.659+32T=
c.659+32T=
c.828+32T= (n.828+32T=)
c.294+32T= (n.294+32T=)
18g.31524623T>CCA2641406217DSG2n.659+38T>C
c.659+38T>C
c.828+38T>C (n.828+38T>C)
c.294+38T>C (n.294+38T>C)
 gnomAD v4
18g.31524626A=CA2293857188DSG2n.659+41A=
c.659+41A=
c.828+41A= (n.828+41A=)
c.294+41A= (n.294+41A=)
18g.31524626A>GCA2293857189DSG2n.659+41A>G
c.659+41A>G
c.828+41A>G (n.828+41A>G)
c.294+41A>G (n.294+41A>G)
 dbSNP gnomAD v4
18g.31524628T>CCA2576480512DSG2n.659+43T>C
c.659+43T>C
c.828+43T>C (n.828+43T>C)
c.294+43T>C (n.294+43T>C)
18g.31524630C>TCA2734853171DSG2n.659+45C>T
c.659+45C>T
c.828+45C>T (n.828+45C>T)
c.294+45C>T (n.294+45C>T)
 dbSNP
18g.31524632G>CCA2741576437DSG2n.659+47G>C
c.659+47G>C
c.828+47G>C (n.828+47G>C)
c.294+47G>C (n.294+47G>C)
18g.31524632G=CA2293857192DSG2n.659+47G=
c.659+47G=
c.828+47G= (n.828+47G=)
c.294+47G= (n.294+47G=)
18g.31524632G>TCA629148145DSG2n.659+47G>T
c.659+47G>T
c.828+47G>T (n.828+47G>T)
c.294+47G>T (n.294+47G>T)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
18g.31524633T>CCA050165DSG2n.659+48T>C
c.659+48T>C
c.828+48T>C (n.828+48T>C)
c.294+48T>C (n.294+48T>C)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.31524633T=CA2293857194DSG2n.659+48T=
c.659+48T=
c.828+48T= (n.828+48T=)
c.294+48T= (n.294+48T=)
18g.31524634C>ACA2641406218DSG2n.659+49C>A
c.659+49C>A
c.828+49C>A (n.828+49C>A)
c.294+49C>A (n.294+49C>A)
 gnomAD v4
18g.31524635C>ACA2641406219DSG2n.659+50C>A
c.659+50C>A
c.828+50C>A (n.828+50C>A)
c.294+50C>A (n.294+50C>A)
 gnomAD v4
18g.31524636T>GCA2641406220DSG2n.659+51T>G
c.659+51T>G
c.828+51T>G (n.828+51T>G)
c.294+51T>G (n.294+51T>G)
 gnomAD v4
18g.31524639T>GCA2641406221DSG2n.659+54T>G
c.659+54T>G
c.828+54T>G (n.828+54T>G)
c.294+54T>G (n.294+54T>G)
 gnomAD v4
18g.31524645dupCA2641406222DSG2n.660-58dup
c.660-58dup
c.829-58dup (n.829-58dup)
c.295-58dup (n.295-58dup)
 gnomAD v4
18g.31524645_31524646delinsATCA2293857197DSG2n.660-58_660-57delinsAT
c.660-58_660-57delinsAT
c.829-58_829-57delinsAT (n.829-58_829-57delinsAT)
c.295-58_295-57delinsAT (n.295-58_295-57delinsAT)
18g.31524646delCA778437062DSG2n.660-57del
c.660-57del
c.829-57del (n.829-57del)
c.295-57del (n.295-57del)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
18g.31524646T>ACA297732002DSG2n.660-57T>A
c.660-57T>A
c.829-57T>A (n.829-57T>A)
c.295-57T>A (n.295-57T>A)
 dbSNP
18g.31524646T=CA2293857204DSG2n.660-57T=
c.660-57T=
c.829-57T= (n.829-57T=)
c.295-57T= (n.295-57T=)
18g.31524647A>GCA2641406223DSG2n.660-56A>G
c.660-56A>G
c.829-56A>G (n.829-56A>G)
c.295-56A>G (n.295-56A>G)
 gnomAD v4
18g.31524648T>CCA2293857209DSG2n.660-55T>C
c.660-55T>C
c.829-55T>C (n.829-55T>C)
c.295-55T>C (n.295-55T>C)
 dbSNP
18g.31524648T=CA2293857208DSG2n.660-55T=
c.660-55T=
c.829-55T= (n.829-55T=)
c.295-55T= (n.295-55T=)
18g.31524649A>GCA2641406224DSG2n.660-54A>G
c.660-54A>G
c.829-54A>G (n.829-54A>G)
c.295-54A>G (n.295-54A>G)
 gnomAD v4
18g.31524651C>ACA297732003DSG2n.660-52C>A
c.660-52C>A
c.829-52C>A (n.829-52C>A)
c.295-52C>A (n.295-52C>A)
 dbSNP gnomAD v3 gnomAD v4
18g.31524651C=CA2293857211DSG2n.660-52C=
c.660-52C=
c.829-52C= (n.829-52C=)
c.295-52C= (n.295-52C=)
18g.31524651C>TCA2293857212DSG2n.660-52C>T
c.660-52C>T
c.829-52C>T (n.829-52C>T)
c.295-52C>T (n.295-52C>T)
 dbSNP
18g.31524652A=CA2293857214DSG2n.660-51A=
c.660-51A=
c.829-51A= (n.829-51A=)
c.295-51A= (n.295-51A=)
18g.31524652A>TCA629148146DSG2n.660-51A>T
c.660-51A>T
c.829-51A>T (n.829-51A>T)
c.295-51A>T (n.295-51A>T)
 dbSNP gnomAD v2 gnomAD v3 gnomAD v4
18g.31524653C>ACA2641406225DSG2n.660-50C>A
c.660-50C>A
c.829-50C>A (n.829-50C>A)
c.295-50C>A (n.295-50C>A)
 gnomAD v4
18g.31524653C=CA2293857220DSG2n.660-50C=
c.660-50C=
c.829-50C= (n.829-50C=)
c.295-50C= (n.295-50C=)

Number of alleles fetched