Colon Cancer: Gene >> FAM126A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000432176
Start	22984019:22984019(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.78T>G
AA Mutation	p.Asn26Lys(p.N26K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000432176
Start	22960315:22960315(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs148168726
CDS Mutation	c.932G>A
AA Mutation	p.Arg311Gln(p.R311Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000432176
Start	22984009:22984009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.88A>C
AA Mutation	p.Asn30His(p.N30H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000432176
Start	22960351:22960351(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.896G>T
AA Mutation	p.Arg299Met(p.R299M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000432176
Start	22946022:22946022(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1133G>A
AA Mutation	p.Gly378Glu(p.G378E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000432176
Start	22978312:22978312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.290G>A
AA Mutation	p.Ser97Asn(p.S97N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000432176
Start	22964470:22964470(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.688A>T
AA Mutation	p.Ile230Leu(p.I230L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000432176
Start	22945815:22945815(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs777996428
CDS Mutation	c.1340C>T
AA Mutation	p.Ala447Val(p.A447V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000432176
Start	22978431:22978431(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.171T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	stop_gained
Transcription ID	ENST00000432176
Start	22961254:22961254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.812T>G
AA Mutation	p.Leu271Ter(p.L271*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	start_lost
Transcription ID	ENST00000432176
Start	22991109:22991109(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.3G>A
AA Mutation	p.Met1?(p.M1?)
Mutation Classification	Translation_Start_Site
Feature Type	Transcript

Rectum Cancer: Gene >> FAM126A

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000432176
Start	22976694:22976694(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.529C>T
AA Mutation	p.Arg177Trp(p.R177W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000432176
Start	22978364:22978364(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.238C>T
AA Mutation	p.Pro80Ser(p.P80S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000432176
Start	22978289:22978289(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.313C>A
AA Mutation	p.Leu105Ile(p.L105I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000432176
Start	22991074:22991074(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.38T>G
AA Mutation	p.Leu13Trp(p.L13W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000432176
Start	22960323:22960323(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.924T>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	stop_gained;splice_region_variant
Transcription ID	ENST00000432176
Start	22977421:22977421(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.334G>T
AA Mutation	p.Glu112Ter(p.E112*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	stop_gained
Transcription ID	ENST00000432176
Start	22961258:22961258(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.808G>T
AA Mutation	p.Glu270Ter(p.E270*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript