Colon Cancer: Gene >> C1R

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000542285
Start	7090120:7090120(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.360C>A
AA Mutation	p.Phe120Leu(p.F120L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000542285
Start	7081006:7081006(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1644G>T
AA Mutation	p.Gln548His(p.Q548H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000542285
Start	7080705:7080705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1945G>A
AA Mutation	p.Ala649Thr(p.A649T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000542285
Start	7090220:7090220(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.260G>T
AA Mutation	p.Arg87Met(p.R87M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000542285
Start	7080964:7080964(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1686G>T
AA Mutation	p.Glu562Asp(p.E562D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000542285
Start	7080819:7080819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772664204
CDS Mutation	c.1831C>T
AA Mutation	p.Arg611Cys(p.R611C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000542285
Start	7088699:7088699(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772306231
CDS Mutation	c.949G>A
AA Mutation	p.Glu317Lys(p.E317K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000542285
Start	7080769:7080769(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1881G>T
AA Mutation	p.Lys627Asn(p.K627N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000542285
Start	7088842:7088842(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767341899
CDS Mutation	c.913G>A
AA Mutation	p.Glu305Lys(p.E305K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000542285
Start	7089464:7089464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs369628991
CDS Mutation	c.597G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000542285
Start	7081255:7081255(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs755994555
CDS Mutation	c.1395C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000542285
Start	7080661:7080661(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147540938
CDS Mutation	c.1989G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000542285
Start	7088960:7088960(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.795C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000542285
Start	7089414:7089414(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.647delC
AA Mutation	p.Pro216LeufsTer100(p.P216Lfs*100)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000542285
Start	7090181:7090181(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.299delC
AA Mutation	p.Pro100ArgfsTer15(p.P100Rfs*15)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> C1R

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000542285
Start	7091649:7091649(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.34T>C
AA Mutation	p.Phe12Leu(p.F12L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000542285
Start	7080975:7080975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776015455
CDS Mutation	c.1675G>A
AA Mutation	p.Ala559Thr(p.A559T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000542285
Start	7080736:7080736(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1914C>A
AA Mutation	p.Phe638Leu(p.F638L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript