Colon Cancer: Gene >> VGLL4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000273038
Start	11559409:11559409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.524G>A
AA Mutation	p.Cys175Tyr(p.C175Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000273038
Start	11564993:11564993(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112232182
CDS Mutation	c.281G>A
AA Mutation	p.Arg94His(p.R94H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000273038
Start	11564954:11564954(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757243456
CDS Mutation	c.320G>A
AA Mutation	p.Arg107His(p.R107H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000273038
Start	11702971:11702971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752998676
CDS Mutation	c.64C>T
AA Mutation	p.Arg22Cys(p.R22C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000273038
Start	11558807:11558807(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.622G>A
AA Mutation	p.Val208Met(p.V208M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000273038
Start	11559442:11559442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.491T>C
AA Mutation	p.Val164Ala(p.V164A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000273038
Start	11559416:11559416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.517C>T
AA Mutation	p.Arg173Cys(p.R173C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000273038
Start	11564805:11564805(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770798622
CDS Mutation	c.469C>T
AA Mutation	p.Arg157Trp(p.R157W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000273038
Start	11601962:11601962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.125G>A
AA Mutation	p.Ser42Asn(p.S42N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273038
Start	11564857:11564857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.417C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> VGLL4

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000273038
Start	11602020:11602020(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748118489
CDS Mutation	c.67G>A
AA Mutation	p.Glu23Lys(p.E23K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript