Colon Cancer: Gene >> MAPK10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359221
Start	86101172:86101172(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.610A>G
AA Mutation	p.Lys204Glu(p.K204E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359221
Start	86067789:86067789(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.969G>T
AA Mutation	p.Glu323Asp(p.E323D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359221
Start	86101102:86101102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752620406
CDS Mutation	c.680G>A
AA Mutation	p.Arg227His(p.R227H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359221
Start	86102001:86102001(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.457T>G
AA Mutation	p.Leu153Val(p.L153V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359221
Start	86067799:86067799(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757125320
CDS Mutation	c.959C>T
AA Mutation	p.Ala320Val(p.A320V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359221
Start	86103241:86103241(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.370A>T
AA Mutation	p.Ile124Phe(p.I124F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000359221
Start	86103216:86103216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.395C>T
AA Mutation	p.Pro132Leu(p.P132L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000359221
Start	86017349:86017349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1274A>G
AA Mutation	p.Glu425Gly(p.E425G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000359221
Start	86101981:86101981(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.477G>A
AA Mutation	p.Met159Ile(p.M159I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359221
Start	86017285:86017285(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1338A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359221
Start	86101074:86101074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.708G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000359221
Start	86031377:86031377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1165G>T
AA Mutation	p.Glu389Ter(p.E389*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MAPK10

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000359221
Start	86107350:86107350(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.239C>T
AA Mutation	p.Ala80Val(p.A80V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359221
Start	86101139:86101139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.643G>A
AA Mutation	p.Gly215Ser(p.G215S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359221
Start	86159456:86159456(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.78A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000359221
Start	86101965:86101965(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.493C>T
AA Mutation	p.Arg165Ter(p.R165*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000359221
Start	86029242:86029242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1207G>T
AA Mutation	p.Glu403Ter(p.E403*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript