Colon Cancer: Gene >> ERF

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000222329
Start	42249142:42249142(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.970T>A
AA Mutation	p.Tyr324Asn(p.Y324N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000222329
Start	42249610:42249610(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.502T>C
AA Mutation	p.Ser168Pro(p.S168P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000222329
Start	42249496:42249496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs767080643
CDS Mutation	c.616G>A
AA Mutation	p.Ala206Thr(p.A206T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000222329
Start	42249899:42249899(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs769239795
CDS Mutation	c.301C>T
AA Mutation	p.Arg101Trp(p.R101W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000222329
Start	42250428:42250428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.160G>A
AA Mutation	p.Glu54Lys(p.E54K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000222329
Start	42250355:42250355(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.233A>G
AA Mutation	p.Tyr78Cys(p.Y78C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000222329
Start	42248542:42248542(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1570C>G
AA Mutation	p.Pro524Ala(p.P524A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000222329
Start	42248853:42248853(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1259C>T
AA Mutation	p.Pro420Leu(p.P420L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000222329
Start	42250379:42250379(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370521331
CDS Mutation	c.209G>A
AA Mutation	p.Arg70His(p.R70H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000222329
Start	42248484:42248484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1628T>C
AA Mutation	p.Leu543Pro(p.L543P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222329
Start	42248630:42248630(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs138540323
CDS Mutation	c.1482C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222329
Start	42249026:42249026(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1086C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000222329
Start	42248543:42248543(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1569delG
AA Mutation	p.Leu525SerfsTer6(p.L525Sfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000222329
Start	42249393:42249393(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.719delG
AA Mutation	p.Gly240ValfsTer31(p.G240Vfs*31)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000222329
Start	42249216:42249216(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	rs780487406
CDS Mutation	c.896delG
AA Mutation	p.Gly299GlufsTer12(p.G299Efs*12)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000222329
Start	42248539:42248539(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1573delC
AA Mutation	p.Leu525SerfsTer6(p.L525Sfs*6)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> ERF

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222329
Start	42249533:42249533(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.579G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222329
Start	42250384:42250384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772092372
CDS Mutation	c.204C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000222329
Start	42250423:42250423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776977688
CDS Mutation	c.165C>T
Mutation Classification	Silent
Feature Type	Transcript