Colon Cancer: Gene >> MAP3K14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344686
Start	45286841:45286841(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.742G>A
AA Mutation	p.Gly248Arg(p.G248R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000344686
Start	45267651:45267651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755630489
CDS Mutation	c.2081C>T
AA Mutation	p.Ser694Leu(p.S694L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000344686
Start	45286610:45286610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370661357
CDS Mutation	c.973C>T
AA Mutation	p.Arg325Cys(p.R325C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000344686
Start	45271155:45271155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1724C>T
AA Mutation	p.Ala575Val(p.A575V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000344686
Start	45286951:45286951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.632A>T
AA Mutation	p.Lys211Met(p.K211M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000344686
Start	45286435:45286435(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1148C>T
AA Mutation	p.Thr383Ile(p.T383I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000344686
Start	45266539:45266539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371527687
CDS Mutation	c.2576A>G
AA Mutation	p.Asn859Ser(p.N859S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000344686
Start	45270464:45270464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1921C>T
AA Mutation	p.Arg641Cys(p.R641C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000344686
Start	45286930:45286930(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199558586
CDS Mutation	c.653G>A
AA Mutation	p.Arg218Gln(p.R218Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000344686
Start	45265216:45265216(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2626C>T
AA Mutation	p.Arg876Trp(p.R876W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000344686
Start	45290660:45290660(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs55820104
CDS Mutation	c.86C>T
AA Mutation	p.Thr29Met(p.T29M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000344686
Start	45271099:45271099(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1780C>T
AA Mutation	p.His594Tyr(p.H594Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344686
Start	45267125:45267125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2400C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344686
Start	45270546:45270546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs572439695
CDS Mutation	c.1839G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344686
Start	45286517:45286517(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759193300
CDS Mutation	c.1066C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> MAP3K14

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000344686
Start	45289245:45289245(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.317A>C
AA Mutation	p.Lys106Thr(p.K106T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000344686
Start	45286842:45286842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754605998
CDS Mutation	c.741C>T
Mutation Classification	Silent
Feature Type	Transcript