Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MATN3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000407540
Start	20006134:20006134(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.400G>A
AA Mutation	p.Glu134Lys(p.E134K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000407540
Start	20006025:20006025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.509T>C
AA Mutation	p.Met170Thr(p.M170T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000407540
Start	20006185:20006185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs563628955
CDS Mutation	c.349C>T
AA Mutation	p.Pro117Ser(p.P117S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000407540
Start	20005863:20005863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201491595
CDS Mutation	c.671G>A
AA Mutation	p.Arg224Gln(p.R224Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000407540
Start	20000454:20000454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1155A>T
AA Mutation	p.Lys385Asn(p.K385N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407540
Start	20005769:20005769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.765C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000407540
Start	20000450:20000450(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1159delA
AA Mutation	p.Thr387HisfsTer10(p.T387Hfs*10)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MATN3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000407540
Start	20003215:20003215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376404727
CDS Mutation	c.862C>T
AA Mutation	p.His288Tyr(p.H288Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000407540
Start	20005767:20005767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.767C>T
AA Mutation	p.Ser256Phe(p.S256F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000407540
Start	19997228:19997228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1200T>G
Mutation Classification	Silent
Feature Type	Transcript