Colon Cancer: Gene >> GRHL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000350501
Start	24342725:24342725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1238G>A
AA Mutation	p.Arg413Gln(p.R413Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000350501
Start	24334663:24334663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.223A>G
AA Mutation	p.Ile75Val(p.I75V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000350501
Start	24342934:24342934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140365190
CDS Mutation	c.1328C>T
AA Mutation	p.Thr443Met(p.T443M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350501
Start	24342905:24342905(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1299C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350501
Start	24338012:24338012(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.861C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350501
Start	24346628:24346628(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760661018
CDS Mutation	c.1530C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000350501
Start	24337137:24337137(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.675delC
AA Mutation	p.Ser226AlafsTer58(p.S226Afs*58)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> GRHL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000350501
Start	24342127:24342127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375437963
CDS Mutation	c.1060G>A
AA Mutation	p.Val354Ile(p.V354I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript