Colon Cancer: Gene >> TKTL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369915
Start	154310846:154310846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.361T>G
AA Mutation	p.Phe121Val(p.F121V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000369915
Start	154311227:154311227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.659G>A
AA Mutation	p.Arg220Gln(p.R220Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000369915
Start	154312681:154312681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.772C>A
AA Mutation	p.Leu258Ile(p.L258I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000369915
Start	154311011:154311011(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.526C>T
AA Mutation	p.Arg176Cys(p.R176C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369915
Start	154327680:154327680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145236754
CDS Mutation	c.1491G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369915
Start	154315235:154315235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.927C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369915
Start	154323211:154323211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781847361
CDS Mutation	c.1191C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369915
Start	154320901:154320901(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1177delG
AA Mutation	p.Val393TyrfsTer16(p.V393Yfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TKTL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000369915
Start	154320887:154320887(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1160T>C
AA Mutation	p.Ile387Thr(p.I387T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000369915
Start	154309431:154309431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782116452
CDS Mutation	c.339C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000369915
Start	154327947:154327947(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1607delA
AA Mutation	p.His536ProfsTer52(p.H536Pfs*52)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript