Colon Cancer: Gene >> WASF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000618852
Start	27408259:27408259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1427G>A
AA Mutation	p.Arg476His(p.R476H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000618852
Start	27409998:27409998(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1033G>T
AA Mutation	p.Gly345Trp(p.G345W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000618852
Start	27414917:27414917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.584A>C
AA Mutation	p.Lys195Thr(p.K195T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000618852
Start	27414889:27414889(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.612G>T
AA Mutation	p.Glu204Asp(p.E204D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000618852
Start	27418956:27418956(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.263A>G
AA Mutation	p.Glu88Gly(p.E88G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000618852
Start	27416029:27416029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.493C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000618852
Start	27409843:27409843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1188T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000618852
Start	27409885:27409885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1146C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000618852
Start	27418415:27418415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.273G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> WASF2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000618852
Start	27418327:27418327(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.361T>C
Mutation Classification	Silent
Feature Type	Transcript