Colon Cancer: Gene >> APMAP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000217456
Start	24973663:24973663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.403T>G
AA Mutation	p.Phe135Val(p.F135V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000217456
Start	24969008:24969008(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs774016612
CDS Mutation	c.925C>T
AA Mutation	p.Arg309Trp(p.R309W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000217456
Start	24963959:24963959(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1105G>A
AA Mutation	p.Asp369Asn(p.D369N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000217456
Start	24969569:24969569(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.805G>T
AA Mutation	p.Asp269Tyr(p.D269Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000217456
Start	24971537:24971537(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.461G>A
AA Mutation	p.Gly154Asp(p.G154D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000217456
Start	24968987:24968987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.946T>C
AA Mutation	p.Tyr316His(p.Y316H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000217456
Start	24969004:24969004(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.929C>A
AA Mutation	p.Pro310His(p.P310H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217456
Start	24963978:24963978(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371057635
CDS Mutation	c.1086C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000217456
Start	24969598:24969598(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.776delC
AA Mutation	p.Pro259ArgfsTer31(p.P259Rfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000217456
Start	24968895:24968895(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1038delT
AA Mutation	p.Phe346LeufsTer9(p.F346Lfs*9)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	start_lost
Transcription ID	ENST00000217456
Start	24992688:24992688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1A>G
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> APMAP

No Mutation Annotation!