Primary Site >> Pancreatic Cancer

Gene >> THBS1

ID 1
Mutation Consequence missense_variant
Transcription ID ENST00000260356
Start 39593450:39593450(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs566389840
CDS Mutation c.3049G>A
AA Mutation p.Glu1017Lys(p.E1017K)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 2
Mutation Consequence missense_variant
Transcription ID ENST00000260356
Start 39584340:39584340(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.944C>T
AA Mutation p.Pro315Leu(p.P315L)
Mutation Classification Missense_Mutation
Feature Type Transcript
ID 3
Mutation Consequence synonymous_variant
Transcription ID ENST00000260356
Start 39589816:39589816(version: GRCh38)
Mutation Type SNP
dbSNP_RS null
CDS Mutation c.1938C>T
Mutation Classification Silent
Feature Type Transcript
ID 4
Mutation Consequence synonymous_variant
Transcription ID ENST00000260356
Start 39593449:39593449(version: GRCh38)
Mutation Type SNP
dbSNP_RS rs766425737
CDS Mutation c.3048C>T
Mutation Classification Silent
Feature Type Transcript
ID 5
Mutation Consequence synonymous_variant
Transcription ID ENST00000260356
Start 39594349:39594349(version: GRCh38)
Mutation Type SNP
dbSNP_RS novel
CDS Mutation c.3414C>T
Mutation Classification Silent
Feature Type Transcript