Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MARCH8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319836
Start	45461284:45461284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751632778
CDS Mutation	c.370G>A
AA Mutation	p.Glu124Lys(p.E124K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000319836
Start	45458244:45458244(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138249794
CDS Mutation	c.871G>A
AA Mutation	p.Val291Ile(p.V291I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000319836
Start	45459204:45459204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573798318
CDS Mutation	c.487G>A
AA Mutation	p.Val163Ile(p.V163I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000319836
Start	45459237:45459237(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.454C>T
AA Mutation	p.Arg152Cys(p.R152C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000319836
Start	45533207:45533207(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.5G>A
AA Mutation	p.Ser2Asn(p.S2N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319836
Start	45458311:45458311(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.804C>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MARCH8

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000319836
Start	45458301:45458301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.814G>A
AA Mutation	p.Asp272Asn(p.D272N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000319836
Start	45461284:45461284(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751632778
CDS Mutation	c.370G>A
AA Mutation	p.Glu124Lys(p.E124K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000319836
Start	45464262:45464262(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.219G>A
Mutation Classification	Silent
Feature Type	Transcript