Colon Cancer: Gene >> CCR6

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000341935
Start	167136379:167136379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.149C>T
AA Mutation	p.Pro50Leu(p.P50L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000341935
Start	167137173:167137173(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.943C>T
AA Mutation	p.Leu315Phe(p.L315F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000341935
Start	167137060:167137060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752574574
CDS Mutation	c.830C>T
AA Mutation	p.Thr277Met(p.T277M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000341935
Start	167136469:167136469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.239T>G
AA Mutation	p.Met80Arg(p.M80R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341935
Start	167137340:167137340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773654249
CDS Mutation	c.1110G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341935
Start	167137220:167137220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.990C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341935
Start	167137157:167137157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.927C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341935
Start	167136623:167136623(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143644849
CDS Mutation	c.393C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341935
Start	167136986:167136986(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.756C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341935
Start	167136257:167136257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774953497
CDS Mutation	c.27C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341935
Start	167136755:167136755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.525A>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> CCR6

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000341935
Start	167136641:167136641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.411T>C
Mutation Classification	Silent
Feature Type	Transcript