Colon Cancer: Gene >> CD34

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310833
Start	207899945:207899945(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.138G>T
AA Mutation	p.Gln46His(p.Q46H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310833
Start	207889561:207889561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.658G>A
AA Mutation	p.Ala220Thr(p.A220T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000310833
Start	207888787:207888787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.867G>T
AA Mutation	p.Lys289Asn(p.K289N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000310833
Start	207888764:207888764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.890C>T
AA Mutation	p.Ser297Leu(p.S297L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310833
Start	207887804:207887804(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147168836
CDS Mutation	c.1092C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310833
Start	207889535:207889535(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.684A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000310833
Start	207889203:207889203(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.765C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000310833
Start	207889183:207889183(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.785delA
AA Mutation	p.Lys262SerfsTer6(p.K262Sfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000310833
Start	207899001:207899001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.488C>A
AA Mutation	p.Ser163Ter(p.S163*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CD34

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000310833
Start	207888787:207888787(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.867G>T
AA Mutation	p.Lys289Asn(p.K289N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000310833
Start	207899199:207899199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.290C>A
AA Mutation	p.Ser97Tyr(p.S97Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript