Colon Cancer: Gene >> ST7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000446490
Start	117229969:117229969(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1544A>G
AA Mutation	p.Asp515Gly(p.D515G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265437
Start	117209842:117209842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1310G>T
AA Mutation	p.Gly437Val(p.G437V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000265437
Start	117221973:117221973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1549C>A
AA Mutation	p.Leu517Ile(p.L517I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000265437
Start	117219089:117219089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772278439
CDS Mutation	c.1411C>T
AA Mutation	p.Arg471Trp(p.R471W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000265437
Start	117129808:117129808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs528877219
CDS Mutation	c.410G>A
AA Mutation	p.Arg137Gln(p.R137Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000265437
Start	117222907:117222907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1685A>G
AA Mutation	p.Lys562Arg(p.K562R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265437
Start	117222962:117222962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1740T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000265437
Start	117222035:117222035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs137974019
CDS Mutation	c.1611G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ST7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000265437
Start	117119627:117119627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.301T>G
AA Mutation	p.Leu101Val(p.L101V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000265437
Start	117136142:117136142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.772A>G
AA Mutation	p.Lys258Glu(p.K258E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript