Colon Cancer: Gene >> IL4R

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395762
Start	27362658:27362658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1306T>C
AA Mutation	p.Ser436Pro(p.S436P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000395762
Start	27362565:27362565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376032165
CDS Mutation	c.1213C>T
AA Mutation	p.Arg405Trp(p.R405W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000395762
Start	27355861:27355861(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773871414
CDS Mutation	c.724A>G
AA Mutation	p.Ile242Val(p.I242V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000395762
Start	27363610:27363610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs530539235
CDS Mutation	c.2258C>T
AA Mutation	p.Ser753Leu(p.S753L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000395762
Start	27362398:27362398(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1046C>T
AA Mutation	p.Thr349Ile(p.T349I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000395762
Start	27362743:27362743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1391C>A
AA Mutation	p.Pro464His(p.P464H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395762
Start	27363248:27363248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1896G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395762
Start	27342158:27342158(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs17548704
CDS Mutation	c.108C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395762
Start	27340236:27340236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.33T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395762
Start	27362642:27362642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1290A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000395762
Start	27363398:27363398(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2050delG
AA Mutation	p.Glu684LysfsTer3(p.E684Kfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> IL4R

No Mutation Annotation!