Colon Cancer: Gene >> MMP14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311852
Start	22843358:22843358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.790A>G
AA Mutation	p.Met264Val(p.M264V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311852
Start	22836822:22836822(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5C>A
AA Mutation	p.Ser2Tyr(p.S2Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000311852
Start	22842462:22842462(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.433C>T
AA Mutation	p.Arg145Cys(p.R145C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000311852
Start	22842474:22842474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748601843
CDS Mutation	c.445C>T
AA Mutation	p.Arg149Cys(p.R149C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000311852
Start	22842555:22842555(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145801508
CDS Mutation	c.526G>A
AA Mutation	p.Asp176Asn(p.D176N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311852
Start	22845901:22845901(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760876083
CDS Mutation	c.1611G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311852
Start	22845892:22845892(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1602C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311852
Start	22844682:22844682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1203G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311852
Start	22842683:22842683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371769574
CDS Mutation	c.654C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MMP14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000311852
Start	22845897:22845897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758484236
CDS Mutation	c.1607C>T
AA Mutation	p.Ala536Val(p.A536V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000311852
Start	22844770:22844770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770392329
CDS Mutation	c.1291C>T
AA Mutation	p.Arg431Cys(p.R431C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311852
Start	22843285:22843285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs548260059
CDS Mutation	c.717C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000311852
Start	22842617:22842617(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368784954
CDS Mutation	c.588C>T
Mutation Classification	Silent
Feature Type	Transcript