Colon Cancer: Gene >> ZNF622

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308683
Start	16465275:16465275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.391G>A
AA Mutation	p.Ala131Thr(p.A131T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308683
Start	16465301:16465301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.365G>A
AA Mutation	p.Ser122Asn(p.S122N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000308683
Start	16465190:16465190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.476T>C
AA Mutation	p.Val159Ala(p.V159A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000308683
Start	16451734:16451734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1357T>A
AA Mutation	p.Ser453Thr(p.S453T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000308683
Start	16453088:16453088(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777954248
CDS Mutation	c.1231G>A
AA Mutation	p.Ala411Thr(p.A411T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000308683
Start	16453112:16453112(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771709029
CDS Mutation	c.1207C>T
AA Mutation	p.Arg403Ter(p.R403*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ZNF622

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000308683
Start	16458563:16458563(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1116G>T
AA Mutation	p.Lys372Asn(p.K372N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000308683
Start	16463582:16463582(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.786C>A
AA Mutation	p.Ser262Arg(p.S262R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000308683
Start	16465111:16465111(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.555G>A
Mutation Classification	Silent
Feature Type	Transcript