Colon Cancer: Gene >> ALOXE3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000448843
Start	8096743:8096743(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375389989
CDS Mutation	c.2020G>A
AA Mutation	p.Ala674Thr(p.A674T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000448843
Start	8109186:8109186(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1550C>T
AA Mutation	p.Ala517Val(p.A517V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000448843
Start	8116875:8116875(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.253A>G
AA Mutation	p.Ser85Gly(p.S85G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000448843
Start	8096697:8096697(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs761555598
CDS Mutation	c.2066G>A
AA Mutation	p.Arg689Gln(p.R689Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000448843
Start	8114523:8114523(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.641C>T
AA Mutation	p.Ala214Val(p.A214V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000448843
Start	8116874:8116874(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.254G>A
AA Mutation	p.Ser85Asn(p.S85N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000448843
Start	8111484:8111484(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758981995
CDS Mutation	c.832T>C
AA Mutation	p.Tyr278His(p.Y278H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000448843
Start	8115678:8115678(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.363T>G
AA Mutation	p.Ile121Met(p.I121M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000448843
Start	8108529:8108529(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773541451
CDS Mutation	c.1623G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000448843
Start	8116858:8116858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.270C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000448843
Start	8096651:8096651(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2112C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000448843
Start	8116813:8116813(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.315T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000448843
Start	8115027:8115027(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770504844
CDS Mutation	c.465C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000448843
Start	8116858:8116858(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.270C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000448843
Start	8103337:8103337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1942G>T
AA Mutation	p.Glu648Ter(p.E648*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ALOXE3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000448843
Start	8112131:8112131(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.746T>C
AA Mutation	p.Met249Thr(p.M249T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000448843
Start	8103337:8103337(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1942G>T
AA Mutation	p.Glu648Ter(p.E648*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	stop_gained
Transcription ID	ENST00000448843
Start	8108579:8108579(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1573G>T
AA Mutation	p.Glu525Ter(p.E525*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript