Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> IL20RA

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000316649
Start	137009318:137009318(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs142288648
CDS Mutation	c.578C>T
AA Mutation	p.Thr193Met(p.T193M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000316649
Start	137001688:137001688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1532G>T
AA Mutation	p.Gly511Val(p.G511V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000316649
Start	137001706:137001706(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1514A>C
AA Mutation	p.Glu505Ala(p.E505A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000316649
Start	137017062:137017062(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.130A>G
AA Mutation	p.Thr44Ala(p.T44A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000316649
Start	137002078:137002078(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1142C>A
AA Mutation	p.Ser381Tyr(p.S381Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000316649
Start	137002184:137002184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751829168
CDS Mutation	c.1036G>A
AA Mutation	p.Gly346Arg(p.G346R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000316649
Start	137001985:137001985(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1235C>T
AA Mutation	p.Ala412Val(p.A412V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> IL20RA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000316649
Start	137009382:137009382(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.514A>G
AA Mutation	p.Met172Val(p.M172V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000316649
Start	137002113:137002113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1107T>G
AA Mutation	p.Ile369Met(p.I369M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000316649
Start	137002228:137002228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.992G>T
AA Mutation	p.Gly331Val(p.G331V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316649
Start	137001963:137001963(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1257C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316649
Start	137001747:137001747(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1473T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000316649
Start	137017090:137017090(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.102T>G
Mutation Classification	Silent
Feature Type	Transcript