Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.7128877T>ACA403671716INSRc.2920A>T (p.Ser974Cys)
c.2884A>T (p.Ser962Cys)
c.2995A>T (p.Ser999Cys)
c.2959A>T (p.Ser987Cys)
c.2917A>T (p.Ser973Cys)
c.2881A>T (p.Ser961Cys)
19g.7128877T>CCA403671715INSRc.2920A>G (p.Ser974Gly)
c.2884A>G (p.Ser962Gly)
c.2995A>G (p.Ser999Gly)
c.2959A>G (p.Ser987Gly)
c.2917A>G (p.Ser973Gly)
c.2881A>G (p.Ser961Gly)
19g.7128877T>GCA403671714INSRc.2920A>C (p.Ser974Arg)
c.2884A>C (p.Ser962Arg)
c.2995A>C (p.Ser999Arg)
c.2959A>C (p.Ser987Arg)
c.2917A>C (p.Ser973Arg)
c.2881A>C (p.Ser961Arg)
19g.7128878T>ACA505217375INSRc.2919A>T (p.Gly973=)
c.2883A>T (p.Gly961=)
c.2994A>T (p.Gly998=)
c.2958A>T (p.Gly986=)
c.2916A>T (p.Gly972=)
c.2880A>T (p.Gly960=)
19g.7128878T>CCA505217374INSRc.2919A>G (p.Gly973=)
c.2883A>G (p.Gly961=)
c.2994A>G (p.Gly998=)
c.2958A>G (p.Gly986=)
c.2916A>G (p.Gly972=)
c.2880A>G (p.Gly960=)
19g.7128878T>GCA505217376INSRc.2919A>C (p.Gly973=)
c.2883A>C (p.Gly961=)
c.2994A>C (p.Gly998=)
c.2958A>C (p.Gly986=)
c.2916A>C (p.Gly972=)
c.2880A>C (p.Gly960=)
19g.7128879C>ACA403671717INSRc.2918G>T (p.Gly973Val)
c.2882G>T (p.Gly961Val)
c.2993G>T (p.Gly998Val)
c.2957G>T (p.Gly986Val)
c.2915G>T (p.Gly972Val)
c.2879G>T (p.Gly960Val)
19g.7128879C>GCA403671718INSRc.2918G>C (p.Gly973Ala)
c.2882G>C (p.Gly961Ala)
c.2993G>C (p.Gly998Ala)
c.2957G>C (p.Gly986Ala)
c.2915G>C (p.Gly972Ala)
c.2879G>C (p.Gly960Ala)
gnomAD v4
19g.7128879C>TCA403671719INSRc.2918G>A (p.Gly973Glu)
c.2882G>A (p.Gly961Glu)
c.2993G>A (p.Gly998Glu)
c.2957G>A (p.Gly986Glu)
c.2915G>A (p.Gly972Glu)
c.2879G>A (p.Gly960Glu)
19g.7128880C>ACA403671720INSRc.2917G>T (p.Gly973Ter)
c.2881G>T (p.Gly961Ter)
c.2992G>T (p.Gly998Ter)
c.2956G>T (p.Gly986Ter)
c.2914G>T (p.Gly972Ter)
c.2878G>T (p.Gly960Ter)
19g.7128880C>GCA403671721INSRc.2917G>C (p.Gly973Arg)
c.2881G>C (p.Gly961Arg)
c.2992G>C (p.Gly998Arg)
c.2956G>C (p.Gly986Arg)
c.2914G>C (p.Gly972Arg)
c.2878G>C (p.Gly960Arg)
19g.7128880C>TCA403671722INSRc.2917G>A (p.Gly973Arg)
c.2881G>A (p.Gly961Arg)
c.2992G>A (p.Gly998Arg)
c.2956G>A (p.Gly986Arg)
c.2914G>A (p.Gly972Arg)
c.2878G>A (p.Gly960Arg)
gnomAD v4
19g.7128881A>CCA403671723INSRc.2916T>G (p.Ile972Met)
c.2880T>G (p.Ile960Met)
c.2991T>G (p.Ile997Met)
c.2955T>G (p.Ile985Met)
c.2913T>G (p.Ile971Met)
c.2877T>G (p.Ile959Met)
19g.7128881A>GCA505217377INSRc.2916T>C (p.Ile972=)
c.2880T>C (p.Ile960=)
c.2991T>C (p.Ile997=)
c.2955T>C (p.Ile985=)
c.2913T>C (p.Ile971=)
c.2877T>C (p.Ile959=)
19g.7128881A>TCA505217378INSRc.2916T>A (p.Ile972=)
c.2880T>A (p.Ile960=)
c.2991T>A (p.Ile997=)
c.2955T>A (p.Ile985=)
c.2913T>A (p.Ile971=)
c.2877T>A (p.Ile959=)
19g.7128882A>CCA403671724INSRc.2915T>G (p.Ile972Ser)
c.2879T>G (p.Ile960Ser)
c.2990T>G (p.Ile997Ser)
c.2954T>G (p.Ile985Ser)
c.2912T>G (p.Ile971Ser)
c.2876T>G (p.Ile959Ser)
19g.7128882A>GCA403671725INSRc.2915T>C (p.Ile972Thr)
c.2879T>C (p.Ile960Thr)
c.2990T>C (p.Ile997Thr)
c.2954T>C (p.Ile985Thr)
c.2912T>C (p.Ile971Thr)
c.2876T>C (p.Ile959Thr)
gnomAD v4
19g.7128882A>TCA403671726INSRc.2915T>A (p.Ile972Asn)
c.2879T>A (p.Ile960Asn)
c.2990T>A (p.Ile997Asn)
c.2954T>A (p.Ile985Asn)
c.2912T>A (p.Ile971Asn)
c.2876T>A (p.Ile959Asn)
19g.7128883T>ACA403671727INSRc.2914A>T (p.Ile972Phe)
c.2878A>T (p.Ile960Phe)
c.2989A>T (p.Ile997Phe)
c.2953A>T (p.Ile985Phe)
c.2911A>T (p.Ile971Phe)
c.2875A>T (p.Ile959Phe)
19g.7128883T>CCA403671728INSRc.2914A>G (p.Ile972Val)
c.2878A>G (p.Ile960Val)
c.2989A>G (p.Ile997Val)
c.2953A>G (p.Ile985Val)
c.2911A>G (p.Ile971Val)
c.2875A>G (p.Ile959Val)
dbSNP gnomAD v3 gnomAD v4
19g.7128883T>GCA403671729INSRc.2914A>C (p.Ile972Leu)
c.2878A>C (p.Ile960Leu)
c.2989A>C (p.Ile997Leu)
c.2953A>C (p.Ile985Leu)
c.2911A>C (p.Ile971Leu)
c.2875A>C (p.Ile959Leu)
19g.7128883T=CA2320769466INSRc.2914A= (p.Ile972=)
c.2878A= (p.Ile960=)
c.2989A= (p.Ile997=)
c.2953A= (p.Ile985=)
c.2911A= (p.Ile971=)
c.2875A= (p.Ile959=)
19g.7128884C>ACA505217380INSRc.2913G>T (p.Val971=)
c.2877G>T (p.Val959=)
c.2988G>T (p.Val996=)
c.2952G>T (p.Val984=)
c.2910G>T (p.Val970=)
c.2874G>T (p.Val958=)
19g.7128884C>GCA505217381INSRc.2913G>C (p.Val971=)
c.2877G>C (p.Val959=)
c.2988G>C (p.Val996=)
c.2952G>C (p.Val984=)
c.2910G>C (p.Val970=)
c.2874G>C (p.Val958=)
19g.7128884C>TCA505217379INSRc.2913G>A (p.Val971=)
c.2877G>A (p.Val959=)
c.2988G>A (p.Val996=)
c.2952G>A (p.Val984=)
c.2910G>A (p.Val970=)
c.2874G>A (p.Val958=)
19g.7128885A=CA2320769467INSRc.2912T= (p.Val971=)
c.2876T= (p.Val959=)
c.2987T= (p.Val996=)
c.2951T= (p.Val984=)
c.2909T= (p.Val970=)
c.2873T= (p.Val958=)
19g.7128885A>CCA403671731INSRc.2912T>G (p.Val971Gly)
c.2876T>G (p.Val959Gly)
c.2987T>G (p.Val996Gly)
c.2951T>G (p.Val984Gly)
c.2909T>G (p.Val970Gly)
c.2873T>G (p.Val958Gly)
19g.7128885A>GCA304876008INSRc.2912T>C (p.Val971Ala)
c.2876T>C (p.Val959Ala)
c.2987T>C (p.Val996Ala)
c.2951T>C (p.Val984Ala)
c.2909T>C (p.Val970Ala)
c.2873T>C (p.Val958Ala)
dbSNP
19g.7128885A>TCA403671730INSRc.2912T>A (p.Val971Glu)
c.2876T>A (p.Val959Glu)
c.2987T>A (p.Val996Glu)
c.2951T>A (p.Val984Glu)
c.2909T>A (p.Val970Glu)
c.2873T>A (p.Val958Glu)
19g.7128886C>ACA403671732INSRc.2911G>T (p.Val971Leu)
c.2875G>T (p.Val959Leu)
c.2986G>T (p.Val996Leu)
c.2950G>T (p.Val984Leu)
c.2908G>T (p.Val970Leu)
c.2872G>T (p.Val958Leu)
19g.7128886C>GCA403671734INSRc.2911G>C (p.Val971Leu)
c.2875G>C (p.Val959Leu)
c.2986G>C (p.Val996Leu)
c.2950G>C (p.Val984Leu)
c.2908G>C (p.Val970Leu)
c.2872G>C (p.Val958Leu)
19g.7128886C>TCA403671733INSRc.2911G>A (p.Val971Met)
c.2875G>A (p.Val959Met)
c.2986G>A (p.Val996Met)
c.2950G>A (p.Val984Met)
c.2908G>A (p.Val970Met)
c.2872G>A (p.Val958Met)
gnomAD v4
19g.7128887A>CCA505217384INSRc.2910T>G (p.Val970=)
c.2874T>G (p.Val958=)
c.2985T>G (p.Val995=)
c.2949T>G (p.Val983=)
c.2907T>G (p.Val969=)
c.2871T>G (p.Val957=)
19g.7128887A>GCA505217385INSRc.2910T>C (p.Val970=)
c.2874T>C (p.Val958=)
c.2985T>C (p.Val995=)
c.2949T>C (p.Val983=)
c.2907T>C (p.Val969=)
c.2871T>C (p.Val957=)
19g.7128887A>TCA505217386INSRc.2910T>A (p.Val970=)
c.2874T>A (p.Val958=)
c.2985T>A (p.Val995=)
c.2949T>A (p.Val983=)
c.2907T>A (p.Val969=)
c.2871T>A (p.Val957=)
19g.7128888A>CCA403671735INSRc.2909T>G (p.Val970Gly)
c.2873T>G (p.Val958Gly)
c.2984T>G (p.Val995Gly)
c.2948T>G (p.Val983Gly)
c.2906T>G (p.Val969Gly)
c.2870T>G (p.Val957Gly)
19g.7128888A>GCA403671736INSRc.2909T>C (p.Val970Ala)
c.2873T>C (p.Val958Ala)
c.2984T>C (p.Val995Ala)
c.2948T>C (p.Val983Ala)
c.2906T>C (p.Val969Ala)
c.2870T>C (p.Val957Ala)
19g.7128888A>TCA403671737INSRc.2909T>A (p.Val970Asp)
c.2873T>A (p.Val958Asp)
c.2984T>A (p.Val995Asp)
c.2948T>A (p.Val983Asp)
c.2906T>A (p.Val969Asp)
c.2870T>A (p.Val957Asp)
19g.7128889C>ACA403671738INSRc.2908G>T (p.Val970Phe)
c.2872G>T (p.Val958Phe)
c.2983G>T (p.Val995Phe)
c.2947G>T (p.Val983Phe)
c.2905G>T (p.Val969Phe)
c.2869G>T (p.Val957Phe)
dbSNP gnomAD v2
19g.7128889C=CA2320769468INSRc.2908G= (p.Val970=)
c.2872G= (p.Val958=)
c.2983G= (p.Val995=)
c.2947G= (p.Val983=)
c.2905G= (p.Val969=)
c.2869G= (p.Val957=)
19g.7128889C>GCA403671739INSRc.2908G>C (p.Val970Leu)
c.2872G>C (p.Val958Leu)
c.2983G>C (p.Val995Leu)
c.2947G>C (p.Val983Leu)
c.2905G>C (p.Val969Leu)
c.2869G>C (p.Val957Leu)
19g.7128889C>TCA403671740INSRc.2908G>A (p.Val970Ile)
c.2872G>A (p.Val958Ile)
c.2983G>A (p.Val995Ile)
c.2947G>A (p.Val983Ile)
c.2905G>A (p.Val969Ile)
c.2869G>A (p.Val957Ile)
19g.7128890A>CCA403671741INSRc.2907T>G (p.Ser969Arg)
c.2871T>G (p.Ser957Arg)
c.2982T>G (p.Ser994Arg)
c.2946T>G (p.Ser982Arg)
c.2904T>G (p.Ser968Arg)
c.2868T>G (p.Ser956Arg)
19g.7128890A>GCA505217387INSRc.2907T>C (p.Ser969=)
c.2871T>C (p.Ser957=)
c.2982T>C (p.Ser994=)
c.2946T>C (p.Ser982=)
c.2904T>C (p.Ser968=)
c.2868T>C (p.Ser956=)
19g.7128890A>TCA403671742INSRc.2907T>A (p.Ser969Arg)
c.2871T>A (p.Ser957Arg)
c.2982T>A (p.Ser994Arg)
c.2946T>A (p.Ser982Arg)
c.2904T>A (p.Ser968Arg)
c.2868T>A (p.Ser956Arg)
19g.7128891C>ACA403671743INSRc.2906G>T (p.Ser969Ile)
c.2870G>T (p.Ser957Ile)
c.2981G>T (p.Ser994Ile)
c.2945G>T (p.Ser982Ile)
c.2903G>T (p.Ser968Ile)
c.2867G>T (p.Ser956Ile)
19g.7128891C>GCA403671744INSRc.2906G>C (p.Ser969Thr)
c.2870G>C (p.Ser957Thr)
c.2981G>C (p.Ser994Thr)
c.2945G>C (p.Ser982Thr)
c.2903G>C (p.Ser968Thr)
c.2867G>C (p.Ser956Thr)
19g.7128891C>TCA403671745INSRc.2906G>A (p.Ser969Asn)
c.2870G>A (p.Ser957Asn)
c.2981G>A (p.Ser994Asn)
c.2945G>A (p.Ser982Asn)
c.2903G>A (p.Ser968Asn)
c.2867G>A (p.Ser956Asn)
19g.7128892T>ACA403671748INSRc.2905A>T (p.Ser969Cys)
c.2869A>T (p.Ser957Cys)
c.2980A>T (p.Ser994Cys)
c.2944A>T (p.Ser982Cys)
c.2902A>T (p.Ser968Cys)
c.2866A>T (p.Ser956Cys)
19g.7128892T>CCA403671747INSRc.2905A>G (p.Ser969Gly)
c.2869A>G (p.Ser957Gly)
c.2980A>G (p.Ser994Gly)
c.2944A>G (p.Ser982Gly)
c.2902A>G (p.Ser968Gly)
c.2866A>G (p.Ser956Gly)
gnomAD v4

Number of alleles fetched