Colon Cancer: Gene >> SFXN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000321442
Start	175492261:175492261(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.158A>G
AA Mutation	p.Asp53Gly(p.D53G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321442
Start	175510115:175510115(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759387895
CDS Mutation	c.342G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321442
Start	175511517:175511517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.501A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000321442
Start	175511469:175511469(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs184377169
CDS Mutation	c.453C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> SFXN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000321442
Start	175511491:175511491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374767128
CDS Mutation	c.475G>A
AA Mutation	p.Val159Ile(p.V159I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript