Colon Cancer: Gene >> CEACAM7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000006724
Start	41677445:41677445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.765G>T
AA Mutation	p.Met255Ile(p.M255I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000006724
Start	41687165:41687165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374301472
CDS Mutation	c.121G>A
AA Mutation	p.Val41Met(p.V41M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000006724
Start	41686914:41686914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138765616
CDS Mutation	c.372C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000006724
Start	41684059:41684059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.432G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000006724
Start	41688115:41688115(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.51delG
AA Mutation	p.Leu18SerfsTer8(p.L18Sfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CEACAM7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000006724
Start	41687167:41687167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.119T>C
AA Mutation	p.Val40Ala(p.V40A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000006724
Start	41687053:41687053(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201819691
CDS Mutation	c.233G>A
AA Mutation	p.Arg78Gln(p.R78Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript