Colon Cancer: Gene >> ULBP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000229708
Start	149968865:149968865(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.344C>T
AA Mutation	p.Pro115Leu(p.P115L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000229708
Start	149964116:149964116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.67T>C
AA Mutation	p.Ser23Pro(p.S23P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000229708
Start	149968810:149968810(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs115012653
CDS Mutation	c.289G>A
AA Mutation	p.Val97Met(p.V97M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000229708
Start	149968625:149968625(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.104A>G
AA Mutation	p.Tyr35Cys(p.Y35C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000229708
Start	149964068:149964068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.19C>A
AA Mutation	p.Pro7Thr(p.P7T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000229708
Start	149970031:149970031(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.644delC
AA Mutation	p.Pro215GlnfsTer27(p.P215Qfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000229708
Start	149969321:149969321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.586G>T
AA Mutation	p.Glu196Ter(p.E196*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ULBP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000229708
Start	149969287:149969287(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.552G>T
AA Mutation	p.Lys184Asn(p.K184N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript