Colon Cancer: Gene >> TPRG1L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378344
Start	3628595:3628595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.811G>T
AA Mutation	p.Gly271Cys(p.G271C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378344
Start	3625243:3625243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.171C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000378344
Start	3627519:3627519(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151278945
CDS Mutation	c.490C>T
AA Mutation	p.Arg164Ter(p.R164*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TPRG1L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378344
Start	3627520:3627520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778701998
CDS Mutation	c.491G>A
AA Mutation	p.Arg164Gln(p.R164Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378344
Start	3625763:3625763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.344A>C
AA Mutation	p.Gln115Pro(p.Q115P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript