Colon Cancer: Gene >> WISP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000190983
Start	44727255:44727255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.701C>A
AA Mutation	p.Ser234Tyr(p.S234Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000190983
Start	44724770:44724770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.310G>A
AA Mutation	p.Gly104Ser(p.G104S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000190983
Start	44719901:44719901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759003113
CDS Mutation	c.65G>A
AA Mutation	p.Arg22His(p.R22H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000190983
Start	44724809:44724809(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349T>C
AA Mutation	p.Cys117Arg(p.C117R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000190983
Start	44724976:44724976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.516G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> WISP2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000190983
Start	44727197:44727197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763203992
CDS Mutation	c.643C>T
AA Mutation	p.Arg215Trp(p.R215W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000190983
Start	44719901:44719901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759003113
CDS Mutation	c.65G>A
AA Mutation	p.Arg22His(p.R22H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript