Colon Cancer: Gene >> CSF1R

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000286301
Start	150073304:150073304(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767493560
CDS Mutation	c.1079A>G
AA Mutation	p.Tyr360Cys(p.Y360C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000286301
Start	150057306:150057306(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2300C>T
AA Mutation	p.Ala767Val(p.A767V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000286301
Start	150080153:150080153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.491T>C
AA Mutation	p.Ile164Thr(p.I164T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000286301
Start	150080289:150080289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.355G>A
AA Mutation	p.Glu119Lys(p.E119K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000286301
Start	150080982:150080982(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.92T>C
AA Mutation	p.Val31Ala(p.V31A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000286301
Start	150073442:150073442(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.941C>T
AA Mutation	p.Thr314Ile(p.T314I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000286301
Start	150059824:150059824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2008G>A
AA Mutation	p.Asp670Asn(p.D670N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000286301
Start	150056068:150056068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2512G>A
AA Mutation	p.Val838Ile(p.V838I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000286301
Start	150061803:150061803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1673G>A
AA Mutation	p.Gly558Asp(p.G558D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000286301
Start	150056113:150056113(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2467G>C
AA Mutation	p.Ala823Pro(p.A823P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286301
Start	150068281:150068281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767351282
CDS Mutation	c.1560C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286301
Start	150077280:150077280(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.885G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286301
Start	150078175:150078175(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759716223
CDS Mutation	c.666C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000286301
Start	150080855:150080855(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777507344
CDS Mutation	c.219C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000286301
Start	150069907:150069907(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1476delG
AA Mutation	p.Ser493ValfsTer119(p.S493Vfs*119)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000286301
Start	150070546:150070546(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1108delC
AA Mutation	p.Arg370AlafsTer2(p.R370Afs*2)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000286301
Start	150070296:150070296(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1205delC
AA Mutation	p.Pro402GlnfsTer3(p.P402Qfs*3)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	18
Mutation Consequence	stop_gained
Transcription ID	ENST00000286301
Start	150078195:150078195(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758322216
CDS Mutation	c.646C>T
AA Mutation	p.Arg216Ter(p.R216*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CSF1R

No Mutation Annotation!