Colon Cancer: Gene >> MAP3K9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000554752
Start	70801017:70801017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.470A>T
AA Mutation	p.Lys157Met(p.K157M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000554752
Start	70800907:70800907(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.580C>G
AA Mutation	p.Leu194Val(p.L194V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000554752
Start	70761038:70761038(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770124979
CDS Mutation	c.965G>A
AA Mutation	p.Arg322Gln(p.R322Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000554752
Start	70730688:70730688(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758186971
CDS Mutation	c.3007C>T
AA Mutation	p.Arg1003Trp(p.R1003W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000554752
Start	70732709:70732709(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772906765
CDS Mutation	c.2660G>A
AA Mutation	p.Arg887His(p.R887H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000554752
Start	70808924:70808924(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.248C>T
AA Mutation	p.Ser83Phe(p.S83F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000554752
Start	70732961:70732961(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756820633
CDS Mutation	c.2408G>A
AA Mutation	p.Arg803His(p.R803H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000554752
Start	70738296:70738296(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs572761925
CDS Mutation	c.1793C>T
AA Mutation	p.Thr598Met(p.T598M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000554752
Start	70742474:70742474(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1444C>T
AA Mutation	p.Arg482Trp(p.R482W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000554752
Start	70730649:70730649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201827381
CDS Mutation	c.3046C>T
AA Mutation	p.Arg1016Cys(p.R1016C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000554752
Start	70733242:70733242(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2127C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000554752
Start	70800857:70800857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.630T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000554752
Start	70800764:70800764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.723C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000554752
Start	70732651:70732651(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs774413853
CDS Mutation	c.2718delC
AA Mutation	p.Ser907ArgfsTer21(p.S907Rfs*21)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000554752
Start	70730786:70730786(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.2909delC
AA Mutation	p.Pro970GlnfsTer74(p.P970Qfs*74)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	stop_gained
Transcription ID	ENST00000554752
Start	70761005:70761005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.998G>A
AA Mutation	p.Trp333Ter(p.W333*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000554752
Start	70736023:70736024(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1850dupC
AA Mutation	p.Gln618SerfsTer4(p.Q618Sfs*4)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> MAP3K9

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000554752
Start	70730636:70730636(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3059C>A
AA Mutation	p.Pro1020Gln(p.P1020Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000554752
Start	70733167:70733167(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2202G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000554752
Start	70750035:70750035(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1048C>T
AA Mutation	p.Arg350Ter(p.R350*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript