Colon Cancer: Gene >> ZKSCAN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324306
Start	100033863:100033863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1358G>A
AA Mutation	p.Arg453His(p.R453H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000324306
Start	100024250:100024250(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.523G>A
AA Mutation	p.Ala175Thr(p.A175T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324306
Start	100023632:100023632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.126C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324306
Start	100033897:100033897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1392T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000324306
Start	100033882:100033882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1377A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000324306
Start	100033517:100033517(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1018delA
AA Mutation	p.Thr340ProfsTer21(p.T340Pfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000324306
Start	100034003:100034003(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747747537
CDS Mutation	c.1498C>T
AA Mutation	p.Arg500Ter(p.R500*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ZKSCAN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000324306
Start	100033388:100033388(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.883G>A
AA Mutation	p.Gly295Arg(p.G295R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript