Colon Cancer: Gene >> OXER1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378661
Start	42763818:42763818(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs141097062
CDS Mutation	c.362C>T
AA Mutation	p.Thr121Met(p.T121M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378661
Start	42764166:42764166(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140987475
CDS Mutation	c.14G>A
AA Mutation	p.Arg5His(p.R5H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000378661
Start	42763681:42763681(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.499G>T
AA Mutation	p.Val167Phe(p.V167F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000378661
Start	42763137:42763137(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1043G>A
AA Mutation	p.Ser348Asn(p.S348N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000378661
Start	42763621:42763621(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.559G>A
AA Mutation	p.Ala187Thr(p.A187T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378661
Start	42763124:42763124(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs182457573
CDS Mutation	c.1056C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378661
Start	42763361:42763361(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.819G>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000378661
Start	42763205:42763205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769126172
CDS Mutation	c.975C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378661
Start	42763949:42763949(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs753912794
CDS Mutation	c.231delG
AA Mutation	p.Ser78ProfsTer64(p.S78Pfs*64)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000378661
Start	42763948:42763949(version: GRCh38)
Mutation Type	INS
dbSNP_RS	rs764276620
CDS Mutation	c.231dupG
AA Mutation	p.Ser78ValfsTer61(p.S78Vfs*61)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> OXER1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000378661
Start	42763197:42763197(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750491796
CDS Mutation	c.983G>A
AA Mutation	p.Arg328Gln(p.R328Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000378661
Start	42763372:42763372(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.808T>C
AA Mutation	p.Phe270Leu(p.F270L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript