Colon Cancer: Gene >> STK32C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000298630
Start	132228089:132228089(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.358G>A
AA Mutation	p.Ala120Thr(p.A120T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000298630
Start	132225292:132225292(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.817T>C
AA Mutation	p.Ser273Pro(p.S273P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000298630
Start	132208015:132208015(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780331333
CDS Mutation	c.1456G>A
AA Mutation	p.Gly486Ser(p.G486S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000298630
Start	132209096:132209096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1257T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant;stop_lost
Transcription ID	ENST00000368619
Start	132324235:132324236(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.438_439dupGT
AA Mutation	p.Ter147Cys(p.*147C)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> STK32C

No Mutation Annotation!