Colon Cancer: Gene >> DBT

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000370132
Start	100218645:100218645(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs766629953
CDS Mutation	c.536G>A
AA Mutation	p.Arg179His(p.R179H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000370132
Start	100230816:100230816(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.350T>C
AA Mutation	p.Val117Ala(p.V117A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000370132
Start	100214870:100214870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.886C>A
AA Mutation	p.Pro296Thr(p.P296T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000370132
Start	100215984:100215984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.771A>C
AA Mutation	p.Lys257Asn(p.K257N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000370132
Start	100216042:100216042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.713C>A
AA Mutation	p.Pro238His(p.P238H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000370132
Start	100216171:100216171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.584G>T
AA Mutation	p.Gly195Val(p.G195V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000370132
Start	100196268:100196268(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1436T>C
AA Mutation	p.Leu479Pro(p.L479P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000370132
Start	100206491:100206491(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1163C>T
AA Mutation	p.Thr388Ile(p.T388I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000370132
Start	100230894:100230894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.272C>T
AA Mutation	p.Thr91Ile(p.T91I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370132
Start	100214841:100214841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.915C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000370132
Start	100196285:100196285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1419C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370132
Start	100230806:100230806(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs398123668
CDS Mutation	c.360delA
AA Mutation	p.Lys120AsnfsTer6(p.K120Nfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000370132
Start	100196276:100196276(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1428delT
AA Mutation	p.Phe476LeufsTer4(p.F476Lfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	stop_gained
Transcription ID	ENST00000370132
Start	100214879:100214879(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.877G>T
AA Mutation	p.Glu293Ter(p.E293*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> DBT

No Mutation Annotation!