Colon Cancer: Gene >> ALDH18A1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000371224
Start	95606803:95606803(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2347C>A
AA Mutation	p.Leu783Ile(p.L783I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000371224
Start	95626746:95626746(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1109C>T
AA Mutation	p.Ala370Val(p.A370V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000371224
Start	95606908:95606908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773903524
CDS Mutation	c.2242G>A
AA Mutation	p.Ala748Thr(p.A748T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000371224
Start	95637358:95637358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.382C>T
AA Mutation	p.Arg128Cys(p.R128C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000371224
Start	95614095:95614095(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1672C>T
AA Mutation	p.Arg558Cys(p.R558C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000371224
Start	95643068:95643068(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.227A>G
AA Mutation	p.Lys76Arg(p.K76R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000371224
Start	95613751:95613751(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1914A>C
AA Mutation	p.Arg638Ser(p.R638S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000371224
Start	95633564:95633564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.644T>C
AA Mutation	p.Ile215Thr(p.I215T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371224
Start	95637332:95637332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.408C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000371224
Start	95621221:95621221(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1277T>A
AA Mutation	p.Leu426Ter(p.L426*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	stop_gained
Transcription ID	ENST00000371224
Start	95606857:95606857(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2293C>T
AA Mutation	p.Arg765Ter(p.R765*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ALDH18A1

Mutation ID	1
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000371224
Start	95627530:95627530(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.990A>C
Mutation Classification	Silent
Feature Type	Transcript