Colon Cancer: Gene >> MACROD2

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000217246
Start	13995777:13995777(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.14A>G
AA Mutation	p.Asn5Ser(p.N5S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000217246
Start	14002338:14002338(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.97G>T
AA Mutation	p.Asp33Tyr(p.D33Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000217246
Start	15933332:15933332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.832G>T
AA Mutation	p.Asp278Tyr(p.D278Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000217246
Start	14002290:14002290(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.49C>T
AA Mutation	p.Arg17Cys(p.R17C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000217246
Start	15986737:15986737(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.996T>A
AA Mutation	p.Asn332Lys(p.N332K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000217246
Start	15986774:15986774(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1033T>C
AA Mutation	p.Ser345Pro(p.S345P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000217246
Start	14085728:14085728(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.271G>T
AA Mutation	p.Ala91Ser(p.A91S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000217246
Start	15431423:15431423(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.559A>G
AA Mutation	p.Thr187Ala(p.T187A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000217246
Start	15885766:15885766(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.730G>A
AA Mutation	p.Asp244Asn(p.D244N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217246
Start	15431428:15431428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.564C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217246
Start	15499796:15499796(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.594A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217246
Start	15937498:15937498(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.861G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217246
Start	15986734:15986734(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.993G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217246
Start	15230022:15230022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs368006162
CDS Mutation	c.501A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	splice_acceptor_variant
Transcription ID	ENST00000217246
Start	15987065:15987065(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1061-1G>T
Mutation Classification	Splice_Site
Feature Type	Transcript

Rectum Cancer: Gene >> MACROD2

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000217246
Start	15885811:15885811(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.775G>T
AA Mutation	p.Asp259Tyr(p.D259Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000217246
Start	15229966:15229966(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.445G>T
AA Mutation	p.Ala149Ser(p.A149S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript