Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> EMILIN3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332312
Start	41361588:41361588(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1981C>T
AA Mutation	p.Leu661Phe(p.L661F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332312
Start	41362401:41362401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1168T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332312
Start	41362564:41362564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1005G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332312
Start	41363750:41363750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753229547
CDS Mutation	c.402G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332312
Start	41361778:41361778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145897278
CDS Mutation	c.1791G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000332312
Start	41362138:41362138(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140838664
CDS Mutation	c.1431C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000332312
Start	41362316:41362317(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1252dupG
AA Mutation	p.Asp418GlyfsTer2(p.D418Gfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> EMILIN3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000332312
Start	41362010:41362010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1559C>T
AA Mutation	p.Ser520Leu(p.S520L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000332312
Start	41362339:41362339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1230G>T
AA Mutation	p.Arg410Ser(p.R410S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript