Colon Cancer: Gene >> TCFL5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335351
Start	62842052:62842052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1426C>A
AA Mutation	p.Leu476Met(p.L476M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335351
Start	62860216:62860216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778322425
CDS Mutation	c.740C>T
AA Mutation	p.Ala247Val(p.A247V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335351
Start	62861457:62861457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.214G>A
AA Mutation	p.Glu72Lys(p.E72K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000335351
Start	62842009:62842009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1469G>A
AA Mutation	p.Ser490Asn(p.S490N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000335351
Start	62857591:62857591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767486884
CDS Mutation	c.1042C>T
AA Mutation	p.Arg348Cys(p.R348C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000335351
Start	62859456:62859456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.902C>A
AA Mutation	p.Ser301Tyr(p.S301Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000335351
Start	62857632:62857632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1001C>T
AA Mutation	p.Ala334Val(p.A334V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335351
Start	62857535:62857535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1098C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335351
Start	62857631:62857631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs193288319
CDS Mutation	c.1002G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000335351
Start	62857567:62857567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1066C>T
AA Mutation	p.Arg356Ter(p.R356*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TCFL5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335351
Start	62842039:62842039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1439A>G
AA Mutation	p.Asp480Gly(p.D480G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript