Colon Cancer: Gene >> THPO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000204615
Start	184375961:184375961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.68C>T
AA Mutation	p.Pro23Leu(p.P23L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000204615
Start	184372661:184372661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148499454
CDS Mutation	c.914C>T
AA Mutation	p.Thr305Met(p.T305M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000204615
Start	184373017:184373017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.558C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000204615
Start	184372678:184372678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.897T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000204615
Start	184372750:184372750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.825C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000204615
Start	184372645:184372645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.930A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> THPO

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000204615
Start	184372821:184372821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780672946
CDS Mutation	c.754G>A
AA Mutation	p.Glu252Lys(p.E252K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000204615
Start	184372534:184372534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1041G>T
AA Mutation	p.Gln347His(p.Q347H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript