Colon Cancer: Gene >> TNFRSF25

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000356876
Start	6461705:6461705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.983T>C
AA Mutation	p.Met328Thr(p.M328T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000356876
Start	6462068:6462068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.851G>A
AA Mutation	p.Gly284Asp(p.G284D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000356876
Start	6466073:6466073(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.35C>T
AA Mutation	p.Ala12Val(p.A12V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356876
Start	6465477:6465477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.123G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356876
Start	6466072:6466072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.36G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356876
Start	6464703:6464703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.312G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TNFRSF25

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000356876
Start	6461689:6461689(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.999G>A
Mutation Classification	Silent
Feature Type	Transcript