Colon Cancer: Gene >> FAM133B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000445716
Start	92566043:92566043(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.628A>G
AA Mutation	p.Lys210Glu(p.K210E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000445716
Start	92578322:92578322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.273A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000445716
Start	92578370:92578370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.225A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000445716
Start	92566020:92566020(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.651delA
AA Mutation	p.Ala218GlnfsTer52(p.A218Qfs*52)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000445716
Start	92578324:92578324(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.271delA
AA Mutation	p.Arg91AspfsTer68(p.R91Dfs*68)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000445716
Start	92590285:92590286(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.6dupG
AA Mutation	p.Lys3GlufsTer58(p.K3Efs*58)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000445716
Start	92578323:92578324(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.271dupA
AA Mutation	p.Arg91LysfsTer13(p.R91Kfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000445716
Start	92577701:92577703(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs769332443
CDS Mutation	c.324_326delTTC
AA Mutation	p.Ser112del(p.S112del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> FAM133B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000445716
Start	92578161:92578161(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.298A>C
AA Mutation	p.Lys100Gln(p.K100Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript