Colon Cancer: Gene >> CCL16

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000611905
Start	35978176:35978176(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.164G>T
AA Mutation	p.Arg55Ile(p.R55I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000611905
Start	35977654:35977654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.275A>G
AA Mutation	p.Asn92Ser(p.N92S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000611905
Start	35977609:35977609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.320T>A
AA Mutation	p.Ile107Asn(p.I107N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000611905
Start	35978178:35978178(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.162C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CCL16

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000611905
Start	35981365:35981365(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199602184
CDS Mutation	c.56C>T
AA Mutation	p.Ser19Leu(p.S19L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000611905
Start	35978171:35978171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.169G>A
AA Mutation	p.Ala57Thr(p.A57T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000611905
Start	35977725:35977725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.204C>G
Mutation Classification	Silent
Feature Type	Transcript