Colon Cancer: Gene >> FAM129A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367511
Start	184894155:184894155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.238T>G
AA Mutation	p.Ser80Ala(p.S80A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367511
Start	184818702:184818702(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1109A>T
AA Mutation	p.Glu370Val(p.E370V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367511
Start	184806017:184806017(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1375T>G
AA Mutation	p.Ser459Ala(p.S459A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367511
Start	184795254:184795254(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2510A>G
AA Mutation	p.Asp837Gly(p.D837G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000367511
Start	184795308:184795308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751972614
CDS Mutation	c.2456C>T
AA Mutation	p.Ala819Val(p.A819V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000367511
Start	184795452:184795452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2312G>A
AA Mutation	p.Arg771Lys(p.R771K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000367511
Start	184899231:184899231(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs562448693
CDS Mutation	c.134G>A
AA Mutation	p.Arg45His(p.R45H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000367511
Start	184823281:184823281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.871T>G
AA Mutation	p.Leu291Val(p.L291V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000367511
Start	184899188:184899188(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.177G>T
AA Mutation	p.Leu59Phe(p.L59F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000367511
Start	184884674:184884674(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.560T>G
AA Mutation	p.Phe187Cys(p.F187C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant
Transcription ID	ENST00000367511
Start	184803601:184803601(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs750889582
CDS Mutation	c.1538C>T
AA Mutation	p.Ala513Val(p.A513V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367511
Start	184808200:184808200(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs149201304
CDS Mutation	c.1209C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367511
Start	184795427:184795427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2337G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367511
Start	184795334:184795334(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.2430C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367511
Start	184884652:184884652(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs751710345
CDS Mutation	c.582C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000367511
Start	184798125:184798125(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1620C>G
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000367511
Start	184808079:184808079(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1330C>T
AA Mutation	p.Gln444Ter(p.Q444*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FAM129A

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000367511
Start	184899193:184899193(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.172T>A
AA Mutation	p.Phe58Ile(p.F58I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000367511
Start	184795900:184795900(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1864T>G
AA Mutation	p.Ser622Ala(p.S622A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000367511
Start	184818677:184818677(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1134G>T
AA Mutation	p.Gln378His(p.Q378H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000367511
Start	184823294:184823294(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.858A>C
AA Mutation	p.Gln286His(p.Q286H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript