Colon Cancer: Gene >> TMEM8B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377988
Start	35853511:35853511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1090C>T
AA Mutation	p.Arg364Cys(p.R364C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377988
Start	35853554:35853554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1133G>T
AA Mutation	p.Arg378Leu(p.R378L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377988
Start	35846940:35846940(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775431408
CDS Mutation	c.764G>A
AA Mutation	p.Arg255Gln(p.R255Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377988
Start	35846536:35846536(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.565G>A
AA Mutation	p.Asp189Asn(p.D189N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377988
Start	35842503:35842503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.65C>A
AA Mutation	p.Pro22His(p.P22H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377988
Start	35842687:35842687(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369754805
CDS Mutation	c.249C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377988
Start	35842558:35842558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548793454
CDS Mutation	c.120G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TMEM8B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377988
Start	35842538:35842538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.100C>A
AA Mutation	p.His34Asn(p.H34N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript