Colon Cancer: Gene >> HHLA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357759
Start	108357919:108357919(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.761A>G
AA Mutation	p.Gln254Arg(p.Q254R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000357759
Start	108376520:108376520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768241814
CDS Mutation	c.1187G>A
AA Mutation	p.Arg396His(p.R396H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000357759
Start	108353673:108353673(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771206254
CDS Mutation	c.311C>T
AA Mutation	p.Ala104Val(p.A104V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000357759
Start	108357869:108357869(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.711A>C
AA Mutation	p.Glu237Asp(p.E237D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357759
Start	108358133:108358133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.975T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357759
Start	108357872:108357872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138516182
CDS Mutation	c.714C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357759
Start	108355338:108355338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.642T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000357759
Start	108362376:108362376(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1038C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HHLA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000357759
Start	108358022:108358022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.864C>A
AA Mutation	p.Phe288Leu(p.F288L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript