Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MMP10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000279441
Start	102779592:102779592(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.259C>T
AA Mutation	p.Arg87Cys(p.R87C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000279441
Start	102776326:102776326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139185475
CDS Mutation	c.886G>A
AA Mutation	p.Asp296Asn(p.D296N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000279441
Start	102776650:102776650(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.749T>G
AA Mutation	p.Leu250Arg(p.L250R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000279441
Start	102779243:102779243(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.466G>C
AA Mutation	p.Ala156Pro(p.A156P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000279441
Start	102778735:102778736(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.510_511delTT
AA Mutation	p.Phe170LeufsTer4(p.F170Lfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000279441
Start	102776764:102776767(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.632_635delTATT
AA Mutation	p.Leu211SerfsTer23(p.L211Sfs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000279441
Start	102779664:102779664(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.187delA
AA Mutation	p.Ile63SerfsTer12(p.I63Sfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MMP10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000279441
Start	102779644:102779644(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.207C>A
AA Mutation	p.Phe69Leu(p.F69L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000279441
Start	102776296:102776296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.916C>A
AA Mutation	p.Leu306Met(p.L306M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000279441
Start	102776401:102776401(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.811G>T
AA Mutation	p.Glu271Ter(p.E271*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript