Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MAT2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000321757
Start	163518224:163518224(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147499303
CDS Mutation	c.866G>A
AA Mutation	p.Arg289His(p.R289H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000321757
Start	163518293:163518293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768283411
CDS Mutation	c.935G>A
AA Mutation	p.Arg312Gln(p.R312Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000321757
Start	163513976:163513976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.508G>A
AA Mutation	p.Val170Ile(p.V170I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000321757
Start	163516578:163516578(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.587C>T
AA Mutation	p.Ala196Val(p.A196V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000321757
Start	163517643:163517643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.803C>T
AA Mutation	p.Ala268Val(p.A268V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000321757
Start	163517607:163517607(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.767T>C
AA Mutation	p.Met256Thr(p.M256T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000321757
Start	163518280:163518280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.922C>T
AA Mutation	p.Arg308Ter(p.R308*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MAT2B

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000321757
Start	163518293:163518293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768283411
CDS Mutation	c.935G>A
AA Mutation	p.Arg312Gln(p.R312Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000321757
Start	163518230:163518230(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.872G>T
AA Mutation	p.Arg291Ile(p.R291I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000321757
Start	163516568:163516568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200525612
CDS Mutation	c.577G>A
AA Mutation	p.Glu193Lys(p.E193K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript