Colon Cancer: Gene >> AATF

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000619387
Start	37021013:37021013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199725061
CDS Mutation	c.1546C>T
AA Mutation	p.Arg516Trp(p.R516W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000619387
Start	37031619:37031619(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1553A>G
AA Mutation	p.His518Arg(p.H518R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000619387
Start	36986725:36986725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200375945
CDS Mutation	c.941C>T
AA Mutation	p.Ala314Val(p.A314V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000619387
Start	36986617:36986617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.833G>A
AA Mutation	p.Ser278Asn(p.S278N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000619387
Start	36953796:36953796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.721A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000619387
Start	36950278:36950278(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.156A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000619387
Start	36986637:36986637(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.853T>C
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> AATF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000619387
Start	36952893:36952893(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.291A>C
AA Mutation	p.Glu97Asp(p.E97D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript