Colon Cancer: Gene >> TAT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355962
Start	71568799:71568799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1136A>G
AA Mutation	p.Glu379Gly(p.E379G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355962
Start	71575976:71575976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.286G>A
AA Mutation	p.Ala96Thr(p.A96T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355962
Start	71570312:71570312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771408463
CDS Mutation	c.998G>A
AA Mutation	p.Arg333His(p.R333H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355962
Start	71576306:71576306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.110G>T
AA Mutation	p.Arg37Ile(p.R37I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000355962
Start	71568220:71568220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750638957
CDS Mutation	c.1289C>T
AA Mutation	p.Ala430Val(p.A430V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000355962
Start	71568751:71568751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1184G>A
AA Mutation	p.Arg395Gln(p.R395Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000355962
Start	71572666:71572666(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.431G>A
AA Mutation	p.Cys144Tyr(p.C144Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000355962
Start	71576193:71576193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.223T>G
AA Mutation	p.Ser75Ala(p.S75A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355962
Start	71568270:71568270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146926467
CDS Mutation	c.1239G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355962
Start	71576359:71576359(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777582600
CDS Mutation	c.57C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355962
Start	71568210:71568210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1299G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355962
Start	71576356:71576356(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.60G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355962
Start	71572605:71572605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.492T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355962
Start	71568159:71568159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1350G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000355962
Start	71576028:71576028(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.236-2delA
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> TAT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355962
Start	71568782:71568782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1153G>A
AA Mutation	p.Glu385Lys(p.E385K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000355962
Start	71576024:71576024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.238G>A
AA Mutation	p.Asp80Asn(p.D80N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355962
Start	71576347:71576347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370850249
CDS Mutation	c.69C>T
Mutation Classification	Silent
Feature Type	Transcript