Colon Cancer: Gene >> MID1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317552
Start	10454909:10454909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1616G>A
AA Mutation	p.Gly539Asp(p.G539D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317552
Start	10566941:10566941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.607C>T
AA Mutation	p.Arg203Trp(p.R203W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000317552
Start	10567246:10567246(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs202142461
CDS Mutation	c.302G>A
AA Mutation	p.Arg101His(p.R101H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000317552
Start	10449564:10449564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750682655
CDS Mutation	c.1808G>A
AA Mutation	p.Arg603His(p.R603H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000317552
Start	10523180:10523180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.668T>C
AA Mutation	p.Leu223Ser(p.L223S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317552
Start	10469767:10469767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775126734
CDS Mutation	c.1215C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317552
Start	10449683:10449683(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1689G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317552
Start	10567254:10567254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.294C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MID1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000317552
Start	10449426:10449426(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1946C>T
AA Mutation	p.Thr649Met(p.T649M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000317552
Start	10566891:10566891(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.657G>T
AA Mutation	p.Leu219Phe(p.L219F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317552
Start	10459740:10459740(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748126421
CDS Mutation	c.1353C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317552
Start	10449482:10449482(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1890C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000317552
Start	10567299:10567299(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.249C>T
Mutation Classification	Silent
Feature Type	Transcript