Colon Cancer: Gene >> MAPK4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000400384
Start	50729487:50729487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1397C>T
AA Mutation	p.Ala466Val(p.A466V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000400384
Start	50729282:50729282(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764772500
CDS Mutation	c.1192C>T
AA Mutation	p.Arg398Cys(p.R398C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000400384
Start	50729723:50729723(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1633C>T
AA Mutation	p.Arg545Cys(p.R545C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000400384
Start	50726120:50726120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1012G>A
AA Mutation	p.Val338Met(p.V338M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000400384
Start	50729355:50729355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1265C>A
AA Mutation	p.Ala422Asp(p.A422D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000400384
Start	50664082:50664082(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.124G>A
AA Mutation	p.Ala42Thr(p.A42T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000400384
Start	50729663:50729663(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1573C>T
AA Mutation	p.Arg525Cys(p.R525C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400384
Start	50663976:50663976(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.18C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400384
Start	50715165:50715165(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.633C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400384
Start	50729392:50729392(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1302G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400384
Start	50664363:50664363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370089598
CDS Mutation	c.405C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400384
Start	50726119:50726119(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1011C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000400384
Start	50729680:50729680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1590C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000400384
Start	50721937:50721937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.692-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MAPK4

No Mutation Annotation!