Colon Cancer: Gene >> SEC13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000350697
Start	10304111:10304111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.770T>G
AA Mutation	p.Leu257Trp(p.L257W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000350697
Start	10304081:10304081(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754797935
CDS Mutation	c.800A>G
AA Mutation	p.His267Arg(p.H267R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350697
Start	10312079:10312079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.336C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350697
Start	10315380:10315380(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.105G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350697
Start	10305111:10305111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138539081
CDS Mutation	c.630G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000350697
Start	10301303:10301303(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139150328
CDS Mutation	c.927C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000350697
Start	10312075:10312075(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.340delC
AA Mutation	p.His114MetfsTer5(p.H114Mfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SEC13

No Mutation Annotation!