Colon Cancer: Gene >> MMP26

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300762
Start	4992118:4992118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.750T>G
AA Mutation	p.His250Gln(p.H250Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300762
Start	4991440:4991440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.539G>A
AA Mutation	p.Gly180Glu(p.G180E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000300762
Start	4991436:4991436(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.535T>A
AA Mutation	p.Ser179Thr(p.S179T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000300762
Start	4991463:4991463(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.562G>T
AA Mutation	p.Asp188Tyr(p.D188Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000300762
Start	4990632:4990632(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764121875
CDS Mutation	c.355G>A
AA Mutation	p.Ala119Thr(p.A119T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000300762
Start	4990698:4990698(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.421C>G
AA Mutation	p.Gln141Glu(p.Q141E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300762
Start	4989863:4989863(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.315T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000300762
Start	4988259:4988259(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757679480
CDS Mutation	c.48C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000300762
Start	4990646:4990647(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.375_376delTA
AA Mutation	p.Tyr125Ter(p.Y125*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000300762
Start	4991472:4991472(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.571G>T
AA Mutation	p.Glu191Ter(p.E191*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MMP26

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000300762
Start	4990654:4990654(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.377A>C
AA Mutation	p.Asn126Thr(p.N126T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000300762
Start	4990641:4990641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.364G>T
AA Mutation	p.Asp122Tyr(p.D122Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000300762
Start	4990641:4990641(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.364G>A
AA Mutation	p.Asp122Asn(p.D122N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000300762
Start	4992058:4992058(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.690C>A
AA Mutation	p.Tyr230Ter(p.Y230*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript