Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
---|---|---|---|---|---|
17 | g.50185812C>A | CA400191507 | COL1A1 | c.4214G>T (p.Arg1405Leu) c.3944G>T (p.Arg1315Leu) c.3296G>T (p.Arg1099Leu) c.4016G>T (p.Arg1339Leu) | |
17 | g.50185812C= | CA2263913860 | COL1A1 | c.4214G= (p.Arg1405=) c.3944G= (p.Arg1315=) c.3296G= (p.Arg1099=) c.4016G= (p.Arg1339=) | |
17 | g.50185812C>G | CA400191512 | COL1A1 | c.4214G>C (p.Arg1405Pro) c.3944G>C (p.Arg1315Pro) c.3296G>C (p.Arg1099Pro) c.4016G>C (p.Arg1339Pro) | gnomAD v4 |
17 | g.50185812C>T | CA8644226 | COL1A1 | c.4214G>A (p.Arg1405His) c.3944G>A (p.Arg1315His) c.3296G>A (p.Arg1099His) c.4016G>A (p.Arg1339His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 COSMIC |
17 | g.50185813G>A | CA400191518 | COL1A1 | c.4213C>T (p.Arg1405Cys) c.3943C>T (p.Arg1315Cys) c.3295C>T (p.Arg1099Cys) c.4015C>T (p.Arg1339Cys) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.50185813G>C | CA400191521 | COL1A1 | c.4213C>G (p.Arg1405Gly) c.3943C>G (p.Arg1315Gly) c.3295C>G (p.Arg1099Gly) c.4015C>G (p.Arg1339Gly) | |
17 | g.50185813G= | CA2263913861 | COL1A1 | c.4213C= (p.Arg1405=) c.3943C= (p.Arg1315=) c.3295C= (p.Arg1099=) c.4015C= (p.Arg1339=) | |
17 | g.50185813G>T | CA400191524 | COL1A1 | c.4213C>A (p.Arg1405Ser) c.3943C>A (p.Arg1315Ser) c.3295C>A (p.Arg1099Ser) c.4015C>A (p.Arg1339Ser) | ClinVar |
17 | g.50185814G>A | CA8644227 | COL1A1 | c.4212C>T (p.Ser1404=) c.3942C>T (p.Ser1314=) c.3294C>T (p.Ser1098=) c.4014C>T (p.Ser1338=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.50185814G>C | CA400191529 | COL1A1 | c.4212C>G (p.Ser1404Arg) c.3942C>G (p.Ser1314Arg) c.3294C>G (p.Ser1098Arg) c.4014C>G (p.Ser1338Arg) | |
17 | g.50185814G= | CA2263913862 | COL1A1 | c.4212C= (p.Ser1404=) c.3942C= (p.Ser1314=) c.3294C= (p.Ser1098=) c.4014C= (p.Ser1338=) | |
17 | g.50185814G>T | CA400191527 | COL1A1 | c.4212C>A (p.Ser1404Arg) c.3942C>A (p.Ser1314Arg) c.3294C>A (p.Ser1098Arg) c.4014C>A (p.Ser1338Arg) | gnomAD v4 |
17 | g.50185815C>A | CA400191532 | COL1A1 | c.4211G>T (p.Ser1404Ile) c.3941G>T (p.Ser1314Ile) c.3293G>T (p.Ser1098Ile) c.4013G>T (p.Ser1338Ile) | |
17 | g.50185815C= | CA2263913863 | COL1A1 | c.4211G= (p.Ser1404=) c.3941G= (p.Ser1314=) c.3293G= (p.Ser1098=) c.4013G= (p.Ser1338=) | |
17 | g.50185815C>G | CA400191533 | COL1A1 | c.4211G>C (p.Ser1404Thr) c.3941G>C (p.Ser1314Thr) c.3293G>C (p.Ser1098Thr) c.4013G>C (p.Ser1338Thr) | |
17 | g.50185815C>T | CA8644228 | COL1A1 | c.4211G>A (p.Ser1404Asn) c.3941G>A (p.Ser1314Asn) c.3293G>A (p.Ser1098Asn) c.4013G>A (p.Ser1338Asn) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.50185816T>A | CA400191540 | COL1A1 | c.4210A>T (p.Ser1404Cys) c.3940A>T (p.Ser1314Cys) c.3292A>T (p.Ser1098Cys) c.4012A>T (p.Ser1338Cys) | |
17 | g.50185816T>C | CA8644229 | COL1A1 | c.4210A>G (p.Ser1404Gly) c.3940A>G (p.Ser1314Gly) c.3292A>G (p.Ser1098Gly) c.4012A>G (p.Ser1338Gly) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.50185816T>G | CA400191546 | COL1A1 | c.4210A>C (p.Ser1404Arg) c.3940A>C (p.Ser1314Arg) c.3292A>C (p.Ser1098Arg) c.4012A>C (p.Ser1338Arg) | |
17 | g.50185816T= | CA2263913864 | COL1A1 | c.4210A= (p.Ser1404=) c.3940A= (p.Ser1314=) c.3292A= (p.Ser1098=) c.4012A= (p.Ser1338=) | |
17 | g.50185817G>A | CA291542791 | COL1A1 | c.4209C>T (p.Asn1403=) c.3939C>T (p.Asn1313=) c.3291C>T (p.Asn1097=) c.4011C>T (p.Asn1337=) | dbSNP gnomAD v4 |
17 | g.50185817G>C | CA400191552 | COL1A1 | c.4209C>G (p.Asn1403Lys) c.3939C>G (p.Asn1313Lys) c.3291C>G (p.Asn1097Lys) c.4011C>G (p.Asn1337Lys) | |
17 | g.50185817G= | CA2263913865 | COL1A1 | c.4209C= (p.Asn1403=) c.3939C= (p.Asn1313=) c.3291C= (p.Asn1097=) c.4011C= (p.Asn1337=) | |
17 | g.50185817G>T | CA400191555 | COL1A1 | c.4209C>A (p.Asn1403Lys) c.3939C>A (p.Asn1313Lys) c.3291C>A (p.Asn1097Lys) c.4011C>A (p.Asn1337Lys) | |
17 | g.50185817_50185818insGGG | CA291542790 | COL1A1 | c.4209_4210insCCC (p.Asn1403_Ser1404insPro) c.3939_3940insCCC (p.Asn1313_Ser1314insPro) c.3291_3292insCCC (p.Asn1097_Ser1098insPro) c.4011_4012insCCC (p.Asn1337_Ser1338insPro) | dbSNP |
17 | g.50185818T>A | CA400191559 | COL1A1 | c.4208A>T (p.Asn1403Ile) c.3938A>T (p.Asn1313Ile) c.3290A>T (p.Asn1097Ile) c.4010A>T (p.Asn1337Ile) | |
17 | g.50185818T>C | CA400191563 | COL1A1 | c.4208A>G (p.Asn1403Ser) c.3938A>G (p.Asn1313Ser) c.3290A>G (p.Asn1097Ser) c.4010A>G (p.Asn1337Ser) | |
17 | g.50185818T>G | CA8644230 | COL1A1 | c.4208A>C (p.Asn1403Thr) c.3938A>C (p.Asn1313Thr) c.3290A>C (p.Asn1097Thr) c.4010A>C (p.Asn1337Thr) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.50185818T= | CA2263913866 | COL1A1 | c.4208A= (p.Asn1403=) c.3938A= (p.Asn1313=) c.3290A= (p.Asn1097=) c.4010A= (p.Asn1337=) | |
17 | g.50185819T>A | CA400191575 | COL1A1 | c.4207A>T (p.Asn1403Tyr) c.3937A>T (p.Asn1313Tyr) c.3289A>T (p.Asn1097Tyr) c.4009A>T (p.Asn1337Tyr) | |
17 | g.50185819T>C | CA400191581 | COL1A1 | c.4207A>G (p.Asn1403Asp) c.3937A>G (p.Asn1313Asp) c.3289A>G (p.Asn1097Asp) c.4009A>G (p.Asn1337Asp) | |
17 | g.50185819T>G | CA400191579 | COL1A1 | c.4207A>C (p.Asn1403His) c.3937A>C (p.Asn1313His) c.3289A>C (p.Asn1097His) c.4009A>C (p.Asn1337His) | |
17 | g.50185820G>A | CA500991601 | COL1A1 | c.4206C>T (p.Gly1402=) c.3936C>T (p.Gly1312=) c.3288C>T (p.Gly1096=) c.4008C>T (p.Gly1336=) | |
17 | g.50185820G>C | CA500991599 | COL1A1 | c.4206C>G (p.Gly1402=) c.3936C>G (p.Gly1312=) c.3288C>G (p.Gly1096=) c.4008C>G (p.Gly1336=) | |
17 | g.50185820G>T | CA500991594 | COL1A1 | c.4206C>A (p.Gly1402=) c.3936C>A (p.Gly1312=) c.3288C>A (p.Gly1096=) c.4008C>A (p.Gly1336=) | |
17 | g.50185821_50185957dup | CA2697560244 | COL1A1 | c.4070_4206dup (p.Asn1403Ter) c.3800_3936dup (p.Asn1313Ter) c.3152_3288dup (p.Asn1097Ter) c.3872_4008dup (p.Asn1337Ter) | ClinVar |
17 | g.50185821C>A | CA400191586 | COL1A1 | c.4205G>T (p.Gly1402Val) c.3935G>T (p.Gly1312Val) c.3287G>T (p.Gly1096Val) c.4007G>T (p.Gly1336Val) | |
17 | g.50185821C>G | CA400191591 | COL1A1 | c.4205G>C (p.Gly1402Ala) c.3935G>C (p.Gly1312Ala) c.3287G>C (p.Gly1096Ala) c.4007G>C (p.Gly1336Ala) | |
17 | g.50185821C>T | CA400191588 | COL1A1 | c.4205G>A (p.Gly1402Asp) c.3935G>A (p.Gly1312Asp) c.3287G>A (p.Gly1096Asp) c.4007G>A (p.Gly1336Asp) | |
17 | g.50185822C>A | CA400191594 | COL1A1 | c.4204G>T (p.Gly1402Cys) c.3934G>T (p.Gly1312Cys) c.3286G>T (p.Gly1096Cys) c.4006G>T (p.Gly1336Cys) | |
17 | g.50185822C>G | CA400191597 | COL1A1 | c.4204G>C (p.Gly1402Arg) c.3934G>C (p.Gly1312Arg) c.3286G>C (p.Gly1096Arg) c.4006G>C (p.Gly1336Arg) | |
17 | g.50185822C>T | CA400191595 | COL1A1 | c.4204G>A (p.Gly1402Ser) c.3934G>A (p.Gly1312Ser) c.3286G>A (p.Gly1096Ser) c.4006G>A (p.Gly1336Ser) | gnomAD v4 |
17 | g.50185823C>A | CA400191601 | COL1A1 | c.4203G>T (p.Glu1401Asp) c.3933G>T (p.Glu1311Asp) c.3285G>T (p.Glu1095Asp) c.4005G>T (p.Glu1335Asp) | |
17 | g.50185823C= | CA2263913867 | COL1A1 | c.4203G= (p.Glu1401=) c.3933G= (p.Glu1311=) c.3285G= (p.Glu1095=) c.4005G= (p.Glu1335=) | |
17 | g.50185823C>G | CA400191602 | COL1A1 | c.4203G>C (p.Glu1401Asp) c.3933G>C (p.Glu1311Asp) c.3285G>C (p.Glu1095Asp) c.4005G>C (p.Glu1335Asp) | dbSNP gnomAD v3 gnomAD v4 |
17 | g.50185823C>T | CA500991602 | COL1A1 | c.4203G>A (p.Glu1401=) c.3933G>A (p.Glu1311=) c.3285G>A (p.Glu1095=) c.4005G>A (p.Glu1335=) | dbSNP gnomAD v4 |
17 | g.50185824T>A | CA400191605 | COL1A1 | c.4202A>T (p.Glu1401Val) c.3932A>T (p.Glu1311Val) c.3284A>T (p.Glu1095Val) c.4004A>T (p.Glu1335Val) | |
17 | g.50185824T>C | CA400191610 | COL1A1 | c.4202A>G (p.Glu1401Gly) c.3932A>G (p.Glu1311Gly) c.3284A>G (p.Glu1095Gly) c.4004A>G (p.Glu1335Gly) | |
17 | g.50185824T>G | CA400191607 | COL1A1 | c.4202A>C (p.Glu1401Ala) c.3932A>C (p.Glu1311Ala) c.3284A>C (p.Glu1095Ala) c.4004A>C (p.Glu1335Ala) | |
17 | g.50185825C>A | CA400191614 | COL1A1 | c.4201G>T (p.Glu1401Ter) c.3931G>T (p.Glu1311Ter) c.3283G>T (p.Glu1095Ter) c.4003G>T (p.Glu1335Ter) | ClinVar |
17 | g.50185825C= | CA2263913868 | COL1A1 | c.4201G= (p.Glu1401=) c.3931G= (p.Glu1311=) c.3283G= (p.Glu1095=) c.4003G= (p.Glu1335=) | |
17 | g.50185825C>G | CA400191619 | COL1A1 | c.4201G>C (p.Glu1401Gln) c.3931G>C (p.Glu1311Gln) c.3283G>C (p.Glu1095Gln) c.4003G>C (p.Glu1335Gln) | |
17 | g.50185825C>T | CA8644231 | COL1A1 | c.4201G>A (p.Glu1401Lys) c.3931G>A (p.Glu1311Lys) c.3283G>A (p.Glu1095Lys) c.4003G>A (p.Glu1335Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 COSMIC |
17 | g.50185826G>A | CA8644232 | COL1A1 | c.4200C>T (p.Ala1400=) c.3930C>T (p.Ala1310=) c.3282C>T (p.Ala1094=) c.4002C>T (p.Ala1334=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.50185826G>C | CA500991606 | COL1A1 | c.4200C>G (p.Ala1400=) c.3930C>G (p.Ala1310=) c.3282C>G (p.Ala1094=) c.4002C>G (p.Ala1334=) | |
17 | g.50185826G= | CA2263913869 | COL1A1 | c.4200C= (p.Ala1400=) c.3930C= (p.Ala1310=) c.3282C= (p.Ala1094=) c.4002C= (p.Ala1334=) | |
17 | g.50185826G>T | CA500991607 | COL1A1 | c.4200C>A (p.Ala1400=) c.3930C>A (p.Ala1310=) c.3282C>A (p.Ala1094=) c.4002C>A (p.Ala1334=) | gnomAD v4 COSMIC |
17 | g.50185827G>A | CA400191624 | COL1A1 | c.4199C>T (p.Ala1400Val) c.3929C>T (p.Ala1310Val) c.3281C>T (p.Ala1094Val) c.4001C>T (p.Ala1334Val) | |
17 | g.50185827G>C | CA400191627 | COL1A1 | c.4199C>G (p.Ala1400Gly) c.3929C>G (p.Ala1310Gly) c.3281C>G (p.Ala1094Gly) c.4001C>G (p.Ala1334Gly) | dbSNP |
17 | g.50185827G= | CA2263913870 | COL1A1 | c.4199C= (p.Ala1400=) c.3929C= (p.Ala1310=) c.3281C= (p.Ala1094=) c.4001C= (p.Ala1334=) | |
17 | g.50185827G>T | CA400191629 | COL1A1 | c.4199C>A (p.Ala1400Asp) c.3929C>A (p.Ala1310Asp) c.3281C>A (p.Ala1094Asp) c.4001C>A (p.Ala1334Asp) | ClinVar dbSNP |
17 | g.50185828C>A | CA400191634 | COL1A1 | c.4198G>T (p.Ala1400Ser) c.3928G>T (p.Ala1310Ser) c.3280G>T (p.Ala1094Ser) c.4000G>T (p.Ala1334Ser) | |
17 | g.50185828C= | CA2263913871 | COL1A1 | c.4198G= (p.Ala1400=) c.3928G= (p.Ala1310=) c.3280G= (p.Ala1094=) c.4000G= (p.Ala1334=) | |
17 | g.50185828C>G | CA8644233 | COL1A1 | c.4198G>C (p.Ala1400Pro) c.3928G>C (p.Ala1310Pro) c.3280G>C (p.Ala1094Pro) c.4000G>C (p.Ala1334Pro) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.50185828C>T | CA400191639 | COL1A1 | c.4198G>A (p.Ala1400Thr) c.3928G>A (p.Ala1310Thr) c.3280G>A (p.Ala1094Thr) c.4000G>A (p.Ala1334Thr) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.50185829G>A | CA8644234 | COL1A1 | c.4197C>T (p.Arg1399=) c.3927C>T (p.Arg1309=) c.3279C>T (p.Arg1093=) c.3999C>T (p.Arg1333=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.50185829G>C | CA500991608 | COL1A1 | c.4197C>G (p.Arg1399=) c.3927C>G (p.Arg1309=) c.3279C>G (p.Arg1093=) c.3999C>G (p.Arg1333=) | dbSNP |
17 | g.50185829G= | CA2263913872 | COL1A1 | c.4197C= (p.Arg1399=) c.3927C= (p.Arg1309=) c.3279C= (p.Arg1093=) c.3999C= (p.Arg1333=) | |
17 | g.50185829G>T | CA500991609 | COL1A1 | c.4197C>A (p.Arg1399=) c.3927C>A (p.Arg1309=) c.3279C>A (p.Arg1093=) c.3999C>A (p.Arg1333=) | |
17 | g.50185830C>A | CA400191651 | COL1A1 | c.4196G>T (p.Arg1399Leu) c.3926G>T (p.Arg1309Leu) c.3278G>T (p.Arg1093Leu) c.3998G>T (p.Arg1333Leu) | |
17 | g.50185830C= | CA2263913873 | COL1A1 | c.4196G= (p.Arg1399=) c.3926G= (p.Arg1309=) c.3278G= (p.Arg1093=) c.3998G= (p.Arg1333=) | |
17 | g.50185830C>G | CA400191648 | COL1A1 | c.4196G>C (p.Arg1399Pro) c.3926G>C (p.Arg1309Pro) c.3278G>C (p.Arg1093Pro) c.3998G>C (p.Arg1333Pro) | |
17 | g.50185830C>T | CA8644235 | COL1A1 | c.4196G>A (p.Arg1399His) c.3926G>A (p.Arg1309His) c.3278G>A (p.Arg1093His) c.3998G>A (p.Arg1333His) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.50185831G>A | CA8644236 | COL1A1 | c.4195C>T (p.Arg1399Cys) c.3925C>T (p.Arg1309Cys) c.3277C>T (p.Arg1093Cys) c.3997C>T (p.Arg1333Cys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.50185831G>C | CA400191657 | COL1A1 | c.4195C>G (p.Arg1399Gly) c.3925C>G (p.Arg1309Gly) c.3277C>G (p.Arg1093Gly) c.3997C>G (p.Arg1333Gly) | |
17 | g.50185831G= | CA2263913874 | COL1A1 | c.4195C= (p.Arg1399=) c.3925C= (p.Arg1309=) c.3277C= (p.Arg1093=) c.3997C= (p.Arg1333=) | |
17 | g.50185831G>T | CA400191660 | COL1A1 | c.4195C>A (p.Arg1399Ser) c.3925C>A (p.Arg1309Ser) c.3277C>A (p.Arg1093Ser) c.3997C>A (p.Arg1333Ser) | dbSNP |
17 | g.50185832G>A | CA500991615 | COL1A1 | c.4194C>T (p.Ile1398=) c.3924C>T (p.Ile1308=) c.3276C>T (p.Ile1092=) c.3996C>T (p.Ile1332=) | |
17 | g.50185832G>C | CA400191664 | COL1A1 | c.4194C>G (p.Ile1398Met) c.3924C>G (p.Ile1308Met) c.3276C>G (p.Ile1092Met) c.3996C>G (p.Ile1332Met) | |
17 | g.50185832G>T | CA500991617 | COL1A1 | c.4194C>A (p.Ile1398=) c.3924C>A (p.Ile1308=) c.3276C>A (p.Ile1092=) c.3996C>A (p.Ile1332=) | |
17 | g.50185833A>C | CA400191667 | COL1A1 | c.4193T>G (p.Ile1398Ser) c.3923T>G (p.Ile1308Ser) c.3275T>G (p.Ile1092Ser) c.3995T>G (p.Ile1332Ser) | ClinVar |
17 | g.50185833A>G | CA400191669 | COL1A1 | c.4193T>C (p.Ile1398Thr) c.3923T>C (p.Ile1308Thr) c.3275T>C (p.Ile1092Thr) c.3995T>C (p.Ile1332Thr) | |
17 | g.50185833A>T | CA400191671 | COL1A1 | c.4193T>A (p.Ile1398Asn) c.3923T>A (p.Ile1308Asn) c.3275T>A (p.Ile1092Asn) c.3995T>A (p.Ile1332Asn) | |
17 | g.50185834T>A | CA8644237 | COL1A1 | c.4192A>T (p.Ile1398Phe) c.3922A>T (p.Ile1308Phe) c.3274A>T (p.Ile1092Phe) c.3994A>T (p.Ile1332Phe) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.50185834T>C | CA400191675 | COL1A1 | c.4192A>G (p.Ile1398Val) c.3922A>G (p.Ile1308Val) c.3274A>G (p.Ile1092Val) c.3994A>G (p.Ile1332Val) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
17 | g.50185834T>G | CA400191677 | COL1A1 | c.4192A>C (p.Ile1398Leu) c.3922A>C (p.Ile1308Leu) c.3274A>C (p.Ile1092Leu) c.3994A>C (p.Ile1332Leu) | dbSNP |
17 | g.50185834T= | CA2263913875 | COL1A1 | c.4192A= (p.Ile1398=) c.3922A= (p.Ile1308=) c.3274A= (p.Ile1092=) c.3994A= (p.Ile1332=) | |
17 | g.50185835C>A | CA400191680 | COL1A1 | c.4191G>T (p.Glu1397Asp) c.3921G>T (p.Glu1307Asp) c.3273G>T (p.Glu1091Asp) c.3993G>T (p.Glu1331Asp) | ClinVar |
17 | g.50185835C>G | CA400191683 | COL1A1 | c.4191G>C (p.Glu1397Asp) c.3921G>C (p.Glu1307Asp) c.3273G>C (p.Glu1091Asp) c.3993G>C (p.Glu1331Asp) | |
17 | g.50185835C>T | CA500991621 | COL1A1 | c.4191G>A (p.Glu1397=) c.3921G>A (p.Glu1307=) c.3273G>A (p.Glu1091=) c.3993G>A (p.Glu1331=) | gnomAD v4 |
17 | g.50185836T>A | CA400191687 | COL1A1 | c.4190A>T (p.Glu1397Val) c.3920A>T (p.Glu1307Val) c.3272A>T (p.Glu1091Val) c.3992A>T (p.Glu1331Val) | |
17 | g.50185836T>C | CA400191686 | COL1A1 | c.4190A>G (p.Glu1397Gly) c.3920A>G (p.Glu1307Gly) c.3272A>G (p.Glu1091Gly) c.3992A>G (p.Glu1331Gly) | |
17 | g.50185836T>G | CA400191685 | COL1A1 | c.4190A>C (p.Glu1397Ala) c.3920A>C (p.Glu1307Ala) c.3272A>C (p.Glu1091Ala) c.3992A>C (p.Glu1331Ala) | |
17 | g.50185837C>A | CA400191688 | COL1A1 | c.4189G>T (p.Glu1397Ter) c.3919G>T (p.Glu1307Ter) c.3271G>T (p.Glu1091Ter) c.3991G>T (p.Glu1331Ter) | ClinVar dbSNP |
17 | g.50185837C= | CA2263913876 | COL1A1 | c.4189G= (p.Glu1397=) c.3919G= (p.Glu1307=) c.3271G= (p.Glu1091=) c.3991G= (p.Glu1331=) | |
17 | g.50185837C>G | CA291542792 | COL1A1 | c.4189G>C (p.Glu1397Gln) c.3919G>C (p.Glu1307Gln) c.3271G>C (p.Glu1091Gln) c.3991G>C (p.Glu1331Gln) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.50185837C>T | CA400191690 | COL1A1 | c.4189G>A (p.Glu1397Lys) c.3919G>A (p.Glu1307Lys) c.3271G>A (p.Glu1091Lys) c.3991G>A (p.Glu1331Lys) | ClinVar gnomAD v4 |
17 | g.50185838G>A | CA8644238 | COL1A1 | c.4188C>T (p.Ile1396=) c.3918C>T (p.Ile1306=) c.3270C>T (p.Ile1090=) c.3990C>T (p.Ile1330=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.50185838G>C | CA400191694 | COL1A1 | c.4188C>G (p.Ile1396Met) c.3918C>G (p.Ile1306Met) c.3270C>G (p.Ile1090Met) c.3990C>G (p.Ile1330Met) | gnomAD v4 |
17 | g.50185838G= | CA2263913877 | COL1A1 | c.4188C= (p.Ile1396=) c.3918C= (p.Ile1306=) c.3270C= (p.Ile1090=) c.3990C= (p.Ile1330=) | |
17 | g.50185838G>T | CA500991627 | COL1A1 | c.4188C>A (p.Ile1396=) c.3918C>A (p.Ile1306=) c.3270C>A (p.Ile1090=) c.3990C>A (p.Ile1330=) | |
17 | g.50185839A= | CA2263913878 | COL1A1 | c.4187T= (p.Ile1396=) c.3917T= (p.Ile1306=) c.3269T= (p.Ile1090=) c.3989T= (p.Ile1330=) | |
17 | g.50185839A>C | CA400191695 | COL1A1 | c.4187T>G (p.Ile1396Ser) c.3917T>G (p.Ile1306Ser) c.3269T>G (p.Ile1090Ser) c.3989T>G (p.Ile1330Ser) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.50185839A>G | CA400191698 | COL1A1 | c.4187T>C (p.Ile1396Thr) c.3917T>C (p.Ile1306Thr) c.3269T>C (p.Ile1090Thr) c.3989T>C (p.Ile1330Thr) | |
17 | g.50185839A>T | CA400191699 | COL1A1 | c.4187T>A (p.Ile1396Asn) c.3917T>A (p.Ile1306Asn) c.3269T>A (p.Ile1090Asn) c.3989T>A (p.Ile1330Asn) | |
17 | g.50185840T>A | CA400191701 | COL1A1 | c.4186A>T (p.Ile1396Phe) c.3916A>T (p.Ile1306Phe) c.3268A>T (p.Ile1090Phe) c.3988A>T (p.Ile1330Phe) | |
17 | g.50185840T>C | CA400191703 | COL1A1 | c.4186A>G (p.Ile1396Val) c.3916A>G (p.Ile1306Val) c.3268A>G (p.Ile1090Val) c.3988A>G (p.Ile1330Val) | |
17 | g.50185840T>G | CA400191706 | COL1A1 | c.4186A>C (p.Ile1396Leu) c.3916A>C (p.Ile1306Leu) c.3268A>C (p.Ile1090Leu) c.3988A>C (p.Ile1330Leu) | |
17 | g.50185841C>A | CA400191709 | COL1A1 | c.4185G>T (p.Glu1395Asp) c.3915G>T (p.Glu1305Asp) c.3267G>T (p.Glu1089Asp) c.3987G>T (p.Glu1329Asp) | |
17 | g.50185841C>G | CA400191711 | COL1A1 | c.4185G>C (p.Glu1395Asp) c.3915G>C (p.Glu1305Asp) c.3267G>C (p.Glu1089Asp) c.3987G>C (p.Glu1329Asp) | |
17 | g.50185841C>T | CA500991630 | COL1A1 | c.4185G>A (p.Glu1395=) c.3915G>A (p.Glu1305=) c.3267G>A (p.Glu1089=) c.3987G>A (p.Glu1329=) | |
17 | g.50185842T>A | CA400191718 | COL1A1 | c.4184A>T (p.Glu1395Val) c.3914A>T (p.Glu1305Val) c.3266A>T (p.Glu1089Val) c.3986A>T (p.Glu1329Val) | |
17 | g.50185842T>C | CA400191714 | COL1A1 | c.4184A>G (p.Glu1395Gly) c.3914A>G (p.Glu1305Gly) c.3266A>G (p.Glu1089Gly) c.3986A>G (p.Glu1329Gly) | |
17 | g.50185842T>G | CA400191716 | COL1A1 | c.4184A>C (p.Glu1395Ala) c.3914A>C (p.Glu1305Ala) c.3266A>C (p.Glu1089Ala) c.3986A>C (p.Glu1329Ala) | |
17 | g.50185843C>A | CA400191720 | COL1A1 | c.4183G>T (p.Glu1395Ter) c.3913G>T (p.Glu1305Ter) c.3265G>T (p.Glu1089Ter) c.3985G>T (p.Glu1329Ter) | ClinVar COSMIC |
17 | g.50185843C= | CA2263913879 | COL1A1 | c.4183G= (p.Glu1395=) c.3913G= (p.Glu1305=) c.3265G= (p.Glu1089=) c.3985G= (p.Glu1329=) | |
17 | g.50185843C>G | CA400191722 | COL1A1 | c.4183G>C (p.Glu1395Gln) c.3913G>C (p.Glu1305Gln) c.3265G>C (p.Glu1089Gln) c.3985G>C (p.Glu1329Gln) | |
17 | g.50185843C>T | CA8644239 | COL1A1 | c.4183G>A (p.Glu1395Lys) c.3913G>A (p.Glu1305Lys) c.3265G>A (p.Glu1089Lys) c.3985G>A (p.Glu1329Lys) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.50185843_50185846delinsCGTT | CA2263913880 | COL1A1 | c.4180_4183delinsAACG (p.Asn1394=) c.3910_3913delinsAACG (p.Asn1304=) c.3262_3265delinsAACG (p.Asn1088=) c.3982_3985delinsAACG (p.Asn1328=) | |
17 | g.50185844G>A | CA8644240 | COL1A1 | c.4182C>T (p.Asn1394=) n.1147C>T c.3912C>T (p.Asn1304=) c.3264C>T (p.Asn1088=) c.3984C>T (p.Asn1328=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.50185844G>C | CA400191728 | COL1A1 | c.4182C>G (p.Asn1394Lys) n.1147C>G c.3912C>G (p.Asn1304Lys) c.3264C>G (p.Asn1088Lys) c.3984C>G (p.Asn1328Lys) | |
17 | g.50185844G= | CA2263913881 | COL1A1 | c.4182C= (p.Asn1394=) n.1147C= c.3912C= (p.Asn1304=) c.3264C= (p.Asn1088=) c.3984C= (p.Asn1328=) | |
17 | g.50185844G>T | CA8644241 | COL1A1 | c.4182C>A (p.Asn1394Lys) n.1147C>A c.3912C>A (p.Asn1304Lys) c.3264C>A (p.Asn1088Lys) c.3984C>A (p.Asn1328Lys) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.50185845_50185847del | CA984452345 | COL1A1 | c.4180_4182del (p.Asn1394del) n.1145_1147del c.3910_3912del (p.Asn1304del) c.3262_3264del (p.Asn1088del) c.3982_3984del (p.Asn1328del) | ClinVar dbSNP gnomAD v3 gnomAD v4 |
17 | g.50185845T>A | CA400191732 | COL1A1 | c.4181A>T (p.Asn1394Ile) n.1146A>T c.3911A>T (p.Asn1304Ile) c.3263A>T (p.Asn1088Ile) c.3983A>T (p.Asn1328Ile) | |
17 | g.50185845T>C | CA8644242 | COL1A1 | c.4181A>G (p.Asn1394Ser) n.1146A>G c.3911A>G (p.Asn1304Ser) c.3263A>G (p.Asn1088Ser) c.3983A>G (p.Asn1328Ser) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.50185845T>G | CA400191734 | COL1A1 | c.4181A>C (p.Asn1394Thr) n.1146A>C c.3911A>C (p.Asn1304Thr) c.3263A>C (p.Asn1088Thr) c.3983A>C (p.Asn1328Thr) | |
17 | g.50185845T= | CA2263913882 | COL1A1 | c.4181A= (p.Asn1394=) n.1146A= c.3911A= (p.Asn1304=) c.3263A= (p.Asn1088=) c.3983A= (p.Asn1328=) | |
17 | g.50185846T>A | CA400191736 | COL1A1 | c.4180A>T (p.Asn1394Tyr) n.1145A>T c.3910A>T (p.Asn1304Tyr) c.3262A>T (p.Asn1088Tyr) c.3982A>T (p.Asn1328Tyr) | |
17 | g.50185846T>C | CA400191738 | COL1A1 | c.4180A>G (p.Asn1394Asp) n.1145A>G c.3910A>G (p.Asn1304Asp) c.3262A>G (p.Asn1088Asp) c.3982A>G (p.Asn1328Asp) | |
17 | g.50185846T>G | CA400191739 | COL1A1 | c.4180A>C (p.Asn1394His) n.1145A>C c.3910A>C (p.Asn1304His) c.3262A>C (p.Asn1088His) c.3982A>C (p.Asn1328His) | |
17 | g.50185847G>A | CA8644243 | COL1A1 | c.4179C>T (p.Ser1393=) n.1144C>T c.3909C>T (p.Ser1303=) c.3261C>T (p.Ser1087=) c.3981C>T (p.Ser1327=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.50185847G>C | CA500991640 | COL1A1 | c.4179C>G (p.Ser1393=) n.1144C>G c.3909C>G (p.Ser1303=) c.3261C>G (p.Ser1087=) c.3981C>G (p.Ser1327=) | |
17 | g.50185847G= | CA2263913883 | COL1A1 | c.4179C= (p.Ser1393=) n.1144C= c.3909C= (p.Ser1303=) c.3261C= (p.Ser1087=) c.3981C= (p.Ser1327=) | |
17 | g.50185847G>T | CA500991642 | COL1A1 | c.4179C>A (p.Ser1393=) n.1144C>A c.3909C>A (p.Ser1303=) c.3261C>A (p.Ser1087=) c.3981C>A (p.Ser1327=) | |
17 | g.50185848G>A | CA8644244 | COL1A1 | c.4178C>T (p.Ser1393Phe) n.1143C>T c.3908C>T (p.Ser1303Phe) c.3260C>T (p.Ser1087Phe) c.3980C>T (p.Ser1327Phe) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.50185848G>C | CA400191740 | COL1A1 | c.4178C>G (p.Ser1393Cys) n.1143C>G c.3908C>G (p.Ser1303Cys) c.3260C>G (p.Ser1087Cys) c.3980C>G (p.Ser1327Cys) | |
17 | g.50185848G= | CA2263913884 | COL1A1 | c.4178C= (p.Ser1393=) n.1143C= c.3908C= (p.Ser1303=) c.3260C= (p.Ser1087=) c.3980C= (p.Ser1327=) | |
17 | g.50185848G>T | CA400191741 | COL1A1 | c.4178C>A (p.Ser1393Tyr) n.1143C>A c.3908C>A (p.Ser1303Tyr) c.3260C>A (p.Ser1087Tyr) c.3980C>A (p.Ser1327Tyr) | |
17 | g.50185849A= | CA2263913885 | COL1A1 | c.4177T= (p.Ser1393=) n.1142T= c.3907T= (p.Ser1303=) c.3259T= (p.Ser1087=) c.3979T= (p.Ser1327=) | |
17 | g.50185849A>C | CA400191742 | COL1A1 | c.4177T>G (p.Ser1393Ala) n.1142T>G c.3907T>G (p.Ser1303Ala) c.3259T>G (p.Ser1087Ala) c.3979T>G (p.Ser1327Ala) | dbSNP |
17 | g.50185849A>G | CA400191744 | COL1A1 | c.4177T>C (p.Ser1393Pro) n.1142T>C c.3907T>C (p.Ser1303Pro) c.3259T>C (p.Ser1087Pro) c.3979T>C (p.Ser1327Pro) | |
17 | g.50185849A>T | CA400191746 | COL1A1 | c.4177T>A (p.Ser1393Thr) n.1142T>A c.3907T>A (p.Ser1303Thr) c.3259T>A (p.Ser1087Thr) c.3979T>A (p.Ser1327Thr) | ClinVar gnomAD v4 |
17 | g.50185850G>A | CA8644245 | COL1A1 | c.4176C>T (p.Gly1392=) n.1141C>T c.3906C>T (p.Gly1302=) c.3258C>T (p.Gly1086=) c.3978C>T (p.Gly1326=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.50185850G>C | CA500991646 | COL1A1 | c.4176C>G (p.Gly1392=) n.1141C>G c.3906C>G (p.Gly1302=) c.3258C>G (p.Gly1086=) c.3978C>G (p.Gly1326=) | |
17 | g.50185850G= | CA2263913886 | COL1A1 | c.4176C= (p.Gly1392=) n.1141C= c.3906C= (p.Gly1302=) c.3258C= (p.Gly1086=) c.3978C= (p.Gly1326=) | |
17 | g.50185850G>T | CA500991647 | COL1A1 | c.4176C>A (p.Gly1392=) n.1141C>A c.3906C>A (p.Gly1302=) c.3258C>A (p.Gly1086=) c.3978C>A (p.Gly1326=) | dbSNP |
17 | g.50185851C>A | CA400191753 | COL1A1 | c.4175G>T (p.Gly1392Val) n.1140G>T c.3905G>T (p.Gly1302Val) c.3257G>T (p.Gly1086Val) c.3977G>T (p.Gly1326Val) | |
17 | g.50185851C= | CA2263913887 | COL1A1 | c.4175G= (p.Gly1392=) n.1140G= c.3905G= (p.Gly1302=) c.3257G= (p.Gly1086=) c.3977G= (p.Gly1326=) | |
17 | g.50185851C>G | CA8644246 | COL1A1 | c.4175G>C (p.Gly1392Ala) n.1140G>C c.3905G>C (p.Gly1302Ala) c.3257G>C (p.Gly1086Ala) c.3977G>C (p.Gly1326Ala) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.50185851C>T | CA400191751 | COL1A1 | c.4175G>A (p.Gly1392Asp) n.1140G>A c.3905G>A (p.Gly1302Asp) c.3257G>A (p.Gly1086Asp) c.3977G>A (p.Gly1326Asp) | |
17 | g.50185852C>A | CA400191756 | COL1A1 | c.4174G>T (p.Gly1392Cys) n.1139G>T c.3904G>T (p.Gly1302Cys) c.3256G>T (p.Gly1086Cys) c.3976G>T (p.Gly1326Cys) | |
17 | g.50185852C= | CA2263913888 | COL1A1 | c.4174G= (p.Gly1392=) n.1139G= c.3904G= (p.Gly1302=) c.3256G= (p.Gly1086=) c.3976G= (p.Gly1326=) | |
17 | g.50185852C>G | CA400191758 | COL1A1 | c.4174G>C (p.Gly1392Arg) n.1139G>C c.3904G>C (p.Gly1302Arg) c.3256G>C (p.Gly1086Arg) c.3976G>C (p.Gly1326Arg) | |
17 | g.50185852C>T | CA291542793 | COL1A1 | c.4174G>A (p.Gly1392Ser) n.1139G>A c.3904G>A (p.Gly1302Ser) c.3256G>A (p.Gly1086Ser) c.3976G>A (p.Gly1326Ser) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.50185853C>A | CA400191762 | COL1A1 | c.4173G>T (p.Gln1391His) n.1138G>T c.3903G>T (p.Gln1301His) c.3255G>T (p.Gln1085His) c.3975G>T (p.Gln1325His) | |
17 | g.50185853C>G | CA400191764 | COL1A1 | c.4173G>C (p.Gln1391His) n.1138G>C c.3903G>C (p.Gln1301His) c.3255G>C (p.Gln1085His) c.3975G>C (p.Gln1325His) | |
17 | g.50185853C>T | CA500991654 | COL1A1 | c.4173G>A (p.Gln1391=) n.1138G>A c.3903G>A (p.Gln1301=) c.3255G>A (p.Gln1085=) c.3975G>A (p.Gln1325=) | |
17 | g.50185854T>A | CA400191767 | COL1A1 | c.4172A>T (p.Gln1391Leu) n.1137A>T c.3902A>T (p.Gln1301Leu) c.3254A>T (p.Gln1085Leu) c.3974A>T (p.Gln1325Leu) | |
17 | g.50185854T>C | CA8644247 | COL1A1 | c.4172A>G (p.Gln1391Arg) n.1137A>G c.3902A>G (p.Gln1301Arg) c.3254A>G (p.Gln1085Arg) c.3974A>G (p.Gln1325Arg) | dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.50185854T>G | CA400191766 | COL1A1 | c.4172A>C (p.Gln1391Pro) n.1137A>C c.3902A>C (p.Gln1301Pro) c.3254A>C (p.Gln1085Pro) c.3974A>C (p.Gln1325Pro) | |
17 | g.50185854T= | CA2263913889 | COL1A1 | c.4172A= (p.Gln1391=) n.1137A= c.3902A= (p.Gln1301=) c.3254A= (p.Gln1085=) c.3974A= (p.Gln1325=) | |
17 | g.50185855G>A | CA400191768 | COL1A1 | c.4171C>T (p.Gln1391Ter) n.1136C>T c.3901C>T (p.Gln1301Ter) c.3253C>T (p.Gln1085Ter) c.3973C>T (p.Gln1325Ter) | ClinVar dbSNP |
17 | g.50185855G>C | CA400191770 | COL1A1 | c.4171C>G (p.Gln1391Glu) n.1136C>G c.3901C>G (p.Gln1301Glu) c.3253C>G (p.Gln1085Glu) c.3973C>G (p.Gln1325Glu) | |
17 | g.50185855G= | CA2263913890 | COL1A1 | c.4171C= (p.Gln1391=) n.1136C= c.3901C= (p.Gln1301=) c.3253C= (p.Gln1085=) c.3973C= (p.Gln1325=) | |
17 | g.50185855G>T | CA291542794 | COL1A1 | c.4171C>A (p.Gln1391Lys) n.1136C>A c.3901C>A (p.Gln1301Lys) c.3253C>A (p.Gln1085Lys) c.3973C>A (p.Gln1325Lys) | dbSNP |
17 | g.50185856G>A | CA8644248 | COL1A1 | c.4170C>T (p.Leu1390=) n.1135C>T c.3900C>T (p.Leu1300=) c.3252C>T (p.Leu1084=) c.3972C>T (p.Leu1324=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.50185856G>C | CA500991656 | COL1A1 | c.4170C>G (p.Leu1390=) n.1135C>G c.3900C>G (p.Leu1300=) c.3252C>G (p.Leu1084=) c.3972C>G (p.Leu1324=) | |
17 | g.50185856G= | CA2263913891 | COL1A1 | c.4170C= (p.Leu1390=) n.1135C= c.3900C= (p.Leu1300=) c.3252C= (p.Leu1084=) c.3972C= (p.Leu1324=) | |
17 | g.50185856G>T | CA500991657 | COL1A1 | c.4170C>A (p.Leu1390=) n.1135C>A c.3900C>A (p.Leu1300=) c.3252C>A (p.Leu1084=) c.3972C>A (p.Leu1324=) | |
17 | g.50185857A>C | CA400191772 | COL1A1 | c.4169T>G (p.Leu1390Arg) n.1134T>G c.3899T>G (p.Leu1300Arg) c.3251T>G (p.Leu1084Arg) c.3971T>G (p.Leu1324Arg) | |
17 | g.50185857A>G | CA400191774 | COL1A1 | c.4169T>C (p.Leu1390Pro) n.1134T>C c.3899T>C (p.Leu1300Pro) c.3251T>C (p.Leu1084Pro) c.3971T>C (p.Leu1324Pro) | |
17 | g.50185857A>T | CA400191775 | COL1A1 | c.4169T>A (p.Leu1390His) n.1134T>A c.3899T>A (p.Leu1300His) c.3251T>A (p.Leu1084His) c.3971T>A (p.Leu1324His) | |
17 | g.50185858G>A | CA8644249 | COL1A1 | c.4168C>T (p.Leu1390Phe) n.1133C>T c.3898C>T (p.Leu1300Phe) c.3250C>T (p.Leu1084Phe) c.3970C>T (p.Leu1324Phe) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.50185858G>C | CA400191785 | COL1A1 | c.4168C>G (p.Leu1390Val) n.1133C>G c.3898C>G (p.Leu1300Val) c.3250C>G (p.Leu1084Val) c.3970C>G (p.Leu1324Val) | |
17 | g.50185858G= | CA2263913892 | COL1A1 | c.4168C= (p.Leu1390=) n.1133C= c.3898C= (p.Leu1300=) c.3250C= (p.Leu1084=) c.3970C= (p.Leu1324=) | |
17 | g.50185858G>T | CA400191787 | COL1A1 | c.4168C>A (p.Leu1390Ile) n.1133C>A c.3898C>A (p.Leu1300Ile) c.3250C>A (p.Leu1084Ile) c.3970C>A (p.Leu1324Ile) | |
17 | g.50185859G>A | CA500991662 | COL1A1 | c.4167C>T (p.Leu1389=) n.1132C>T c.3897C>T (p.Leu1299=) c.3249C>T (p.Leu1083=) c.3969C>T (p.Leu1323=) | |
17 | g.50185859G>C | CA500991661 | COL1A1 | c.4167C>G (p.Leu1389=) n.1132C>G c.3897C>G (p.Leu1299=) c.3249C>G (p.Leu1083=) c.3969C>G (p.Leu1323=) | dbSNP |
17 | g.50185859G= | CA2263913893 | COL1A1 | c.4167C= (p.Leu1389=) n.1132C= c.3897C= (p.Leu1299=) c.3249C= (p.Leu1083=) c.3969C= (p.Leu1323=) | |
17 | g.50185859G>T | CA500991659 | COL1A1 | c.4167C>A (p.Leu1389=) n.1132C>A c.3897C>A (p.Leu1299=) c.3249C>A (p.Leu1083=) c.3969C>A (p.Leu1323=) | |
17 | g.50185860A>C | CA400191789 | COL1A1 | c.4166T>G (p.Leu1389Arg) n.1131T>G c.3896T>G (p.Leu1299Arg) c.3248T>G (p.Leu1083Arg) c.3968T>G (p.Leu1323Arg) | |
17 | g.50185860A>G | CA400191791 | COL1A1 | c.4166T>C (p.Leu1389Pro) n.1131T>C c.3896T>C (p.Leu1299Pro) c.3248T>C (p.Leu1083Pro) c.3968T>C (p.Leu1323Pro) | ClinVar dbSNP |
17 | g.50185860A>T | CA400191794 | COL1A1 | c.4166T>A (p.Leu1389His) n.1131T>A c.3896T>A (p.Leu1299His) c.3248T>A (p.Leu1083His) c.3968T>A (p.Leu1323His) | |
17 | g.50185861G>A | CA400191797 | COL1A1 | c.4165C>T (p.Leu1389Phe) n.1130C>T c.3895C>T (p.Leu1299Phe) c.3247C>T (p.Leu1083Phe) c.3967C>T (p.Leu1323Phe) | |
17 | g.50185861G>C | CA400191800 | COL1A1 | c.4165C>G (p.Leu1389Val) n.1130C>G c.3895C>G (p.Leu1299Val) c.3247C>G (p.Leu1083Val) c.3967C>G (p.Leu1323Val) | |
17 | g.50185861G>T | CA400191798 | COL1A1 | c.4165C>A (p.Leu1389Ile) n.1130C>A c.3895C>A (p.Leu1299Ile) c.3247C>A (p.Leu1083Ile) c.3967C>A (p.Leu1323Ile) | |
17 | g.50185862C>A | CA500991668 | COL1A1 | c.4164G>T (p.Leu1388=) n.1129G>T c.3894G>T (p.Leu1298=) c.3246G>T (p.Leu1082=) c.3966G>T (p.Leu1322=) | dbSNP gnomAD v4 |
17 | g.50185862C= | CA2263913894 | COL1A1 | c.4164G= (p.Leu1388=) n.1129G= c.3894G= (p.Leu1298=) c.3246G= (p.Leu1082=) c.3966G= (p.Leu1322=) | |
17 | g.50185862C>G | CA500991667 | COL1A1 | c.4164G>C (p.Leu1388=) n.1129G>C c.3894G>C (p.Leu1298=) c.3246G>C (p.Leu1082=) c.3966G>C (p.Leu1322=) | |
17 | g.50185862C>T | CA500991666 | COL1A1 | c.4164G>A (p.Leu1388=) n.1129G>A c.3894G>A (p.Leu1298=) c.3246G>A (p.Leu1082=) c.3966G>A (p.Leu1322=) | |
17 | g.50185863A= | CA2263913895 | COL1A1 | c.4163T= (p.Leu1388=) n.1128T= c.3893T= (p.Leu1298=) c.3245T= (p.Leu1082=) c.3965T= (p.Leu1322=) | |
17 | g.50185863A>C | CA291542795 | COL1A1 | c.4163T>G (p.Leu1388Arg) n.1128T>G c.3893T>G (p.Leu1298Arg) c.3245T>G (p.Leu1082Arg) c.3965T>G (p.Leu1322Arg) | dbSNP |
17 | g.50185863A>G | CA400191803 | COL1A1 | c.4163T>C (p.Leu1388Pro) n.1128T>C c.3893T>C (p.Leu1298Pro) c.3245T>C (p.Leu1082Pro) c.3965T>C (p.Leu1322Pro) | ClinVar dbSNP |
17 | g.50185863A>T | CA400191804 | COL1A1 | c.4163T>A (p.Leu1388Gln) n.1128T>A c.3893T>A (p.Leu1298Gln) c.3245T>A (p.Leu1082Gln) c.3965T>A (p.Leu1322Gln) | |
17 | g.50185864G>A | CA500991671 | COL1A1 | c.4162C>T (p.Leu1388=) n.1127C>T c.3892C>T (p.Leu1298=) c.3244C>T (p.Leu1082=) c.3964C>T (p.Leu1322=) | COSMIC |
17 | g.50185864G>C | CA400191806 | COL1A1 | c.4162C>G (p.Leu1388Val) n.1127C>G c.3892C>G (p.Leu1298Val) c.3244C>G (p.Leu1082Val) c.3964C>G (p.Leu1322Val) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.50185864G= | CA2263913896 | COL1A1 | c.4162C= (p.Leu1388=) n.1127C= c.3892C= (p.Leu1298=) c.3244C= (p.Leu1082=) c.3964C= (p.Leu1322=) | |
17 | g.50185864G>T | CA400191808 | COL1A1 | c.4162C>A (p.Leu1388Met) n.1127C>A c.3892C>A (p.Leu1298Met) c.3244C>A (p.Leu1082Met) c.3964C>A (p.Leu1322Met) | |
17 | g.50185865G>A | CA500991673 | COL1A1 | c.4161C>T (p.Ala1387=) n.1126C>T c.3891C>T (p.Ala1297=) c.3243C>T (p.Ala1081=) c.3963C>T (p.Ala1321=) | dbSNP gnomAD v3 gnomAD v4 COSMIC |
17 | g.50185865G>C | CA500991675 | COL1A1 | c.4161C>G (p.Ala1387=) n.1126C>G c.3891C>G (p.Ala1297=) c.3243C>G (p.Ala1081=) c.3963C>G (p.Ala1321=) | |
17 | g.50185865G= | CA2263913897 | COL1A1 | c.4161C= (p.Ala1387=) n.1126C= c.3891C= (p.Ala1297=) c.3243C= (p.Ala1081=) c.3963C= (p.Ala1321=) | |
17 | g.50185865G>T | CA500991674 | COL1A1 | c.4161C>A (p.Ala1387=) n.1126C>A c.3891C>A (p.Ala1297=) c.3243C>A (p.Ala1081=) c.3963C>A (p.Ala1321=) | |
17 | g.50185866G>A | CA261266 | COL1A1 | c.4160C>T (p.Ala1387Val) n.1125C>T c.3890C>T (p.Ala1297Val) c.3242C>T (p.Ala1081Val) c.3962C>T (p.Ala1321Val) | ClinVar dbSNP |
17 | g.50185866G>C | CA400191810 | COL1A1 | c.4160C>G (p.Ala1387Gly) n.1125C>G c.3890C>G (p.Ala1297Gly) c.3242C>G (p.Ala1081Gly) c.3962C>G (p.Ala1321Gly) | |
17 | g.50185866G= | CA2263913898 | COL1A1 | c.4160C= (p.Ala1387=) n.1125C= c.3890C= (p.Ala1297=) c.3242C= (p.Ala1081=) c.3962C= (p.Ala1321=) | |
17 | g.50185866G>T | CA400191811 | COL1A1 | c.4160C>A (p.Ala1387Asp) n.1125C>A c.3890C>A (p.Ala1297Asp) c.3242C>A (p.Ala1081Asp) c.3962C>A (p.Ala1321Asp) | |
17 | g.50185867C>A | CA400191813 | COL1A1 | c.4159G>T (p.Ala1387Ser) n.1124G>T c.3889G>T (p.Ala1297Ser) c.3241G>T (p.Ala1081Ser) c.3961G>T (p.Ala1321Ser) | dbSNP |
17 | g.50185867C= | CA2263913899 | COL1A1 | c.4159G= (p.Ala1387=) n.1124G= c.3889G= (p.Ala1297=) c.3241G= (p.Ala1081=) c.3961G= (p.Ala1321=) | |
17 | g.50185867C>G | CA400191815 | COL1A1 | c.4159G>C (p.Ala1387Pro) n.1124G>C c.3889G>C (p.Ala1297Pro) c.3241G>C (p.Ala1081Pro) c.3961G>C (p.Ala1321Pro) | |
17 | g.50185867C>T | CA400191818 | COL1A1 | c.4159G>A (p.Ala1387Thr) n.1124G>A c.3889G>A (p.Ala1297Thr) c.3241G>A (p.Ala1081Thr) c.3961G>A (p.Ala1321Thr) | ClinVar dbSNP |
17 | g.50185868del | CA645569622 | COL1A1 | c.4159del (p.Ala1387ProfsTer?) n.1124del c.3889del (p.Ala1297ProfsTer?) c.3241del (p.Ala1081ProfsTer?) c.3961del (p.Ala1321ProfsTer?) | COSMIC |
17 | g.50185868C>A | CA400191821 | COL1A1 | c.4158G>T (p.Lys1386Asn) n.1123G>T c.3888G>T (p.Lys1296Asn) c.3240G>T (p.Lys1080Asn) c.3960G>T (p.Lys1320Asn) | |
17 | g.50185868C= | CA2263913900 | COL1A1 | c.4158G= (p.Lys1386=) n.1123G= c.3888G= (p.Lys1296=) c.3240G= (p.Lys1080=) c.3960G= (p.Lys1320=) | |
17 | g.50185868C>G | CA400191823 | COL1A1 | c.4158G>C (p.Lys1386Asn) n.1123G>C c.3888G>C (p.Lys1296Asn) c.3240G>C (p.Lys1080Asn) c.3960G>C (p.Lys1320Asn) | |
17 | g.50185868C>T | CA500991678 | COL1A1 | c.4158G>A (p.Lys1386=) n.1123G>A c.3888G>A (p.Lys1296=) c.3240G>A (p.Lys1080=) c.3960G>A (p.Lys1320=) | dbSNP |
17 | g.50185869T>A | CA400191830 | COL1A1 | c.4157A>T (p.Lys1386Met) n.1122A>T c.3887A>T (p.Lys1296Met) c.3239A>T (p.Lys1080Met) c.3959A>T (p.Lys1320Met) | |
17 | g.50185869T>C | CA400191826 | COL1A1 | c.4157A>G (p.Lys1386Arg) n.1122A>G c.3887A>G (p.Lys1296Arg) c.3239A>G (p.Lys1080Arg) c.3959A>G (p.Lys1320Arg) | |
17 | g.50185869T>G | CA400191828 | COL1A1 | c.4157A>C (p.Lys1386Thr) n.1122A>C c.3887A>C (p.Lys1296Thr) c.3239A>C (p.Lys1080Thr) c.3959A>C (p.Lys1320Thr) | |
17 | g.50185870T>A | CA400191834 | COL1A1 | c.4156A>T (p.Lys1386Ter) n.1121A>T c.3886A>T (p.Lys1296Ter) c.3238A>T (p.Lys1080Ter) c.3958A>T (p.Lys1320Ter) | |
17 | g.50185870T>C | CA400191836 | COL1A1 | c.4156A>G (p.Lys1386Glu) n.1121A>G c.3886A>G (p.Lys1296Glu) c.3238A>G (p.Lys1080Glu) c.3958A>G (p.Lys1320Glu) | |
17 | g.50185870T>G | CA400191838 | COL1A1 | c.4156A>C (p.Lys1386Gln) n.1121A>C c.3886A>C (p.Lys1296Gln) c.3238A>C (p.Lys1080Gln) c.3958A>C (p.Lys1320Gln) | |
17 | g.50185871C>A | CA400191840 | COL1A1 | c.4155G>T (p.Lys1385Asn) n.1120G>T c.3885G>T (p.Lys1295Asn) c.3237G>T (p.Lys1079Asn) c.3957G>T (p.Lys1319Asn) | |
17 | g.50185871C>G | CA400191842 | COL1A1 | c.4155G>C (p.Lys1385Asn) n.1120G>C c.3885G>C (p.Lys1295Asn) c.3237G>C (p.Lys1079Asn) c.3957G>C (p.Lys1319Asn) | |
17 | g.50185871C>T | CA500991682 | COL1A1 | c.4155G>A (p.Lys1385=) n.1120G>A c.3885G>A (p.Lys1295=) c.3237G>A (p.Lys1079=) c.3957G>A (p.Lys1319=) | ClinVar |
17 | g.50185872T>A | CA400191845 | COL1A1 | c.4154A>T (p.Lys1385Met) n.1119A>T c.3884A>T (p.Lys1295Met) c.3236A>T (p.Lys1079Met) c.3956A>T (p.Lys1319Met) | |
17 | g.50185872T>C | CA8644250 | COL1A1 | c.4154A>G (p.Lys1385Arg) n.1119A>G c.3884A>G (p.Lys1295Arg) c.3236A>G (p.Lys1079Arg) c.3956A>G (p.Lys1319Arg) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.50185872T>G | CA400191848 | COL1A1 | c.4154A>C (p.Lys1385Thr) n.1119A>C c.3884A>C (p.Lys1295Thr) c.3236A>C (p.Lys1079Thr) c.3956A>C (p.Lys1319Thr) | |
17 | g.50185872T= | CA2263913901 | COL1A1 | c.4154A= (p.Lys1385=) n.1119A= c.3884A= (p.Lys1295=) c.3236A= (p.Lys1079=) c.3956A= (p.Lys1319=) | |
17 | g.50185873T>A | CA400191851 | COL1A1 | c.4153A>T (p.Lys1385Ter) n.1118A>T c.3883A>T (p.Lys1295Ter) c.3235A>T (p.Lys1079Ter) c.3955A>T (p.Lys1319Ter) | |
17 | g.50185873T>C | CA400191853 | COL1A1 | c.4153A>G (p.Lys1385Glu) n.1118A>G c.3883A>G (p.Lys1295Glu) c.3235A>G (p.Lys1079Glu) c.3955A>G (p.Lys1319Glu) | |
