Colon Cancer: Gene >> ZMIZ1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334512
Start	79311156:79311156(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3068C>T
AA Mutation	p.Ala1023Val(p.A1023V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334512
Start	79304132:79304132(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2243G>A
AA Mutation	p.Arg748His(p.R748H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000334512
Start	79277214:79277214(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.314G>A
AA Mutation	p.Arg105His(p.R105H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000334512
Start	79216254:79216254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.260A>G
AA Mutation	p.Lys87Arg(p.K87R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000334512
Start	79311044:79311044(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2956C>T
AA Mutation	p.Pro986Ser(p.P986S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000334512
Start	79298416:79298416(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1502C>T
AA Mutation	p.Pro501Leu(p.P501L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334512
Start	79216264:79216264(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368416414
CDS Mutation	c.270G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334512
Start	79304157:79304157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs116799693
CDS Mutation	c.2268C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334512
Start	79277251:79277251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373895979
CDS Mutation	c.351C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334512
Start	79311142:79311142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3054C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334512
Start	79299096:79299096(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756844568
CDS Mutation	c.1713C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334512
Start	79300822:79300822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765411461
CDS Mutation	c.1899C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334512
Start	79306310:79306310(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2634A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000334512
Start	79296545:79296545(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1305C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000334512
Start	79312689:79312689(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs767811057
CDS Mutation	c.3150delC
AA Mutation	p.Asp1051ThrfsTer73(p.D1051Tfs*73)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ZMIZ1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000334512
Start	79291023:79291023(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.605C>T
AA Mutation	p.Ser202Leu(p.S202L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000334512
Start	79291133:79291133(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.715T>C
AA Mutation	p.Tyr239His(p.Y239H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript