Colon Cancer: Gene >> SPOP

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000347630
Start	49607257:49607257(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.830C>T
AA Mutation	p.Ala277Val(p.A277V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000347630
Start	49622770:49622770(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.41C>T
AA Mutation	p.Ser14Leu(p.S14L)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant;splice_region_variant
Transcription ID	ENST00000347630
Start	49607876:49607876(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.712A>G
AA Mutation	p.Lys238Glu(p.K238E)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347630
Start	49601951:49601951(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146116174
CDS Mutation	c.894C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000347630
Start	49618984:49618984(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs375093038
CDS Mutation	c.477C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000347630
Start	49600403:49600403(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.1100delC
AA Mutation	p.Pro367HisfsTer5(p.P367Hfs*5)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	frameshift_variant
Transcription ID	ENST00000347630
Start	49607334:49607334(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.753delT
AA Mutation	p.Phe251LeufsTer4(p.F251Lfs*4)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Rectum Cancer: Gene >> SPOP

No Mutation Annotation!