Colon Cancer: Gene >> FAM129C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335393
Start	17553363:17553363(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1894A>G
AA Mutation	p.Thr632Ala(p.T632A)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000335393
Start	17533591:17533591(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.410A>T
AA Mutation	p.Tyr137Phe(p.Y137F)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000335393
Start	17532309:17532309(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs76766278
CDS Mutation	c.326G>A
AA Mutation	p.Arg109Gln(p.R109Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000335393
Start	17543332:17543332(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs758503031
CDS Mutation	c.1438G>A
AA Mutation	p.Val480Met(p.V480M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000335393
Start	17539643:17539643(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.950C>G
AA Mutation	p.Ser317Cys(p.S317C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000335393
Start	17543336:17543336(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1442C>T
AA Mutation	p.Ala481Val(p.A481V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000335393
Start	17527275:17527275(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.28C>A
AA Mutation	p.Leu10Met(p.L10M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000335393
Start	17549464:17549464(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1780G>A
AA Mutation	p.Ala594Thr(p.A594T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	missense_variant
Transcription ID	ENST00000335393
Start	17532308:17532308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536652149
CDS Mutation	c.325C>T
AA Mutation	p.Arg109Trp(p.R109W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	missense_variant
Transcription ID	ENST00000335393
Start	17537454:17537454(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs746166080
CDS Mutation	c.599G>A
AA Mutation	p.Arg200His(p.R200H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000335393
Start	17546686:17546686(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1648G>A
AA Mutation	p.Glu550Lys(p.E550K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335393
Start	17543400:17543400(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1506G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335393
Start	17553473:17553473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.2004C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335393
Start	17546775:17546775(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1737C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335393
Start	17532358:17532358(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143668756
CDS Mutation	c.375C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000335393
Start	17546700:17546700(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs752996617
CDS Mutation	c.1662C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	17
Mutation Consequence	stop_gained
Transcription ID	ENST00000335393
Start	17527281:17527281(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.34C>T
AA Mutation	p.Arg12Ter(p.R12*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> FAM129C

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000335393
Start	17532308:17532308(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs536652149
CDS Mutation	c.325C>T
AA Mutation	p.Arg109Trp(p.R109W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	stop_gained
Transcription ID	ENST00000335393
Start	17530868:17530868(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.262C>T
AA Mutation	p.Gln88Ter(p.Q88*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript