Colon Cancer: Gene >> MYOD1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000250003
Start	17720131:17720131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.349C>T
AA Mutation	p.Arg117Cys(p.R117C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000250003
Start	17719943:17719943(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.161G>A
AA Mutation	p.Gly54Asp(p.G54D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000250003
Start	17720192:17720192(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.410C>T
AA Mutation	p.Ser137Leu(p.S137L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000250003
Start	17719813:17719813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781508900
CDS Mutation	c.31G>A
AA Mutation	p.Val11Ile(p.V11I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000250003
Start	17720104:17720104(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.322G>A
AA Mutation	p.Ala108Thr(p.A108T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000250003
Start	17720929:17720929(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.658G>A
AA Mutation	p.Ala220Thr(p.A220T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000250003
Start	17719888:17719888(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.106G>A
AA Mutation	p.Asp36Asn(p.D36N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250003
Start	17719926:17719926(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.144G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250003
Start	17719959:17719959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.177C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250003
Start	17720190:17720190(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.408G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250003
Start	17719896:17719896(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.114G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250003
Start	17721289:17721289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.744C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250003
Start	17719911:17719911(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.129C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250003
Start	17720211:17720211(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.429G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000250003
Start	17720238:17720238(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.456C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MYOD1

No Mutation Annotation!