Colon Cancer: Gene >> MAP3K5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359015
Start	136656433:136656433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1554T>G
AA Mutation	p.Ile518Met(p.I518M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359015
Start	136669328:136669328(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1321G>T
AA Mutation	p.Ala441Ser(p.A441S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359015
Start	136697260:136697260(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.934G>T
AA Mutation	p.Asp312Tyr(p.D312Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359015
Start	136791757:136791757(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.401A>C
AA Mutation	p.Lys134Thr(p.K134T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359015
Start	136605349:136605349(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2539G>A
AA Mutation	p.Ala847Thr(p.A847T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000359015
Start	136592202:136592202(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3196G>A
AA Mutation	p.Val1066Met(p.V1066M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000359015
Start	136659324:136659324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1421G>A
AA Mutation	p.Ser474Asn(p.S474N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000359015
Start	136567779:136567779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3613C>G
AA Mutation	p.Gln1205Glu(p.Q1205E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000359015
Start	136697319:136697319(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.875T>C
AA Mutation	p.Leu292Ser(p.L292S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000359015
Start	136580390:136580390(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3428G>A
AA Mutation	p.Arg1143Gln(p.R1143Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000359015
Start	136694249:136694249(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770548145
CDS Mutation	c.1144G>A
AA Mutation	p.Glu382Lys(p.E382K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000359015
Start	136601844:136601844(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2815A>C
AA Mutation	p.Lys939Gln(p.K939Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000359015
Start	136605270:136605270(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2618A>C
AA Mutation	p.Glu873Ala(p.E873A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant
Transcription ID	ENST00000359015
Start	136613142:136613142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2393A>G
AA Mutation	p.Gln798Arg(p.Q798R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359015
Start	136583576:136583576(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3390A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359015
Start	136639572:136639572(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1905C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359015
Start	136592589:136592589(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749467328
CDS Mutation	c.2904G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359015
Start	136698539:136698539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.756T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359015
Start	136601941:136601941(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs267600833
CDS Mutation	c.2718C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000359015
Start	136592227:136592227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368851337
CDS Mutation	c.3171C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359015
Start	136583737:136583737(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3229delG
AA Mutation	p.Ala1077LeufsTer6(p.A1077Lfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359015
Start	136669387:136669387(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1262delA
AA Mutation	p.Lys421ArgfsTer37(p.K421Rfs*37)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359015
Start	136583570:136583571(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.3395_3396delTT
AA Mutation	p.Phe1132TrpfsTer8(p.F1132Wfs*8)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> MAP3K5

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000359015
Start	136557774:136557774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4109G>A
AA Mutation	p.Arg1370Gln(p.R1370Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000359015
Start	136557776:136557776(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.4107T>G
AA Mutation	p.Phe1369Leu(p.F1369L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000359015
Start	136592181:136592181(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3217T>A
AA Mutation	p.Leu1073Ile(p.L1073I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000359015
Start	136562539:136562539(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3838G>A
AA Mutation	p.Glu1280Lys(p.E1280K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000359015
Start	136637373:136637373(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1968G>T
AA Mutation	p.Glu656Asp(p.E656D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained
Transcription ID	ENST00000359015
Start	136583680:136583680(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3286G>T
AA Mutation	p.Glu1096Ter(p.E1096*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000359015
Start	136592288:136592289(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.3109_3110insG
AA Mutation	p.Lys1037ArgfsTer13(p.K1037Rfs*13)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript