Colon Cancer: Gene >> SLC35A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000247138
Start	48909924:48909924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.164G>A
AA Mutation	p.Arg55His(p.R55H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000247138
Start	48904846:48904846(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376547003
CDS Mutation	c.1063G>A
AA Mutation	p.Ala355Thr(p.A355T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000247138
Start	48905440:48905440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782219505
CDS Mutation	c.469G>A
AA Mutation	p.Val157Met(p.V157M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247138
Start	48909962:48909962(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.126G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SLC35A2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000247138
Start	48905451:48905451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.458C>T
AA Mutation	p.Ala153Val(p.A153V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247138
Start	48905036:48905036(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781917175
CDS Mutation	c.873C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000247138
Start	48906539:48906539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782206039
CDS Mutation	c.279C>T
Mutation Classification	Silent
Feature Type	Transcript