Colon Cancer: Gene >> TMEM37

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000306406
Start	119437171:119437171(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771071832
CDS Mutation	c.304G>A
AA Mutation	p.Ala102Thr(p.A102T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000306406
Start	119436920:119436920(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780577316
CDS Mutation	c.53G>A
AA Mutation	p.Arg18His(p.R18H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000306406
Start	119437103:119437103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.236C>T
AA Mutation	p.Ala79Val(p.A79V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000306406
Start	119436922:119436922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747500777
CDS Mutation	c.55C>T
AA Mutation	p.Arg19Trp(p.R19W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000306406
Start	119437152:119437152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs567745556
CDS Mutation	c.285C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> TMEM37

No Mutation Annotation!