Colon Cancer: Gene >> CD1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000289429
Start	158257444:158257444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.907A>G
AA Mutation	p.Ile303Val(p.I303V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000289429
Start	158256072:158256072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529984822
CDS Mutation	c.394C>A
AA Mutation	p.Gln132Lys(p.Q132K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000289429
Start	158256989:158256989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143177914
CDS Mutation	c.808G>A
AA Mutation	p.Ala270Thr(p.A270T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000289429
Start	158255121:158255121(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.96C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000289429
Start	158256926:158256926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149659983
CDS Mutation	c.745C>T
AA Mutation	p.Arg249Ter(p.R249*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CD1A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000289429
Start	158256971:158256971(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778216345
CDS Mutation	c.790G>A
AA Mutation	p.Ala264Thr(p.A264T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000289429
Start	158255122:158255122(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140904380
CDS Mutation	c.97G>A
AA Mutation	p.Ala33Thr(p.A33T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000289429
Start	158257491:158257491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768867270
CDS Mutation	c.954G>A
Mutation Classification	Silent
Feature Type	Transcript