Colon Cancer: Gene >> GRHL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324907
Start	9961099:9961099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.332G>T
AA Mutation	p.Arg111Ile(p.R111I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324907
Start	9951846:9951846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.13T>C
AA Mutation	p.Tyr5His(p.Y5H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000324907
Start	9964020:9964020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.881A>C
AA Mutation	p.His294Pro(p.H294P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000324907
Start	9992024:9992024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1339C>T
AA Mutation	p.Pro447Ser(p.P447S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000324907
Start	9961116:9961116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.349A>G
AA Mutation	p.Asn117Asp(p.N117D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000324907
Start	9954964:9954964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370119892
CDS Mutation	c.70C>T
AA Mutation	p.Arg24Trp(p.R24W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324907
Start	9992113:9992113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs575432176
CDS Mutation	c.1428C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324907
Start	9954933:9954933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.39T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324907
Start	9961277:9961277(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.515delC
AA Mutation	p.Pro172GlnfsTer66(p.P172Qfs*66)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324907
Start	9958791:9958792(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.221_222dupGA
AA Mutation	p.Arg75GlufsTer26(p.R75Efs*26)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	inframe_insertion
Transcription ID	ENST00000324907
Start	9986197:9986198(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1184_1185insCAC
AA Mutation	p.Ile395_Gln396insThr(p.I395_Q396insT)
Mutation Classification	In_Frame_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> GRHL1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324907
Start	9961326:9961326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773330664
CDS Mutation	c.559G>A
AA Mutation	p.Asp187Asn(p.D187N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000324907
Start	9958786:9958786(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.208G>A
AA Mutation	p.Val70Ile(p.V70I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324907
Start	9965324:9965324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs367582209
CDS Mutation	c.1053C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324907
Start	9963955:9963955(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766799953
CDS Mutation	c.816G>A
Mutation Classification	Silent
Feature Type	Transcript