Colon Cancer: Gene >> MCAM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264036
Start	119314567:119314567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.481T>C
AA Mutation	p.Cys161Arg(p.C161R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264036
Start	119311561:119311561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1376G>A
AA Mutation	p.Arg459Gln(p.R459Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264036
Start	119312385:119312385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772127034
CDS Mutation	c.905A>G
AA Mutation	p.Asn302Ser(p.N302S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264036
Start	119310441:119310441(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201149343
CDS Mutation	c.1819G>A
AA Mutation	p.Glu607Lys(p.E607K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000264036
Start	119312358:119312358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140965114
CDS Mutation	c.932G>A
AA Mutation	p.Arg311Gln(p.R311Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000264036
Start	119315155:119315155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.176A>G
AA Mutation	p.His59Arg(p.H59R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000264036
Start	119309900:119309900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1927G>A
AA Mutation	p.Asp643Asn(p.D643N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264036
Start	119312587:119312587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201305960
CDS Mutation	c.801C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264036
Start	119312115:119312115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1080C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264036
Start	119311560:119311560(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778246760
CDS Mutation	c.1377G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264036
Start	119311575:119311575(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202027486
CDS Mutation	c.1362G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264036
Start	119311097:119311097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1638C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264036
Start	119310358:119310358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773872862
CDS Mutation	c.1902G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000264036
Start	119310760:119310760(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1789G>T
AA Mutation	p.Glu597Ter(p.E597*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MCAM

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264036
Start	119312359:119312359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200709459
CDS Mutation	c.931C>T
AA Mutation	p.Arg311Trp(p.R311W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript