Colon Cancer: Gene >> MAP2K7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7911031:7911031(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.727G>A
AA Mutation	p.Asp243Asn(p.D243N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7911139:7911139(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.835G>A
AA Mutation	p.Gly279Ser(p.G279S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7910778:7910778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.650G>A
AA Mutation	p.Arg217His(p.R217H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7912396:7912396(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs775112625
CDS Mutation	c.1225G>A
AA Mutation	p.Val409Ile(p.V409I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7911479:7911479(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.980C>T
AA Mutation	p.Thr327Met(p.T327M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7911047:7911047(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.743A>G
AA Mutation	p.Asn248Ser(p.N248S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000397979
Start	7910697:7910697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs377648179
CDS Mutation	c.569C>T
AA Mutation	p.Thr190Met(p.T190M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7911085:7911085(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.781G>A
AA Mutation	p.Asp261Asn(p.D261N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7910489:7910489(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.484C>T
AA Mutation	p.Arg162Cys(p.R162C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7912367:7912367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201368825
CDS Mutation	c.1196C>T
AA Mutation	p.Ala399Val(p.A399V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397979
Start	7910710:7910710(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200708722
CDS Mutation	c.582C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397979
Start	7911492:7911492(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.993C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397979
Start	7910467:7910467(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs373551377
CDS Mutation	c.462C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397979
Start	7910280:7910280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369656037
CDS Mutation	c.354C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397979
Start	7912320:7912320(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200201904
CDS Mutation	c.1149C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397979
Start	7911030:7911030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376803808
CDS Mutation	c.726C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000397979
Start	7911264:7911264(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.875delC
AA Mutation	p.Pro292GlnfsTer119(p.P292Qfs*119)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000397979
Start	7903966:7903966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.22C>T
AA Mutation	p.Gln8Ter(p.Q8*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MAP2K7

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7911029:7911029(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.725G>A
AA Mutation	p.Arg242His(p.R242H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000397979
Start	7912367:7912367(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201368825
CDS Mutation	c.1196C>T
AA Mutation	p.Ala399Val(p.A399V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000397979
Start	7910307:7910307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.381C>G
Mutation Classification	Silent
Feature Type	Transcript