Colon Cancer: Gene >> SUZ12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322652
Start	31998733:31998733(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1950G>T
AA Mutation	p.Lys650Asn(p.K650N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000322652
Start	31998755:31998755(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1972C>A
AA Mutation	p.Leu658Ile(p.L658I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000322652
Start	31947657:31947657(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.427A>G
AA Mutation	p.Lys143Glu(p.K143E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000322652
Start	31940319:31940319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.308G>A
AA Mutation	p.Arg103Gln(p.R103Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000322652
Start	31993983:31993983(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1412A>G
AA Mutation	p.His471Arg(p.H471R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000322652
Start	31940467:31940467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.367T>C
AA Mutation	p.Ser123Pro(p.S123P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SUZ12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000322652
Start	31988335:31988335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1039G>A
AA Mutation	p.Glu347Lys(p.E347K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000322652
Start	31947636:31947636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.406G>T
AA Mutation	p.Asp136Tyr(p.D136Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000322652
Start	31983001:31983001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.920G>A
AA Mutation	p.Arg307His(p.R307H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000322652
Start	31940462:31940462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.362G>A
AA Mutation	p.Arg121Gln(p.R121Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000322652
Start	31988394:31988394(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1098T>C
Mutation Classification	Silent
Feature Type	Transcript