Colon Cancer: Gene >> SHISA2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319420
Start	26047031:26047031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746308107
CDS Mutation	c.370G>A
AA Mutation	p.Val124Met(p.V124M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000319420
Start	26047022:26047022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs779132447
CDS Mutation	c.379G>A
AA Mutation	p.Ala127Thr(p.A127T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000319420
Start	26047024:26047024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.377T>A
AA Mutation	p.Val126Asp(p.V126D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000319420
Start	26046752:26046752(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.649T>C
AA Mutation	p.Tyr217His(p.Y217H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319420
Start	26046900:26046900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.501C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319420
Start	26046648:26046648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369705662
CDS Mutation	c.753G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000319420
Start	26046906:26046906(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.495delC
AA Mutation	p.Met166Ter(p.M166*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SHISA2

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319420
Start	26046774:26046774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138455555
CDS Mutation	c.627G>A
Mutation Classification	Silent
Feature Type	Transcript