Colon Cancer: Gene >> MC4R

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299766
Start	60371369:60371369(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.981C>G
AA Mutation	p.Asp327Glu(p.D327E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299766
Start	60371531:60371531(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760380326
CDS Mutation	c.819G>T
AA Mutation	p.Gln273His(p.Q273H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000299766
Start	60371928:60371928(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.422T>A
AA Mutation	p.Leu141His(p.L141H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000299766
Start	60371499:60371499(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.851T>C
AA Mutation	p.Phe284Ser(p.F284S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000299766
Start	60371805:60371805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.545T>C
AA Mutation	p.Ile182Thr(p.I182T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000299766
Start	60371376:60371376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.974T>C
AA Mutation	p.Leu325Pro(p.L325P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000299766
Start	60372131:60372131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.219G>T
AA Mutation	p.Lys73Asn(p.K73N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299766
Start	60371600:60371600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.750G>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MC4R

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299766
Start	60372298:60372298(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749768113
CDS Mutation	c.52C>T
AA Mutation	p.Arg18Cys(p.R18C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299766
Start	60371988:60371988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.362T>G
AA Mutation	p.Ile121Ser(p.I121S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript