Colon Cancer: Gene >> IL31RA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000447346
Start	55872322:55872322(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.325A>C
AA Mutation	p.Asn109His(p.N109H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000447346
Start	55914917:55914917(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1807G>A
AA Mutation	p.Asp603Asn(p.D603N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000447346
Start	55872410:55872410(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769522205
CDS Mutation	c.413T>C
AA Mutation	p.Val138Ala(p.V138A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000447346
Start	55896415:55896415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768209580
CDS Mutation	c.838C>T
AA Mutation	p.Arg280Trp(p.R280W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000447346
Start	55851623:55851623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs183626277
CDS Mutation	c.53C>T
AA Mutation	p.Pro18Leu(p.P18L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000447346
Start	55916678:55916678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1853T>C
AA Mutation	p.Val618Ala(p.V618A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000447346
Start	55916731:55916731(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1906G>T
AA Mutation	p.Val636Leu(p.V636L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000447346
Start	55906215:55906215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs547992094
CDS Mutation	c.1179G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000447346
Start	55859553:55859553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.108C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000447346
Start	55872338:55872339(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.347dupT
AA Mutation	p.Leu117ProfsTer9(p.L117Pfs*9)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> IL31RA

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000447346
Start	55900070:55900070(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1007C>A
AA Mutation	p.Ser336Tyr(p.S336Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000447346
Start	55851602:55851602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.32C>T
AA Mutation	p.Thr11Met(p.T11M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000447346
Start	55883063:55883063(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.474G>T
AA Mutation	p.Lys158Asn(p.K158N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000447346
Start	55900099:55900099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1036G>A
AA Mutation	p.Ala346Thr(p.A346T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000447346
Start	55914847:55914847(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1737C>A
AA Mutation	p.Asn579Lys(p.N579K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000447346
Start	55896415:55896415(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768209580
CDS Mutation	c.838C>T
AA Mutation	p.Arg280Trp(p.R280W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000447346
Start	55916691:55916691(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1866C>T
Mutation Classification	Silent
Feature Type	Transcript