Chr Mutation (hg38) CAid Gene Transcript Linkouts
18g.31524582_31524585delinsAGTGCA2293857133DSG2n.656_659delinsAGTG
c.656_659delinsAGTG
c.825_828delinsAGTG (p.Lys275=)
c.291_294delinsAGTG (p.Lys97=)
18g.31524585_31524587delCA050140DSG2n.659_659+2del
c.659_659+2del
c.828_828+2del
c.294_294+2del
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v4
18g.31524585G>ACA503599186DSG2n.659G>A
c.659G>A
c.828G>A (p.Val276=)
c.294G>A (p.Val98=)
18g.31524585G>CCA503599187DSG2n.659G>C
c.659G>C
c.828G>C (p.Val276=)
c.294G>C (p.Val98=)
18g.31524585G>TCA503599188DSG2n.659G>T
c.659G>T
c.828G>T (p.Val276=)
c.294G>T (p.Val98=)
18g.31524586G>ACA402135324DSG2n.659+1G>A
c.659+1G>A
c.828+1G>A (n.828+1G>A)
c.294+1G>A (n.294+1G>A)
18g.31524586G>CCA402135326DSG2n.659+1G>C
c.659+1G>C
c.828+1G>C (n.828+1G>C)
c.294+1G>C (n.294+1G>C)
18g.31524586G>TCA402135328DSG2n.659+1G>T
c.659+1G>T
c.828+1G>T (n.828+1G>T)
c.294+1G>T (n.294+1G>T)
18g.31524587T>ACA402135329DSG2n.659+2T>A
c.659+2T>A
c.828+2T>A (n.828+2T>A)
c.294+2T>A (n.294+2T>A)
18g.31524587T>CCA402135331DSG2n.659+2T>C
c.659+2T>C
c.828+2T>C (n.828+2T>C)
c.294+2T>C (n.294+2T>C)
18g.31524587T>GCA402135333DSG2n.659+2T>G
c.659+2T>G
c.828+2T>G (n.828+2T>G)
c.294+2T>G (n.294+2T>G)
18g.31524590C=CA2293857140DSG2n.659+5C=
c.659+5C=
c.828+5C= (n.828+5C=)
c.294+5C= (n.294+5C=)
18g.31524590C>TCA050171DSG2n.659+5C>T
c.659+5C>T
c.828+5C>T (n.828+5C>T)
c.294+5C>T (n.294+5C>T)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.31524590_31524593delinsCTATCA2293857142DSG2n.659+5_659+8delinsCTAT
c.659+5_659+8delinsCTAT
c.828+5_828+8delinsCTAT (n.828+5_828+8delinsCTAT)
c.294+5_294+8delinsCTAT (n.294+5_294+8delinsCTAT)
18g.31524595_31524597delCA629148137DSG2n.659+10_659+12del
c.659+10_659+12del
c.828+10_828+12del (n.828+10_828+12del)
c.294+10_294+12del (n.294+10_294+12del)
 dbSNP gnomAD v2 gnomAD v4
18g.31524592A=CA2293857146DSG2n.659+7A=
c.659+7A=
c.828+7A= (n.828+7A=)
c.294+7A= (n.294+7A=)
18g.31524592A>GCA629148138DSG2n.659+7A>G
c.659+7A>G
c.828+7A>G (n.828+7A>G)
c.294+7A>G (n.294+7A>G)
 ClinVar dbSNP gnomAD v2 gnomAD v4
18g.31524593T>CCA2641406211DSG2n.659+8T>C
c.659+8T>C
c.828+8T>C (n.828+8T>C)
c.294+8T>C (n.294+8T>C)
 gnomAD v4
18g.31524593_31524594insACCCA2576480507DSG2n.659+8_659+9insACC
c.659+8_659+9insACC
c.828+8_828+9insACC (n.828+8_828+9insACC)
c.294+8_294+9insACC (n.294+8_294+9insACC)
18g.31524595A=CA2293857152DSG2n.659+10A=
c.659+10A=
c.828+10A= (n.828+10A=)
c.294+10A= (n.294+10A=)
18g.31524595A>CCA10641361DSG2n.659+10A>C
c.659+10A>C
