| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 3 | g.30674130C>A | CA351808917 | TGFBR2 | c.1280C>A (p.Pro427Gln) n.2876C>A n.158C>A c.1355C>A (p.Pro452Gln) c.1307C>A (p.Pro436Gln) c.1232C>A (p.Pro411Gln) c.1175C>A (p.Pro392Gln) | dbSNP |
| 3 | g.30674130C= | CA1354873998 | TGFBR2 | c.1280C= (p.Pro427=) n.2876C= n.158C= c.1355C= (p.Pro452=) c.1307C= (p.Pro436=) c.1232C= (p.Pro411=) c.1175C= (p.Pro392=) | |
| 3 | g.30674130C>G | CA351808918 | TGFBR2 | c.1280C>G (p.Pro427Arg) n.2876C>G n.158C>G c.1355C>G (p.Pro452Arg) c.1307C>G (p.Pro436Arg) c.1232C>G (p.Pro411Arg) c.1175C>G (p.Pro392Arg) | dbSNP |
| 3 | g.30674130C>T | CA020649 | TGFBR2 | c.1280C>T (p.Pro427Leu) n.2876C>T n.158C>T c.1355C>T (p.Pro452Leu) c.1307C>T (p.Pro436Leu) c.1232C>T (p.Pro411Leu) c.1175C>T (p.Pro392Leu) | ClinVar dbSNP |
| 3 | g.30674131A= | CA1354873999 | TGFBR2 | c.1281A= (p.Pro427=) n.2877A= n.159A= c.1356A= (p.Pro452=) c.1308A= (p.Pro436=) c.1233A= (p.Pro411=) c.1176A= (p.Pro392=) | |
| 3 | g.30674131A>C | CA432917700 | TGFBR2 | c.1281A>C (p.Pro427=) n.2877A>C n.159A>C c.1356A>C (p.Pro452=) c.1308A>C (p.Pro436=) c.1233A>C (p.Pro411=) c.1176A>C (p.Pro392=) | |
| 3 | g.30674131A>G | CA432917702 | TGFBR2 | c.1281A>G (p.Pro427=) n.2877A>G n.159A>G c.1356A>G (p.Pro452=) c.1308A>G (p.Pro436=) c.1233A>G (p.Pro411=) c.1176A>G (p.Pro392=) | dbSNP gnomAD v4 |
| 3 | g.30674131A>T | CA432917701 | TGFBR2 | c.1281A>T (p.Pro427=) n.2877A>T n.159A>T c.1356A>T (p.Pro452=) c.1308A>T (p.Pro436=) c.1233A>T (p.Pro411=) c.1176A>T (p.Pro392=) | |
| 3 | g.30674132G>A | CA351808919 | TGFBR2 | c.1282G>A (p.Glu428Lys) n.2878G>A n.160G>A c.1357G>A (p.Glu453Lys) c.1309G>A (p.Glu437Lys) c.1234G>A (p.Glu412Lys) c.1177G>A (p.Glu393Lys) | dbSNP |
| 3 | g.30674132G>C | CA020653 | TGFBR2 | c.1282G>C (p.Glu428Gln) n.2878G>C n.160G>C c.1357G>C (p.Glu453Gln) c.1309G>C (p.Glu437Gln) c.1234G>C (p.Glu412Gln) c.1177G>C (p.Glu393Gln) | ClinVar dbSNP |
| 3 | g.30674132G= | CA1354874000 | TGFBR2 | c.1282G= (p.Glu428=) n.2878G= n.160G= c.1357G= (p.Glu453=) c.1309G= (p.Glu437=) c.1234G= (p.Glu412=) c.1177G= (p.Glu393=) | |
| 3 | g.30674132G>T | CA351808920 | TGFBR2 | c.1282G>T (p.Glu428Ter) n.2878G>T n.160G>T c.1357G>T (p.Glu453Ter) c.1309G>T (p.Glu437Ter) c.1234G>T (p.Glu412Ter) c.1177G>T (p.Glu393Ter) | |
| 3 | g.30674133A>C | CA351808921 | TGFBR2 | c.1283A>C (p.Glu428Ala) n.2879A>C n.161A>C c.1358A>C (p.Glu453Ala) c.1310A>C (p.Glu437Ala) c.1235A>C (p.Glu412Ala) c.1178A>C (p.Glu393Ala) | |
| 3 | g.30674133A>G | CA351808922 | TGFBR2 | c.1283A>G (p.Glu428Gly) n.2879A>G n.161A>G c.1358A>G (p.Glu453Gly) c.1310A>G (p.Glu437Gly) c.1235A>G (p.Glu412Gly) c.1178A>G (p.Glu393Gly) | dbSNP |
| 3 | g.30674133A>T | CA351808923 | TGFBR2 | c.1283A>T (p.Glu428Val) n.2879A>T n.161A>T c.1358A>T (p.Glu453Val) c.1310A>T (p.Glu437Val) c.1235A>T (p.Glu412Val) c.1178A>T (p.Glu393Val) | |
| 3 | g.30674134A>C | CA351808924 | TGFBR2 | c.1284A>C (p.Glu428Asp) n.2880A>C n.162A>C c.1359A>C (p.Glu453Asp) c.1311A>C (p.Glu437Asp) c.1236A>C (p.Glu412Asp) c.1179A>C (p.Glu393Asp) | |
| 3 | g.30674134A>G | CA432917703 | TGFBR2 | c.1284A>G (p.Glu428=) n.2880A>G n.162A>G c.1359A>G (p.Glu453=) c.1311A>G (p.Glu437=) c.1236A>G (p.Glu412=) c.1179A>G (p.Glu393=) | |
| 3 | g.30674134A>T | CA351808925 | TGFBR2 | c.1284A>T (p.Glu428Asp) n.2880A>T n.162A>T c.1359A>T (p.Glu453Asp) c.1311A>T (p.Glu437Asp) c.1236A>T (p.Glu412Asp) c.1179A>T (p.Glu393Asp) | |
| 3 | g.30674135G>A | CA351808926 | TGFBR2 | c.1285G>A (p.Val429Ile) n.2881G>A n.163G>A c.1360G>A (p.Val454Ile) c.1312G>A (p.Val438Ile) c.1237G>A (p.Val413Ile) c.1180G>A (p.Val394Ile) | dbSNP |
| 3 | g.30674135G>C | CA351808927 | TGFBR2 | c.1285G>C (p.Val429Leu) n.2881G>C n.163G>C c.1360G>C (p.Val454Leu) c.1312G>C (p.Val438Leu) c.1237G>C (p.Val413Leu) c.1180G>C (p.Val394Leu) | dbSNP |
| 3 | g.30674135G>T | CA351808928 | TGFBR2 | c.1285G>T (p.Val429Phe) n.2881G>T n.163G>T c.1360G>T (p.Val454Phe) c.1312G>T (p.Val438Phe) c.1237G>T (p.Val413Phe) c.1180G>T (p.Val394Phe) | |
| 3 | g.30674136T>A | CA351808929 | TGFBR2 | c.1286T>A (p.Val429Asp) n.2882T>A n.164T>A c.1361T>A (p.Val454Asp) c.1313T>A (p.Val438Asp) c.1238T>A (p.Val413Asp) c.1181T>A (p.Val394Asp) | dbSNP |
| 3 | g.30674136T>C | CA351808930 | TGFBR2 | c.1286T>C (p.Val429Ala) n.2882T>C n.164T>C c.1361T>C (p.Val454Ala) c.1313T>C (p.Val438Ala) c.1238T>C (p.Val413Ala) c.1181T>C (p.Val394Ala) | |
| 3 | g.30674136T>G | CA351808931 | TGFBR2 | c.1286T>G (p.Val429Gly) n.2882T>G n.164T>G c.1361T>G (p.Val454Gly) c.1313T>G (p.Val438Gly) c.1238T>G (p.Val413Gly) c.1181T>G (p.Val394Gly) | dbSNP |
| 3 | g.30674136T= | CA1354874001 | TGFBR2 | c.1286T= (p.Val429=) n.2882T= n.164T= c.1361T= (p.Val454=) c.1313T= (p.Val438=) c.1238T= (p.Val413=) c.1181T= (p.Val394=) | |
| 3 | g.30674137C>A | CA432917704 | TGFBR2 | c.1287C>A (p.Val429=) n.2883C>A n.165C>A c.1362C>A (p.Val454=) c.1314C>A (p.Val438=) c.1239C>A (p.Val413=) c.1182C>A (p.Val394=) | dbSNP COSMIC COSMIC |
| 3 | g.30674137C= | CA1354874002 | TGFBR2 | c.1287C= (p.Val429=) n.2883C= n.165C= c.1362C= (p.Val454=) c.1314C= (p.Val438=) c.1239C= (p.Val413=) c.1182C= (p.Val394=) | |
| 3 | g.30674137C>G | CA432917705 | TGFBR2 | c.1287C>G (p.Val429=) n.2883C>G n.165C>G c.1362C>G (p.Val454=) c.1314C>G (p.Val438=) c.1239C>G (p.Val413=) c.1182C>G (p.Val394=) | dbSNP |
| 3 | g.30674137C>T | CA432917706 | TGFBR2 | c.1287C>T (p.Val429=) n.2883C>T n.165C>T c.1362C>T (p.Val454=) c.1314C>T (p.Val438=) c.1239C>T (p.Val413=) c.1182C>T (p.Val394=) | dbSNP |
| 3 | g.30674138C>A | CA351808932 | TGFBR2 | c.1288C>A (p.Leu430Ile) n.2884C>A n.166C>A c.1363C>A (p.Leu455Ile) c.1315C>A (p.Leu439Ile) c.1240C>A (p.Leu414Ile) c.1183C>A (p.Leu395Ile) | dbSNP |
| 3 | g.30674138C>G | CA351808933 | TGFBR2 | c.1288C>G (p.Leu430Val) n.2884C>G n.166C>G c.1363C>G (p.Leu455Val) c.1315C>G (p.Leu439Val) c.1240C>G (p.Leu414Val) c.1183C>G (p.Leu395Val) | dbSNP |
| 3 | g.30674138C>T | CA432917707 | TGFBR2 | c.1288C>T (p.Leu430=) n.2884C>T n.166C>T c.1363C>T (p.Leu455=) c.1315C>T (p.Leu439=) c.1240C>T (p.Leu414=) c.1183C>T (p.Leu395=) | dbSNP |
| 3 | g.30674139T>A | CA351808936 | TGFBR2 | c.1289T>A (p.Leu430Gln) n.2885T>A n.167T>A c.1364T>A (p.Leu455Gln) c.1316T>A (p.Leu439Gln) c.1241T>A (p.Leu414Gln) c.1184T>A (p.Leu395Gln) | dbSNP |
| 3 | g.30674139T>C | CA351808934 | TGFBR2 | c.1289T>C (p.Leu430Pro) n.2885T>C n.167T>C c.1364T>C (p.Leu455Pro) c.1316T>C (p.Leu439Pro) c.1241T>C (p.Leu414Pro) c.1184T>C (p.Leu395Pro) | ClinVar dbSNP |
| 3 | g.30674139T>G | CA351808935 | TGFBR2 | c.1289T>G (p.Leu430Arg) n.2885T>G n.167T>G c.1364T>G (p.Leu455Arg) c.1316T>G (p.Leu439Arg) c.1241T>G (p.Leu414Arg) c.1184T>G (p.Leu395Arg) | dbSNP gnomAD v2 gnomAD v4 |
| 3 | g.30674139T= | CA1354874003 | TGFBR2 | c.1289T= (p.Leu430=) n.2885T= n.167T= c.1364T= (p.Leu455=) c.1316T= (p.Leu439=) c.1241T= (p.Leu414=) c.1184T= (p.Leu395=) | |
| 3 | g.30674140A>C | CA432917710 | TGFBR2 | c.1290A>C (p.Leu430=) n.2886A>C n.168A>C c.1365A>C (p.Leu455=) c.1317A>C (p.Leu439=) c.1242A>C (p.Leu414=) c.1185A>C (p.Leu395=) | |
| 3 | g.30674140A>G | CA432917708 | TGFBR2 | c.1290A>G (p.Leu430=) n.2886A>G n.168A>G c.1365A>G (p.Leu455=) c.1317A>G (p.Leu439=) c.1242A>G (p.Leu414=) c.1185A>G (p.Leu395=) | dbSNP |
| 3 | g.30674140A>T | CA432917709 | TGFBR2 | c.1290A>T (p.Leu430=) n.2886A>T n.168A>T c.1365A>T (p.Leu455=) c.1317A>T (p.Leu439=) c.1242A>T (p.Leu414=) c.1185A>T (p.Leu395=) | dbSNP |
| 3 | g.30674141G>A | CA351808937 | TGFBR2 | c.1291G>A (p.Glu431Lys) n.2887G>A n.169G>A c.1366G>A (p.Glu456Lys) c.1318G>A (p.Glu440Lys) c.1243G>A (p.Glu415Lys) c.1186G>A (p.Glu396Lys) | dbSNP COSMIC COSMIC |
| 3 | g.30674141G>C | CA351808938 | TGFBR2 | c.1291G>C (p.Glu431Gln) n.2887G>C n.169G>C c.1366G>C (p.Glu456Gln) c.1318G>C (p.Glu440Gln) c.1243G>C (p.Glu415Gln) c.1186G>C (p.Glu396Gln) | dbSNP |
| 3 | g.30674141G>T | CA351808939 | TGFBR2 | c.1291G>T (p.Glu431Ter) n.2887G>T n.169G>T c.1366G>T (p.Glu456Ter) c.1318G>T (p.Glu440Ter) c.1243G>T (p.Glu415Ter) c.1186G>T (p.Glu396Ter) | dbSNP |
| 3 | g.30674142A>C | CA351808940 | TGFBR2 | c.1292A>C (p.Glu431Ala) n.2888A>C n.170A>C c.1367A>C (p.Glu456Ala) c.1319A>C (p.Glu440Ala) c.1244A>C (p.Glu415Ala) c.1187A>C (p.Glu396Ala) | |
| 3 | g.30674142A>G | CA351808941 | TGFBR2 | c.1292A>G (p.Glu431Gly) n.2888A>G n.170A>G c.1367A>G (p.Glu456Gly) c.1319A>G (p.Glu440Gly) c.1244A>G (p.Glu415Gly) c.1187A>G (p.Glu396Gly) | |
| 3 | g.30674142A>T | CA351808942 | TGFBR2 | c.1292A>T (p.Glu431Val) n.2888A>T n.170A>T c.1367A>T (p.Glu456Val) c.1319A>T (p.Glu440Val) c.1244A>T (p.Glu415Val) c.1187A>T (p.Glu396Val) | |
| 3 | g.30674143A= | CA1354874004 | TGFBR2 | c.1293A= (p.Glu431=) n.2889A= n.171A= c.1368A= (p.Glu456=) c.1320A= (p.Glu440=) c.1245A= (p.Glu415=) c.1188A= (p.Glu396=) | |
| 3 | g.30674143A>C | CA351808943 | TGFBR2 | c.1293A>C (p.Glu431Asp) n.2889A>C n.171A>C c.1368A>C (p.Glu456Asp) c.1320A>C (p.Glu440Asp) c.1245A>C (p.Glu415Asp) c.1188A>C (p.Glu396Asp) | |
| 3 | g.30674143A>G | CA046260 | TGFBR2 | c.1293A>G (p.Glu431=) n.2889A>G n.171A>G c.1368A>G (p.Glu456=) c.1320A>G (p.Glu440=) c.1245A>G (p.Glu415=) c.1188A>G (p.Glu396=) | ClinVar dbSNP ExAC gnomAD v2 gnomAD v3 gnomAD v4 |
| 3 | g.30674143A>T | CA351808944 | TGFBR2 | c.1293A>T (p.Glu431Asp) n.2889A>T n.171A>T c.1368A>T (p.Glu456Asp) c.1320A>T (p.Glu440Asp) c.1245A>T (p.Glu415Asp) c.1188A>T (p.Glu396Asp) | dbSNP |
| 3 | g.30674144T>A | CA351808945 | TGFBR2 | c.1294T>A (p.Ser432Thr) n.2890T>A n.172T>A c.1369T>A (p.Ser457Thr) c.1321T>A (p.Ser441Thr) c.1246T>A (p.Ser416Thr) c.1189T>A (p.Ser397Thr) | dbSNP |