Colon Cancer: Gene >> REXO1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000170168
Start	1827737:1827737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs760529975
CDS Mutation	c.1052C>T
AA Mutation	p.Pro351Leu(p.P351L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000170168
Start	1828118:1828118(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.671A>G
AA Mutation	p.Asp224Gly(p.D224G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000170168
Start	1827477:1827477(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs780025948
CDS Mutation	c.1312T>C
AA Mutation	p.Ser438Pro(p.S438P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000170168
Start	1819991:1819991(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs765143258
CDS Mutation	c.2593G>A
AA Mutation	p.Val865Met(p.V865M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000170168
Start	1817775:1817775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3022G>A
AA Mutation	p.Gly1008Arg(p.G1008R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000170168
Start	1821629:1821629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs759792519
CDS Mutation	c.2284G>A
AA Mutation	p.Gly762Ser(p.G762S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000170168
Start	1828151:1828151(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.638G>A
AA Mutation	p.Ser213Asn(p.S213N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000170168
Start	1816444:1816444(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.3443T>C
AA Mutation	p.Leu1148Pro(p.L1148P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000170168
Start	1827573:1827573(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs562950047
CDS Mutation	c.1216C>T
AA Mutation	p.Arg406Trp(p.R406W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000170168
Start	1818565:1818565(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2933C>A
AA Mutation	p.Thr978Asn(p.T978N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000170168
Start	1828201:1828201(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767396382
CDS Mutation	c.588C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000170168
Start	1827904:1827904(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.885G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000170168
Start	1828554:1828554(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.235delG
AA Mutation	p.Glu79ArgfsTer81(p.E79Rfs*81)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> REXO1

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000170168
Start	1827579:1827579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1210C>T
AA Mutation	p.Arg404Ter(p.R404*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript