Colon Cancer: Gene >> IRF2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393593
Start	184418596:184418596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.300G>T
AA Mutation	p.Lys100Asn(p.K100N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000393593
Start	184419534:184419534(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.122C>T
AA Mutation	p.Ala41Val(p.A41V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000393593
Start	184418646:184418646(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.250G>A
AA Mutation	p.Ala84Thr(p.A84T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000393593
Start	184388975:184388975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377626557
CDS Mutation	c.833C>T
AA Mutation	p.Ala278Val(p.A278V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000393593
Start	184388817:184388817(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753833490
CDS Mutation	c.991C>T
AA Mutation	p.Arg331Trp(p.R331W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000393593
Start	184418573:184418573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.323T>G
AA Mutation	p.Val108Gly(p.V108G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000393593
Start	184390740:184390740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779259983
CDS Mutation	c.704C>T
AA Mutation	p.Thr235Met(p.T235M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000393593
Start	184429040:184429040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.25C>T
AA Mutation	p.Arg9Cys(p.R9C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000393593
Start	184388808:184388808(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1000G>A
AA Mutation	p.Val334Ile(p.V334I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393593
Start	184388914:184388914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141066995
CDS Mutation	c.894G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393593
Start	184428999:184428999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142409473
CDS Mutation	c.66G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393593
Start	184388988:184388988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.820C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000393593
Start	184419506:184419506(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.150delA
AA Mutation	p.Asp51MetfsTer19(p.D51Mfs*19)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000393593
Start	184408187:184408187(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.500delA
AA Mutation	p.Asn167MetfsTer7(p.N167Mfs*7)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000393593
Start	184419469:184419469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.187G>T
AA Mutation	p.Gly63Ter(p.G63*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> IRF2

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000393593
Start	184418190:184418190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.388G>T
AA Mutation	p.Glu130Ter(p.E130*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript