Chr Mutation (hg38) CAid Gene Transcript Linkouts
19g.7122924G>ACA9135303INSRc.3324C>T (p.His1108=)
c.3288C>T (p.His1096=)
n.170C>T
n.235C>T
c.3399C>T (p.His1133=)
c.3363C>T (p.His1121=)
c.3321C>T (p.His1107=)
c.3285C>T (p.His1095=)
ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4
19g.7122924G>CCA403670814INSRc.3324C>G (p.His1108Gln)
c.3288C>G (p.His1096Gln)
n.170C>G
n.235C>G
c.3399C>G (p.His1133Gln)
c.3363C>G (p.His1121Gln)
c.3321C>G (p.His1107Gln)
c.3285C>G (p.His1095Gln)
19g.7122924G=CA2320766500INSRc.3324C= (p.His1108=)
c.3288C= (p.His1096=)
n.170C=
n.235C=
c.3399C= (p.His1133=)
c.3363C= (p.His1121=)
c.3321C= (p.His1107=)
c.3285C= (p.His1095=)
19g.7122924G>TCA403670815INSRc.3324C>A (p.His1108Gln)
c.3288C>A (p.His1096Gln)
n.170C>A
n.235C>A
c.3399C>A (p.His1133Gln)
c.3363C>A (p.His1121Gln)
c.3321C>A (p.His1107Gln)
c.3285C>A (p.His1095Gln)
gnomAD v4
19g.7122925T>ACA403670816INSRc.3323A>T (p.His1108Leu)
c.3287A>T (p.His1096Leu)
n.169A>T
n.234A>T
c.3398A>T (p.His1133Leu)
c.3362A>T (p.His1121Leu)
c.3320A>T (p.His1107Leu)
c.3284A>T (p.His1095Leu)
19g.7122925T>CCA403670817INSRc.3323A>G (p.His1108Arg)
c.3287A>G (p.His1096Arg)
n.169A>G
n.234A>G
c.3398A>G (p.His1133Arg)
c.3362A>G (p.His1121Arg)
c.3320A>G (p.His1107Arg)
c.3284A>G (p.His1095Arg)
19g.7122925T>GCA403670818INSRc.3323A>C (p.His1108Pro)
c.3287A>C (p.His1096Pro)
n.169A>C
n.234A>C
c.3398A>C (p.His1133Pro)
c.3362A>C (p.His1121Pro)
c.3320A>C (p.His1107Pro)
c.3284A>C (p.His1095Pro)
19g.7122926G>ACA403670819INSRc.3322C>T (p.His1108Tyr)
c.3286C>T (p.His1096Tyr)
n.168C>T
n.233C>T
c.3397C>T (p.His1133Tyr)
c.3361C>T (p.His1121Tyr)
c.3319C>T (p.His1107Tyr)
c.3283C>T (p.His1095Tyr)
gnomAD v4
19g.7122926G>CCA403670820INSRc.3322C>G (p.His1108Asp)
c.3286C>G (p.His1096Asp)
n.168C>G
n.233C>G
c.3397C>G (p.His1133Asp)
c.3361C>G (p.His1121Asp)
c.3319C>G (p.His1107Asp)
c.3283C>G (p.His1095Asp)
19g.7122926G>TCA403670821INSRc.3322C>A (p.His1108Asn)
c.3286C>A (p.His1096Asn)
n.168C>A
n.233C>A
c.3397C>A (p.His1133Asn)
c.3361C>A (p.His1121Asn)
c.3319C>A (p.His1107Asn)
c.3283C>A (p.His1095Asn)
19g.7122927A=CA2320766501INSRc.3321T= (p.Ala1107=)
c.3285T= (p.Ala1095=)
n.167T=
n.232T=
c.3396T= (p.Ala1132=)
c.3360T= (p.Ala1120=)
c.3318T= (p.Ala1106=)
c.3282T= (p.Ala1094=)
19g.7122927A>CCA505217077INSRc.3321T>G (p.Ala1107=)
c.3285T>G (p.Ala1095=)
n.167T>G
n.232T>G
c.3396T>G (p.Ala1132=)
c.3360T>G (p.Ala1120=)
c.3318T>G (p.Ala1106=)
c.3282T>G (p.Ala1094=)
19g.7122927A>GCA505217078INSRc.3321T>C (p.Ala1107=)
c.3285T>C (p.Ala1095=)
n.167T>C
n.232T>C
c.3396T>C (p.Ala1132=)
c.3360T>C (p.Ala1120=)
c.3318T>C (p.Ala1106=)
c.3282T>C (p.Ala1094=)
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.7122927A>TCA505217079INSRc.3321T>A (p.Ala1107=)
c.3285T>A (p.Ala1095=)
n.167T>A
n.232T>A
c.3396T>A (p.Ala1132=)
c.3360T>A (p.Ala1120=)
c.3318T>A (p.Ala1106=)
c.3282T>A (p.Ala1094=)
19g.7122928G>ACA9135304INSRc.3320C>T (p.Ala1107Val)
c.3284C>T (p.Ala1095Val)
n.166C>T
n.231C>T
c.3395C>T (p.Ala1132Val)
c.3359C>T (p.Ala1120Val)
c.3317C>T (p.Ala1106Val)
c.3281C>T (p.Ala1094Val)
dbSNP ExAC gnomAD v2
19g.7122928G>CCA403670823INSRc.3320C>G (p.Ala1107Gly)
c.3284C>G (p.Ala1095Gly)
n.166C>G
n.231C>G
c.3395C>G (p.Ala1132Gly)
c.3359C>G (p.Ala1120Gly)
c.3317C>G (p.Ala1106Gly)
c.3281C>G (p.Ala1094Gly)
19g.7122928G=CA2320766502INSRc.3320C= (p.Ala1107=)
c.3284C= (p.Ala1095=)
n.166C=
n.231C=
c.3395C= (p.Ala1132=)
c.3359C= (p.Ala1120=)
c.3317C= (p.Ala1106=)
c.3281C= (p.Ala1094=)
19g.7122928G>TCA403670822INSRc.3320C>A (p.Ala1107Asp)
c.3284C>A (p.Ala1095Asp)
n.166C>A
n.231C>A
c.3395C>A (p.Ala1132Asp)
c.3359C>A (p.Ala1120Asp)
c.3317C>A (p.Ala1106Asp)
c.3281C>A (p.Ala1094Asp)
19g.7122929C>ACA403670824INSRc.3319G>T (p.Ala1107Ser)
c.3283G>T (p.Ala1095Ser)
n.165G>T
n.230G>T
c.3394G>T (p.Ala1132Ser)
c.3358G>T (p.Ala1120Ser)
c.3316G>T (p.Ala1106Ser)
c.3280G>T (p.Ala1094Ser)
19g.7122929C=CA2320766503INSRc.3319G= (p.Ala1107=)
c.3283G= (p.Ala1095=)
n.165G=
n.230G=
c.3394G= (p.Ala1132=)
c.3358G= (p.Ala1120=)
c.3316G= (p.Ala1106=)
c.3280G= (p.Ala1094=)
19g.7122929C>GCA403670825INSRc.3319G>C (p.Ala1107Pro)
c.3283G>C (p.Ala1095Pro)
n.165G>C
n.230G>C
c.3394G>C (p.Ala1132Pro)
c.3358G>C (p.Ala1120Pro)
c.3316G>C (p.Ala1106Pro)
c.3280G>C (p.Ala1094Pro)
19g.7122929C>TCA9135305INSRc.3319G>A (p.Ala1107Thr)
c.3283G>A (p.Ala1095Thr)
n.165G>A
n.230G>A
c.3394G>A (p.Ala1132Thr)
c.3358G>A (p.Ala1120Thr)
c.3316G>A (p.Ala1106Thr)
c.3280G>A (p.Ala1094Thr)
dbSNP ExAC gnomAD v2 gnomAD v4
19g.7122930C>ACA403670827INSRc.3318G>T (p.Met1106Ile)
c.3282G>T (p.Met1094Ile)
n.164G>T
n.229G>T
c.3393G>T (p.Met1131Ile)
c.3357G>T (p.Met1119Ile)
c.3315G>T (p.Met1105Ile)
c.3279G>T (p.Met1093Ile)
gnomAD v4
19g.7122930C>GCA403670828INSRc.3318G>C (p.Met1106Ile)
c.3282G>C (p.Met1094Ile)
n.164G>C
n.229G>C
c.3393G>C (p.Met1131Ile)
c.3357G>C (p.Met1119Ile)
c.3315G>C (p.Met1105Ile)
c.3279G>C (p.Met1093Ile)
19g.7122930C>TCA403670829INSRc.3318G>A (p.Met1106Ile)
c.3282G>A (p.Met1094Ile)
n.164G>A
n.229G>A
c.3393G>A (p.Met1131Ile)
c.3357G>A (p.Met1119Ile)
c.3315G>A (p.Met1105Ile)
c.3279G>A (p.Met1093Ile)
19g.7122931A=CA2320766504INSRc.3317T= (p.Met1106=)
c.3281T= (p.Met1094=)
n.163T=
n.228T=
c.3392T= (p.Met1131=)
c.3356T= (p.Met1119=)
c.3314T= (p.Met1105=)
c.3278T= (p.Met1093=)
19g.7122931A>CCA403670830INSRc.3317T>G (p.Met1106Arg)
c.3281T>G (p.Met1094Arg)
n.163T>G
n.228T>G
c.3392T>G (p.Met1131Arg)
c.3356T>G (p.Met1119Arg)
c.3314T>G (p.Met1105Arg)
c.3278T>G (p.Met1093Arg)
dbSNP
19g.7122931A>GCA403670831INSRc.3317T>C (p.Met1106Thr)
c.3281T>C (p.Met1094Thr)
n.163T>C
n.228T>C
c.3392T>C (p.Met1131Thr)
c.3356T>C (p.Met1119Thr)
c.3314T>C (p.Met1105Thr)
c.3278T>C (p.Met1093Thr)
19g.7122931A>TCA403670832INSRc.3317T>A (p.Met1106Lys)
c.3281T>A (p.Met1094Lys)
n.163T>A
n.228T>A
c.3392T>A (p.Met1131Lys)
c.3356T>A (p.Met1119Lys)
c.3314T>A (p.Met1105Lys)
c.3278T>A (p.Met1093Lys)
19g.7122932T>ACA403670833INSRc.3316A>T (p.Met1106Leu)
c.3280A>T (p.Met1094Leu)
n.162A>T
n.227A>T
c.3391A>T (p.Met1131Leu)
c.3355A>T (p.Met1119Leu)
c.3313A>T (p.Met1105Leu)
c.3277A>T (p.Met1093Leu)
gnomAD v4
19g.7122932T>CCA403670834INSRc.3316A>G (p.Met1106Val)
c.3280A>G (p.Met1094Val)
n.162A>G
n.227A>G
c.3391A>G (p.Met1131Val)
c.3355A>G (p.Met1119Val)
c.3313A>G (p.Met1105Val)
c.3277A>G (p.Met1093Val)
19g.7122932T>GCA403670835INSRc.3316A>C (p.Met1106Leu)
c.3280A>C (p.Met1094Leu)
n.162A>C
n.227A>C
c.3391A>C (p.Met1131Leu)
c.3355A>C (p.Met1119Leu)
c.3313A>C (p.Met1105Leu)
c.3277A>C (p.Met1093Leu)
19g.7122933C>ACA505217082INSRc.3315G>T (p.Leu1105=)
c.3279G>T (p.Leu1093=)
n.161G>T
n.226G>T
c.3390G>T (p.Leu1130=)
c.3354G>T (p.Leu1118=)
c.3312G>T (p.Leu1104=)
c.3276G>T (p.Leu1092=)
dbSNP gnomAD v4
19g.7122933C>GCA505217081INSRc.3315G>C (p.Leu1105=)
c.3279G>C (p.Leu1093=)
n.161G>C
n.226G>C
c.3390G>C (p.Leu1130=)
c.3354G>C (p.Leu1118=)
c.3312G>C (p.Leu1104=)
c.3276G>C (p.Leu1092=)
19g.7122933C>TCA505217080INSRc.3315G>A (p.Leu1105=)
c.3279G>A (p.Leu1093=)
n.161G>A
n.226G>A
c.3390G>A (p.Leu1130=)
c.3354G>A (p.Leu1118=)
c.3312G>A (p.Leu1104=)
c.3276G>A (p.Leu1092=)
19g.7122934A>CCA403670838INSRc.3314T>G (p.Leu1105Arg)
c.3278T>G (p.Leu1093Arg)
n.160T>G
n.225T>G
c.3389T>G (p.Leu1130Arg)
c.3353T>G (p.Leu1118Arg)
c.3311T>G (p.Leu1104Arg)
c.3275T>G (p.Leu1092Arg)
19g.7122934A>GCA403670837INSRc.3314T>C (p.Leu1105Pro)
c.3278T>C (p.Leu1093Pro)
n.160T>C
n.225T>C
c.3389T>C (p.Leu1130Pro)
c.3353T>C (p.Leu1118Pro)
c.3311T>C (p.Leu1104Pro)
c.3275T>C (p.Leu1092Pro)
19g.7122934A>TCA403670836INSRc.3314T>A (p.Leu1105Gln)
c.3278T>A (p.Leu1093Gln)
n.160T>A
n.225T>A
c.3389T>A (p.Leu1130Gln)
c.3353T>A (p.Leu1118Gln)
c.3311T>A (p.Leu1104Gln)
c.3275T>A (p.Leu1092Gln)
19g.7122935G>ACA505217083INSRc.3313C>T (p.Leu1105=)
c.3277C>T (p.Leu1093=)
n.159C>T
n.224C>T
c.3388C>T (p.Leu1130=)
c.3352C>T (p.Leu1118=)
c.3310C>T (p.Leu1104=)
c.3274C>T (p.Leu1092=)
dbSNP gnomAD v2 gnomAD v3 gnomAD v4
19g.7122935G>CCA403670839INSRc.3313C>G (p.Leu1105Val)
c.3277C>G (p.Leu1093Val)
n.159C>G
n.224C>G
c.3388C>G (p.Leu1130Val)
c.3352C>G (p.Leu1118Val)
c.3310C>G (p.Leu1104Val)
c.3274C>G (p.Leu1092Val)
19g.7122935G=CA2320766505INSRc.3313C= (p.Leu1105=)
c.3277C= (p.Leu1093=)
n.159C=
n.224C=
c.3388C= (p.Leu1130=)
c.3352C= (p.Leu1118=)
c.3310C= (p.Leu1104=)
c.3274C= (p.Leu1092=)
19g.7122935G>TCA403670840INSRc.3313C>A (p.Leu1105Met)
c.3277C>A (p.Leu1093Met)
n.159C>A
n.224C>A
c.3388C>A (p.Leu1130Met)
c.3352C>A (p.Leu1118Met)
c.3310C>A (p.Leu1104Met)
c.3274C>A (p.Leu1092Met)
19g.7122936C>ACA403670841INSRc.3312G>T (p.Glu1104Asp)
c.3276G>T (p.Glu1092Asp)
n.158G>T
n.223G>T
c.3387G>T (p.Glu1129Asp)
c.3351G>T (p.Glu1117Asp)
c.3309G>T (p.Glu1103Asp)
c.3273G>T (p.Glu1091Asp)
19g.7122936C=CA2320766506INSRc.3312G= (p.Glu1104=)
c.3276G= (p.Glu1092=)
n.158G=
n.223G=
c.3387G= (p.Glu1129=)
c.3351G= (p.Glu1117=)
c.3309G= (p.Glu1103=)
c.3273G= (p.Glu1091=)
19g.7122936C>GCA403670842INSRc.3312G>C (p.Glu1104Asp)
c.3276G>C (p.Glu1092Asp)
n.158G>C
n.223G>C
c.3387G>C (p.Glu1129Asp)
c.3351G>C (p.Glu1117Asp)
c.3309G>C (p.Glu1103Asp)
c.3273G>C (p.Glu1091Asp)
19g.7122936C>TCA505217084INSRc.3312G>A (p.Glu1104=)
c.3276G>A (p.Glu1092=)
n.158G>A
n.223G>A
c.3387G>A (p.Glu1129=)
c.3351G>A (p.Glu1117=)
c.3309G>A (p.Glu1103=)
c.3273G>A (p.Glu1091=)
ClinVar dbSNP gnomAD v3 gnomAD v4
19g.7122937_7122938dupCA2587921682INSRc.3311_3312dup (p.Leu1105SerfsTer2)
c.3275_3276dup (p.Leu1093SerfsTer2)
n.157_158dup
n.222_223dup
c.3386_3387dup (p.Leu1130SerfsTer2)
c.3350_3351dup (p.Leu1118SerfsTer2)
c.3308_3309dup (p.Leu1104SerfsTer2)
c.3272_3273dup (p.Leu1092SerfsTer2)
gnomAD v4
19g.7122937T>ACA403670843INSRc.3311A>T (p.Glu1104Val)
c.3275A>T (p.Glu1092Val)
n.157A>T
n.222A>T
c.3386A>T (p.Glu1129Val)
c.3350A>T (p.Glu1117Val)
c.3308A>T (p.Glu1103Val)
c.3272A>T (p.Glu1091Val)
19g.7122937T>CCA403670844INSRc.3311A>G (p.Glu1104Gly)
c.3275A>G (p.Glu1092Gly)
n.157A>G
n.222A>G
c.3386A>G (p.Glu1129Gly)
c.3350A>G (p.Glu1117Gly)
c.3308A>G (p.Glu1103Gly)
c.3272A>G (p.Glu1091Gly)
19g.7122937T>GCA403670845INSRc.3311A>C (p.Glu1104Ala)
c.3275A>C (p.Glu1092Ala)
n.157A>C
n.222A>C
c.3386A>C (p.Glu1129Ala)
c.3350A>C (p.Glu1117Ala)
c.3308A>C (p.Glu1103Ala)
c.3272A>C (p.Glu1091Ala)

Number of alleles fetched