c.828+10A>C (n.828+10A>C)
c.294+10A>C (n.294+10A>C)
 ClinVar dbSNP
18g.31524595A>GCA2576480508DSG2n.659+10A>G
c.659+10A>G
c.828+10A>G (n.828+10A>G)
c.294+10A>G (n.294+10A>G)
18g.31524595_31524601delinsATTCTTCCA2293857150DSG2n.659+10_659+16delinsATTCTTC
c.659+10_659+16delinsATTCTTC
c.828+10_828+16delinsATTCTTC (n.828+10_828+16delinsATTCTTC)
c.294+10_294+16delinsATTCTTC (n.294+10_294+16delinsATTCTTC)
18g.31524596T>CCA050148DSG2n.659+11T>C
c.659+11T>C
c.828+11T>C (n.828+11T>C)
c.294+11T>C (n.294+11T>C)
 dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.31524596T>GCA2641406212DSG2n.659+11T>G
c.659+11T>G
c.828+11T>G (n.828+11T>G)
c.294+11T>G (n.294+11T>G)
 gnomAD v4
18g.31524596T=CA2293857154DSG2n.659+11T=
c.659+11T=
c.828+11T= (n.828+11T=)
c.294+11T= (n.294+11T=)
18g.31524597dupCA2576480509DSG2n.659+12dup
c.659+12dup
c.828+12dup (n.828+12dup)
c.294+12dup (n.294+12dup)
18g.31524597_31524602delCA778437048DSG2n.659+12_659+17del
c.659+12_659+17del
c.828+12_828+17del (n.828+12_828+17del)
c.294+12_294+17del (n.294+12_294+17del)
 dbSNP gnomAD v3 gnomAD v4
18g.31524597T>CCA2641406213DSG2n.659+12T>C
c.659+12T>C
c.828+12T>C (n.828+12T>C)
c.294+12T>C (n.294+12T>C)
 gnomAD v4
18g.31524598C>ACA297731970DSG2n.659+13C>A
c.659+13C>A
c.828+13C>A (n.828+13C>A)
c.294+13C>A (n.294+13C>A)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
18g.31524598C=CA2293857159DSG2n.659+13C=
c.659+13C=
c.828+13C= (n.828+13C=)
c.294+13C= (n.294+13C=)
18g.31524598C>TCA16607923DSG2n.659+13C>T
c.659+13C>T
c.828+13C>T (n.828+13C>T)
c.294+13C>T (n.294+13C>T)
 ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4
18g.31524599T>ACA2293857163DSG2n.659+14T>A
c.659+14T>A
c.828+14T>A (n.828+14T>A)
c.294+14T>A (n.294+14T>A)
 dbSNP
18g.31524599T>CCA2293857164DSG2n.659+14T>C
c.659+14T>C
c.828+14T>C (n.828+14T>C)
c.294+14T>C (n.294+14T>C)
 ClinVar dbSNP
18g.31524599T=CA2293857162DSG2n.659+14T=
c.659+14T=
c.828+14T= (n.828+14T=)
c.294+14T= (n.294+14T=)
18g.31524601C>ACA050154DSG2n.659+16C>A
c.659+16C>A
c.828+16C>A (n.828+16C>A)
c.294+16C>A (n.294+16C>A)
 ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
18g.31524601C=CA2293857167DSG2n.659+16C=
c.659+16C=
c.828+16C= (n.828+16C=)
c.294+16C= (n.294+16C=)
18g.31524601C>GCA2576480510DSG2n.659+16C>G
c.659+16C>G
c.828+16C>G (n.828+16C>G)
c.294+16C>G (n.294+16C>G)
 ClinVar
18g.31524601C>TCA2581341668DSG2n.659+16C>T
c.659+16C>T
c.828+16C>T (n.828+16C>T)
c.294+16C>T (n.294+16C>T)
 gnomAD v4
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

Number of alleles fetched