Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> XYLT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000017003
Start	50358520:50358520(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775076771
CDS Mutation	c.2255G>A
AA Mutation	p.Arg752His(p.R752H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000017003
Start	50353745:50353745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766625947
CDS Mutation	c.251G>A
AA Mutation	p.Arg84His(p.R84H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000017003
Start	50358220:50358220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1955G>T
AA Mutation	p.Trp652Leu(p.W652L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000017003
Start	50358243:50358243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761317517
CDS Mutation	c.1978C>T
AA Mutation	p.Arg660Trp(p.R660W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000017003
Start	50353884:50353884(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.390G>T
AA Mutation	p.Glu130Asp(p.E130D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000017003
Start	50353667:50353667(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.173G>T
AA Mutation	p.Gly58Val(p.G58V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000017003
Start	50358237:50358237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1972C>A
AA Mutation	p.Leu658Ile(p.L658I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000017003
Start	50359989:50359989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141313233
CDS Mutation	c.2296G>A
AA Mutation	p.Ala766Thr(p.A766T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000017003
Start	50354974:50354974(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.925C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000017003
Start	50357171:50357171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776734491
CDS Mutation	c.1860G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000017003
Start	50355513:50355513(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1020G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000017003
Start	50356606:50356606(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1584delC
AA Mutation	p.Gly529AlafsTer78(p.G529Afs*78)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_lost
Transcription ID	ENST00000017003
Start	50360291:50360291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2598G>T
AA Mutation	p.Ter866TyrextTer57(p.866Yext57)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> XYLT2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000017003
Start	50354562:50354562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.783C>A
AA Mutation	p.Phe261Leu(p.F261L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript