Colon Cancer: Gene >> ZNF346

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358149
Start	177050791:177050791(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.558C>A
AA Mutation	p.Phe186Leu(p.F186L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000358149
Start	177041194:177041194(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.244C>T
AA Mutation	p.Leu82Phe(p.L82F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000358149
Start	177044522:177044522(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.506C>T
AA Mutation	p.Thr169Ile(p.T169I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000358149
Start	177041800:177041800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.302T>C
AA Mutation	p.Val101Ala(p.V101A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000358149
Start	177041199:177041199(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.249T>G
AA Mutation	p.Ile83Met(p.I83M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000358149
Start	177064545:177064545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.831G>T
AA Mutation	p.Gln277His(p.Q277H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358149
Start	177062068:177062068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.714C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF346

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000358149
Start	177050783:177050783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.550G>T
AA Mutation	p.Asp184Tyr(p.D184Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000358149
Start	177041187:177041187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200491700
CDS Mutation	c.237C>T
Mutation Classification	Silent
Feature Type	Transcript