Colon Cancer: Gene >> CD1C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368170
Start	158292133:158292133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761108555
CDS Mutation	c.378G>T
AA Mutation	p.Lys126Asn(p.K126N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368170
Start	158292272:158292272(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146158051
CDS Mutation	c.517G>A
AA Mutation	p.Val173Ile(p.V173I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368170
Start	158292796:158292796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.811G>A
AA Mutation	p.Ala271Thr(p.A271T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368170
Start	158292842:158292842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.857G>A
AA Mutation	p.Ser286Asn(p.S286N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368170
Start	158292750:158292750(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.765T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368170
Start	158291162:158291162(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.90C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368170
Start	158290088:158290088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.24G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_lost
Transcription ID	ENST00000368170
Start	158293474:158293474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1000T>C
AA Mutation	p.Ter334ArgextTer5(p.*334Rext*5)
Mutation Classification	Nonstop_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CD1C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368170
Start	158292210:158292210(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.455C>A
AA Mutation	p.Ser152Tyr(p.S152Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368170
Start	158292624:158292624(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.639C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368170
Start	158291396:158291396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116022586
CDS Mutation	c.324G>A
Mutation Classification	Silent
Feature Type	Transcript