Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> VSIG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000217957
Start	108067005:108067005(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.283G>A
AA Mutation	p.Asp95Asn(p.D95N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000217957
Start	108045164:108045164(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.34C>A
AA Mutation	p.Leu12Ile(p.L12I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000217957
Start	108076157:108076157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.769G>A
AA Mutation	p.Ala257Thr(p.A257T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217957
Start	108058060:108058060(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.72G>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217957
Start	108073347:108073347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764140353
CDS Mutation	c.666C>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> VSIG1

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000217957
Start	108077235:108077235(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.1018G>A
AA Mutation	p.Ala340Thr(p.A340T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000217957
Start	108076209:108076209(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.821C>T
AA Mutation	p.Ala274Val(p.A274V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000217957
Start	108073347:108073347(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs764140353
CDS Mutation	c.666C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	stop_gained
Transcription ID	ENST00000217957
Start	108077097:108077097(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.880G>T
AA Mutation	p.Glu294Ter(p.E294*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript