Colon Cancer: Gene >> RHAG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371175
Start	49618177:49618177(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.383C>A
AA Mutation	p.Ser128Tyr(p.S128Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371175
Start	49618107:49618107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.453C>A
AA Mutation	p.Phe151Leu(p.F151L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371175
Start	49614766:49614766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.728C>T
AA Mutation	p.Thr243Met(p.T243M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371175
Start	49619264:49619264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139053593
CDS Mutation	c.256G>A
AA Mutation	p.Val86Ile(p.V86I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371175
Start	49636791:49636791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.22A>G
AA Mutation	p.Met8Val(p.M8V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371175
Start	49614814:49614814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.680C>T
AA Mutation	p.Ser227Leu(p.S227L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371175
Start	49618107:49618107(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.453C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371175
Start	49615646:49615646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372834667
CDS Mutation	c.618C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000371175
Start	49615673:49615673(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.591delG
AA Mutation	p.His198MetfsTer15(p.H198Mfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> RHAG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371175
Start	49619327:49619327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.193T>G
AA Mutation	p.Phe65Val(p.F65V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371175
Start	49614749:49614749(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.745G>A
AA Mutation	p.Ala249Thr(p.A249T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371175
Start	49611123:49611123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.968G>T
AA Mutation	p.Arg323Met(p.R323M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript