Colon Cancer: Gene >> ULBP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367339
Start	150066001:150066001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.250G>A
AA Mutation	p.Ala84Thr(p.A84T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367339
Start	150065452:150065452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.574A>G
AA Mutation	p.Lys192Glu(p.K192E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367339
Start	150065530:150065530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.496G>A
AA Mutation	p.Ala166Thr(p.A166T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367339
Start	150065455:150065455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.571T>C
AA Mutation	p.Cys191Arg(p.C191R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367339
Start	150065422:150065422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.604A>T
AA Mutation	p.Arg202Trp(p.R202W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367339
Start	150065914:150065914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.337G>A
AA Mutation	p.Asp113Asn(p.D113N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000367339
Start	150065899:150065899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.352G>T
AA Mutation	p.Gly118Ter(p.G118*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ULBP3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367339
Start	150065590:150065590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.436G>A
AA Mutation	p.Gly146Arg(p.G146R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript