Colon Cancer: Gene >> ACHE

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000241069
Start	100892446:100892446(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1441G>A
AA Mutation	p.Glu481Lys(p.E481K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000241069
Start	100893995:100893995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.238C>T
AA Mutation	p.Pro80Ser(p.P80S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000241069
Start	100892599:100892599(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1288A>C
AA Mutation	p.Ser430Arg(p.S430R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000241069
Start	100893484:100893484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs768947251
CDS Mutation	c.749G>A
AA Mutation	p.Arg250Gln(p.R250Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000241069
Start	100892406:100892406(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs374462106
CDS Mutation	c.1481G>A
AA Mutation	p.Arg494Gln(p.R494Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241069
Start	100893558:100893558(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs139672629
CDS Mutation	c.675G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241069
Start	100893252:100893252(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs529092085
CDS Mutation	c.981G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241069
Start	100893546:100893546(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151335006
CDS Mutation	c.687G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000241069
Start	100893990:100893990(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs747887610
CDS Mutation	c.243G>A
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> ACHE

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000241069
Start	100892384:100892384(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1503A>C
AA Mutation	p.Lys501Asn(p.K501N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000241069
Start	100892487:100892487(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs771862488
CDS Mutation	c.1400C>T
AA Mutation	p.Thr467Met(p.T467M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript