| Chr | Mutation (hg38) | CAid | Gene | Transcript | Linkouts |
|---|---|---|---|---|---|
| 5 | g.112839201G>C | CA16029253 | APC | c.3272G>C (n.3272G>C) c.3661G>C (p.Gly1221Arg) c.*3613G>C (n.*3613G>C) c.3553G>C (p.Gly1185Arg) c.3607G>C (p.Gly1203Arg) c.1960G>C c.*2929G>C (n.*2929G>C) c.230+10229G>C c.3637G>C (p.Gly1213Arg) c.3532G>C (p.Gly1178Arg) c.3523G>C (p.Gly1175Arg) c.3484G>C (p.Gly1162Arg) c.3430G>C (p.Gly1144Arg) c.3334G>C (p.Gly1112Arg) c.3304G>C (p.Gly1102Arg) c.3229G>C (p.Gly1077Arg) c.3127G>C (p.Gly1043Arg) c.2758G>C (p.Gly920Arg) | ClinVar dbSNP |
| 5 | g.112839201G>A | CA16029252 | APC | c.3272G>A (n.3272G>A) c.3661G>A (p.Gly1221Arg) c.*3613G>A (n.*3613G>A) c.3553G>A (p.Gly1185Arg) c.3607G>A (p.Gly1203Arg) c.1960G>A c.*2929G>A (n.*2929G>A) c.230+10229G>A c.3637G>A (p.Gly1213Arg) c.3532G>A (p.Gly1178Arg) c.3523G>A (p.Gly1175Arg) c.3484G>A (p.Gly1162Arg) c.3430G>A (p.Gly1144Arg) c.3334G>A (p.Gly1112Arg) c.3304G>A (p.Gly1102Arg) c.3229G>A (p.Gly1077Arg) c.3127G>A (p.Gly1043Arg) c.2758G>A (p.Gly920Arg) | dbSNP |
| 5 | g.112839201G>T | CA16029254 | APC | c.3272G>T (n.3272G>T) c.3661G>T (p.Gly1221Ter) c.*3613G>T (n.*3613G>T) c.3553G>T (p.Gly1185Ter) c.3607G>T (p.Gly1203Ter) c.1960G>T c.*2929G>T (n.*2929G>T) c.230+10229G>T c.3637G>T (p.Gly1213Ter) c.3532G>T (p.Gly1178Ter) c.3523G>T (p.Gly1175Ter) c.3484G>T (p.Gly1162Ter) c.3430G>T (p.Gly1144Ter) c.3334G>T (p.Gly1112Ter) c.3304G>T (p.Gly1102Ter) c.3229G>T (p.Gly1077Ter) c.3127G>T (p.Gly1043Ter) c.2758G>T (p.Gly920Ter) | ClinVar dbSNP COSMIC |
| 5 | g.112839201G= | CA1573489350 | APC | c.3272G= (n.3272G=) c.3661G= (p.Gly1221=) c.*3613G= (n.*3613G=) c.3553G= (p.Gly1185=) c.3607G= (p.Gly1203=) c.1960G= c.*2929G= (n.*2929G=) c.230+10229G= c.3637G= (p.Gly1213=) c.3532G= (p.Gly1178=) c.3523G= (p.Gly1175=) c.3484G= (p.Gly1162=) c.3430G= (p.Gly1144=) c.3334G= (p.Gly1112=) c.3304G= (p.Gly1102=) c.3229G= (p.Gly1077=) c.3127G= (p.Gly1043=) c.2758G= (p.Gly920=) | dbSNP |