Colon Cancer: Gene >> MMP20

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260228
Start	102593572:102593572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1114G>A
AA Mutation	p.Gly372Arg(p.G372R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260228
Start	102611769:102611769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781580828
CDS Mutation	c.509C>A
AA Mutation	p.Ser170Tyr(p.S170Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260228
Start	102606579:102606579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145296288
CDS Mutation	c.909C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260228
Start	102609987:102609987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.567A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260228
Start	102609052:102609052(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.696G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260228
Start	102610008:102610008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148659857
CDS Mutation	c.546C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000260228
Start	102609061:102609061(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.687C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260228
Start	102625227:102625227(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.93delC
AA Mutation	p.Arg32GlyfsTer37(p.R32Gfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MMP20

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000260228
Start	102616891:102616891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.295C>A
AA Mutation	p.Arg99Ser(p.R99S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000260228
Start	102577397:102577397(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1381A>G
AA Mutation	p.Thr461Ala(p.T461A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000260228
Start	102616827:102616827(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.359delA
AA Mutation	p.Asn120IlefsTer3(p.N120Ifs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript