Mutation

Primary Site >> Colorectal Cancer

Colon Cancer: Gene >> SGK3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345714
Start	66793800:66793800(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs146507110
CDS Mutation	c.64G>A
AA Mutation	p.Asp22Asn(p.D22N)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000345714
Start	66822452:66822452(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	null
CDS Mutation	c.410C>A
AA Mutation	p.Ser137Tyr(p.S137Y)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	missense_variant
Transcription ID	ENST00000345714
Start	66813885:66813885(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs772372105
CDS Mutation	c.286G>A
AA Mutation	p.Glu96Lys(p.E96K)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	4
Mutation Consequence	frameshift_variant;splice_region_variant
Transcription ID	ENST00000345714
Start	66840004:66840004(version: GRCh38)
Mutation Type	DEL
dbSNP_RS	null
CDS Mutation	c.749delT
AA Mutation	p.Phe250SerfsTer33(p.F250Sfs*33)
Mutation Classification	Frame_Shift_Del
Feature Type	Transcript

Mutation ID	5
Mutation Consequence	stop_gained
Transcription ID	ENST00000345714
Start	66813870:66813870(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs756034666
CDS Mutation	c.271C>T
AA Mutation	p.Arg91Ter(p.R91*)
Mutation Classification	Nonsense_Mutation
Feature Type	Transcript

Rectum Cancer: Gene >> SGK3

Mutation ID	1
Mutation Consequence	missense_variant
Transcription ID	ENST00000345714
Start	66798554:66798554(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.109C>A
AA Mutation	p.Leu37Met(p.L37M)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	2
Mutation Consequence	missense_variant
Transcription ID	ENST00000345714
Start	66859427:66859427(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	rs150440508
CDS Mutation	c.1337T>C
AA Mutation	p.Ile446Thr(p.I446T)
Mutation Classification	Missense_Mutation
Feature Type	Transcript

Mutation ID	3
Mutation Consequence	synonymous_variant
Transcription ID	ENST00000345714
Start	66835975:66835975(version: GRCh38)
Mutation Type	SNP
dbSNP_RS	novel
CDS Mutation	c.642C>A
Mutation Classification	Silent
Feature Type	Transcript