Colon Cancer: Gene >> CCL28

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000361115
Start	43388392:43388392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775586405
CDS Mutation	c.149G>A
AA Mutation	p.Arg50His(p.R50H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000361115
Start	43381873:43381873(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.371A>C
AA Mutation	p.Lys124Thr(p.K124T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361115
Start	43412260:43412260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.57C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000361115
Start	43382013:43382013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.231C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CCL28

No Mutation Annotation!