Colon Cancer: Gene >> MTMR7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000180173
Start	17302257:17302257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750208861
CDS Mutation	c.1517G>A
AA Mutation	p.Arg506His(p.R506H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000180173
Start	17371130:17371130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750007122
CDS Mutation	c.217C>T
AA Mutation	p.Arg73Cys(p.R73C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000180173
Start	17299897:17299897(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1948C>T
AA Mutation	p.Arg650Trp(p.R650W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000180173
Start	17371069:17371069(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.278T>C
AA Mutation	p.Val93Ala(p.V93A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000180173
Start	17371148:17371148(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.199G>A
AA Mutation	p.Gly67Arg(p.G67R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000180173
Start	17304490:17304490(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1382C>T
AA Mutation	p.Ala461Val(p.A461V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000180173
Start	17331241:17331241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.774G>T
AA Mutation	p.Glu258Asp(p.E258D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000180173
Start	17300060:17300060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1785A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000180173
Start	17373136:17373136(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747268193
CDS Mutation	c.129C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000180173
Start	17371164:17371164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.183G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MTMR7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000180173
Start	17331248:17331248(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.767G>A
AA Mutation	p.Gly256Asp(p.G256D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000180173
Start	17331263:17331263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376725869
CDS Mutation	c.752G>A
AA Mutation	p.Arg251His(p.R251H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript