Colon Cancer: Gene >> TIMP4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000287814
Start	12157407:12157407(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368380293
CDS Mutation	c.215G>A
AA Mutation	p.Arg72Gln(p.R72Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000287814
Start	12153557:12153557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.633C>A
AA Mutation	p.His211Gln(p.H211Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000287814
Start	12153678:12153678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755266079
CDS Mutation	c.512C>T
AA Mutation	p.Ser171Leu(p.S171L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000287814
Start	12153586:12153586(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.604G>T
AA Mutation	p.Asp202Tyr(p.D202Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000287814
Start	12154340:12154340(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.464A>C
AA Mutation	p.Asn155Thr(p.N155T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000287814
Start	12154355:12154355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.449A>G
AA Mutation	p.His150Arg(p.H150R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287814
Start	12157445:12157445(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755939718
CDS Mutation	c.177G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287814
Start	12153643:12153643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.547T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287814
Start	12153584:12153584(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765096492
CDS Mutation	c.606C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TIMP4

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000287814
Start	12157408:12157408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750080317
CDS Mutation	c.214C>A
Mutation Classification	Silent
Feature Type	Transcript