Colon Cancer: Gene >> MMP13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260302
Start	102955451:102955451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.163A>C
AA Mutation	p.Ile55Leu(p.I55L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260302
Start	102944306:102944306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1376T>G
AA Mutation	p.Ile459Ser(p.I459S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000260302
Start	102944309:102944309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1373G>A
AA Mutation	p.Arg458His(p.R458H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000260302
Start	102955448:102955448(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.166C>A
AA Mutation	p.Leu56Met(p.L56M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000260302
Start	102955493:102955493(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767829684
CDS Mutation	c.121C>T
AA Mutation	p.Arg41Cys(p.R41C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000260302
Start	102955282:102955282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.332T>G
AA Mutation	p.Leu111Arg(p.L111R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000260302
Start	102945736:102945736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1225A>G
AA Mutation	p.Asn409Asp(p.N409D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000260302
Start	102955492:102955492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.122G>A
AA Mutation	p.Arg41His(p.R41H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260302
Start	102952139:102952139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782295095
CDS Mutation	c.672C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260302
Start	102955326:102955326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.288C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260302
Start	102954567:102954567(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs576919878
CDS Mutation	c.402C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000260302
Start	102947894:102947894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1208G>A
AA Mutation	p.Trp403Ter(p.W403*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260302
Start	102947993:102947994(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.1108dupA
AA Mutation	p.Ile370AsnfsTer3(p.I370Nfs*3)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MMP13

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260302
Start	102944301:102944301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1381C>T
AA Mutation	p.Arg461Cys(p.R461C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260302
Start	102952139:102952139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782295095
CDS Mutation	c.672C>T
Mutation Classification	Silent
Feature Type	Transcript