Colon Cancer: Gene >> MAPK14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000229794
Start	36073703:36073703(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.430G>A
AA Mutation	p.Ala144Thr(p.A144T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000229794
Start	36107550:36107550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.937G>A
AA Mutation	p.Asp313Asn(p.D313N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000229794
Start	36052826:36052826(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.244A>C
AA Mutation	p.Asn82His(p.N82H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000229794
Start	36059307:36059307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.265G>A
AA Mutation	p.Val89Ile(p.V89I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000229794
Start	36072970:36072970(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.403C>A
AA Mutation	p.Leu135Ile(p.L135I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000229794
Start	36076568:36076568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.642C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000229794
Start	36107562:36107562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.949G>T
AA Mutation	p.Glu317Ter(p.E317*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000229794
Start	36072892:36072893(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.326dupT
AA Mutation	p.Met109IlefsTer17(p.M109Ifs*17)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MAPK14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000229794
Start	36072937:36072937(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.370G>A
AA Mutation	p.Asp124Asn(p.D124N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript