Colon Cancer: Gene >> RGMB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000513185
Start	98793179:98793179(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.740C>T
AA Mutation	p.Thr247Ile(p.T247I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000513185
Start	98793220:98793220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.781G>T
AA Mutation	p.Val261Leu(p.V261L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000513185
Start	98779587:98779587(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.144C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000513185
Start	98779680:98779681(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.237_238delTG
AA Mutation	p.Glu80ValfsTer34(p.E80Vfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000513185
Start	98793704:98793704(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1265T>A
AA Mutation	p.Leu422Ter(p.L422*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000513185
Start	98793614:98793615(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1177dupG
AA Mutation	p.Glu393GlyfsTer29(p.E393Gfs*29)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000513185
Start	98793723:98793724(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1285dupA
AA Mutation	p.Thr429AsnfsTer33(p.T429Nfs*33)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000513185
Start	98779753:98779754(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.311_313dupTAT
AA Mutation	p.Val104_Tyr105insLeu(p.V104_Y105insL)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> RGMB

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000513185
Start	98793598:98793598(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs550569565
CDS Mutation	c.1159G>A
AA Mutation	p.Ala387Thr(p.A387T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000513185
Start	98793675:98793676(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1238dupA
AA Mutation	p.Asn413LysfsTer9(p.N413Kfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript