Colon Cancer: Gene >> MAP2K1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307102
Start	66387409:66387409(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.62A>C
AA Mutation	p.Asn21Thr(p.N21T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000307102
Start	66481878:66481878(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.692C>T
AA Mutation	p.Ser231Leu(p.S231L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000307102
Start	66443290:66443290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.449C>T
AA Mutation	p.Ser150Phe(p.S150F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000307102
Start	66436824:66436824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.370C>T
AA Mutation	p.Pro124Ser(p.P124S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000307102
Start	66435103:66435103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.157T>C
AA Mutation	p.Phe53Leu(p.F53L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000307102
Start	66435092:66435092(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.146G>A
AA Mutation	p.Arg49His(p.R49H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000307102
Start	66436837:66436837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.383G>A
AA Mutation	p.Gly128Asp(p.G128D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000307102
Start	66435113:66435113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.167A>C
AA Mutation	p.Gln56Pro(p.Q56P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000307102
Start	66435145:66435145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs727504317
CDS Mutation	c.199G>A
AA Mutation	p.Asp67Asn(p.D67N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000307102
Start	66436833:66436833(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.379G>A
AA Mutation	p.Val127Met(p.V127M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307102
Start	66435180:66435180(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.234T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000307102
Start	66490609:66490609(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781328871
CDS Mutation	c.1176C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000307102
Start	66485144:66485145(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.848_849insT
AA Mutation	p.Ala284GlyfsTer2(p.A284Gfs*2)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MAP2K1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000307102
Start	66435145:66435145(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs727504317
CDS Mutation	c.199G>A
AA Mutation	p.Asp67Asn(p.D67N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000307102
Start	66435103:66435103(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.157T>G
AA Mutation	p.Phe53Val(p.F53V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000307102
Start	66489252:66489252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.998A>C
AA Mutation	p.Glu333Ala(p.E333A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript