Colon Cancer: Gene >> TMEM201

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000340381
Start	9598558:9598558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.539G>A
AA Mutation	p.Arg180His(p.R180H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000340381
Start	9597039:9597039(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752313181
CDS Mutation	c.415G>A
AA Mutation	p.Ala139Thr(p.A139T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000340381
Start	9613022:9613022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1940C>T
AA Mutation	p.Ala647Val(p.A647V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000340381
Start	9598620:9598620(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.601G>A
AA Mutation	p.Ala201Thr(p.A201T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000340381
Start	9607745:9607745(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1349G>A
AA Mutation	p.Ser450Asn(p.S450N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000340381
Start	9607756:9607756(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1360T>C
AA Mutation	p.Ser454Pro(p.S454P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340381
Start	9611784:9611784(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1797C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340381
Start	9596924:9596924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.300C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000340381
Start	9597032:9597032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.408C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000340381
Start	9610676:9610676(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1640delC
AA Mutation	p.Pro547LeufsTer38(p.P547Lfs*38)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> TMEM201

No Mutation Annotation!