Colon Cancer: Gene >> CA13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000321764
Start	85250839:85250839(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767404207
CDS Mutation	c.137G>A
AA Mutation	p.Arg46Gln(p.R46Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000321764
Start	85281242:85281242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.682C>T
AA Mutation	p.Arg228Cys(p.R228C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000321764
Start	85250927:85250927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.225G>T
AA Mutation	p.Glu75Asp(p.E75D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000321764
Start	85250890:85250890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.188G>A
AA Mutation	p.Ser63Asn(p.S63N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321764
Start	85259485:85259485(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775391404
CDS Mutation	c.300C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321764
Start	85250891:85250891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548734922
CDS Mutation	c.189C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000321764
Start	85266695:85266695(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.446delT
AA Mutation	p.Leu149TyrfsTer65(p.L149Yfs*65)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CA13

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000321764
Start	85250814:85250814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.112G>T
AA Mutation	p.Glu38Ter(p.E38*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript