Colon Cancer: Gene >> CD38

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000226279
Start	15778553:15778553(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.139C>T
AA Mutation	p.Arg47Cys(p.R47C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000226279
Start	15824990:15824990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.473C>A
AA Mutation	p.Thr158Lys(p.T158K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000226279
Start	15778545:15778545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.131C>T
AA Mutation	p.Pro44Leu(p.P44L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000226279
Start	15840490:15840490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772248233
CDS Mutation	c.791C>T
AA Mutation	p.Ser264Leu(p.S264L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226279
Start	15778567:15778567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.153C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226279
Start	15778495:15778495(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.81C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226279
Start	15778480:15778480(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.66C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000226279
Start	15778552:15778552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.138G>A
AA Mutation	p.Trp46Ter(p.W46*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CD38

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000226279
Start	15838156:15838156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.650A>G
AA Mutation	p.Asp217Gly(p.D217G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000226279
Start	15848599:15848599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.900C>A
Mutation Classification	Silent
Feature Type	Transcript