Colon Cancer: Gene >> STAT4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358470
Start	191076316:191076316(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.283C>A
AA Mutation	p.His95Asn(p.H95N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358470
Start	191041111:191041111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758109437
CDS Mutation	c.1289C>T
AA Mutation	p.Thr430Met(p.T430M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358470
Start	191033591:191033591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779069171
CDS Mutation	c.1751G>T
AA Mutation	p.Arg584Leu(p.R584L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358470
Start	191036238:191036238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1496G>A
AA Mutation	p.Ser499Asn(p.S499N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358470
Start	191033080:191033080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1922T>G
AA Mutation	p.Ile641Ser(p.I641S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000358470
Start	191066450:191066450(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.610A>C
AA Mutation	p.Ser204Arg(p.S204R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000358470
Start	191073109:191073109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.454A>C
AA Mutation	p.Asn152His(p.N152H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000358470
Start	191066494:191066494(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.566C>T
AA Mutation	p.Ala189Val(p.A189V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358470
Start	191073173:191073173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.390C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358470
Start	191064857:191064857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs557179689
CDS Mutation	c.732C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000358470
Start	191148185:191148185(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.19delG
AA Mutation	p.Val7SerfsTer4(p.V7Sfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> STAT4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358470
Start	191054517:191054517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1224G>C
AA Mutation	p.Lys408Asn(p.K408N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358470
Start	191148160:191148160(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.44T>G
AA Mutation	p.Leu15Trp(p.L15W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358470
Start	191064918:191064918(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.671A>C
AA Mutation	p.Asp224Ala(p.D224A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358470
Start	191029856:191029856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2231C>A
AA Mutation	p.Pro744His(p.P744H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358470
Start	191033007:191033007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1995T>G
AA Mutation	p.Ile665Met(p.I665M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript