Colon Cancer: Gene >> CD1D

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368171
Start	158183047:158183047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.777G>T
AA Mutation	p.Glu259Asp(p.E259D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368171
Start	158182082:158182082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.379G>A
AA Mutation	p.Ala127Thr(p.A127T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000368171
Start	158182923:158182923(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147417067
CDS Mutation	c.653G>A
AA Mutation	p.Gly218Asp(p.G218D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000368171
Start	158183045:158183045(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs182855664
CDS Mutation	c.775G>A
AA Mutation	p.Glu259Lys(p.E259K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000368171
Start	158184142:158184142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777157013
CDS Mutation	c.1000G>A
AA Mutation	p.Val334Ile(p.V334I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368171
Start	158182231:158182231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.528G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368171
Start	158181658:158181658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.265C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368171
Start	158182168:158182168(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.465C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000368171
Start	158181537:158181537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.144G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000368171
Start	158182215:158182215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.512G>A
AA Mutation	p.Trp171Ter(p.W171*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CD1D

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000368171
Start	158184142:158184142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777157013
CDS Mutation	c.1000G>A
AA Mutation	p.Val334Ile(p.V334I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000368171
Start	158182888:158182888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.618G>T
AA Mutation	p.Lys206Asn(p.K206N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript