Colon Cancer: Gene >> WEE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000450114
Start	9577149:9577149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1027G>A
AA Mutation	p.Ala343Thr(p.A343T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000450114
Start	9588495:9588495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1834G>A
AA Mutation	p.Ala612Thr(p.A612T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000450114
Start	9576015:9576015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.704T>G
AA Mutation	p.Ile235Ser(p.I235S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000450114
Start	9577168:9577168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1046C>T
AA Mutation	p.Ala349Val(p.A349V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000450114
Start	9577191:9577191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1069T>G
AA Mutation	p.Ser357Ala(p.S357A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000450114
Start	9586529:9586529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750751257
CDS Mutation	c.1551G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000450114
Start	9577247:9577247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1125G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000450114
Start	9586782:9586782(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377274614
CDS Mutation	c.1713C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> WEE1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000450114
Start	9576605:9576605(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.965G>A
AA Mutation	p.Gly322Glu(p.G322E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000450114
Start	9586734:9586734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1665G>A
Mutation Classification	Silent
Feature Type	Transcript