Colon Cancer: Gene >> TMED10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303575
Start	75176463:75176463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767047055
CDS Mutation	c.117C>G
AA Mutation	p.Asn39Lys(p.N39K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303575
Start	75176413:75176413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.167G>A
AA Mutation	p.Gly56Asp(p.G56D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000303575
Start	75135841:75135841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.457C>T
AA Mutation	p.Arg153Cys(p.R153C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303575
Start	75152072:75152072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.297T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000303575
Start	75147679:75147679(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.396G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TMED10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000303575
Start	75135808:75135808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.490G>T
AA Mutation	p.Asp164Tyr(p.D164Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000303575
Start	75147702:75147702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.373G>T
AA Mutation	p.Asp125Tyr(p.D125Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript