Colon Cancer: Gene >> CCDC34

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328697
Start	27341424:27341424(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.733G>C
AA Mutation	p.Ala245Pro(p.A245P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000328697
Start	27362885:27362885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.310G>A
AA Mutation	p.Glu104Lys(p.E104K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000328697
Start	27362908:27362908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.287T>A
AA Mutation	p.Val96Glu(p.V96E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328697
Start	27363006:27363006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.189C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328697
Start	27341437:27341437(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.720A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328697
Start	27363096:27363096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.99C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000328697
Start	27357502:27357502(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.399A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000328697
Start	27341426:27341426(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.731delA
AA Mutation	p.Asn244MetfsTer28(p.N244Mfs*28)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000328697
Start	27363032:27363037(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.158_163delCGCCGC
AA Mutation	p.Pro53_Pro54del(p.P53_P54del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CCDC34

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000328697
Start	27357511:27357511(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.390A>C
AA Mutation	p.Glu130Asp(p.E130D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript