Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MS4A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345732
Start	60467010:60467010(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.625G>A
AA Mutation	p.Ala209Thr(p.A209T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000345732
Start	60466013:60466013(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.429T>G
AA Mutation	p.Ile143Met(p.I143M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000345732
Start	60468345:60468345(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.771G>T
AA Mutation	p.Lys257Asn(p.K257N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000345732
Start	60467041:60467041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs188842906
CDS Mutation	c.656C>T
AA Mutation	p.Thr219Met(p.T219M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345732
Start	60468405:60468405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.831G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000345732
Start	60466024:60466024(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs538978795
CDS Mutation	c.440T>A
AA Mutation	p.Leu147Ter(p.L147*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MS4A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345732
Start	60466021:60466021(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.437T>G
AA Mutation	p.Phe146Cys(p.F146C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000345732
Start	60462406:60462406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.32C>A
AA Mutation	p.Thr11Asn(p.T11N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345732
Start	60468405:60468405(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.831G>A
Mutation Classification	Silent
Feature Type	Transcript