Colon Cancer: Gene >> KCTD11

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000333751
Start	7353427:7353427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.485G>A
AA Mutation	p.Arg162His(p.R162H)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000333751
Start	7353144:7353144(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.202C>T
AA Mutation	p.Pro68Ser(p.P68S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000333751
Start	7353157:7353157(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.215C>T
AA Mutation	p.Ala72Val(p.A72V)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000333751
Start	7352953:7352953(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.11C>A
AA Mutation	p.Ala4Asp(p.A4D)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000333751
Start	7353291:7353291(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs754017618
CDS Mutation	c.349G>A
AA Mutation	p.Val117Ile(p.V117I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000333751
Start	7353042:7353042(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs781114097
CDS Mutation	c.100C>T
AA Mutation	p.Arg34Trp(p.R34W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	missense_variant
Transcription ID	ENST00000333751
Start	7353564:7353564(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.622G>A
AA Mutation	p.Gly208Ser(p.G208S)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333751
Start	7353041:7353041(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.99C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333751
Start	7353155:7353155(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.213C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000333751
Start	7353503:7353503(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.561G>T
Mutation Classification	Silent
Feature Type	Transcript

Rectum Cancer: Gene >> KCTD11

No Mutation Annotation!