Colon Cancer: Gene >> TBX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000240328
Start	61408225:61408225(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373091690
CDS Mutation	c.1858C>T
AA Mutation	p.Arg620Cys(p.R620C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000240328
Start	61405555:61405555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1405G>A
AA Mutation	p.Ala469Thr(p.A469T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000240328
Start	61405550:61405550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1400G>A
AA Mutation	p.Gly467Asp(p.G467D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000240328
Start	61405537:61405537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1387G>A
AA Mutation	p.Gly463Arg(p.G463R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000240328
Start	61401686:61401686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.398G>A
AA Mutation	p.Arg133Gln(p.R133Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000240328
Start	61401797:61401797(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.509C>T
AA Mutation	p.Ser170Leu(p.S170L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000240328
Start	61404668:61404668(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.950G>T
AA Mutation	p.Gly317Val(p.G317V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000240328
Start	61401848:61401848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.560A>G
AA Mutation	p.Tyr187Cys(p.Y187C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000240328
Start	61403151:61403151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.754A>G
AA Mutation	p.Thr252Ala(p.T252A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000240328
Start	61400444:61400444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.268C>T
AA Mutation	p.Arg90Cys(p.R90C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000240328
Start	61405431:61405431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548613583
CDS Mutation	c.1281C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000240328
Start	61408119:61408119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1752C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TBX2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000240328
Start	61408382:61408382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780953070
CDS Mutation	c.2015G>A
AA Mutation	p.Arg672His(p.R672H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript