Colon Cancer: Gene >> TMEM173

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000330794
Start	139476371:139476371(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1030G>T
AA Mutation	p.Gly344Cys(p.G344C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000330794
Start	139478335:139478335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767228149
CDS Mutation	c.694C>T
AA Mutation	p.His232Tyr(p.H232Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000330794
Start	139478271:139478271(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148833313
CDS Mutation	c.758G>A
AA Mutation	p.Arg253Gln(p.R253Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330794
Start	139480815:139480815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746690249
CDS Mutation	c.495C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000330794
Start	139481249:139481249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.321C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000330794
Start	139481600:139481600(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.105delG
AA Mutation	p.Leu36Ter(p.L36*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000330794
Start	139481324:139481324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770660580
CDS Mutation	c.246G>A
AA Mutation	p.Trp82Ter(p.W82*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> TMEM173

No Mutation Annotation!