Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> KIR2DL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342376
Start	54752500:54752500(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1007T>G
AA Mutation	p.Leu336Arg(p.L336R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342376
Start	54747378:54747378(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200347365
CDS Mutation	c.708C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342376
Start	54742032:54742032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.123A>G
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> KIR2DL3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000342376
Start	54742045:54742045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.136A>G
AA Mutation	p.Ile46Val(p.I46V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342376
Start	54747360:54747360(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.690A>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000342376
Start	54744021:54744021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747953308
CDS Mutation	c.597C>T
Mutation Classification	Silent
Feature Type	Transcript