Colon Cancer: Gene >> KCTD15

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000430256
Start	33811403:33811403(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.544G>A
AA Mutation	p.Ala182Thr(p.A182T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000430256
Start	33801185:33801185(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.85C>T
AA Mutation	p.Arg29Trp(p.R29W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000430256
Start	33812883:33812883(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs770573450
CDS Mutation	c.787C>T
AA Mutation	p.Arg263Trp(p.R263W)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	missense_variant
Transcription ID	ENST00000430256
Start	33801314:33801314(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.214G>A
AA Mutation	p.Ala72Thr(p.A72T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	missense_variant
Transcription ID	ENST00000430256
Start	33806957:33806957(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs199530630
CDS Mutation	c.337G>A
AA Mutation	p.Val113Ile(p.V113I)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	6
Mutation Consequence	missense_variant
Transcription ID	ENST00000430256
Start	33806867:33806867(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.247A>C
AA Mutation	p.Ser83Arg(p.S83R)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	7
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000430256
Start	33811501:33811501(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.642G>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	8
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000430256
Start	33812843:33812843(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.747C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	9
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000430256
Start	33800514:33800514(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.60C>A
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	10
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000430256
Start	33800496:33800496(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.42C>T
Mutation Classification	Silent
Feature Type	Transcript

Mutation ID	11
Mutation Consequence	inframe_deletion
Transcription ID	ENST00000430256
Start	33806915:33806917(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	novel
CDS Mutation	c.297_299delACA
AA Mutation	p.Gln99del(p.Q99del)
Mutation Classification	In_Frame_Del
Feature Type	Transcript

Rectum Cancer: Gene >> KCTD15

Mutation ID	1
Mutation Consequence	stop_gained
Transcription ID	ENST00000430256
Start	33812922:33812922(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs757471584
CDS Mutation	c.826C>T
AA Mutation	p.Arg276Ter(p.R276*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript