Colon Cancer: Gene >> CREB3L4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000271889
Start	153968966:153968966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.211C>T
AA Mutation	p.Leu71Phe(p.L71F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000271889
Start	153973400:153973400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150049615
CDS Mutation	c.833G>A
AA Mutation	p.Arg278His(p.R278H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000271889
Start	153974004:153974004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764666056
CDS Mutation	c.1127T>C
AA Mutation	p.Met376Thr(p.M376T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000271889
Start	153969370:153969370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777111235
CDS Mutation	c.458G>A
AA Mutation	p.Cys153Tyr(p.C153Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000271889
Start	153973051:153973051(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.716A>C
AA Mutation	p.Lys239Thr(p.K239T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000271889
Start	153973248:153973248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.797T>G
AA Mutation	p.Leu266Arg(p.L266R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000271889
Start	153969155:153969155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.400G>T
AA Mutation	p.Gly134Cys(p.G134C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000271889
Start	153973915:153973915(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1038T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000271889
Start	153973046:153973048(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs749320152
CDS Mutation	c.715_717delAAG
AA Mutation	p.Lys239del(p.K239del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000271889
Start	153973257:153973259(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs760103702
CDS Mutation	c.809_811delACA
AA Mutation	p.Asn270del(p.N270del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CREB3L4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000271889
Start	153969000:153969000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.245A>G
AA Mutation	p.Glu82Gly(p.E82G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000271889
Start	153968595:153968595(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.70T>C
AA Mutation	p.Ser24Pro(p.S24P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript