Colon Cancer: Gene >> ALOX12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000251535
Start	7001788:7001788(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1138C>A
AA Mutation	p.Pro380Thr(p.P380T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000251535
Start	6996125:6996125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.8G>T
AA Mutation	p.Arg3Leu(p.R3L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000251535
Start	7010048:7010048(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1734G>A
AA Mutation	p.Met578Ile(p.M578I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000251535
Start	6996152:6996152(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.35C>T
AA Mutation	p.Ala12Val(p.A12V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000251535
Start	7010257:7010257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1826A>G
AA Mutation	p.His609Arg(p.H609R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000251535
Start	7010110:7010110(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1796G>C
AA Mutation	p.Arg599Pro(p.R599P)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251535
Start	6996840:6996840(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.150T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251535
Start	7001781:7001781(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777502068
CDS Mutation	c.1131G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251535
Start	7009778:7009778(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1572A>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251535
Start	7009802:7009802(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs151263719
CDS Mutation	c.1596C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251535
Start	6996894:6996894(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.204C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251535
Start	6996909:6996909(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.219C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251535
Start	7000341:7000341(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs763759102
CDS Mutation	c.813T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000251535
Start	7010312:7010312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1881C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	stop_gained
Transcription ID	ENST00000251535
Start	6999440:6999440(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.781C>T
AA Mutation	p.Gln261Ter(p.Q261*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> ALOX12

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000251535
Start	7009999:7009999(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs776380897
CDS Mutation	c.1685G>A
AA Mutation	p.Arg562Gln(p.R562Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	splice_donor_variant
Transcription ID	ENST00000251535
Start	7010127:7010127(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1812+1G>A
Mutation Classification	Splice_Site
Feature Type	Transcript