Primary Site >> Pancreatic Cancer
Gene >> FLNA
| ID | 1 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369850 |
| Start | 154354907:154354907(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5135A>G |
| AA Mutation | p.Tyr1712Cys(p.Y1712C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 2 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369850 |
| Start | 154364716:154364716(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.1832T>C |
| AA Mutation | p.Phe611Ser(p.F611S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 3 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369850 |
| Start | 154351924:154351924(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.6867G>T |
| AA Mutation | p.Lys2289Asn(p.K2289N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 4 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369850 |
| Start | 154360317:154360317(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.3478G>T |
| AA Mutation | p.Ala1160Ser(p.A1160S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 5 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369850 |
| Start | 154362257:154362257(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2641G>A |
| AA Mutation | p.Gly881Ser(p.G881S) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 6 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369850 |
| Start | 154364032:154364032(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2270G>A |
| AA Mutation | p.Ser757Asn(p.S757N) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 7 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369850 |
| Start | 154359399:154359399(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.4150G>T |
| AA Mutation | p.Gly1384Cys(p.G1384C) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 8 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369850 |
| Start | 154353385:154353385(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.5933C>A |
| AA Mutation | p.Thr1978Lys(p.T1978K) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 9 |
| Mutation Consequence | missense_variant |
| Transcription ID | ENST00000369850 |
| Start | 154348865:154348865(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | rs782641074 |
| CDS Mutation | c.7928G>A |
| AA Mutation | p.Arg2643His(p.R2643H) |
| Mutation Classification | Missense_Mutation |
| Feature Type | Transcript |
| ID | 10 |
| Mutation Consequence | synonymous_variant |
| Transcription ID | ENST00000369850 |
| Start | 154364058:154364058(version: GRCh38) |
| Mutation Type | SNP |
| dbSNP_RS | novel |
| CDS Mutation | c.2244C>A |
| Mutation Classification | Silent |
| Feature Type | Transcript |