Colon Cancer: Gene >> TBX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329705
Start	19764159:19764159(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.517G>A
AA Mutation	p.Ala173Thr(p.A173T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000329705
Start	19761129:19761129(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.259G>A
AA Mutation	p.Glu87Lys(p.E87K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329705
Start	19761206:19761206(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.336G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329705
Start	19765086:19765086(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61730282
CDS Mutation	c.813C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329705
Start	19764314:19764314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367657296
CDS Mutation	c.672C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329705
Start	19764254:19764254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778071107
CDS Mutation	c.612G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329705
Start	19761185:19761185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.315G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000329705
Start	19779274:19779275(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1072_1073dupGA
AA Mutation	p.Val359LysfsTer5(p.V359Kfs*5)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> TBX1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000329705
Start	19779384:19779384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1174A>G
AA Mutation	p.Thr392Ala(p.T392A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000329705
Start	19763316:19763316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764371266
CDS Mutation	c.486C>T
Mutation Classification	Silent
Feature Type	Transcript