17 | g.50185873T>G | CA400191857 | COL1A1 | c.4153A>C (p.Lys1385Gln) n.1118A>C c.3883A>C (p.Lys1295Gln) c.3235A>C (p.Lys1079Gln) c.3955A>C (p.Lys1319Gln) | gnomAD v4 |
17 | g.50185874G>A | CA500991687 | COL1A1 | c.4152C>T (p.Leu1384=) n.1117C>T c.3882C>T (p.Leu1294=) c.3234C>T (p.Leu1078=) c.3954C>T (p.Leu1318=) | |
17 | g.50185874G>C | CA500991688 | COL1A1 | c.4152C>G (p.Leu1384=) n.1117C>G c.3882C>G (p.Leu1294=) c.3234C>G (p.Leu1078=) c.3954C>G (p.Leu1318=) | dbSNP |
17 | g.50185874G= | CA2263913902 | COL1A1 | c.4152C= (p.Leu1384=) n.1117C= c.3882C= (p.Leu1294=) c.3234C= (p.Leu1078=) c.3954C= (p.Leu1318=) | |
17 | g.50185874G>T | CA500991690 | COL1A1 | c.4152C>A (p.Leu1384=) n.1117C>A c.3882C>A (p.Leu1294=) c.3234C>A (p.Leu1078=) c.3954C>A (p.Leu1318=) | |
17 | g.50185875A>C | CA400191861 | COL1A1 | c.4151T>G (p.Leu1384Arg) n.1116T>G c.3881T>G (p.Leu1294Arg) c.3233T>G (p.Leu1078Arg) c.3953T>G (p.Leu1318Arg) | |
17 | g.50185875A>G | CA400191867 | COL1A1 | c.4151T>C (p.Leu1384Pro) n.1116T>C c.3881T>C (p.Leu1294Pro) c.3233T>C (p.Leu1078Pro) c.3953T>C (p.Leu1318Pro) | |
17 | g.50185875A>T | CA400191864 | COL1A1 | c.4151T>A (p.Leu1384His) n.1116T>A c.3881T>A (p.Leu1294His) c.3233T>A (p.Leu1078His) c.3953T>A (p.Leu1318His) | |
17 | g.50185876G>A | CA291542796 | COL1A1 | c.4150C>T (p.Leu1384Phe) n.1115C>T c.3880C>T (p.Leu1294Phe) c.3232C>T (p.Leu1078Phe) c.3952C>T (p.Leu1318Phe) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.50185876G>C | CA400191873 | COL1A1 | c.4150C>G (p.Leu1384Val) n.1115C>G c.3880C>G (p.Leu1294Val) c.3232C>G (p.Leu1078Val) c.3952C>G (p.Leu1318Val) | COSMIC |
17 | g.50185876G= | CA2263913903 | COL1A1 | c.4150C= (p.Leu1384=) n.1115C= c.3880C= (p.Leu1294=) c.3232C= (p.Leu1078=) c.3952C= (p.Leu1318=) | |
17 | g.50185876G>T | CA400191878 | COL1A1 | c.4150C>A (p.Leu1384Ile) n.1115C>A c.3880C>A (p.Leu1294Ile) c.3232C>A (p.Leu1078Ile) c.3952C>A (p.Leu1318Ile) | |
17 | g.50185877G>A | CA8644251 | COL1A1 | c.4149C>T (p.Asn1383=) n.1114C>T c.3879C>T (p.Asn1293=) c.3231C>T (p.Asn1077=) c.3951C>T (p.Asn1317=) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.50185877G>C | CA400191885 | COL1A1 | c.4149C>G (p.Asn1383Lys) n.1114C>G c.3879C>G (p.Asn1293Lys) c.3231C>G (p.Asn1077Lys) c.3951C>G (p.Asn1317Lys) | |
17 | g.50185877G= | CA2263913904 | COL1A1 | c.4149C= (p.Asn1383=) n.1114C= c.3879C= (p.Asn1293=) c.3231C= (p.Asn1077=) c.3951C= (p.Asn1317=) | |
17 | g.50185877G>T | CA400191887 | COL1A1 | c.4149C>A (p.Asn1383Lys) n.1114C>A c.3879C>A (p.Asn1293Lys) c.3231C>A (p.Asn1077Lys) c.3951C>A (p.Asn1317Lys) | |
17 | g.50185878T>A | CA400191899 | COL1A1 | c.4148A>T (p.Asn1383Ile) n.1113A>T c.3878A>T (p.Asn1293Ile) c.3230A>T (p.Asn1077Ile) c.3950A>T (p.Asn1317Ile) | |
17 | g.50185878T>C | CA400191894 | COL1A1 | c.4148A>G (p.Asn1383Ser) n.1113A>G c.3878A>G (p.Asn1293Ser) c.3230A>G (p.Asn1077Ser) c.3950A>G (p.Asn1317Ser) | ClinVar dbSNP |
17 | g.50185878T>G | CA400191893 | COL1A1 | c.4148A>C (p.Asn1383Thr) n.1113A>C c.3878A>C (p.Asn1293Thr) c.3230A>C (p.Asn1077Thr) c.3950A>C (p.Asn1317Thr) | |
17 | g.50185878T= | CA2263913905 | COL1A1 | c.4148A= (p.Asn1383=) n.1113A= c.3878A= (p.Asn1293=) c.3230A= (p.Asn1077=) c.3950A= (p.Asn1317=) | |
17 | g.50185879T>A | CA400191903 | COL1A1 | c.4147A>T (p.Asn1383Tyr) n.1112A>T c.3877A>T (p.Asn1293Tyr) c.3229A>T (p.Asn1077Tyr) c.3949A>T (p.Asn1317Tyr) | |
17 | g.50185879T>C | CA400191910 | COL1A1 | c.4147A>G (p.Asn1383Asp) n.1112A>G c.3877A>G (p.Asn1293Asp) c.3229A>G (p.Asn1077Asp) c.3949A>G (p.Asn1317Asp) | |
17 | g.50185879T>G | CA400191913 | COL1A1 | c.4147A>C (p.Asn1383His) n.1112A>C c.3877A>C (p.Asn1293His) c.3229A>C (p.Asn1077His) c.3949A>C (p.Asn1317His) | |
17 | g.50185880G>A | CA500991697 | COL1A1 | c.4146C>T (p.Gly1382=) n.1111C>T c.3876C>T (p.Gly1292=) c.3228C>T (p.Gly1076=) c.3948C>T (p.Gly1316=) | |
17 | g.50185880G>C | CA500991698 | COL1A1 | c.4146C>G (p.Gly1382=) n.1111C>G c.3876C>G (p.Gly1292=) c.3228C>G (p.Gly1076=) c.3948C>G (p.Gly1316=) | |
17 | g.50185880G>T | CA500991696 | COL1A1 | c.4146C>A (p.Gly1382=) n.1111C>A c.3876C>A (p.Gly1292=) c.3228C>A (p.Gly1076=) c.3948C>A (p.Gly1316=) | |
17 | g.50185881C>A | CA400191917 | COL1A1 | c.4145G>T (p.Gly1382Val) n.1110G>T c.3875G>T (p.Gly1292Val) c.3227G>T (p.Gly1076Val) c.3947G>T (p.Gly1316Val) | |
17 | g.50185881C>G | CA400191920 | COL1A1 | c.4145G>C (p.Gly1382Ala) n.1110G>C c.3875G>C (p.Gly1292Ala) c.3227G>C (p.Gly1076Ala) c.3947G>C (p.Gly1316Ala) | |
17 | g.50185881C>T | CA400191923 | COL1A1 | c.4145G>A (p.Gly1382Asp) n.1110G>A c.3875G>A (p.Gly1292Asp) c.3227G>A (p.Gly1076Asp) c.3947G>A (p.Gly1316Asp) | COSMIC |
17 | g.50185882C>A | CA8644252 | COL1A1 | c.4144G>T (p.Gly1382Cys) n.1109G>T c.3874G>T (p.Gly1292Cys) c.3226G>T (p.Gly1076Cys) c.3946G>T (p.Gly1316Cys) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.50185882C= | CA2263913906 | COL1A1 | c.4144G= (p.Gly1382=) n.1109G= c.3874G= (p.Gly1292=) c.3226G= (p.Gly1076=) c.3946G= (p.Gly1316=) | |
17 | g.50185882C>G | CA400191931 | COL1A1 | c.4144G>C (p.Gly1382Arg) n.1109G>C c.3874G>C (p.Gly1292Arg) c.3226G>C (p.Gly1076Arg) c.3946G>C (p.Gly1316Arg) | |
17 | g.50185882C>T | CA400191928 | COL1A1 | c.4144G>A (p.Gly1382Ser) n.1109G>A c.3874G>A (p.Gly1292Ser) c.3226G>A (p.Gly1076Ser) c.3946G>A (p.Gly1316Ser) | |
17 | g.50185883A>C | CA500991705 | COL1A1 | c.4143T>G (p.Thr1381=) n.1108T>G c.3873T>G (p.Thr1291=) c.3225T>G (p.Thr1075=) c.3945T>G (p.Thr1315=) | |
17 | g.50185883A>G | CA500991706 | COL1A1 | c.4143T>C (p.Thr1381=) n.1108T>C c.3873T>C (p.Thr1291=) c.3225T>C (p.Thr1075=) c.3945T>C (p.Thr1315=) | |
17 | g.50185883A>T | CA500991707 | COL1A1 | c.4143T>A (p.Thr1381=) n.1108T>A c.3873T>A (p.Thr1291=) c.3225T>A (p.Thr1075=) c.3945T>A (p.Thr1315=) | |
17 | g.50185884G>A | CA400191934 | COL1A1 | c.4142C>T (p.Thr1381Ile) n.1107C>T c.3872C>T (p.Thr1291Ile) c.3224C>T (p.Thr1075Ile) c.3944C>T (p.Thr1315Ile) | |
17 | g.50185884G>C | CA400191936 | COL1A1 | c.4142C>G (p.Thr1381Ser) n.1107C>G c.3872C>G (p.Thr1291Ser) c.3224C>G (p.Thr1075Ser) c.3944C>G (p.Thr1315Ser) | |
17 | g.50185884G>T | CA400191938 | COL1A1 | c.4142C>A (p.Thr1381Asn) n.1107C>A c.3872C>A (p.Thr1291Asn) c.3224C>A (p.Thr1075Asn) c.3944C>A (p.Thr1315Asn) | |
17 | g.50185885T>A | CA400191942 | COL1A1 | c.4141A>T (p.Thr1381Ser) n.1106A>T c.3871A>T (p.Thr1291Ser) c.3223A>T (p.Thr1075Ser) c.3943A>T (p.Thr1315Ser) | |
17 | g.50185885T>C | CA291542797 | COL1A1 | c.4141A>G (p.Thr1381Ala) n.1106A>G c.3871A>G (p.Thr1291Ala) c.3223A>G (p.Thr1075Ala) c.3943A>G (p.Thr1315Ala) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
17 | g.50185885T>G | CA400191943 | COL1A1 | c.4141A>C (p.Thr1381Pro) n.1106A>C c.3871A>C (p.Thr1291Pro) c.3223A>C (p.Thr1075Pro) c.3943A>C (p.Thr1315Pro) | |
17 | g.50185885T= | CA2263913907 | COL1A1 | c.4141A= (p.Thr1381=) n.1106A= c.3871A= (p.Thr1291=) c.3223A= (p.Thr1075=) c.3943A= (p.Thr1315=) | |
17 | g.50185886C>A | CA400191944 | COL1A1 | c.4140G>T (p.Gln1380His) n.1105G>T c.3870G>T (p.Gln1290His) c.3222G>T (p.Gln1074His) c.3942G>T (p.Gln1314His) | |
17 | g.50185886C= | CA2263913908 | COL1A1 | c.4140G= (p.Gln1380=) n.1105G= c.3870G= (p.Gln1290=) c.3222G= (p.Gln1074=) c.3942G= (p.Gln1314=) | |
17 | g.50185886C>G | CA10640064 | COL1A1 | c.4140G>C (p.Gln1380His) n.1105G>C c.3870G>C (p.Gln1290His) c.3222G>C (p.Gln1074His) c.3942G>C (p.Gln1314His) | ClinVar dbSNP gnomAD v2 gnomAD v4 |
17 | g.50185886C>T | CA500991710 | COL1A1 | c.4140G>A (p.Gln1380=) n.1105G>A c.3870G>A (p.Gln1290=) c.3222G>A (p.Gln1074=) c.3942G>A (p.Gln1314=) | |
17 | g.50185887T>A | CA400191949 | COL1A1 | c.4139A>T (p.Gln1380Leu) n.1104A>T c.3869A>T (p.Gln1290Leu) c.3221A>T (p.Gln1074Leu) c.3941A>T (p.Gln1314Leu) | |
17 | g.50185887T>C | CA400191954 | COL1A1 | c.4139A>G (p.Gln1380Arg) n.1104A>G c.3869A>G (p.Gln1290Arg) c.3221A>G (p.Gln1074Arg) c.3941A>G (p.Gln1314Arg) | |
17 | g.50185887T>G | CA400191957 | COL1A1 | c.4139A>C (p.Gln1380Pro) n.1104A>C c.3869A>C (p.Gln1290Pro) c.3221A>C (p.Gln1074Pro) c.3941A>C (p.Gln1314Pro) | |
17 | g.50185888G>A | CA400191964 | COL1A1 | c.4138C>T (p.Gln1380Ter) n.1103C>T c.3868C>T (p.Gln1290Ter) c.3220C>T (p.Gln1074Ter) c.3940C>T (p.Gln1314Ter) | |
17 | g.50185888G>C | CA400191961 | COL1A1 | c.4138C>G (p.Gln1380Glu) n.1103C>G c.3868C>G (p.Gln1290Glu) c.3220C>G (p.Gln1074Glu) c.3940C>G (p.Gln1314Glu) | |
17 | g.50185888G>T | CA400191963 | COL1A1 | c.4138C>A (p.Gln1380Lys) n.1103C>A c.3868C>A (p.Gln1290Lys) c.3220C>A (p.Gln1074Lys) c.3940C>A (p.Gln1314Lys) | |
17 | g.50185889C>A | CA400191968 | COL1A1 | c.4137G>T (p.Gln1379His) n.1102G>T c.3867G>T (p.Gln1289His) c.3219G>T (p.Gln1073His) c.3939G>T (p.Gln1313His) | |
17 | g.50185889C= | CA2263913909 | COL1A1 | c.4137G= (p.Gln1379=) n.1102G= c.3867G= (p.Gln1289=) c.3219G= (p.Gln1073=) c.3939G= (p.Gln1313=) | |
17 | g.50185889C>G | CA400191971 | COL1A1 | c.4137G>C (p.Gln1379His) n.1102G>C c.3867G>C (p.Gln1289His) c.3219G>C (p.Gln1073His) c.3939G>C (p.Gln1313His) | |
17 | g.50185889C>T | CA500991711 | COL1A1 | c.4137G>A (p.Gln1379=) n.1102G>A c.3867G>A (p.Gln1289=) c.3219G>A (p.Gln1073=) c.3939G>A (p.Gln1313=) | dbSNP |
17 | g.50185890T>A | CA400191975 | COL1A1 | c.4136A>T (p.Gln1379Leu) n.1101A>T c.3866A>T (p.Gln1289Leu) c.3218A>T (p.Gln1073Leu) c.3938A>T (p.Gln1313Leu) | |
17 | g.50185890T>C | CA400191977 | COL1A1 | c.4136A>G (p.Gln1379Arg) n.1101A>G c.3866A>G (p.Gln1289Arg) c.3218A>G (p.Gln1073Arg) c.3938A>G (p.Gln1313Arg) | dbSNP |
17 | g.50185890T>G | CA400191982 | COL1A1 | c.4136A>C (p.Gln1379Pro) n.1101A>C c.3866A>C (p.Gln1289Pro) c.3218A>C (p.Gln1073Pro) c.3938A>C (p.Gln1313Pro) | |
17 | g.50185890T= | CA2263913910 | COL1A1 | c.4136A= (p.Gln1379=) n.1101A= c.3866A= (p.Gln1289=) c.3218A= (p.Gln1073=) c.3938A= (p.Gln1313=) | |
17 | g.50185891G>A | CA400191991 | COL1A1 | c.4135C>T (p.Gln1379Ter) n.1100C>T c.3865C>T (p.Gln1289Ter) c.3217C>T (p.Gln1073Ter) c.3937C>T (p.Gln1313Ter) | ClinVar COSMIC |
17 | g.50185891G>C | CA400191987 | COL1A1 | c.4135C>G (p.Gln1379Glu) n.1100C>G c.3865C>G (p.Gln1289Glu) c.3217C>G (p.Gln1073Glu) c.3937C>G (p.Gln1313Glu) | |
17 | g.50185891G= | CA2263913911 | COL1A1 | c.4135C= (p.Gln1379=) n.1100C= c.3865C= (p.Gln1289=) c.3217C= (p.Gln1073=) c.3937C= (p.Gln1313=) | |
17 | g.50185891G>T | CA291542798 | COL1A1 | c.4135C>A (p.Gln1379Lys) n.1100C>A c.3865C>A (p.Gln1289Lys) c.3217C>A (p.Gln1073Lys) c.3937C>A (p.Gln1313Lys) | dbSNP gnomAD v4 |
17 | g.50185892G>A | CA291542799 | COL1A1 | c.4134C>T (p.Asp1378=) n.1099C>T c.3864C>T (p.Asp1288=) c.3216C>T (p.Asp1072=) c.3936C>T (p.Asp1312=) | dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.50185892G>C | CA400191994 | COL1A1 | c.4134C>G (p.Asp1378Glu) n.1099C>G c.3864C>G (p.Asp1288Glu) c.3216C>G (p.Asp1072Glu) c.3936C>G (p.Asp1312Glu) | gnomAD v4 |
17 | g.50185892G= | CA2263913912 | COL1A1 | c.4134C= (p.Asp1378=) n.1099C= c.3864C= (p.Asp1288=) c.3216C= (p.Asp1072=) c.3936C= (p.Asp1312=) | |
17 | g.50185892G>T | CA400191996 | COL1A1 | c.4134C>A (p.Asp1378Glu) n.1099C>A c.3864C>A (p.Asp1288Glu) c.3216C>A (p.Asp1072Glu) c.3936C>A (p.Asp1312Glu) | |
17 | g.50185893T>A | CA400191997 | COL1A1 | c.4133A>T (p.Asp1378Val) n.1098A>T c.3863A>T (p.Asp1288Val) c.3215A>T (p.Asp1072Val) c.3935A>T (p.Asp1312Val) | |
17 | g.50185893T>C | CA400191998 | COL1A1 | c.4133A>G (p.Asp1378Gly) n.1098A>G c.3863A>G (p.Asp1288Gly) c.3215A>G (p.Asp1072Gly) c.3935A>G (p.Asp1312Gly) | |
17 | g.50185893T>G | CA400192000 | COL1A1 | c.4133A>C (p.Asp1378Ala) n.1098A>C c.3863A>C (p.Asp1288Ala) c.3215A>C (p.Asp1072Ala) c.3935A>C (p.Asp1312Ala) | |
17 | g.50185894C>A | CA400192005 | COL1A1 | c.4132G>T (p.Asp1378Tyr) n.1097G>T c.3862G>T (p.Asp1288Tyr) c.3214G>T (p.Asp1072Tyr) c.3934G>T (p.Asp1312Tyr) | |
17 | g.50185894C= | CA2263913913 | COL1A1 | c.4132G= (p.Asp1378=) n.1097G= c.3862G= (p.Asp1288=) c.3214G= (p.Asp1072=) c.3934G= (p.Asp1312=) | |
17 | g.50185894C>G | CA400192010 | COL1A1 | c.4132G>C (p.Asp1378His) n.1097G>C c.3862G>C (p.Asp1288His) c.3214G>C (p.Asp1072His) c.3934G>C (p.Asp1312His) | |
17 | g.50185894C>T | CA8644253 | COL1A1 | c.4132G>A (p.Asp1378Asn) n.1097G>A c.3862G>A (p.Asp1288Asn) c.3214G>A (p.Asp1072Asn) c.3934G>A (p.Asp1312Asn) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.50185895C>A | CA400192013 | COL1A1 | c.4131G>T (p.Met1377Ile) n.1096G>T c.3861G>T (p.Met1287Ile) c.3213G>T (p.Met1071Ile) c.3933G>T (p.Met1311Ile) | |
17 | g.50185895C>G | CA400192015 | COL1A1 | c.4131G>C (p.Met1377Ile) n.1096G>C c.3861G>C (p.Met1287Ile) c.3213G>C (p.Met1071Ile) c.3933G>C (p.Met1311Ile) | |
17 | g.50185895C>T | CA400192019 | COL1A1 | c.4131G>A (p.Met1377Ile) n.1096G>A c.3861G>A (p.Met1287Ile) c.3213G>A (p.Met1071Ile) c.3933G>A (p.Met1311Ile) | |
17 | g.50185896A= | CA2263913914 | COL1A1 | c.4130T= (p.Met1377=) n.1095T= c.3860T= (p.Met1287=) c.3212T= (p.Met1071=) c.3932T= (p.Met1311=) | |
17 | g.50185896A>C | CA400192022 | COL1A1 | c.4130T>G (p.Met1377Arg) n.1095T>G c.3860T>G (p.Met1287Arg) c.3212T>G (p.Met1071Arg) c.3932T>G (p.Met1311Arg) | gnomAD v4 |
17 | g.50185896A>G | CA291542800 | COL1A1 | c.4130T>C (p.Met1377Thr) n.1095T>C c.3860T>C (p.Met1287Thr) c.3212T>C (p.Met1071Thr) c.3932T>C (p.Met1311Thr) | dbSNP |
17 | g.50185896A>T | CA400192023 | COL1A1 | c.4130T>A (p.Met1377Lys) n.1095T>A c.3860T>A (p.Met1287Lys) c.3212T>A (p.Met1071Lys) c.3932T>A (p.Met1311Lys) | |
17 | g.50185897T>A | CA400192024 | COL1A1 | c.4129A>T (p.Met1377Leu) n.1094A>T c.3859A>T (p.Met1287Leu) c.3211A>T (p.Met1071Leu) c.3931A>T (p.Met1311Leu) | |
17 | g.50185897T>C | CA400192027 | COL1A1 | c.4129A>G (p.Met1377Val) n.1094A>G c.3859A>G (p.Met1287Val) c.3211A>G (p.Met1071Val) c.3931A>G (p.Met1311Val) | gnomAD v4 |
17 | g.50185897T>G | CA400192030 | COL1A1 | c.4129A>C (p.Met1377Leu) n.1094A>C c.3859A>C (p.Met1287Leu) c.3211A>C (p.Met1071Leu) c.3931A>C (p.Met1311Leu) | |
17 | g.50185898G>A | CA500991715 | COL1A1 | c.4128C>T (p.Tyr1376=) n.1093C>T c.3858C>T (p.Tyr1286=) c.3210C>T (p.Tyr1070=) c.3930C>T (p.Tyr1310=) | |
17 | g.50185898G>C | CA400192033 | COL1A1 | c.4128C>G (p.Tyr1376Ter) n.1093C>G c.3858C>G (p.Tyr1286Ter) c.3210C>G (p.Tyr1070Ter) c.3930C>G (p.Tyr1310Ter) | |
17 | g.50185898G>T | CA400192035 | COL1A1 | c.4128C>A (p.Tyr1376Ter) n.1093C>A c.3858C>A (p.Tyr1286Ter) c.3210C>A (p.Tyr1070Ter) c.3930C>A (p.Tyr1310Ter) | |
17 | g.50185899_50185901del | CA645569624 | COL1A1 | c.4126_4128del (p.Tyr1376del) n.1091_1093del c.3856_3858del (p.Tyr1286del) c.3208_3210del (p.Tyr1070del) c.3928_3930del (p.Tyr1310del) | COSMIC |
17 | g.50185899T>A | CA400192039 | COL1A1 | c.4127A>T (p.Tyr1376Phe) n.1092A>T c.3857A>T (p.Tyr1286Phe) c.3209A>T (p.Tyr1070Phe) c.3929A>T (p.Tyr1310Phe) | |
17 | g.50185899T>C | CA400192044 | COL1A1 | c.4127A>G (p.Tyr1376Cys) n.1092A>G c.3857A>G (p.Tyr1286Cys) c.3209A>G (p.Tyr1070Cys) c.3929A>G (p.Tyr1310Cys) | |
17 | g.50185899T>G | CA400192042 | COL1A1 | c.4127A>C (p.Tyr1376Ser) n.1092A>C c.3857A>C (p.Tyr1286Ser) c.3209A>C (p.Tyr1070Ser) c.3929A>C (p.Tyr1310Ser) | |
17 | g.50185900A>C | CA400192047 | COL1A1 | c.4126T>G (p.Tyr1376Asp) n.1091T>G c.3856T>G (p.Tyr1286Asp) c.3208T>G (p.Tyr1070Asp) c.3928T>G (p.Tyr1310Asp) | |
17 | g.50185900A>G | CA400192053 | COL1A1 | c.4126T>C (p.Tyr1376His) n.1091T>C c.3856T>C (p.Tyr1286His) c.3208T>C (p.Tyr1070His) c.3928T>C (p.Tyr1310His) | gnomAD v4 |
17 | g.50185900A>T | CA400192051 | COL1A1 | c.4126T>A (p.Tyr1376Asn) n.1091T>A c.3856T>A (p.Tyr1286Asn) c.3208T>A (p.Tyr1070Asn) c.3928T>A (p.Tyr1310Asn) | |
17 | g.50185901G>A | CA500991717 | COL1A1 | c.4125C>T (p.Ala1375=) n.1090C>T c.3855C>T (p.Ala1285=) c.3207C>T (p.Ala1069=) c.3927C>T (p.Ala1309=) | gnomAD v4 |
17 | g.50185901G>C | CA500991718 | COL1A1 | c.4125C>G (p.Ala1375=) n.1090C>G c.3855C>G (p.Ala1285=) c.3207C>G (p.Ala1069=) c.3927C>G (p.Ala1309=) | |
17 | g.50185901G>T | CA500991720 | COL1A1 | c.4125C>A (p.Ala1375=) n.1090C>A c.3855C>A (p.Ala1285=) c.3207C>A (p.Ala1069=) c.3927C>A (p.Ala1309=) | |
17 | g.50185902G>A | CA400192058 | COL1A1 | c.4124C>T (p.Ala1375Val) n.1089C>T c.3854C>T (p.Ala1285Val) c.3206C>T (p.Ala1069Val) c.3926C>T (p.Ala1309Val) | |
17 | g.50185902G>C | CA400192061 | COL1A1 | c.4124C>G (p.Ala1375Gly) n.1089C>G c.3854C>G (p.Ala1285Gly) c.3206C>G (p.Ala1069Gly) c.3926C>G (p.Ala1309Gly) | |
17 | g.50185902G>T | CA400192065 | COL1A1 | c.4124C>A (p.Ala1375Asp) n.1089C>A c.3854C>A (p.Ala1285Asp) c.3206C>A (p.Ala1069Asp) c.3926C>A (p.Ala1309Asp) | |
17 | g.50185903C>A | CA400192069 | COL1A1 | c.4123G>T (p.Ala1375Ser) n.1088G>T c.3853G>T (p.Ala1285Ser) c.3205G>T (p.Ala1069Ser) c.3925G>T (p.Ala1309Ser) | |
17 | g.50185903C>G | CA400192072 | COL1A1 | c.4123G>C (p.Ala1375Pro) n.1088G>C c.3853G>C (p.Ala1285Pro) c.3205G>C (p.Ala1069Pro) c.3925G>C (p.Ala1309Pro) | |
17 | g.50185903C>T | CA400192074 | COL1A1 | c.4123G>A (p.Ala1375Thr) n.1088G>A c.3853G>A (p.Ala1285Thr) c.3205G>A (p.Ala1069Thr) c.3925G>A (p.Ala1309Thr) | |
17 | g.50185904C>A | CA500991721 | COL1A1 | c.4122G>T (p.Val1374=) n.1087G>T c.3852G>T (p.Val1284=) c.3204G>T (p.Val1068=) c.3924G>T (p.Val1308=) | |
17 | g.50185904C= | CA2263913915 | COL1A1 | c.4122G= (p.Val1374=) n.1087G= c.3852G= (p.Val1284=) c.3204G= (p.Val1068=) c.3924G= (p.Val1308=) | |
17 | g.50185904C>G | CA500991722 | COL1A1 | c.4122G>C (p.Val1374=) n.1087G>C c.3852G>C (p.Val1284=) c.3204G>C (p.Val1068=) c.3924G>C (p.Val1308=) | |
17 | g.50185904C>T | CA500991724 | COL1A1 | c.4122G>A (p.Val1374=) n.1087G>A c.3852G>A (p.Val1284=) c.3204G>A (p.Val1068=) c.3924G>A (p.Val1308=) | dbSNP gnomAD v4 |
17 | g.50185905A>C | CA400192079 | COL1A1 | c.4121T>G (p.Val1374Gly) n.1086T>G c.3851T>G (p.Val1284Gly) c.3203T>G (p.Val1068Gly) c.3923T>G (p.Val1308Gly) | |
17 | g.50185905A>G | CA400192081 | COL1A1 | c.4121T>C (p.Val1374Ala) n.1086T>C c.3851T>C (p.Val1284Ala) c.3203T>C (p.Val1068Ala) c.3923T>C (p.Val1308Ala) | |
17 | g.50185905A>T | CA400192083 | COL1A1 | c.4121T>A (p.Val1374Glu) n.1086T>A c.3851T>A (p.Val1284Glu) c.3203T>A (p.Val1068Glu) c.3923T>A (p.Val1308Glu) | |
17 | g.50185906C>A | CA400192086 | COL1A1 | c.4120G>T (p.Val1374Leu) n.1085G>T c.3850G>T (p.Val1284Leu) c.3202G>T (p.Val1068Leu) c.3922G>T (p.Val1308Leu) | |
17 | g.50185906C= | CA2263913916 | COL1A1 | c.4120G= (p.Val1374=) n.1085G= c.3850G= (p.Val1284=) c.3202G= (p.Val1068=) c.3922G= (p.Val1308=) | |
17 | g.50185906C>G | CA400192090 | COL1A1 | c.4120G>C (p.Val1374Leu) n.1085G>C c.3850G>C (p.Val1284Leu) c.3202G>C (p.Val1068Leu) c.3922G>C (p.Val1308Leu) | |
17 | g.50185906C>T | CA291542801 | COL1A1 | c.4120G>A (p.Val1374Met) n.1085G>A c.3850G>A (p.Val1284Met) c.3202G>A (p.Val1068Met) c.3922G>A (p.Val1308Met) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.50185907G>A | CA291542802 | COL1A1 | c.4119C>T (p.Ser1373=) n.1084C>T c.3849C>T (p.Ser1283=) c.3201C>T (p.Ser1067=) c.3921C>T (p.Ser1307=) | ClinVar dbSNP gnomAD v2 gnomAD v3 gnomAD v4 |
17 | g.50185907G>C | CA400192099 | COL1A1 | c.4119C>G (p.Ser1373Arg) n.1084C>G c.3849C>G (p.Ser1283Arg) c.3201C>G (p.Ser1067Arg) c.3921C>G (p.Ser1307Arg) | |
17 | g.50185907G= | CA2263913917 | COL1A1 | c.4119C= (p.Ser1373=) n.1084C= c.3849C= (p.Ser1283=) c.3201C= (p.Ser1067=) c.3921C= (p.Ser1307=) | |
17 | g.50185907G>T | CA400192096 | COL1A1 | c.4119C>A (p.Ser1373Arg) n.1084C>A c.3849C>A (p.Ser1283Arg) c.3201C>A (p.Ser1067Arg) c.3921C>A (p.Ser1307Arg) | |
17 | g.50185908C>A | CA400192104 | COL1A1 | c.4118G>T (p.Ser1373Ile) n.1083G>T c.3848G>T (p.Ser1283Ile) c.3200G>T (p.Ser1067Ile) c.3920G>T (p.Ser1307Ile) | |
17 | g.50185908C>G | CA400192106 | COL1A1 | c.4118G>C (p.Ser1373Thr) n.1083G>C c.3848G>C (p.Ser1283Thr) c.3200G>C (p.Ser1067Thr) c.3920G>C (p.Ser1307Thr) | ClinVar |
17 | g.50185908C>T | CA400192108 | COL1A1 | c.4118G>A (p.Ser1373Asn) n.1083G>A c.3848G>A (p.Ser1283Asn) c.3200G>A (p.Ser1067Asn) c.3920G>A (p.Ser1307Asn) | |
17 | g.50185909T>A | CA400192112 | COL1A1 | c.4117A>T (p.Ser1373Cys) n.1082A>T c.3847A>T (p.Ser1283Cys) c.3199A>T (p.Ser1067Cys) c.3919A>T (p.Ser1307Cys) | |
17 | g.50185909T>C | CA400192125 | COL1A1 | c.4117A>G (p.Ser1373Gly) n.1082A>G c.3847A>G (p.Ser1283Gly) c.3199A>G (p.Ser1067Gly) c.3919A>G (p.Ser1307Gly) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.50185909T>G | CA400192128 | COL1A1 | c.4117A>C (p.Ser1373Arg) n.1082A>C c.3847A>C (p.Ser1283Arg) c.3199A>C (p.Ser1067Arg) c.3919A>C (p.Ser1307Arg) | |
17 | g.50185909T= | CA2263913918 | COL1A1 | c.4117A= (p.Ser1373=) n.1082A= c.3847A= (p.Ser1283=) c.3199A= (p.Ser1067=) c.3919A= (p.Ser1307=) | |
17 | g.50185910G>A | CA500991729 | COL1A1 | c.4116C>T (p.Asn1372=) n.1081C>T c.3846C>T (p.Asn1282=) c.3198C>T (p.Asn1066=) c.3918C>T (p.Asn1306=) | dbSNP gnomAD v2 gnomAD v4 |
17 | g.50185910G>C | CA400192131 | COL1A1 | c.4116C>G (p.Asn1372Lys) n.1081C>G c.3846C>G (p.Asn1282Lys) c.3198C>G (p.Asn1066Lys) c.3918C>G (p.Asn1306Lys) | |
17 | g.50185910G= | CA2263913919 | COL1A1 | c.4116C= (p.Asn1372=) n.1081C= c.3846C= (p.Asn1282=) c.3198C= (p.Asn1066=) c.3918C= (p.Asn1306=) | |
17 | g.50185910G>T | CA400192134 | COL1A1 | c.4116C>A (p.Asn1372Lys) n.1081C>A c.3846C>A (p.Asn1282Lys) c.3198C>A (p.Asn1066Lys) c.3918C>A (p.Asn1306Lys) | |
17 | g.50185911T>A | CA400192138 | COL1A1 | c.4115A>T (p.Asn1372Ile) n.1080A>T c.3845A>T (p.Asn1282Ile) c.3197A>T (p.Asn1066Ile) c.3917A>T (p.Asn1306Ile) | |
17 | g.50185911T>C | CA400192141 | COL1A1 | c.4115A>G (p.Asn1372Ser) n.1080A>G c.3845A>G (p.Asn1282Ser) c.3197A>G (p.Asn1066Ser) c.3917A>G (p.Asn1306Ser) | |
17 | g.50185911T>G | CA400192143 | COL1A1 | c.4115A>C (p.Asn1372Thr) n.1080A>C c.3845A>C (p.Asn1282Thr) c.3197A>C (p.Asn1066Thr) c.3917A>C (p.Asn1306Thr) | |
17 | g.50185912T>A | CA400192155 | COL1A1 | c.4114A>T (p.Asn1372Tyr) n.1079A>T c.3844A>T (p.Asn1282Tyr) c.3196A>T (p.Asn1066Tyr) c.3916A>T (p.Asn1306Tyr) | |
17 | g.50185912T>C | CA8644254 | COL1A1 | c.4114A>G (p.Asn1372Asp) n.1079A>G c.3844A>G (p.Asn1282Asp) c.3196A>G (p.Asn1066Asp) c.3916A>G (p.Asn1306Asp) | dbSNP ExAC gnomAD v2 gnomAD v4 |
17 | g.50185912T>G | CA400192148 | COL1A1 | c.4114A>C (p.Asn1372His) n.1079A>C c.3844A>C (p.Asn1282His) c.3196A>C (p.Asn1066His) c.3916A>C (p.Asn1306His) | |
17 | g.50185912T= | CA2263913920 | COL1A1 | c.4114A= (p.Asn1372=) n.1079A= c.3844A= (p.Asn1282=) c.3196A= (p.Asn1066=) c.3916A= (p.Asn1306=) |