Colon Cancer: Gene >> HLA-DMA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374843
Start	32949316:32949316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768509769
CDS Mutation	c.736G>A
AA Mutation	p.Val246Met(p.V246M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374843
Start	32950642:32950642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148138044
CDS Mutation	c.250G>A
AA Mutation	p.Glu84Lys(p.E84K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374843
Start	32950566:32950566(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.326T>A
AA Mutation	p.Ile109Asn(p.I109N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374843
Start	32950529:32950529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs113629270
CDS Mutation	c.363G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374843
Start	32949350:32949350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756562366
CDS Mutation	c.702C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374843
Start	32949713:32949714(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.549_550insCAGAA
AA Mutation	p.Phe184GlnfsTer9(p.F184Qfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374843
Start	32950565:32950566(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.326_327insGAGAA
AA Mutation	p.Ile109MetfsTer6(p.I109Mfs*6)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> HLA-DMA

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374843
Start	32949663:32949663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.600C>T
Mutation Classification	Silent
Feature Type	Transcript