Colon Cancer: Gene >> MAP2K2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262948
Start	4099236:4099236(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs531584619
CDS Mutation	c.884C>T
AA Mutation	p.Ser295Leu(p.S295L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000262948
Start	4117627:4117627(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.95C>A
AA Mutation	p.Ala32Glu(p.A32E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262948
Start	4099377:4099377(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761669626
CDS Mutation	c.743C>T
AA Mutation	p.Ser248Leu(p.S248L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262948
Start	4117526:4117526(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371852537
CDS Mutation	c.196G>A
AA Mutation	p.Glu66Lys(p.E66K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262948
Start	4099408:4099408(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.712C>T
AA Mutation	p.Arg238Trp(p.R238W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262948
Start	4110557:4110557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753713281
CDS Mutation	c.402C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262948
Start	4099265:4099265(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs778350557
CDS Mutation	c.855C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262948
Start	4101263:4101263(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141402203
CDS Mutation	c.546G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262948
Start	4110608:4110608(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.351C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262948
Start	4099217:4099217(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.903delC
AA Mutation	p.Arg303AlafsTer24(p.R303Afs*24)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000262948
Start	4101232:4101232(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.577C>T
AA Mutation	p.Arg193Ter(p.R193*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MAP2K2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262948
Start	4110648:4110648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.311A>G
AA Mutation	p.His104Arg(p.H104R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript