Colon Cancer: Gene >> PBXIP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368463
Start	154951303:154951303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.338G>A
AA Mutation	p.Gly113Asp(p.G113D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368463
Start	154948189:154948189(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762352663
CDS Mutation	c.587A>G
AA Mutation	p.Asn196Ser(p.N196S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368463
Start	154946410:154946410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147560334
CDS Mutation	c.1264G>A
AA Mutation	p.Gly422Arg(p.G422R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368463
Start	154948279:154948279(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.497A>G
AA Mutation	p.Glu166Gly(p.E166G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368463
Start	154948297:154948297(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376731001
CDS Mutation	c.479G>A
AA Mutation	p.Arg160Gln(p.R160Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000368463
Start	154945046:154945046(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2174A>G
AA Mutation	p.His725Arg(p.H725R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000368463
Start	154951860:154951860(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.113T>C
AA Mutation	p.Leu38Pro(p.L38P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000368463
Start	154946370:154946370(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1304G>T
AA Mutation	p.Arg435Ile(p.R435I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000368463
Start	154945902:154945902(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1772T>C
AA Mutation	p.Val591Ala(p.V591A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368463
Start	154948329:154948329(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776039240
CDS Mutation	c.447C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000368463
Start	154951858:154951858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.115C>T
AA Mutation	p.Gln39Ter(p.Q39*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> PBXIP1

No Mutation Annotation!