Colon Cancer: Gene >> FAM172A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395965
Start	93881576:93881576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373351314
CDS Mutation	c.680G>A
AA Mutation	p.Arg227Gln(p.R227Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000395965
Start	93784479:93784479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.927T>G
AA Mutation	p.Asp309Glu(p.D309E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395965
Start	93824187:93824187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763583872
CDS Mutation	c.867C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395965
Start	93964515:93964515(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.318G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000395965
Start	94074667:94074667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.85G>T
AA Mutation	p.Glu29Ter(p.E29*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained;frameshift_variant
Transcription ID	ENST00000395965
Start	94053214:94053215(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.119_120insATAGATAGATA
AA Mutation	p.Ile41Ter(p.I41*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000395965
Start	93784477:93784478(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.928_929insCTCACACCCATTCATCTCAGCAC
AA Mutation	p.Val310AlafsTer9(p.V310Afs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> FAM172A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395965
Start	94074695:94074695(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.57A>C
AA Mutation	p.Gln19His(p.Q19H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395965
Start	93824187:93824187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763583872
CDS Mutation	c.867C>T
Mutation Classification	Silent
Feature Type	Transcript