Colon Cancer: Gene >> TKT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000423525
Start	53240282:53240282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.406G>A
AA Mutation	p.Ala136Thr(p.A136T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000423525
Start	53235115:53235115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.497C>T
AA Mutation	p.Ala166Val(p.A166V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000423525
Start	53241221:53241221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.250G>A
AA Mutation	p.Ala84Thr(p.A84T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000423525
Start	53242217:53242217(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782597207
CDS Mutation	c.133G>A
AA Mutation	p.Ala45Thr(p.A45T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000423525
Start	53241133:53241133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.338C>T
AA Mutation	p.Pro113Leu(p.P113L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000423525
Start	53226809:53226809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1643G>A
AA Mutation	p.Ser548Asn(p.S548N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000423525
Start	53229305:53229305(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150763423
CDS Mutation	c.1239C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000423525
Start	53229284:53229284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1260C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000423525
Start	53229335:53229335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs144151385
CDS Mutation	c.1209C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000423525
Start	53226844:53226844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1608C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000423525
Start	53242160:53242160(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.190delC
AA Mutation	p.Arg64GlyfsTer35(p.R64Gfs*35)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TKT

No Mutation Annotation!