Colon Cancer: Gene >> MC3R

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000243911
Start	56249168:56249168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767240745
CDS Mutation	c.325G>A
AA Mutation	p.Glu109Lys(p.E109K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000243911
Start	56249773:56249773(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.930T>G
AA Mutation	p.Phe310Leu(p.F310L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000243911
Start	56249330:56249330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.487A>G
AA Mutation	p.Thr163Ala(p.T163A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000243911
Start	56249343:56249343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.500C>A
AA Mutation	p.Ala167Asp(p.A167D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000243911
Start	56249607:56249607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.764G>T
AA Mutation	p.Trp255Leu(p.W255L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000243911
Start	56249763:56249763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.920G>A
AA Mutation	p.Arg307His(p.R307H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000243911
Start	56249289:56249289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs552943206
CDS Mutation	c.446C>T
AA Mutation	p.Ala149Val(p.A149V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000243911
Start	56249191:56249191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.348G>T
AA Mutation	p.Met116Ile(p.M116I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000243911
Start	56249537:56249537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.694C>T
AA Mutation	p.Pro232Ser(p.P232S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000243911
Start	56249590:56249590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.747C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000243911
Start	56249791:56249791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.948C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MC3R

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000243911
Start	56248866:56248866(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.23C>A
AA Mutation	p.Pro8His(p.P8H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript