Colon Cancer: Gene >> ZSCAN30

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000333206
Start	35253908:35253908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1027G>A
AA Mutation	p.Asp343Asn(p.D343N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000333206
Start	35264269:35264269(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.84T>A
AA Mutation	p.Asn28Lys(p.N28K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000333206
Start	35254267:35254267(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749290517
CDS Mutation	c.668G>A
AA Mutation	p.Arg223Gln(p.R223Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000333206
Start	35254340:35254340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.595G>T
AA Mutation	p.Glu199Ter(p.E199*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ZSCAN30

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000333206
Start	35253973:35253973(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200243252
CDS Mutation	c.962G>T
AA Mutation	p.Arg321Ile(p.R321I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000333206
Start	35253658:35253658(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1277C>A
AA Mutation	p.Ser426Tyr(p.S426Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333206
Start	35264332:35264332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.21C>T
Mutation Classification	Silent
Feature Type	Transcript