Colon Cancer: Gene >> RGMA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329082
Start	93045507:93045507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.844G>A
AA Mutation	p.Val282Met(p.V282M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329082
Start	93052211:93052211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763987490
CDS Mutation	c.427G>A
AA Mutation	p.Glu143Lys(p.E143K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000329082
Start	93045564:93045564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.787G>A
AA Mutation	p.Glu263Lys(p.E263K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000329082
Start	93045080:93045080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752421802
CDS Mutation	c.1271C>T
AA Mutation	p.Ala424Val(p.A424V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000329082
Start	93052139:93052139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756255260
CDS Mutation	c.499G>A
AA Mutation	p.Gly167Arg(p.G167R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329082
Start	93045190:93045190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763397042
CDS Mutation	c.1161C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329082
Start	93052242:93052242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368386612
CDS Mutation	c.396C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> RGMA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329082
Start	93045402:93045402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763103195
CDS Mutation	c.949C>T
AA Mutation	p.Arg317Trp(p.R317W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript