Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> ULBP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367351
Start	149946426:149946426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.404G>A
AA Mutation	p.Ser135Asn(p.S135N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367351
Start	149945366:149945366(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772380793
CDS Mutation	c.143G>A
AA Mutation	p.Arg48Gln(p.R48Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367351
Start	149946545:149946545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.523G>T
AA Mutation	p.Asp175Tyr(p.D175Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367351
Start	149945500:149945500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.277G>T
AA Mutation	p.Val93Leu(p.V93L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367351
Start	149946489:149946489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.467G>T
AA Mutation	p.Arg156Ile(p.R156I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367351
Start	149946385:149946385(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.363G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ULBP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367351
Start	149946613:149946613(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.591C>A
AA Mutation	p.Phe197Leu(p.F197L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367351
Start	149946472:149946472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.450C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367351
Start	149945337:149945337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.114C>A
Mutation Classification	Silent
Feature Type	Transcript