Colon Cancer: Gene >> CSE1L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262982
Start	49074819:49074819(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1101G>C
AA Mutation	p.Glu367Asp(p.E367D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000262982
Start	49085293:49085293(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1630G>A
AA Mutation	p.Ala544Thr(p.A544T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000262982
Start	49067227:49067227(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.514G>A
AA Mutation	p.Glu172Lys(p.E172K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000262982
Start	49072343:49072343(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149344844
CDS Mutation	c.826G>A
AA Mutation	p.Ala276Thr(p.A276T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000262982
Start	49066486:49066486(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs753618454
CDS Mutation	c.452G>A
AA Mutation	p.Arg151His(p.R151H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000262982
Start	49089335:49089335(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1910T>C
AA Mutation	p.Val637Ala(p.V637A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000262982
Start	49089541:49089541(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1976T>G
AA Mutation	p.Phe659Cys(p.F659C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262982
Start	49072600:49072600(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.969A>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262982
Start	49090828:49090828(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759049407
CDS Mutation	c.2268G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000262982
Start	49084154:49084154(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1611T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000262982
Start	49075371:49075371(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1191delT
AA Mutation	p.Phe397LeufsTer5(p.F397Lfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	stop_gained
Transcription ID	ENST00000262982
Start	49074820:49074820(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1102G>T
AA Mutation	p.Glu368Ter(p.E368*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	stop_gained
Transcription ID	ENST00000262982
Start	49066228:49066228(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.265C>T
AA Mutation	p.Arg89Ter(p.R89*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> CSE1L

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000262982
Start	49085302:49085302(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs748051425
CDS Mutation	c.1639G>A
AA Mutation	p.Ala547Thr(p.A547T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript