Colon Cancer: Gene >> AHRR

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000505113
Start	413432:413432(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.452A>G
AA Mutation	p.Gln151Arg(p.Q151R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000505113
Start	427987:427987(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762740242
CDS Mutation	c.901G>A
AA Mutation	p.Ala301Thr(p.A301T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000505113
Start	422774:422774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.499G>A
AA Mutation	p.Asp167Asn(p.D167N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000505113
Start	433951:433951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201569850
CDS Mutation	c.1223C>T
AA Mutation	p.Ala408Val(p.A408V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000505113
Start	434317:434317(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs762929753
CDS Mutation	c.1589C>T
AA Mutation	p.Thr530Met(p.T530M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000505113
Start	427934:427934(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201569519
CDS Mutation	c.848C>T
AA Mutation	p.Ala283Val(p.A283V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000505113
Start	413384:413384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763403491
CDS Mutation	c.404C>T
AA Mutation	p.Thr135Met(p.T135M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000505113
Start	434550:434550(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs201956288
CDS Mutation	c.1822C>T
AA Mutation	p.Arg608Cys(p.R608C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000505113
Start	434098:434098(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773041292
CDS Mutation	c.1370C>T
AA Mutation	p.Pro457Leu(p.P457L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000505113
Start	432854:432854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1031A>G
AA Mutation	p.Asp344Gly(p.D344G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000505113
Start	427886:427886(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs749711222
CDS Mutation	c.800G>A
AA Mutation	p.Arg267Gln(p.R267Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	missense_variant
Transcription ID	ENST00000505113
Start	434095:434095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61757545
CDS Mutation	c.1367C>T
AA Mutation	p.Pro456Leu(p.P456L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000505113
Start	434507:434507(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs370473413
CDS Mutation	c.1779C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000505113
Start	427922:427923(version: GRCh38)
Mutation Type	INS
dbSNP_RS	null
CDS Mutation	c.840dupC
AA Mutation	p.Ser281LeufsTer64(p.S281Lfs*64)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000505113
Start	427806:427806(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.721-1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000505113
Start	433851:433851(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1125-2A>G
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> AHRR

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000505113
Start	353735:353735(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.80C>A
AA Mutation	p.Pro27His(p.P27H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000505113
Start	434153:434153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs61753896
CDS Mutation	c.1425C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000505113
Start	434504:434504(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1776G>C
Mutation Classification	Silent
Feature Type	Transcript