Colon Cancer: Gene >> TBATA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000299290
Start	70772545:70772545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.939G>T
AA Mutation	p.Lys313Asn(p.K313N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000299290
Start	70781926:70781926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768147593
CDS Mutation	c.152G>A
AA Mutation	p.Arg51Gln(p.R51Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000299290
Start	70774325:70774325(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.805G>T
AA Mutation	p.Ala269Ser(p.A269S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000299290
Start	70781927:70781927(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199669673
CDS Mutation	c.151C>T
AA Mutation	p.Arg51Trp(p.R51W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000299290
Start	70774351:70774351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.779A>G
AA Mutation	p.Asp260Gly(p.D260G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299290
Start	70772524:70772524(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749992519
CDS Mutation	c.960C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299290
Start	70778599:70778599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.465G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299290
Start	70771397:70771397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141267448
CDS Mutation	c.1035G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000299290
Start	70778559:70778559(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.505G>T
AA Mutation	p.Glu169Ter(p.E169*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000299290
Start	70781960:70781960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.118G>T
AA Mutation	p.Glu40Ter(p.E40*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TBATA

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000299290
Start	70771397:70771397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141267448
CDS Mutation	c.1035G>A
Mutation Classification	Silent
Feature Type	Transcript