Colon Cancer: Gene >> STAT6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300134
Start	57098572:57098572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2092C>T
AA Mutation	p.His698Tyr(p.H698Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300134
Start	57102402:57102402(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775447215
CDS Mutation	c.1400G>A
AA Mutation	p.Arg467Gln(p.R467Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000300134
Start	57100024:57100024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1579C>T
AA Mutation	p.Arg527Cys(p.R527C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000300134
Start	57106548:57106548(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.511A>G
AA Mutation	p.Asn171Asp(p.N171D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300134
Start	57099873:57099873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201779891
CDS Mutation	c.1638C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300134
Start	57106534:57106534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.525A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000300134
Start	57096672:57096672(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2444delG
AA Mutation	p.Gly815GlufsTer27(p.G815Efs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000300134
Start	57106792:57106792(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.379G>T
AA Mutation	p.Glu127Ter(p.E127*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000300134
Start	57106581:57106582(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.479-2_479-1delAG
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> STAT6

No Mutation Annotation!