Colon Cancer: Gene >> SPON2

Mutation ID	1
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000290902
Start	1171852:1171852(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.220G>T
AA Mutation	p.Gly74Trp(p.G74W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000290902
Start	1171872:1171872(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.200C>T
AA Mutation	p.Ala67Val(p.A67V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000290902
Start	1170434:1170434(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs143524322
CDS Mutation	c.779G>A
AA Mutation	p.Ser260Asn(p.S260N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000290902
Start	1171882:1171882(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.190C>T
AA Mutation	p.Arg64Cys(p.R64C)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000290902
Start	1171908:1171908(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.164C>T
AA Mutation	p.Ala55Val(p.A55V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000290902
Start	1170528:1170528(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs376213322
CDS Mutation	c.685C>T
AA Mutation	p.Arg229Trp(p.R229W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000290902
Start	1170451:1170451(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs145897903
CDS Mutation	c.762C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000290902
Start	1171364:1171364(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.343delG
AA Mutation	p.Glu115ArgfsTer96(p.E115Rfs*96)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SPON2

No Mutation Annotation!