Colon Cancer: Gene >> CSRNP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000273153
Start	39144032:39144032(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.793G>A
AA Mutation	p.Ala265Thr(p.A265T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000273153
Start	39143457:39143457(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1368G>T
AA Mutation	p.Glu456Asp(p.E456D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000273153
Start	39144234:39144234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.683A>G
AA Mutation	p.Gln228Arg(p.Q228R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000273153
Start	39143647:39143647(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200794258
CDS Mutation	c.1178G>A
AA Mutation	p.Arg393His(p.R393H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000273153
Start	39145055:39145055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149009984
CDS Mutation	c.407G>A
AA Mutation	p.Arg136Gln(p.R136Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000273153
Start	39143135:39143135(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs112383054
CDS Mutation	c.1690G>A
AA Mutation	p.Ala564Thr(p.A564T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000273153
Start	39144321:39144321(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.596T>C
AA Mutation	p.Leu199Pro(p.L199P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000273153
Start	39144182:39144182(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.735C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000273153
Start	39145176:39145176(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.286delC
AA Mutation	p.Arg96AlafsTer49(p.R96Afs*49)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> CSRNP1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000273153
Start	39146561:39146561(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370236918
CDS Mutation	c.122G>A
AA Mutation	p.Arg41His(p.R41H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript