Colon Cancer: Gene >> ZNF785

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395216
Start	30585457:30585457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.155C>T
AA Mutation	p.Ala52Val(p.A52V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000395216
Start	30582675:30582675(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1103G>A
AA Mutation	p.Arg368Lys(p.R368K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000395216
Start	30583048:30583048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.730G>A
AA Mutation	p.Ala244Thr(p.A244T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000395216
Start	30583156:30583156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.622C>T
AA Mutation	p.Arg208Cys(p.R208C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000395216
Start	30585223:30585223(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773378032
CDS Mutation	c.233T>C
AA Mutation	p.Ile78Thr(p.I78T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000395216
Start	30585191:30585191(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.265A>G
AA Mutation	p.Ser89Gly(p.S89G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000395216
Start	30583009:30583009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.769G>A
AA Mutation	p.Ala257Thr(p.A257T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000395216
Start	30582680:30582680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754271979
CDS Mutation	c.1098C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF785

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000395216
Start	30583156:30583156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.622C>T
AA Mutation	p.Arg208Cys(p.R208C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript