Colon Cancer: Gene >> SYVN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377190
Start	65130307:65130307(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1178C>A
AA Mutation	p.Pro393His(p.P393H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377190
Start	65131147:65131147(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.809G>A
AA Mutation	p.Arg270His(p.R270H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000377190
Start	65131277:65131277(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.755T>C
AA Mutation	p.Met252Thr(p.M252T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000377190
Start	65131562:65131562(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.566T>G
AA Mutation	p.Phe189Cys(p.F189C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000377190
Start	65130301:65130301(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1184C>A
AA Mutation	p.Pro395Gln(p.P395Q)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000377190
Start	65128473:65128473(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1763G>A
AA Mutation	p.Gly588Asp(p.G588D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000377190
Start	65130933:65130933(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.928A>G
AA Mutation	p.Ile310Val(p.I310V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	missense_variant
Transcription ID	ENST00000377190
Start	65133552:65133552(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.50C>A
AA Mutation	p.Ala17Asp(p.A17D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377190
Start	65130123:65130123(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1287T>C
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377190
Start	65131357:65131357(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.675G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377190
Start	65128615:65128615(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs773552759
CDS Mutation	c.1695G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	12
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377190
Start	65131312:65131312(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.720C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	13
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377190
Start	65129779:65129779(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs147803495
CDS Mutation	c.1545C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	14
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377190
Start	65130664:65130664(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1101delC
AA Mutation	p.Asn368ThrfsTer117(p.N368Tfs*117)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	15
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377190
Start	65128707:65128707(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.1603delC
AA Mutation	p.Arg535GlyfsTer96(p.R535Gfs*96)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	16
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000377190
Start	65130663:65130664(version: GRCh38)
Mutation Type	INS
dbSNP_RS	novel
CDS Mutation	c.1101dupC
AA Mutation	p.Asn368GlnfsTer129(p.N368Qfs*129)
Mutation Classification	Frame_Shift_Ins
Feature Type	Transcript

Rectum Cancer: Gene >> SYVN1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000377190
Start	65131476:65131476(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770594418
CDS Mutation	c.652T>C
AA Mutation	p.Phe218Leu(p.F218L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000377190
Start	65132995:65132995(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.305G>A
AA Mutation	p.Arg102His(p.R102H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000377190
Start	65128570:65128570(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1740G>A
Mutation Classification	Silent
Feature Type	Transcript