Colon Cancer: Gene >> MSC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325509
Start	71844106:71844106(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.73G>A
AA Mutation	p.Ala25Thr(p.A25T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000325509
Start	71843848:71843848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.331G>A
AA Mutation	p.Ala111Thr(p.A111T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000325509
Start	71843829:71843829(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.350G>A
AA Mutation	p.Arg117His(p.R117H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000325509
Start	71842719:71842719(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776388351
CDS Mutation	c.563C>T
AA Mutation	p.Pro188Leu(p.P188L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000325509
Start	71842700:71842700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.582A>C
AA Mutation	p.Glu194Asp(p.E194D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000325509
Start	71844085:71844085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759036071
CDS Mutation	c.94C>T
AA Mutation	p.Arg32Cys(p.R32C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000325509
Start	71843980:71843980(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.199G>A
AA Mutation	p.Ala67Thr(p.A67T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325509
Start	71843741:71843741(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.438G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325509
Start	71842682:71842682(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.600A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325509
Start	71843816:71843816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.363C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325509
Start	71843858:71843858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.321G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325509
Start	71843672:71843672(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771055767
CDS Mutation	c.507G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325509
Start	71844080:71844080(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756904680
CDS Mutation	c.99C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325509
Start	71844164:71844164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.15G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MSC

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000325509
Start	71843848:71843848(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.331G>A
AA Mutation	p.Ala111Thr(p.A111T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000325509
Start	71843663:71843663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773546327
CDS Mutation	c.516C>T
Mutation Classification	Silent
Feature Type	Transcript