Colon Cancer: Gene >> WNT16

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222462
Start	121339154:121339154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.907C>A
AA Mutation	p.Pro303Thr(p.P303T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222462
Start	121339082:121339082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747813655
CDS Mutation	c.835A>G
AA Mutation	p.Ile279Val(p.I279V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000222462
Start	121331800:121331800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.469G>A
AA Mutation	p.Gly157Ser(p.G157S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000222462
Start	121329770:121329770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.299C>T
AA Mutation	p.Thr100Ile(p.T100I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000222462
Start	121338911:121338911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773948299
CDS Mutation	c.664C>T
AA Mutation	p.Arg222Cys(p.R222C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000222462
Start	121339049:121339049(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763281050
CDS Mutation	c.802C>T
AA Mutation	p.Arg268Cys(p.R268C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222462
Start	121329367:121329367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.75C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222462
Start	121329612:121329612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.141C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000222462
Start	121331825:121331825(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs773332445
CDS Mutation	c.500delG
AA Mutation	p.Gly167AlafsTer17(p.G167Afs*17)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000222462
Start	121331825:121331826(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.499_500delGG
AA Mutation	p.Gly167LeufsTer4(p.G167Lfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> WNT16

No Mutation Annotation!