Colon Cancer: Gene >> MAPK15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338033
Start	143718072:143718072(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.191T>C
AA Mutation	p.Leu64Pro(p.L64P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338033
Start	143721642:143721642(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372002074
CDS Mutation	c.1298C>T
AA Mutation	p.Ala433Val(p.A433V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000338033
Start	143720806:143720806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs573414435
CDS Mutation	c.883G>A
AA Mutation	p.Ala295Thr(p.A295T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000338033
Start	143718240:143718240(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.224G>C
AA Mutation	p.Ser75Thr(p.S75T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000338033
Start	143717725:143717725(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201487703
CDS Mutation	c.98G>A
AA Mutation	p.Arg33Gln(p.R33Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338033
Start	143718247:143718247(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.231T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000338033
Start	143721850:143721850(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1428C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000338033
Start	143721653:143721653(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1314delC
AA Mutation	p.Leu439Ter(p.L439*)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MAPK15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000338033
Start	143719381:143719381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.620T>A
AA Mutation	p.Ile207Asn(p.I207N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000338033
Start	143721568:143721568(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1224G>T
AA Mutation	p.Lys408Asn(p.K408N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript