Colon Cancer: Gene >> TADA2A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000615182
Start	37426990:37426990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.173A>G
AA Mutation	p.Asp58Gly(p.D58G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000615182
Start	37470453:37470453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.949C>T
AA Mutation	p.Arg317Cys(p.R317C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000615182
Start	37470454:37470454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.950G>A
AA Mutation	p.Arg317His(p.R317H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000615182
Start	37440520:37440520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.300T>A
AA Mutation	p.Asn100Lys(p.N100K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000615182
Start	37467518:37467518(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.892delT
AA Mutation	p.Cys298ValfsTer50(p.C298Vfs*50)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TADA2A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000615182
Start	37476972:37476972(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1322C>A
AA Mutation	p.Thr441Asn(p.T441N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000615182
Start	37465518:37465518(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.800A>G
AA Mutation	p.Asp267Gly(p.D267G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript