Colon Cancer: Gene >> STAT3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264657
Start	42348443:42348443(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.74G>A
AA Mutation	p.Ser25Asn(p.S25N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264657
Start	42329570:42329570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1217C>T
AA Mutation	p.Ala406Val(p.A406V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000264657
Start	42333939:42333939(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.908C>T
AA Mutation	p.Pro303Leu(p.P303L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000264657
Start	42346574:42346574(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.268C>A
AA Mutation	p.Leu90Ile(p.L90I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264657
Start	42333920:42333920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779733888
CDS Mutation	c.927C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000264657
Start	42329413:42329413(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1278T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000264657
Start	42316861:42316861(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2185delC
AA Mutation	p.Arg729AlafsTer3(p.R729Afs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000264657
Start	42324848:42324848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1465-2A>C
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> STAT3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000264657
Start	42323336:42323336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1672G>A
AA Mutation	p.Gly558Ser(p.G558S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000264657
Start	42323013:42323013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1879G>A
AA Mutation	p.Asp627Asn(p.D627N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript