Colon Cancer: Gene >> IL2RG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374202
Start	71107852:71107852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.994G>A
AA Mutation	p.Val332Ile(p.V332I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374202
Start	71110510:71110510(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.448A>C
AA Mutation	p.Asn150His(p.N150H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000374202
Start	71109388:71109388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.597A>T
AA Mutation	p.Glu199Asp(p.E199D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000374202
Start	71109320:71109320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.665G>A
AA Mutation	p.Arg222His(p.R222H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374202
Start	71109361:71109361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.624C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374202
Start	71111453:71111453(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779772745
CDS Mutation	c.87G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374202
Start	71107764:71107764(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs769405722
CDS Mutation	c.1082delC
AA Mutation	p.Pro361HisfsTer5(p.P361Hfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374202
Start	71110599:71110599(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.359delA
AA Mutation	p.Lys120ArgfsTer27(p.K120Rfs*27)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000374202
Start	71108603:71108603(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.850G>T
AA Mutation	p.Glu284Ter(p.E284*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> IL2RG

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374202
Start	71108612:71108612(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.841T>G
AA Mutation	p.Phe281Val(p.F281V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374202
Start	71107764:71107764(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs769405722
CDS Mutation	c.1082delC
AA Mutation	p.Pro361HisfsTer5(p.P361Hfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript