Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SYT10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000228567
Start	33407000:33407000(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.866G>T
AA Mutation	p.Arg289Ile(p.R289I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000228567
Start	33439381:33439381(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.142A>T
AA Mutation	p.Ser48Cys(p.S48C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000228567
Start	33385204:33385204(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1165A>C
AA Mutation	p.Asn389His(p.N389H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000228567
Start	33407040:33407040(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.826C>A
AA Mutation	p.Leu276Ile(p.L276I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228567
Start	33426326:33426326(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.321T>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228567
Start	33406843:33406843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1023C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000228567
Start	33426425:33426425(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.222delT
AA Mutation	p.Phe74LeufsTer16(p.F74Lfs*16)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	stop_gained
Transcription ID	ENST00000228567
Start	33407286:33407286(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.580G>T
AA Mutation	p.Glu194Ter(p.E194*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SYT10

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000228567
Start	33439428:33439428(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.95A>G
AA Mutation	p.Glu32Gly(p.E32G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000228567
Start	33426339:33426339(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.308C>G
AA Mutation	p.Ala103Gly(p.A103G)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000228567
Start	33379854:33379854(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs545012156
CDS Mutation	c.1478C>T
AA Mutation	p.Thr493Met(p.T493M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000228567
Start	33379880:33379880(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.1452G>A
AA Mutation	p.Met484Ile(p.M484I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000228567
Start	33407009:33407009(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146031713
CDS Mutation	c.857G>A
AA Mutation	p.Arg286His(p.R286H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000228567
Start	33426386:33426386(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.261A>G
Mutation Classification	Silent
Feature Type	Transcript