Colon Cancer: Gene >> TRIM15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000376694
Start	30172164:30172164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1213G>A
AA Mutation	p.Asp405Asn(p.D405N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000376694
Start	30168422:30168422(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.600G>T
AA Mutation	p.Lys200Asn(p.K200N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000376694
Start	30171858:30171858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.907G>A
AA Mutation	p.Ala303Thr(p.A303T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000376694
Start	30168427:30168427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.605G>T
AA Mutation	p.Arg202Met(p.R202M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000376694
Start	30171994:30171994(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1043G>A
AA Mutation	p.Arg348His(p.R348H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376694
Start	30170546:30170546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.777C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376694
Start	30171977:30171977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1026G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376694
Start	30171989:30171989(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1038C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376694
Start	30172187:30172187(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1236G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376694
Start	30171995:30171995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1044C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000376694
Start	30163947:30163949(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.266_268delAGA
AA Mutation	p.Lys89del(p.K89del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TRIM15

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000376694
Start	30168308:30168308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.486C>T
Mutation Classification	Silent
Feature Type	Transcript