Colon Cancer: Gene >> HLA-DRA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395388
Start	32443893:32443893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530789959
CDS Mutation	c.748C>T
AA Mutation	p.Arg250Cys(p.R250C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000395388
Start	32443463:32443463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.607T>C
AA Mutation	p.Trp203Arg(p.W203R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000395388
Start	32442462:32442462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.97A>G
AA Mutation	p.Ile33Val(p.I33V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000395388
Start	32443241:32443241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747164620
CDS Mutation	c.385G>A
AA Mutation	p.Val129Ile(p.V129I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000395388
Start	32442570:32442570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751526731
CDS Mutation	c.205C>T
AA Mutation	p.Arg69Trp(p.R69W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000395388
Start	32443840:32443840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.695T>C
AA Mutation	p.Ile232Thr(p.I232T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000395388
Start	32443227:32443227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.371T>C
AA Mutation	p.Leu124Pro(p.L124P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395388
Start	32440010:32440010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.60T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395388
Start	32443396:32443396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.540C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000395388
Start	32442579:32442579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.214G>T
AA Mutation	p.Glu72Ter(p.E72*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000395388
Start	32443223:32443223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.367G>T
AA Mutation	p.Glu123Ter(p.E123*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> HLA-DRA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395388
Start	32443299:32443299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138462914
CDS Mutation	c.443G>A
AA Mutation	p.Arg148Gln(p.R148Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript