Colon Cancer: Gene >> IL12RB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262345
Start	67396007:67396007(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2507C>A
AA Mutation	p.Ser836Tyr(p.S836Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262345
Start	67350903:67350903(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1072C>A
AA Mutation	p.Leu358Ile(p.L358I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262345
Start	67390039:67390039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775260148
CDS Mutation	c.1957C>T
AA Mutation	p.Leu653Phe(p.L653F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262345
Start	67395827:67395827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2327A>G
AA Mutation	p.Asp776Gly(p.D776G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262345
Start	67329602:67329602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374006496
CDS Mutation	c.680C>T
AA Mutation	p.Pro227Leu(p.P227L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262345
Start	67372721:67372721(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1655G>A
AA Mutation	p.Cys552Tyr(p.C552Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262345
Start	67329677:67329677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.755T>C
AA Mutation	p.Val252Ala(p.V252A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000262345
Start	67380040:67380040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771339755
CDS Mutation	c.1772G>A
AA Mutation	p.Arg591Gln(p.R591Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000262345
Start	67320415:67320415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.47T>C
AA Mutation	p.Ile16Thr(p.I16T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000262345
Start	67326827:67326827(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.457T>G
AA Mutation	p.Leu153Val(p.L153V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000262345
Start	67326750:67326750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.380C>T
AA Mutation	p.Pro127Leu(p.P127L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262345
Start	67372629:67372629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1563A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000262345
Start	67367890:67367890(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1324C>T
AA Mutation	p.Gln442Ter(p.Q442*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> IL12RB2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262345
Start	67329701:67329701(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771299847
CDS Mutation	c.779G>A
AA Mutation	p.Arg260Gln(p.R260Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262345
Start	67321770:67321770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.245G>A
AA Mutation	p.Gly82Asp(p.G82D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262345
Start	67326761:67326761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.391T>C
AA Mutation	p.Ser131Pro(p.S131P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript