Colon Cancer: Gene >> CDT1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301019
Start	88805592:88805592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.641C>A
AA Mutation	p.Pro214His(p.P214H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301019
Start	88807092:88807092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761126387
CDS Mutation	c.1164G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301019
Start	88806593:88806593(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs560037813
CDS Mutation	c.1041G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301019
Start	88808209:88808209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760970895
CDS Mutation	c.1572C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301019
Start	88805584:88805584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548341429
CDS Mutation	c.633C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301019
Start	88807421:88807421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1416G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301019
Start	88804634:88804634(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.318T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301019
Start	88805455:88805455(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs534417526
CDS Mutation	c.504C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301019
Start	88807403:88807403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1398G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301019
Start	88804565:88804565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766615832
CDS Mutation	c.249C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000301019
Start	88806036:88806036(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.853delC
AA Mutation	p.Gln285SerfsTer33(p.Q285Sfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CDT1

No Mutation Annotation!