Colon Cancer: Gene >> G6PD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393564
Start	154546130:154546130(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.26G>A
AA Mutation	p.Arg9Gln(p.R9Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000393564
Start	154536017:154536017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs782674059
CDS Mutation	c.187G>A
AA Mutation	p.Glu63Lys(p.E63K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000393564
Start	154533629:154533629(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.811G>A
AA Mutation	p.Val271Met(p.V271M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000393564
Start	154533056:154533056(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150589041
CDS Mutation	c.937G>A
AA Mutation	p.Asp313Asn(p.D313N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000393564
Start	154534102:154534102(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.703C>A
AA Mutation	p.Leu235Ile(p.L235I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000393564
Start	154534126:154534126(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.679C>T
AA Mutation	p.Arg227Trp(p.R227W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000393564
Start	154533590:154533590(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.850G>A
AA Mutation	p.Val284Ile(p.V284I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000393564
Start	154534114:154534114(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.691G>A
AA Mutation	p.Ala231Thr(p.A231T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393564
Start	154546087:154546087(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.69C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393564
Start	154533648:154533648(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.792A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000393564
Start	154534055:154534055(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs140496395
CDS Mutation	c.750C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000393564
Start	154546100:154546107(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.49_56delCGGGAAGA
AA Mutation	p.Arg17AlafsTer23(p.R17Afs*23)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> G6PD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000393564
Start	154532705:154532705(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1149G>T
AA Mutation	p.Gln383His(p.Q383H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript