Colon Cancer: Gene >> HLA-G

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360323
Start	29829830:29829830(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.910C>T
AA Mutation	p.Pro304Ser(p.P304S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000360323
Start	29828816:29828816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.617C>G
AA Mutation	p.Ala206Gly(p.A206G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000360323
Start	29828289:29828289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780775783
CDS Mutation	c.316C>T
AA Mutation	p.Arg106Cys(p.R106C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000360323
Start	29828815:29828815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.616G>A
AA Mutation	p.Ala206Thr(p.A206T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000360323
Start	29828590:29828590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.391G>A
AA Mutation	p.Gly131Arg(p.G131R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000360323
Start	29829502:29829502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147620137
CDS Mutation	c.704C>T
AA Mutation	p.Ala235Val(p.A235V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000360323
Start	29828678:29828678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.479C>T
AA Mutation	p.Ala160Val(p.A160V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000360323
Start	29828231:29828231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.258G>T
AA Mutation	p.Glu86Asp(p.E86D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360323
Start	29828814:29828814(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.615C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000360323
Start	29828718:29828718(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.519G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> HLA-G

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000360323
Start	29827891:29827891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.47C>T
AA Mutation	p.Ala16Val(p.A16V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000360323
Start	29829822:29829822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.902C>A
AA Mutation	p.Ser301Tyr(p.S301Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript