Colon Cancer: Gene >> XIAP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000355640
Start	123900584:123900584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760574724
CDS Mutation	c.1191T>G
AA Mutation	p.Ile397Met(p.I397M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000355640
Start	123886009:123886009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.347A>G
AA Mutation	p.Lys116Arg(p.K116R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000355640
Start	123886132:123886132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.470A>G
AA Mutation	p.Asn157Ser(p.N157S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000355640
Start	123900583:123900583(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1190T>A
AA Mutation	p.Ile397Asn(p.I397N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000355640
Start	123900538:123900538(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1145T>C
AA Mutation	p.Met382Thr(p.M382T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000355640
Start	123907169:123907169(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1482T>G
AA Mutation	p.Ile494Met(p.I494M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000355640
Start	123907166:123907166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1479A>C
AA Mutation	p.Lys493Asn(p.K493N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000355640
Start	123886198:123886198(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.536T>C
AA Mutation	p.Leu179Pro(p.L179P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000355640
Start	123885971:123885971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140230812
CDS Mutation	c.309G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	start_lost
Transcription ID	ENST00000355640
Start	123885664:123885664(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2T>C
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> XIAP

No Mutation Annotation!