Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> MAP4K4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000347699
Start	101866558:101866558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776570846
CDS Mutation	c.2101G>A
AA Mutation	p.Gly701Arg(p.G701R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000347699
Start	101885251:101885251(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3150G>T
AA Mutation	p.Trp1050Cys(p.W1050C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000347699
Start	101831813:101831813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.601G>A
AA Mutation	p.Ala201Thr(p.A201T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000347699
Start	101877116:101877116(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2920G>A
AA Mutation	p.Glu974Lys(p.E974K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000347699
Start	101859059:101859059(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1459C>A
AA Mutation	p.Leu487Ile(p.L487I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000347699
Start	101874201:101874201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375228116
CDS Mutation	c.2755C>T
AA Mutation	p.Arg919Cys(p.R919C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000347699
Start	101877066:101877066(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2870A>C
AA Mutation	p.Lys957Thr(p.K957T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000347699
Start	101831739:101831739(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.527C>A
AA Mutation	p.Ala176Asp(p.A176D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000347699
Start	101869631:101869631(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199996114
CDS Mutation	c.2230G>A
AA Mutation	p.Ala744Thr(p.A744T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000347699
Start	101831743:101831743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.531G>T
AA Mutation	p.Gln177His(p.Q177H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000347699
Start	101869686:101869686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770671445
CDS Mutation	c.2285C>T
AA Mutation	p.Thr762Met(p.T762M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000347699
Start	101870324:101870324(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs372783884
CDS Mutation	c.2426C>T
AA Mutation	p.Thr809Met(p.T809M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	missense_variant
Transcription ID	ENST00000347699
Start	101859030:101859030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1430G>A
AA Mutation	p.Arg477Gln(p.R477Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000347699
Start	101839821:101839821(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.776C>T
AA Mutation	p.Ser259Leu(p.S259L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	missense_variant
Transcription ID	ENST00000347699
Start	101859674:101859674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1514G>T
AA Mutation	p.Arg505Leu(p.R505L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	missense_variant
Transcription ID	ENST00000347699
Start	101888914:101888914(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3615C>A
AA Mutation	p.Phe1205Leu(p.F1205L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	missense_variant
Transcription ID	ENST00000347699
Start	101891184:101891184(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3655C>T
AA Mutation	p.Arg1219Trp(p.R1219W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000347699
Start	101866433:101866433(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1976T>G
AA Mutation	p.Ile659Ser(p.I659S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	19
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347699
Start	101859774:101859774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1614G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	20
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347699
Start	101888824:101888824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3525C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	21
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347699
Start	101885233:101885233(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3132T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	22
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347699
Start	101887864:101887864(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3423G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	23
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347699
Start	101831764:101831764(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.552G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	24
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347699
Start	101887837:101887837(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753534395
CDS Mutation	c.3396G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	25
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347699
Start	101866557:101866557(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376560483
CDS Mutation	c.2100C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	26
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347699
Start	101859699:101859699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1539G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	27
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000347699
Start	101867251:101867251(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.2165delA
AA Mutation	p.Asn722MetfsTer3(p.N722Mfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	28
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000347699
Start	101698101:101698101(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.25delA
AA Mutation	p.Ser9ValfsTer62(p.S9Vfs*62)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	29
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000347699
Start	101888826:101888826(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.3530delG
AA Mutation	p.Gly1177GlufsTer5(p.G1177Efs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	30
Mutation Consequence	stop_gained
Transcription ID	ENST00000347699
Start	101856025:101856025(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1282C>T
AA Mutation	p.Arg428Ter(p.R428*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> MAP4K4

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000347699
Start	101823988:101823988(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.241A>C
AA Mutation	p.Asn81His(p.N81H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000347699
Start	101825403:101825403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.391G>A
AA Mutation	p.Ala131Thr(p.A131T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000347699
Start	101829580:101829580(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.494C>T
AA Mutation	p.Ala165Val(p.A165V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000347699
Start	101887097:101887097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3196G>T
AA Mutation	p.Glu1066Ter(p.E1066*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript