Colon Cancer: Gene >> TMEM245

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000374586
Start	109091114:109091114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.958T>C
AA Mutation	p.Ser320Pro(p.S320P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000374586
Start	109050602:109050602(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1945G>A
AA Mutation	p.Gly649Arg(p.G649R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000374586
Start	109119783:109119783(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.131T>C
AA Mutation	p.Leu44Pro(p.L44P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000374586
Start	109093475:109093475(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.916G>A
AA Mutation	p.Glu306Lys(p.E306K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000374586
Start	109050596:109050596(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1951G>A
AA Mutation	p.Ala651Thr(p.A651T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000374586
Start	109106521:109106521(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.786A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374586
Start	109038049:109038050(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2191_2192delAT
AA Mutation	p.Met731ValfsTer34(p.M731Vfs*34)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000374586
Start	109087327:109087327(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1166delA
AA Mutation	p.Lys389SerfsTer12(p.K389Sfs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TMEM245

No Mutation Annotation!