Colon Cancer: Gene >> MVD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000301012
Start	88652529:88652529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1199C>T
AA Mutation	p.Ala400Val(p.A400V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000301012
Start	88655399:88655399(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.697G>A
AA Mutation	p.Val233Met(p.V233M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000301012
Start	88656275:88656275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.433G>C
AA Mutation	p.Glu145Gln(p.E145Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000301012
Start	88652542:88652542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1186C>T
AA Mutation	p.Pro396Ser(p.P396S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000301012
Start	88655291:88655291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.805G>A
AA Mutation	p.Asp269Asn(p.D269N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000301012
Start	88655222:88655222(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.874A>G
AA Mutation	p.Asn292Asp(p.N292D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000301012
Start	88655363:88655363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780694192
CDS Mutation	c.733C>T
AA Mutation	p.Arg245Trp(p.R245W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000301012
Start	88653330:88653330(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373274334
CDS Mutation	c.1092C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	stop_gained
Transcription ID	ENST00000301012
Start	88656185:88656185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.523C>T
AA Mutation	p.Gln175Ter(p.Q175*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MVD

No Mutation Annotation!