Colon Cancer: Gene >> H6PD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377403
Start	9244942:9244942(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8A>C
AA Mutation	p.Asn3Thr(p.N3T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377403
Start	9262097:9262097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149081812
CDS Mutation	c.784G>A
AA Mutation	p.Asp262Asn(p.D262N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377403
Start	9264234:9264234(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781605545
CDS Mutation	c.1741C>T
AA Mutation	p.Arg581Cys(p.R581C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377403
Start	9245205:9245205(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.271G>A
AA Mutation	p.Ala91Thr(p.A91T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377403
Start	9263895:9263895(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1402G>T
AA Mutation	p.Gly468Cys(p.G468C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377403
Start	9263856:9263856(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs371234309
CDS Mutation	c.1363C>T
AA Mutation	p.Arg455Trp(p.R455W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000377403
Start	9263763:9263763(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1270C>T
AA Mutation	p.Pro424Ser(p.P424S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000377403
Start	9247030:9247030(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.692G>T
AA Mutation	p.Arg231Leu(p.R231L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377403
Start	9264215:9264215(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs200208026
CDS Mutation	c.1722C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377403
Start	9245153:9245153(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.219T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377403
Start	9264824:9264824(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs561393382
CDS Mutation	c.2331C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> H6PD

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377403
Start	9245509:9245509(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.575C>G
AA Mutation	p.Thr192Ser(p.T192S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript