Colon Cancer: Gene >> TRIP10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313244
Start	6741244:6741244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.160C>G
AA Mutation	p.Leu54Val(p.L54V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313244
Start	6746503:6746503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781461983
CDS Mutation	c.1204C>T
AA Mutation	p.Arg402Trp(p.R402W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313244
Start	6746149:6746149(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1105G>C
AA Mutation	p.Val369Leu(p.V369L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313244
Start	6743767:6743767(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371193305
CDS Mutation	c.573G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313244
Start	6751166:6751166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147390840
CDS Mutation	c.1761C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313244
Start	6750408:6750408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373824686
CDS Mutation	c.1512C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313244
Start	6746034:6746034(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.995delC
AA Mutation	p.Pro332HisfsTer31(p.P332Hfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313244
Start	6746048:6746048(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1009delC
AA Mutation	p.Leu337TrpfsTer26(p.L337Wfs*26)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TRIP10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000313244
Start	6744977:6744977(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.967T>A
AA Mutation	p.Phe323Ile(p.F323I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000313244
Start	6744843:6744843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765702512
CDS Mutation	c.833G>A
AA Mutation	p.Arg278His(p.R278H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000313244
Start	6743798:6743798(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.604G>A
AA Mutation	p.Ala202Thr(p.A202T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313244
Start	6743761:6743761(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.567A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000313244
Start	6742988:6742988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148560112
CDS Mutation	c.219C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000313244
Start	6746055:6746055(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1016delG
AA Mutation	p.Gly339AlafsTer24(p.G339Afs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript